U.S. patent application number 12/947008 was filed with the patent office on 2011-08-04 for cosmetic composition containing a polyorganisiloxane polymer.
This patent application is currently assigned to L'Oreal. Invention is credited to Xavier Blin, Veronique FERRARI, Angelike Galdi, Isabelle Hansenne, Shao Xiang Lu, Jean Mondet, Anil Shah, Florence Tournilhac, Wei Yu.
Application Number | 20110189117 12/947008 |
Document ID | / |
Family ID | 46300531 |
Filed Date | 2011-08-04 |
United States Patent
Application |
20110189117 |
Kind Code |
A1 |
FERRARI; Veronique ; et
al. |
August 4, 2011 |
COSMETIC COMPOSITION CONTAINING A POLYORGANISILOXANE POLYMER
Abstract
The invention relates to a physiologically acceptable
composition, especially a cosmetic composition, comprising at least
one polyorganosiloxane containing polymer comprising at least one
moiety which comprises: at least one polyorganosiloxane group
consisting of 1 to about 1000 organosiloxane units in the chain of
the moiety or in the form of graft, and at least two groups capable
of establishing hydrogen interactions.
Inventors: |
FERRARI; Veronique;
(Maisons-Alfort, FR) ; Yu; Wei; (Edison, NJ)
; Lu; Shao Xiang; (Plainsboro, NJ) ; Blin;
Xavier; (Paris, FR) ; Mondet; Jean;
(Aulnay-Sous-Bois, FR) ; Hansenne; Isabelle;
(Westfield, NJ) ; Shah; Anil; (East Windsor,
NJ) ; Galdi; Angelike; (Westfield, NJ) ;
Tournilhac; Florence; (Paris, FR) |
Assignee: |
L'Oreal
Paris
FR
|
Family ID: |
46300531 |
Appl. No.: |
12/947008 |
Filed: |
November 16, 2010 |
Related U.S. Patent Documents
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Application
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Filing Date |
Patent Number |
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10733467 |
Dec 12, 2003 |
7879316 |
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12947008 |
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10622689 |
Jul 21, 2003 |
7321011 |
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10733467 |
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10617048 |
Jul 11, 2003 |
7329699 |
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10622689 |
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10323649 |
Dec 20, 2002 |
6916464 |
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10617048 |
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10320599 |
Dec 17, 2002 |
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10323649 |
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10320599 |
Dec 17, 2002 |
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10320599 |
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10320600 |
Dec 17, 2002 |
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10320599 |
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10323649 |
Dec 20, 2002 |
6916464 |
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10320600 |
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10320599 |
Dec 17, 2002 |
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10323649 |
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10320600 |
Dec 17, 2002 |
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10320599 |
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Dec 17, 2002 |
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10320600 |
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10170549 |
Jun 14, 2002 |
7078026 |
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10320601 |
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10170655 |
Jun 14, 2002 |
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10170549 |
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10170566 |
Jun 14, 2002 |
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10170655 |
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10166648 |
Jun 12, 2002 |
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10170566 |
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10166755 |
Jun 12, 2002 |
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10166648 |
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10166760 |
Jun 12, 2002 |
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10166755 |
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10166650 |
Jun 12, 2002 |
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10166760 |
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Jun 12, 2002 |
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PCT/US2003/018503 |
Jun 12, 2003 |
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10733467 |
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60438782 |
Jan 9, 2003 |
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60438770 |
Jan 9, 2003 |
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Current U.S.
Class: |
424/64 ; 424/63;
424/78.03 |
Current CPC
Class: |
A61K 8/898 20130101;
A61Q 1/02 20130101; A61K 8/894 20130101; A61Q 19/00 20130101; A61K
8/31 20130101; A61Q 1/06 20130101; A61K 8/891 20130101; A61Q 1/04
20130101; A61K 8/42 20130101 |
Class at
Publication: |
424/64 ; 424/63;
424/78.03 |
International
Class: |
A61K 8/89 20060101
A61K008/89; A61Q 1/04 20060101 A61Q001/04; A61Q 1/02 20060101
A61Q001/02 |
Claims
1. A composition comprising at least one at least
polyorganosiloxane containing polymer comprising at least one
moiety which comprises: at least one polyorganosiloxane group
consisting of 1 to about 1000 organosiloxane units in the chain of
the moiety or in the form of graft, and at least two groups capable
of establishing hydrogen interactions; at least one silicone film
former; and at least one volatile oil; wherein the composition is
substantially free of silicone oil.
2. The composition of claim 1, wherein at least one of said
silicone film formers is a polymethylsilsesquioxane.
3. The composition of claim 1, wherein at least one of said
silicone film formers is a trimethylsiloxysilicate.
4. The composition of claim 1, further comprising pigments.
5. The composition of claim 1, wherein said composition is in the
form of a lip composition or a foundation.
6. The composition of claim 1, wherein said volatile oil is a
volatile hydrocarbon oil.
7. The composition of claim 6, wherein said volatile oil is
isododecane.
8. The composition of claim 1, wherein said silicone film former is
present in an amount ranging from about 1% to about 15% by weight
relative to the total weight of the composition.
9. The composition of claim 1, wherein said at least one
polyorganosiloxane containing polymer is a Nylon-611/dimethicone
copolymer.
10. The composition of claim 1, wherein the composition is
anhydrous.
11. The composition of claim 1, wherein the at least one
polyorganosiloxane containing polymer is present in an amount
ranging from about 0.5% to about 10% by weight relative to the
total weight of the composition.
12. The composition of claim 9, wherein at least one of said
silicone film formers is a polymethylsilsesquioxane.
13. The composition of claim 9, wherein at least one of said
silicone film formers is a trimethylsiloxysilicate.
14. The composition of claim 9, further comprising pigments.
15. The composition of claim 9, wherein said volatile oil is a
volatile hydrocarbon oil.
16. The composition of claim 9, wherein said silicone film former
is present in an amount ranging from about 1% to about 15% by
weight relative to the total weight of the composition.
17. The composition of claim 9, wherein the composition is
anhydrous.
18. The composition of claim 9, wherein the at least one
polyorganosiloxane containing polymer is present in an amount
ranging from about 0.5% to about 10% by weight relative to the
total weight of the composition.
19. A method of making up skin comprising applying the composition
of claim 1 to the skin in an amount sufficient to make up the
skin.
20. A method of making up lips comprising applying the composition
of claim 1 to the lips in an amount sufficient to make up the lips.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] The present application is a continuation of U.S. Ser. No.
10/733,467, filed Dec. 12, 2003, which is a continuation-in-part of
U.S. Ser. No. 10/170,566, filed Jun. 14, 2002, and is also a
continuation-in-part of U.S. Ser. No. 10/170,655, filed Jun. 14,
2002, and is also a continuation-in-part of U.S. Ser. No.
10/170,549, filed Jun. 14, 2002, and is also a continuation-in-part
of U.S. Ser. No. 10/320,601, filed Dec. 17, 2002, and is also a
continuation-in-part of U.S. Ser. No. 10/320,600, filed Dec. 17,
2002, and is also a continuation-in-part of U.S. Ser. No.
10/320,599, filed Dec. 17, 2002, and is also a continuation-in-part
of U.S. Ser. No. 10/166,762, filed Jun. 12, 2002, and is also a
continuation-in-part of U.S. Ser. No. 10/166,650, filed Jun. 12,
2002, and is also a continuation-in-part of U.S. Ser. No.
10/166,760, filed Jun. 12, 2002, and is also a continuation-in-part
of U.S. Ser. No. 10/166,755, filed Jun. 12, 2002, and is also a
continuation-in-part of U.S. Ser. No. 10/166,648, filed Jun. 12,
2002, and is also a continuation-in-part of U.S. Ser. No.
10/323,649, filed Dec. 20, 2002, and is also a continuation-in part
of PCT/US03/18503, filed Jun. 12, 2003, and is also a
continuation-in part of U.S. Ser. No. 10/617,048 filed Jul. 11,
2003, and is also a continuation-in part of U.S. Ser. No.
10/622,689 filed Jul. 21, 2003, and also claims the benefit of U.S.
provisional application Ser. No. 60/438,770, filed Jan. 9, 2003,
and also claims the benefit of U.S. provisional application Ser.
No. 60/438,782, filed Jan. 9, 2003, the entire disclosures of all
of which are hereby incorporated by reference.
FIELD OF THE INVENTION
[0002] The present invention relates to compositions, for example,
a transfer resistant cosmetic composition, which may also be
pliable and/or comfortable to wear upon application to a keratinous
substrate, comprising at least one polyorganosiloxane containing
polymer comprising at least one moiety comprising: at least one
polyorganosiloxane group comprising organosiloxane units in the
chain of the moiety or in the form of a graft, and at least two
groups capable of establishing hydrogen interactions.
DISCUSSION OF THE BACKGROUND
[0003] Many cosmetic compositions, including pigmented cosmetics
such as foundations, concealers, lipsticks, mascaras, and other
cosmetic and sunscreen compositions have been developed for longer
wear and transfer resistance properties. This is accomplished by
the use of compositions that form a film after application. Such
compositions generally contain volatile solvents, which evaporate
on contact with the skin or other keratinous tissue, leaving behind
a layer comprising waxes and/or resins, pigments, fillers, and
actives. However, these compositions tend to be uncomfortable for
the wearer as the composition remains on the skin or other
keratinous tissue as a brittle or non-flexible film. Such
compositions may not be pliable or soft, and they may not be
comfortable to wear. There may also be a tendency for such
compositions to flake off because of poor adherence to the skin or
other keratinous tissue. Furthermore, such compositions have a
tendency to be tacky, resulting in poor application, spreadability
and wear characteristics.
[0004] Document EP-A-1 068 856 describes wax-free solid cosmetic
compositions, comprising a liquid fatty phase structured with a
polymer, in which the fatty phase is primarily a non-silicone
oil.
[0005] Presently, the use of fatty phases based on silicone oils
makes it possible to obtain cosmetic compositions with long staying
power when the oils are non-volatile or relatively non-volatile,
namely good staying power over time of the color (no color change
and no fading), and transfer-resistant compositions when the
silicone oils are volatile, namely compositions that do not deposit
onto a support such as a glass, a cup, a fabric or a cigarette,
when placed in contact with the film of makeup.
[0006] In U.S. Pat. No. 5,874,069, U.S. Pat. No. 5,919,441, U.S.
Pat. No. 6,051,216, WO-A-02/17870 and WO-A-02/17871, cosmetic
compositions, such as deodorant gels or sticks, are prepared. These
compositions comprise a silicone oily phase gelled with a wax based
on polysiloxane and polyamide, or with a polymer comprising
siloxane groups and groups capable of hydrogen interactions.
[0007] When these cosmetic compositions are used as deodorants, the
problems of migration of the oily phase into wrinkles and fine
lines, and the problems of the staying power and transfer
resistance of the composition are not significant.
[0008] However, there remains a need for improved long-wearing
cosmetic compositions which transfer little or not at all, i.e.,
"transfer-free" or transfer resistant compositions which also
possess good cosmetic properties such as pliability and comfort.
For example, a composition that is transfer resistant may deposit a
film onto a keratinous substance that may not transfer when the
keratinous substance comes into contact with, for example, skin,
clothes, a cup, paper, cigarette, or a handkerchief.
[0009] Accordingly, one aspect of the present invention is a care
and/or makeup and/or treatment composition for keratinous material
such as the skin and/or the lips, which is able to address or
overcome at least one of the aforementioned problems with the prior
art compositions.
SUMMARY OF THE INVENTION
[0010] The present invention relates to compositions, preferably
cosmetic compositions, comprising at least one polyorganosiloxane
containing polymer chosen from homopolymers and copolymers as well
as to methods for treating, caring for and/or making up keratinous
material by applying such compositions to the keratinous
material.
[0011] The present invention also relates to cosmetic compositions
comprising at least one polyorganosiloxane containing polymer,
preferably a polysilicone-polyamide copolymer, and at least one
volatile oil, preferably a silicone volatile oil, a hydrocarbon
volatile oil, or a mixture thereof.
[0012] The present invention also relates to cosmetic compositions
comprising at least one polyorganosiloxane containing polymer,
preferably a polysilicone-polyamide copolymer, and at least one
film forming agent.
[0013] The present invention also relates to cosmetic compositions
comprising at least one polyorganosiloxane containing polymer,
preferably a polysilicone-polyamide copolymer, at least one
silicone film forming agent, and at least one volatile oil,
preferably a silicone volatile oil, a hydrocarbon volatile oil, or
a mixture thereof.
[0014] The present invention also relates to colored cosmetic
compositions comprising at least one polyorganosiloxane containing
polymer, preferably a silicone-polyamide copolymer. Preferably,
such colored cosmetic compositions are anhydrous lip compositions
(for example, lipstick or liquid lip colors) or foundations.
[0015] The present invention further relates to colored cosmetic
compositions comprising at least one polyorganosiloxane containing
polymer, preferably a silicone-polyamide copolymer, and water.
Preferably, such water-containing colored cosmetic compositions are
lip compositions (for example, lipstick or liquid lip colors),
foundations or mascaras, and are emulsions or dispersions.
[0016] The present invention also relates to methods of treating,
caring for and/or making up keratinous material (for example, skin)
by applying compositions of the present invention to the keratinous
material in an amount sufficient to treat, care for and/or make up
the keratinous material.
[0017] The present invention further relates to covering or hiding
skin defects associated with keratinous material (for example,
skin) by applying compositions of the present invention to the
keratinous material in an amount sufficient to cover or hide such
skin defects.
[0018] The present invention also relates to methods of enhancing
the appearance of keratinous material (for example, skin) by
applying compositions of the present invention to the keratinous
material in an amount sufficient to enhance the appearance of the
keratinous material.
[0019] The present invention further relates to compositions having
improved cosmetic properties such as, for example, improved long
wear, transfer resistance and/or waterproof properties. The
compositions may also possess improved flexibility, wearability,
drying time and/or retention as well as reduced tackiness and/or
migration over time.
[0020] It is to be understood that both the foregoing general
description and the following detailed description are exemplary
and explanatory only, and are not restrictive of the invention.
DETAILED DESCRIPTION OF THE INVENTION
[0021] As used herein, the expression "at least one" means one or
more and thus includes individual components as well as
mixtures/combinations.
[0022] "Film former" or "film forming agent" as used herein means a
polymer that, after dissolution in at least one solvent (such as,
for example, water and organic solvents), leaves a film on the
substrate to which it is applied, for example, once the at least
one solvent evaporates, absorbs and/or dissipates on the
substrate.
[0023] "Transfer resistance" as used herein refers to the quality
exhibited by compositions that are not readily removed by contact
with another material, such as, for example, a glass, an item of
clothing or the skin, for example, when eating or drinking.
Transfer resistance may be evaluated by any method known in the art
for evaluating such. For example, transfer resistance of a
composition may be evaluated by a "kiss" test. The "kiss" test may
involve application of the composition to human lips followed by
"kissing" a material, for example, a sheet of paper, after
expiration of a certain amount of time following application, such
as 2 minutes after application. Similarly, transfer resistance of a
composition may be evaluated by the amount of product transferred
from a wearer to any other substrate, such as transfer from the
neck of an individual to a collar after the expiration of a certain
amount of time following application. The amount of composition
transferred to the substrate (e.g., collar, or paper) may then be
evaluated and compared. For example, a composition may be transfer
resistant if a majority of the product is left on the wearer, e.g.,
lips, neck, etc. Further, the amount transferred may be compared
with that transferred by other compositions, such as commercially
available compositions. In a preferred embodiment of the present
invention, little or no composition is transferred to the
substrate.
[0024] "Long wear" compositions as used herein, refers to
compositions where at least one property chosen from consistency,
texture, and color remains the same as at the time of application,
as viewed by the naked eye, after an extended period of time, such
as, for example, 1 hour, 2 hours, and further such as 8 hours. Long
wear properties may be evaluated by any method known in the art for
evaluating such properties. For example, long wear may be evaluated
by a test involving the application of a composition to human skin
(including lips) and evaluating the consistency, texture and color
of the composition after an extended period of time. For example,
the consistency, texture and color of a lip composition may be
evaluated immediately following application and these
characteristics may then be re-evaluated and compared after an
individual has worn the lip composition for a certain amount of
time. Further, these characteristics may be evaluated with respect
to other compositions, such as commercially available
compositions.
[0025] "Waterproof" as used herein refers to the ability to repel
water and permanence with respect to water. Waterproof properties
may be evaluated by any method known in the art for evaluating such
properties. For example, a mascara composition may be applied to
false eyelashes, which may then be placed in water for a certain
amount of time, such as, for example, 20 minutes. Upon expiration
of the pre-ascertained amount of time, the false eyelashes may be
removed from the water and passed over a material, such as, for
example, a sheet of paper. The extent of residue left on the
material may then be evaluated and compared with other
compositions, such as, for example, commercially available
compositions. Similarly, for example, a composition may be applied
to skin, and the skin may be submerged in water for a certain
amount of time. The amount of composition remaining on the skin
after the pre-ascertained amount of time may then be evaluated and
compared. For example, a composition may be waterproof if a
majority of the product is left on the wearer, e.g., eyelashes,
skin, etc. In a preferred embodiment of the present invention,
little or no composition is transferred from the wearer.
[0026] The cosmetic compositions and methods of the present
invention can comprise, consist of, or consist essentially of the
essential elements and limitations of the invention described
herein, as well as any additional or optional ingredients,
components, or limitations described herein or otherwise useful in
personal care compositions intended for topical application to the
skin.
[0027] In accordance with certain aspects of the present invention,
the phrase "liquid fatty phase" is understood to mean a fatty
phase, which is liquid at room temperature (25.degree. C.) and
atmospheric pressure (760 mmHg), and which comprises one or more
fatty substances that are liquid at room temperature, also known as
oils, which are compatible with one another.
[0028] In accordance with certain aspects of the present invention,
the phrase "structured liquid fatty phase" is understood to mean
that this structured phase does not run between the fingers and is
at least thickened.
[0029] Where the liquid fatty phase is structured, it makes it
possible to limit exudation of the fatty phase from solid
compositions, and furthermore, to limit, after deposition on the
skin or the lips, its migration into the wrinkles and fine lines,
which is desired for compositions such as a lipstick or an
eyeshadow. Significant migration of the liquid fatty phase, laden
with coloring materials, leads to an unaesthetic effect around the
lips or the eyes, which can accentuate the wrinkles and fine lines.
This migration is often mentioned by women as being a major defect
of conventional lipsticks and eyeshadows. The term "migration" is
understood to mean running of the composition deposited on the lips
or skin beyond its initial outline.
[0030] "Gloss" is essentially related to the nature of the liquid
fatty phase. Thus, it is possible to reduce the level of waxes and
fillers in the composition in order to increase the gloss of a
lipstick, but then the migration of the liquid fatty phase
increases. In other words, the levels of waxes and/or of fillers
necessary for preparation of a stick of suitable hardness have been
a restricting factor on the gloss of the deposit.
[0031] "Tackiness" as used herein refers to measuring the maximum
tensile force, F.sub.max, required while separating two surfaces.
Depending on the application envisaged and the formulation being
designed, the desirable value for F.sub.max may vary. In some
embodiments, the substantially non-tacky compositions have a
F.sub.max of less than about 4 Newton (N), less than about 1 N,
less than about 0.5 N, less than about 0.3 N, less than about 0.2 N
or less than 0.1 N. One of ordinary skill in the art can determine
the F.sub.max of the composition by, for example, determining the
maximum force of traction, measured with an extensiometer of the
LLOYD model LR5K type, needed to detach two surfaces.
[0032] For example, two 38 mm.sup.2 surfaces, A and B, which are
solid, rigid, inert, and non-absorbing, are mounted on movable
mounts, facing each other. The surfaces may be movable either
toward or away from each other, or one may move surface A
independently from surface B or vice versa. Prior to insertion into
the extensiometer, surface A is coated with the composition to be
measured, which may be dissolved in a solvent such as aqueous,
hydroalcoholic, hydrocarbon, silicone, and alcoholic solvents in a
concentration of from about 10 to about 30%, preferably 20%, the
surface A is coated in a thickness of from 1 to 10 mil, preferably
1 mil, and the surface is dried for 24 hours at room temperature,
e.g., 22 to 25.degree. C., at a relative humidity of about 50%.
Once inserted in the extensiometer, surface A is subjected for 20
seconds to a compression force of 3 N against surface B and then
subjected for 30 seconds to tensile force at a rate of 20
mm/minute. The amount of force, F.sub.max, needed to obtain initial
separation is then noted. A mean F.sub.max is determined by
carrying out the procedure with multiple pairs, preferably at least
six pairs, of surface A and surface B.
[0033] The composition of the present invention may be in any form.
For example, it may be a paste, a solid, a gel, or a cream. It may
be an emulsion, such as an oil-in-water or water-in-oil emulsion, a
multiple emulsion, such as an oil-in-water-in-oil emulsion or a
water-in-oil-in-water emulsion, or a solid, rigid or supple gel,
including anhydrous gels. The composition can also be in a form
chosen from a translucent anhydrous gel and a transparent anhydrous
gel. The composition of the invention may, for example, comprise an
external or continuous fatty phase. The composition may be
anhydrous. In another embodiment, the composition of the invention
may be transparent or clear, including for example, a composition
without pigments. The composition can also be a molded composition
or cast as a stick or a dish. The composition in one embodiment is
a solid such as a molded stick or a poured stick. The compositions
of the present invention may also be in the form a lip composition
such as a lipstick or a liquid lip color, a foundation or a
mascara, which exhibit excellent and improved properties of
transfer-resistance, flexibility, pliability, adherence and lack of
tackiness.
[0034] Where the composition of the invention is not-liquid, the
structuring of the liquid fatty phase can be controlled by the type
of polyorganosiloxane-containing polymer (or structuring polymer)
used and is such that a rigid structure in the form of a stick, of
good mechanical resistance, can be obtained. These rigid
compositions, when colored, allow for a supple, light,
non-transfer, non-migrating and/or long-wearing applications on a
keratinous surface. Such compositions may contain one or more
structuring polymers.
[0035] As defined herein, stability is tested by placing the
composition in a controlled environment chamber for 8 weeks at
25.degree. C. In this test, the physical condition of the sample is
inspected as it is placed in the chamber. The sample is then
inspected again at 24 hours, 3 days, 1 week, 2 weeks, 4 weeks and 8
weeks. At each inspection, the sample is examined for abnormalities
in the composition such as phase separation if the composition is
in the form of an emulsion, bending or leaning if the composition
is in stick form, melting, or syneresis (or sweating). The
stability is further tested by repeating the 8-week test at
40.degree. C., 37.degree. C., 45.degree. C., 50.degree. C. and
under freeze-thaw conditions. A composition is considered to lack
stability if in any of these tests an abnormality that impedes
functioning of the composition is observed. The skilled artisan
will readily recognize an abnormality that impedes functioning of a
composition based on the intended application.
[0036] Polyorganosiloxane Containing Polymer
[0037] According to the present invention, compositions comprising
at least one polyorganosiloxane containing polymer chosen from
homopolymers and copolymers, preferably, with a weight-average
molecular mass ranging from about 500 to about 2.5.times.10.sup.6
or more, comprising at least one moiety comprising: at least one
polyorganosiloxane group comprising, preferably, from 1 to about
10,000 organosiloxane units in the chain of the moiety or in the
form of a graft, and at least two groups capable of establishing
hydrogen interactions are provided.
[0038] According to preferred embodiments of the present invention,
the polyorganosiloxane-containing polymers used in the composition
of the invention may belong to the following two families:
[0039] a) polyorganosiloxanes comprising at least two groups
capable of establishing hydrogen interactions, these two groups
being located in the polymer chain; and/or
[0040] b) polyorganosiloxanes comprising at least two groups
capable of establishing hydrogen interactions, these two groups
being located on grafts or branches.
[0041] The polyorganosiloxane containing polymers of the present
invention can be liquid or solid at room temperature. Preferably,
the polymers are solid. When the polymers are solid, it is
preferable that they can be dissolved before or during use in a
solvent with hydrogen interaction capable of breaking the hydrogen
interactions of the polymers, for instance C.sub.2 to C.sub.8 lower
alcohols and especially ethanol, n-propanol or isopropanol. It is
also possible to use these hydrogen interaction "breaking" solvents
as co-solvents in the compositions of the present invention. These
solvents may then be stored in the composition or may be removed by
selective evaporation, which is well known to those skilled in the
art.
[0042] The polymers comprising two groups capable of establishing
hydrogen interactions in the polymer chain may be polymers
comprising at least one moiety corresponding to the formula:
##STR00001##
in which:
[0043] 1) R.sup.1, R.sup.2, R.sup.3 and R.sup.4, which may be
identical or different, represent a group chosen from: [0044]
linear, branched or cyclic, saturated or unsaturated, C.sub.1 to
C.sub.40 hydrocarbon-based groups, possibly containing in their
chain one or more oxygen, sulphur and/or nitrogen atoms, and
possibly being partially or totally substituted with fluorine
atoms, [0045] C.sub.6 to C.sub.10 aryl groups, optionally
substituted with one or more C.sub.1 to C.sub.4 alkyl groups,
[0046] polyorganosiloxane chains possibly containing one or more
oxygen, sulphur and/or nitrogen atoms;
[0047] 2) the groups X, which may be identical or different,
represent a linear or branched C.sub.1 to C.sub.30 alkylenediyl
group, possibly containing in its chain one or more oxygen and/or
nitrogen atoms;
[0048] 3) Y is a saturated or unsaturated, C.sub.1 to C.sub.60
linear or branched divalent alkylene, arylene, cycloalkylene,
alkylarylene or arylalkylene group, possibly comprising one or more
oxygen, sulphur and/or nitrogen atoms, and/or bearing as
substituent one of the following atoms or groups of atoms:
fluorine, hydroxyl, C.sub.3 to C.sub.8 cycloalkyl, C.sub.1 to
C.sub.40 alkyl, C.sub.5 to C.sub.10 aryl, phenyl optionally
substituted with 1 to 3 C.sub.1 to C.sub.3 alkyl groups, C.sub.1 to
C.sub.3 hydroxyalkyl and C.sub.1 to C.sub.6 aminoalkyl, or
[0049] 4) Y represents a group corresponding to the formula:
##STR00002##
in which [0050] T represents a linear or branched, saturated or
unsaturated, C.sub.3 to C.sub.24 trivalent or tetravalent
hydrocarbon-based group optionally substituted with a
polyorganosiloxane chain, and possibly containing one or more atoms
chosen from O, N and S, or T represents a trivalent atom chosen
from N, P and Al, and [0051] R.sup.5 represents a linear or
branched C.sub.1 to C.sub.50 alkyl group or a polyorganosiloxane
chain, possibly comprising one or more ester, amide, urethane,
thiocarbamate, urea, thiourea and/or sulphonamide groups, which may
be linked to another chain of the polymer;
[0052] 5) the groups G, which may be identical or different,
represent divalent groups chosen from:
##STR00003##
in which R.sup.6 represents a hydrogen atom or a linear or branched
C.sub.1 to C.sub.20 alkyl group, on condition that at least 50% of
the groups R.sup.6 of the polymer represents a hydrogen atom and
that at least two of the groups G of the polymer are a group other
than:
##STR00004##
[0053] 6) n is an integer of at least 1, for example ranging from 2
to 500 and preferably from 2 to 200, and m is an integer of at
least one, ranging from 1 to 35,000, for example, from 1 to 10,000
and 1 to 2,500, from 1 to 700 and from 6 to 200, including all
values and subranges there between.
[0054] According to the invention, 80% of the groups R.sup.1,
R.sup.2, R.sup.3 and R.sup.4 of the polymer are preferably chosen
from methyl, ethyl, phenyl and 3,3,3-trifluoropropyl groups.
[0055] According to the invention, Y can represent various divalent
groups, furthermore optionally comprising one or two free valencies
to establish bonds with other moieties of the polymer or copolymer.
Preferably, Y represents a group chosen from:
[0056] a) linear C.sub.1 to C.sub.20 and preferably C.sub.1 to
C.sub.10 alkylene groups,
[0057] b) C.sub.30 to C.sub.56 branched alkylene groups possibly
comprising rings and unconjugated unsaturations,
[0058] c) C.sub.5-C.sub.6 cycloalkylene groups,
[0059] d) phenylene groups optionally substituted with one or more
C.sub.1 to C.sub.40 alkyl groups,
[0060] e) C.sub.1 to C.sub.20 alkylene groups comprising from 1 to
5 amide groups,
[0061] f) C.sub.1 to C.sub.20 alkylene groups comprising one or
more substituents chosen from hydroxyl, C.sub.3 to C.sub.8
cycloalkane, C.sub.1 to C.sub.3 hydroxyalkyl and C.sub.1 to C.sub.6
alkylamine groups,
[0062] g) polyorganosiloxane chains of formula:
##STR00005##
in which R.sup.1, R.sup.2, R.sup.3, R.sup.4, T and m are as defined
above, and
[0063] h) polyorganosiloxane chains of formula:
##STR00006##
[0064] The polyorganosiloxanes of the second family may be polymers
comprising at least one moiety corresponding to formula (II):
##STR00007##
in which [0065] R.sup.1 and R.sup.3, which may be identical or
different, are as defined above for formula (I), [0066] R.sup.7
represents a group as defined above for R.sup.1 and R.sup.3, or
represents a group of formula --X-G-R.sup.9 in which X and G are as
defined above for formula (I) and R.sup.9 represents a hydrogen
atom or a linear, branched or cyclic, saturated or unsaturated,
C.sub.1 to C.sub.50 hydrocarbon-based group optionally comprising
in its chain one or more atoms chosen from O, S and N, optionally
substituted with one or more fluorine atoms and/or one or more
hydroxyl groups, or a phenyl group optionally substituted with one
or more C.sub.1 to C.sub.4 alkyl groups, [0067] R.sup.8 represents
a group of formula --X-G-R.sup.9 in which X, G and R.sup.9 are as
defined above, [0068] m.sub.1 is an integer of at least one ranging
from 1 to 35,000, for example, from 1 to 10,000 and 1 to 2,500,
from 1 to 700, and from 6 to 200, including all values and
subranges there between; and [0069] m.sub.2 is an integer of at
least one ranging from 1 to 35,000, for example, from 1 to 10,000
and 1 to 2,500, from 1 to 700, and from 6 to 200, including all
values and subranges there between.
[0070] According to the invention, the polyorganosiloxane
containing polymer may be a homopolymer, that is to say a polymer
comprising several identical moieties, in particular moieties of
formula (I) or of formula (II).
[0071] According to the invention, it is also possible to use a
polymer consisting of a copolymer comprising several different
moieties of formula (I), that is to say a polymer in which at least
one of the groups R.sup.1, R.sup.2, R.sup.3, R.sup.4, X, G, Y, m
and n is different in one of the moieties. The copolymer may also
be formed from several moieties of formula (II), in which at least
one of the groups R.sup.1, R.sup.3, R.sup.7, R.sup.8, m.sub.1 and
m.sub.2 is different in at least one of the moieties.
[0072] It is also possible to use a copolymer comprising at least
one moiety of formula (I) and at least one moiety of formula (II),
the moieties of formula (I) and the moieties of formula (II)
possibly being identical to or different from each other.
[0073] According to preferred embodiments, it is also possible to
use a copolymer comprising at least one hydrocarbon-based moiety
comprising two groups capable of establishing hydrogen
interactions, chosen from ester, amide, sulphonamide, carbamate,
thiocarbamate, urea and thiourea groups, and combinations
thereof.
[0074] These copolymers may be block copolymers or grafted
copolymers.
[0075] According to a first embodiment of the invention, the groups
capable of establishing hydrogen interactions are amide groups of
formulae --C(O)NH-- and --HN--C(O)--.
[0076] In this case, the polymer may comprise at least one moiety
of formula (III) or (IV):
##STR00008##
in which R.sup.1, R.sup.2, R.sup.3, R.sup.4, X, Y, m and n are as
defined above.
[0077] Such a moiety may be obtained: [0078] either by a
condensation reaction between a silicone containing .alpha.,
.omega.-carboxylic acid ends and one or more diamines, according to
the following reaction scheme:
[0078] ##STR00009## [0079] or by reaction of two molecules of
.alpha.-unsaturated carboxylic acid with a diamine according to the
following reaction scheme:
##STR00010##
[0079] followed by the addition of a siloxane to the ethylenic
unsaturations, according to the following scheme:
##STR00011##
in which X.sup.1--(CH.sub.2).sub.2-- corresponds to X defined above
and Y, R.sup.1, R.sup.2, R.sup.3, R.sup.4 and m are as defined
above; [0080] or by reaction of a silicone containing
.alpha.,.omega.-NH.sub.2 ends and a diacid of formula HOOC--Y--COOH
according to the following reaction scheme:
##STR00012##
[0081] In these polyamides of formula (III) or (IV), m is an
integer of at least one as defined above, and preferably in the
range from 1 to 700, for example, from 15 to 500 and from 15 to 45,
including all values and subranges there between; and n is in
particular in the range from 1 to 500, for example, from 1 to 100
and from 4 to 25, including all values and subranges there between;
X is preferably a linear or branched alkylene chain containing from
1 to 30 carbon atoms and in particular 3 to 10 carbon atoms, and Y
is preferably an alkylene chain that is linear or branched or that
possibly comprises rings and/or unsaturations, containing from 1 to
40 carbon atoms, including from 1 to 20 carbon atoms and from 2 to
6 carbon atoms, including all values and subranges there between,
for example, 6 carbon atoms.
[0082] In formulae (III) and (IV), the alkylene group representing
X or Y can optionally contain in its alkylene portion at least one
of the following elements:
[0083] 1) 1 to 5 amide, urea or carbamate groups,
[0084] 2) a C.sub.5 or C.sub.6 cycloalkyl group, and
[0085] 3) a phenylene group optionally substituted with 1 to 3
identical or different C.sub.1 to C.sub.3 alkyl groups.
[0086] In formulae (III) and (IV), the alkylene groups may also be
substituted with at least one element chosen from the group
consisting of: [0087] a hydroxyl group, [0088] a C.sub.3 to C.sub.8
cycloalkyl group, [0089] one to three C.sub.1 to C.sub.40 alkyl
groups, [0090] a phenyl group optionally substituted with one to
three C.sub.1 to C.sub.3 alkyl groups, [0091] a C.sub.1 to C.sub.3
hydroxyalkyl group, and [0092] a C.sub.1 to C.sub.6 aminoalkyl
group.
[0093] In these formulae (III) and (IV), Y may also represent:
##STR00013##
in which R.sup.5 represents a polyorganosiloxane chain and T
represents a group of formula:
##STR00014##
in which a, b and c are, independently, integers ranging from 1 to
10, and R.sup.10 is a hydrogen atom or a group such as those
defined for R.sup.1, R.sup.2, R.sup.3 and R.sup.4.
[0094] In formulae (III) and (IV), R.sup.1, R.sup.2, R.sup.3 and
R.sup.4 preferably represent, independently, a linear or branched
C.sub.1 to C.sub.40 alkyl group, preferably a CH.sub.3,
C.sub.2H.sub.5, n-C.sub.3H.sub.7 or isopropyl group, a
polyorganosiloxane chain or a phenyl group optionally substituted
with one to three methyl or ethyl groups.
[0095] As has been seen previously, the polymer may comprise
identical or different moieties of formula (III) or (IV).
[0096] Thus, the polymer may be a polyamide containing several
moieties of formula (III) or (IV) of different lengths, i.e. a
polyamide corresponding to the formula:
##STR00015##
in which X, Y, n and R.sup.1 to R.sup.4 have the meanings given
above, m.sub.1 and m.sub.2, which are different, are as defined
above, and preferably are chosen in the range from 1 to 1 000, and
p is at least one for example ranging from 2 to 500 and preferably
from 2 to 200.
[0097] In this formula, the moieties may be structured to form
either a block copolymer, or a random copolymer or an alternating
copolymer. In this copolymer, the moieties may be not only of
different lengths, but also of different chemical structures, for
example containing different groups Y. In this case, the copolymer
may correspond to the formula:
##STR00016##
in which R.sup.1 to R.sup.4, X, Y, m.sub.1, m.sub.2, n and p have
the meanings given above and Y.sup.1 is different from Y but chosen
from the groups defined for Y. As previously discussed, the various
moieties may be structured to form either a block copolymer, or a
random copolymer or an alternating copolymer.
[0098] In an embodiment of the invention, the
polyorganosiloxane-containing polymer may also contain a grafted
copolymer. Thus, the polyamide containing silicone units may be
grafted and optionally crosslinked with silicone chains containing
amide groups. Such polymers may be synthesized with trifunctional
amines.
[0099] In this case, the copolymer may comprise at least one moiety
of formula:
##STR00017##
in which X.sup.1 and X.sup.2, which may be identical or different,
have the meaning given for X in formula (I), n is as defined in
formula (I), Y and T are as defined in formula (I), R.sup.11 to
R.sup.18 are groups chosen from the same group as R.sup.1 to
R.sup.4, m.sub.1 and m.sub.2 are numbers in the range from 1 to
1,000, and p is an integer of at least one, for example, p can
range from 2 to 500.
[0100] In formula (VII), it is preferred that: [0101] p is in the
range from 1 to 25, including from 1 to 7, including all values and
subranges there between, [0102] R.sup.11 to R.sup.18 are methyl
groups, [0103] T corresponds to one of the following formulae:
##STR00018##
[0103] in which R.sup.19 is a hydrogen atom or a group chosen from
the groups defined for R.sup.1 to R.sup.4, and R.sup.20, R.sup.21
and R.sup.22 are, independently, linear or branched alkylene
groups, and more preferably corresponds to the formula:
##STR00019##
in particular with R.sup.20, R.sup.21 and R.sup.22 representing
--CH.sub.2--CH.sub.2--, [0104] m.sub.1 and m.sub.2 are in the range
from 15 to 500, including from 15 to 45 and including all values
and subranges there between, [0105] X.sup.1 and X.sup.2 represent
--(CH.sub.2).sub.10--, and [0106] Y represents --CH.sub.2--.
[0107] These polyamides containing a grafted silicone moiety of
formula (VII) may be copolymerized with polyamide-silicones of
formula (II) to form block copolymers, alternating copolymers or
random copolymers. The weight percentage of grafted silicone
moieties (VII) in the copolymer may range from 0.5% to 30% by
weight.
[0108] According to the invention, as has been seen previously, the
siloxane units may be in the main chain or backbone of the polymer,
but they may also be present in grafted or pendent chains. In the
main chain, the siloxane units may be in the form of segments as
described above. In the pendent or grafted chains, the siloxane
units may appear individually or in segments.
[0109] According to the invention, the preferred siloxane-based
polyamides are: [0110] polyamides of formula (III) in which m is
from 15 to 300, for example, 15 to 100, including all values and
subranges there between; [0111] mixtures of two or more polyamides
in which at least one polyamide has a value of m in the range from
15 to 50, including all values and subranges there between and at
least one polyamide has a value of m in the range from 30 to 300,
including all values and subranges there between; [0112] polymers
of formula (V) with m.sub.1 chosen in the range from 15 to 50 and
m.sub.2 chosen in the range from 30 to 500 with the portion
corresponding to m.sub.1 representing 1% to 99% by weight of the
total weight of the polyamide and the corresponding portion m.sub.2
representing 1% to 99% by weight of the total weight of the
polyamide; [0113] mixtures of polyamide of formula (III) combining
[0114] 1) 80% to 99% by weight of a polyamide in which n is equal
to 2 to 10 and in particular 3 to 6, and [0115] 2) 1% to 20% of a
polyamide in which n is in the range from 5 to 500 and in
particular from 6 to 100; [0116] polyamides corresponding to
formula (VI) in which at least one of the groups Y and Y.sup.1
contains at least one hydroxyl substituent; [0117] polyamides of
formula (III) synthesized with at least one portion of an activated
diacid (diacid chloride, dianhydride or diester) instead of the
diacid; [0118] polyamides of formula (III) in which X represents
--(CH.sub.2).sub.3-- or --(CH.sub.2).sub.10; and [0119] polyamides
of formula (III) in which the polyamides end with a monofunctional
chain chosen from the group consisting of monofunctional amines,
monofunctional acids, monofunctional alcohols, including fatty
acids, fatty alcohols and fatty amines, such as, for example,
octylamine, octanol, stearic acid and stearyl alcohol.
[0120] According to the invention, the end groups of the polymer
chain may end with: [0121] a C.sub.1 to C.sub.50 alkyl ester group
by introducing a C.sub.1 to C.sub.50 monoalcohol during the
synthesis, [0122] a C.sub.1 to C.sub.50 alkylamide group by taking
as stopping group a monoacid if the silicone is
.alpha.,.omega.-diaminated, or a monoamine if the silicone is an
.alpha.,.omega.-dicarboxylic acid.
[0123] According to one embodiment of the invention, it is possible
to use a copolymer of silicone polyamide and of hydrocarbon-based
polyamide, i.e. a copolymer comprising moieties of formula (III) or
(IV) and hydrocarbon-based polyamide moieties. In this case, the
polyamide-silicone moieties may be arranged at the ends of the
hydrocarbon-based polyamide.
[0124] Polyamide-based polymers containing silicones may be
produced by silylic amidation of polyamides based on fatty acid
dimer. This approach involves the reaction of free acid sites
existing on a polyamide as end sites, with
organosiloxane-monoamines and/or organosiloxane-diamines (amidation
reaction), or alternatively with oligosiloxane alcohols or
oligosiloxane diols (esterification reaction). The esterification
reaction requires the presence of acid catalysts, as is known in
the art. It is desirable for the polyamide containing free acid
sites, used for the amidation or esterification reaction, to have a
relatively high number of acid end groups (for example polyamides
with high acid numbers, for example from 15 to 20).
[0125] For the amidation of the free acid sites of the
hydrocarbon-based polyamides, siloxane diamines with 1 to 300, more
particularly 2 to 50 and for example, 2, 6, 9.5, 12, 13.5, 23 or 31
siloxane groups, may be used for the reaction with
hydrocarbon-based polyamides based on fatty acid dimers. Siloxane
diamines containing 13.5 siloxane groups are preferred, and the
best results are obtained with the siloxane diamine containing 13.5
siloxane groups and polyamides containing high numbers of
carboxylic acid end groups.
[0126] The reactions may be carried out in xylene to extract the
water produced from the solution by azeotropic distillation, or at
higher temperatures (about 180 to 200.degree. C.) without solvent.
Typically, the efficacy of the amidation and the reaction rates
decrease when the siloxane diamine is longer, that is to say when
the number of siloxane groups is higher. Free amine sites may be
blocked after the initial amidation reaction of the
diaminosiloxanes by reacting them either with a siloxane acid, or
with an organic acid such as benzoic acid.
[0127] For the esterification of the free acid sites on the
polyamides, this may be performed in boiling xylene with about 1%
by weight, relative to the total weight of the reagents, of
para-toluenesulphonic acid as catalyst.
[0128] These reactions carried out on the carboxylic acid end
groups of the polyamide lead to the incorporation of silicone
moieties only at the ends of the polymer chain.
[0129] It is also possible to prepare a copolymer of
polyamide-silicone, using a polyamide containing free amine groups,
by amidation reaction with a siloxane containing an acid group.
[0130] It is also possible to prepare a gelling agent based on a
copolymer between a hydrocarbon-based polyamide and a silicone
polyamide, by transamidation of a polyamide having, for example, an
ethylene-diamine constituent, with an oligosiloxane-am-diamine, at
high temperature (for example 200 to 300.degree. C.), to carry out
a transamidation such that the ethylenediamine component of the
original polyamide is replaced with the oligosiloxane diamine.
[0131] The copolymer of hydrocarbon-based polyamide and of
polyamide-silicone may also be a grafted copolymer comprising a
hydrocarbon-based polyamide backbone with pendent oligosiloxane
groups.
[0132] This may be obtained, for example: [0133] by hydrosilylation
of unsaturated bonds in polyamides based on fatty acid dimers;
[0134] by silylation of the amide groups of a polyamide; or [0135]
by silylation of unsaturated polyamides by means of an oxidation,
that is to say by oxidizing the unsaturated groups into alcohols or
diols, to form hydroxyl groups that are reacted with siloxane
carboxylic acids or siloxane alcohols. The olefinic sites of the
unsaturated polyamides may also be epoxidized and the epoxy groups
may then be reacted with siloxane amines or siloxane alcohols.
[0136] The polyorganosiloxane containing polymers used in the
composition of the invention are most preferably polymers of the
polyorganosiloxane type such as those described in documents U.S.
Pat. No. 5,874,069, U.S. Pat. No. 5,919,441, U.S. Pat. No.
6,051,216 and U.S. Pat. No. 5,981,680, the entire disclosures of
which are hereby incorporated by reference.
[0137] According to another embodiment of the invention, the
polyorganoxiloxane containing polymer is a homopolymer or a
copolymer comprising urethane or urea groups.
[0138] As previously discussed, the polymer may comprise
polyorganosiloxane moieties containing two or more urethane and/or
urea groups, either in the backbone of the polymer or on side
chains or as pendent groups.
[0139] The polymers comprising at least two urethane and/or urea
groups in the backbone may be polymers comprising at least one
moiety corresponding to the following formula:
##STR00020##
in which R.sup.1, R.sup.2, R.sup.3, R.sup.4, X, Y, m and n have the
meanings given above for formula (I), and U represents --O-- or
--NH--, such that:
##STR00021##
corresponds to a urethane or urea group.
[0140] In this formula (VIII), Y may be a linear or branched
C.sub.1 to C.sub.40 alkylene group, optionally substituted with a
C.sub.1 to C.sub.15 alkyl group or a C.sub.5 to C.sub.10 aryl
group. Preferably, a --(CH.sub.2).sub.6-- group is used.
[0141] Y may also represent a C.sub.5 to C.sub.12 cycloaliphatic or
aromatic group that may be substituted with a C.sub.1 to C.sub.15
alkyl group or a C.sub.5 to C.sub.10 aryl group, for example a
radical chosen from the methylene-4,4-biscyclohexyl radical, the
radical derived from isophorone diisocyanate, 2,4- and
2,6-tolylenes, 1,5-naphthylene, p-phenylene and
4,4'-biphenylenemethane. Generally, it is preferred for Y to
represent a linear or branched C.sub.1 to C.sub.40 alkylene radical
or a C.sub.4 to C.sub.12 cycloalkylene radical.
[0142] Y may also represent a polyurethane or polyurea block
corresponding to the condensation of several diisocyanate molecules
with one or more molecules of coupling agents of the diol or
diamine type. In this case, Y comprises several urethane or urea
groups in the alkylene chain.
[0143] It may correspond to the formula:
##STR00022##
in which B.sup.1 is a group chosen from the groups given above for
Y, U is --O-- or --NH-- and B.sup.2 is chosen from:
[0144] linear or branched C.sub.1 to C.sub.40 alkylene groups,
which can optionally bear an ionizable group such as a carboxylic
acid or sulphonic acid group, or a neutralizable or quaternizable
tertiary amine group,
[0145] C.sub.5 to C.sub.12 cycloalkylene groups, optionally bearing
alkyl substituents, for example one to three methyl or ethyl
groups, or alkylene, for example the diol radical:
cyclohexanedimethanol,
[0146] phenylene groups that may optionally bear C.sub.1 to C.sub.3
alkyl substituents, and
[0147] groups of formula:
##STR00023##
in which T is a hydrocarbon-based trivalent radical possibly
containing one or more hetero atoms such as oxygen, sulphur and
nitrogen and R.sup.5 is a polyorganosiloxane chain or a linear or
branched C.sub.1 to C.sub.50 alkyl chain.
[0148] T can represent, for example:
##STR00024##
with w being an integer ranging from 1 to 10 and R.sup.5 being a
polyorganosiloxane chain.
[0149] When Y is a linear or branched C.sub.1 to C.sub.40 alkylene
group, the --(CH.sub.2).sub.2-- and --(CH.sub.2).sub.6-- groups are
preferred.
[0150] In the formula given above for Y, d may be an integer
ranging from 0 to 5, preferably from 0 to 3 and more preferably
equal to 1 or 2.
[0151] Preferably, B.sup.2 is a linear or branched C.sub.1 to
C.sub.40 alkylene group, in particular --(CH.sub.2).sub.2-- or
--(CH.sub.2).sub.6-- or a group:
##STR00025##
with R.sup.5 being a polyorganosiloxane chain.
[0152] As previously discussed, the polyorganosiloxane containing
polymer may be formed from silicone urethane and/or silicone urea
moieties of different length and/or constitution, and may be in the
form of block or random copolymers.
[0153] According to the invention, the silicone may also comprise
urethane and/or urea groups no longer in the backbone but as side
branches.
[0154] In this case, the polymer may comprise at least one moiety
of formula:
##STR00026##
in which R.sup.1, R.sup.2, R.sup.3, m.sub.1 and m.sub.2 have the
meanings given above for formula (I), [0155] U represents O or NH,
[0156] R.sup.23 represents a C.sub.1 to C.sub.40 alkylene group,
optionally comprising one or more hetero atoms chosen from O and N,
or a phenylene group, and [0157] R.sup.24 is chosen from linear,
branched or cyclic, saturated or unsaturated C.sub.1 to C.sub.50
alkyl groups, and phenyl groups optionally substituted with one to
three C.sub.1 to C.sub.3 alkyl groups.
[0158] The polymers comprising at least one moiety of formula (X)
contain siloxane units and urea or urethane groups, and they may be
used, for example, as gelling agents in the compositions of the
invention.
[0159] The siloxane polymers may have a single urea or urethane
group by branching or may have branches containing two urea or
urethane groups, or alternatively they may contain a mixture of
branches containing one urea or urethane group and branches
containing two urea or urethane groups.
[0160] They may be obtained from branched polysiloxanes, comprising
one or two amino groups by branching, by reacting these
polysiloxanes with monoisocyanates.
[0161] As examples of starting polymers of this type containing
amino and diamino branches, mention may be made of the polymers
corresponding to the following formulae:
##STR00027##
[0162] In these formulae, the symbol "/" indicates that the
segments may be of different lengths and in a random order, and R
represents a linear aliphatic group preferably containing 1 to 6
carbon atoms, including 1 to 3 carbon atoms.
[0163] Such polymers containing branching may be formed by reacting
a siloxane polymer, containing at least three amino groups per
polymer molecule, with a compound containing only one
monofunctional group (for example an acid, an isocyanate or an
isothiocyanate) to react this monofunctional group with one of the
amino groups and to form groups capable of establishing hydrogen
interactions. The amino groups may be on side chains extending from
the main chain of the siloxane polymer, such that the groups
capable of establishing hydrogen interactions are formed on these
side chains, or alternatively the amino groups may be at the ends
of the main chain, such that the groups capable of hydrogen
interaction will be end groups of the polymer.
[0164] As a procedure for forming a polymer containing siloxane
units and groups capable of establishing hydrogen interactions,
mention may be made of the reaction of a siloxane diamine and of a
diisocyanate in a silicone solvent so as to provide a gel directly.
The reaction may be performed in a silicone fluid, the resulting
product being dissolved in the silicone fluid, at high temperature,
the temperature of the system then being reduced to form the
gel.
[0165] The polymers that are preferred for incorporation into the
compositions according to the present invention are siloxane-urea
copolymers that are linear and that contain urea groups as groups
capable of establishing hydrogen interactions in the backbone of
the polymer.
[0166] As an illustration of a polysiloxane ending with four urea
groups, mention may be made of the polymer of formula:
##STR00028##
in which Ph is a phenyl group and n is a number larger than 0,
which includes, at least 1, 2 to 500, 2 to 200, from 1 to 300, in
particular from 1 to 100, and all values and subranges there
between, for example 50.
[0167] This polymer is obtained by reacting the following
polysiloxane containing amino groups:
##STR00029##
with phenyl isocyanate.
[0168] The polymers of formula (VIII) comprising urea or urethane
groups in the chain of the silicone polymer may be obtained by
reaction between a silicone containing .alpha.,.omega.-NH.sub.2 or
--OH end groups, of formula:
##STR00030##
in which m, R.sup.1, R.sup.2, R.sup.3, R.sup.4 and X are as defined
for formula (I) and a diisocyanate OCN--Y--NCO in which Y has the
meaning given in formula (I); and optionally a diol or diamine
coupling agent of formula H.sub.2N--B.sup.2--NH.sub.2 or
HO--B.sup.2--OH, in which B.sup.2 is as defined in formula
(IX).
[0169] According to the stoichiometric proportions between the two
reagents, diisocyanate and coupling agent, Y may have the formula
(IX) with d equal to 0 or d equal to 1 to 5.
[0170] As in the case of the polyamide silicones of formula (II) or
(III), it is possible to use in the invention polyurethane or
polyurea silicones containing moieties of different length and
structure, in particular moieties whose lengths differ by the
number of silicone units. In this case, the copolymer may
correspond, for example, to the formula:
##STR00031##
in which R.sup.1, R.sup.2, R.sup.3, R.sup.4, X, Y and U are as
defined for formula (VIII) and m.sub.1, m.sub.2, n and p are as
defined for formula (V).
[0171] Branched polyurethane or polyurea silicones may also be
obtained using, instead of the diisocyanate OCN--Y--NCO, a
triisocyanate of formula:
##STR00032##
[0172] A polyurethane or polyurea silicone containing branches
comprising an organosiloxane chain with groups capable of
establishing hydrogen interactions is thus obtained. Such a polymer
comprises, for example, a moiety corresponding to the formula:
##STR00033##
in which X.sup.1 and X.sup.2, which are identical or different,
have the meaning given for X in formula (I), n is as defined in
formula (I), Y and T are as defined in formula (I), R.sup.11 to
R.sup.18 are groups chosen from the same group as R.sup.1 to
R.sup.4, m.sub.1 and m.sub.2 are as defined above.
[0173] As in the case of the polyamides, this copolymer can also
comprise polyurethane silicone moieties without branching.
[0174] In another embodiment of the invention, the siloxane-based
polyureas and polyurethanes that are preferred are: [0175] polymers
of formula (VIII) in which m is from 15 to 300, for example, 15 to
100 and all values and subranges there between; [0176] mixtures of
two or more polymers in which at least one polymer has a value of m
in the range from 15 to 50 and at least one polymer has a value of
m in the range from 30 to 300, including all values and subranges
there between; [0177] polymers of formula (XII) with m.sub.1 chosen
in the range from 15 to 50 and m.sub.2 chosen in the range from 30
to 500 with the portion corresponding to m.sub.1 representing 1% to
99% by weight of the total weight of the polymer and the portion
corresponding to m.sub.2 representing 1% to 99% by weight of the
total weight of the polymer; [0178] mixtures of polymer of formula
(VIII) combining [0179] 1) 80% to 99% by weight of a polymer in
which n is equal to 2 to 10 and in particular 3 to 6, and [0180] 2)
1% to 20% of a polymer in which n is in the range from 5 to 500 and
in particular from 6 to 100, [0181] copolymers comprising two
moieties of formula (VIII) in which at least one of the groups Y
contains at least one hydroxyl substituent; [0182] polymers of
formula (VIII) synthesized with at least one portion of an
activated diacid (diacid chloride, dianhydride or diester) instead
of the diacid; [0183] polymers of formula (VIII) in which X
represents --(CH.sub.2).sub.3-- or --(CH.sub.2).sub.10--; and
[0184] polymers of formula (VIII) in which the polymers end with a
multifunctional chain chosen from the group consisting of
monofunctional amines, monofunctional acids, monofunctional
alcohols, including fatty acids, fatty alcohols and fatty amines,
such as, for example, octylamine, octanol, stearic acid and stearyl
alcohol.
[0185] As in the case of the polyamides, copolymers of polyurethane
or polyurea silicone and of hydrocarbon-based polyurethane or
polyurea may be used in the invention by performing the reaction
for synthesizing the polymer in the presence of an .alpha.,
.omega.-difunctional block of non-silicone nature, for example a
polyester, a polyether or a polyolefin.
[0186] As has been seen previously, homopolymers or copolymers of
the invention may contain siloxane moieties in the main chain of
the polymer and groups capable of establishing hydrogen
interactions, either in the main chain of the polymer or at the
ends thereof, or on side chains or branches of the main chain. This
may correspond to the following five arrangements:
##STR00034##
in which the continuous line is the main chain of the siloxane
polymer and the squares represent the groups capable of
establishing hydrogen interactions.
[0187] In case (1), the groups capable of establishing hydrogen
interactions are arranged at the ends of the main chain.
[0188] In case (2), two groups capable of establishing hydrogen
interactions are arranged at each of the ends of the main
chain.
[0189] In case (3), the groups capable of establishing hydrogen
interactions are arranged within the main chain in repeating
moieties.
[0190] In cases (4) and (5), these are copolymers in which the
groups capable of establishing hydrogen interactions are arranged
on branches of the main chain of a first series of moieties that
are copolymerized with moieties not comprising groups capable of
establishing hydrogen interactions. Preferably, the values n, x and
y are such that the polymer has the desired properties in terms of
an agent for gelling fatty phases, preferably fatty phases based on
silicone oil.
[0191] As examples of polymers that may be used, mention may be
made of the silicone polyamides obtained in accordance with the
disclosure in U.S. Pat. No. 5,981,680, the entire disclosure of
which is hereby incorporated by reference.
[0192] Further examples of polyorganosiloxane containing polymers
are set forth in U.S. Pat. Nos. 6,503,632 and 6,569,955, both of
which are hereby incorporated by reference in their entirety.
[0193] As noted above, the polymers of the present invention can be
solid or liquid at room temperature. When solid, the polymers
preferably have a softening point from 50 to 130.degree. C. Most
preferably, they have a softening point ranging from 65 to
150.degree. C., including from 70.degree. C. to 130.degree. C. This
softening point is lower than that of other structuring polymers,
which facilitates the use of the polymers that are the subject of
the invention, and limits the deteriorations of the liquid fatty
phase.
[0194] As noted above, the polyorganosiloxane containing polymers
of the present invention contain both siloxane units and at least
two groups capable of establishing hydrogen interactions such as
amide linkages. The siloxane units can provide compatibility with a
silicone fluid, if present, (for example with the cyclomethicones),
while the groups capable of establishing hydrogen interactions and
the spacing and selection of the locations of the amide linkages
can facilitate gelation and the formation of cosmetic products.
[0195] In one embodiment, the polyorganosiloxane containing polymer
of the present invention is present in an amount effective to
provide transfer resistant properties, and may also provide at
least one of the following properties: pliability, softness, and
wearing comfort. In addition, it is preferred that the compositions
of the invention exhibit flexibility and/or good adherence on the
keratinous substance to which the compositions have been applied.
In another preferred embodiment, the compositions of the present
invention when applied to the keratinous substance are
substantially non-tacky.
[0196] In the composition of the present invention, the
polyorganosiloxane-containing polymers are preferably present in an
amount of 0.1-80 percent by weight, more preferably from 0.5 to 30
percent by weight and most preferably from 1 to 20 percent by
weight of the total weight of the composition.
[0197] Depending on the intended application, such as a stick,
hardness of the composition may also be considered. The hardness of
a composition may, for example, be expressed in gramforce (gf). The
composition of the present invention may, for example, have a
hardness ranging from 20 gf to 2000 gf, such as from 20 gf to 900
gf, and further such as from 20 gf to 600 gf.
[0198] This hardness is measured in one of two ways. A first test
for hardness is according to a method of penetrating a probe into
the composition and in particular using a texture analyzer (for
example TA-XT2i from Rheo) equipped with an ebonite cylinder of
height 25 mm and diameter 8 mm. The hardness measurement is carried
out at 20.degree. C. at the center of 5 samples of the composition.
The cylinder is introduced into each sample of composition at a
pre-speed of 2 mm/s and then at a speed of 0.5 mm/s and finally at
a post-speed of 2 mm/s, the total displacement being 1 mm. The
recorded hardness value is that of the maximum peak observed. The
measurement error is .+-.50 gf.
[0199] The second test for hardness is the "cheese wire" method,
which involves cutting an 8.1 mm or preferably 12.7 mm in diameter
stick composition and measuring its hardness at 20.degree. C. using
a DFGHS 2 tensile testing machine from Indelco-Chatillon Co. at a
speed of 100 mm/minute. The hardness value from this method is
expressed in grams as the shear force required to cut a stick under
the above conditions. According to this method, the hardness of
compositions according to the present invention which may be in
stick form may, for example, range from 30 gf to 300 gf, such as
from 30 gf to 250 gf, for a sample of 8.1 mm in diameter stick, and
further such as from 30 gf to 200 gf, and also further such as from
30 gf to 120 gf for a sample of 12.7 mm in diameter stick.
[0200] The hardness of the composition of the present invention may
be such that the compositions are self-supporting and can easily
disintegrate to form a satisfactory deposit on a keratinous
material. In addition, this hardness may impart good impact
strength to the inventive compositions, which may be molded or
cast, for example, in stick or dish form.
[0201] The skilled artisan may choose to evaluate a composition
using at least one of the tests for hardness outlined above based
on the application envisaged and the hardness desired. If one
obtains an acceptable hardness value, in view of the intended
application, from at least one of these hardness tests, the
composition falls within preferred embodiments of the
invention.
[0202] As is evident, the hardness of the composition according to
preferred embodiments of the invention may, for example, be such
that the composition is advantageously self-supporting and can
disintegrate easily to form a satisfactory deposit on the skin
and/or the lips and/or superficial body growths, such as keratinous
fibers. In addition, with this hardness, the composition of the
invention may have good impact strength.
[0203] According to preferred embodiments of the present invention,
the composition in stick form may have the behavior of a
deformable, flexible elastic solid, giving noteworthy elastic
softness on application. The compositions in stick form of the
prior art do not have these properties of elasticity and
flexibility.
[0204] Liquid Fatty Phase
[0205] According to preferred embodiments of the present invention,
cosmetic compositions comprising at least one polyorganosiloxane
containing polymer and a liquid fatty phase are provided,
Preferably, the liquid fatty phase comprises at least one volatile
oil, e.g., a silicone volatile oil, a hydrocarbon volatile oil, or
a mixture thereof.
[0206] In accordance with this embodiment, the liquid fatty phase
may contain, independently or in combinations, volatile silicone
oils, non-volatile silicone oils, volatile non-silicone oils and
non-volatile non-silicone oils. In one embodiment, the compositions
of the present invention are substantially free of silicone oils
(i.e., contain less than about 0.1% silicone oils). In another
embodiment, the compositions are substantially free of non-silicone
oils (i.e., contain less than about 0.1% non-silicone oils). In
another embodiment, the compositions are substantially free of
non-volatile oils (i.e., contain less than about 0.1% non-volatile
oils).
[0207] According to the invention, when volatile oils are present,
these volatile oils permit an easier application of the composition
on the skin, lips or keratinous fibers.
[0208] According to one embodiment, the composition may contain one
or more volatile silicone oils. Examples of such volatile silicone
oils include linear or cyclic silicone oils having a viscosity at
room temperature less than or equal to 6 cSt and having from 2 to 7
silicon atoms, these silicones being optionally substituted with
alkyl or alkoxy groups of 1 to 10 carbon atoms. Specific oils that
may be used in the invention include octamethyltetrasiloxane,
decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane,
heptamethyloctyltrisiloxane, hexamethyldisiloxane,
decamethyltetrasiloxane, dodecamethylpentasiloxane and their
mixtures. Other volatile oils which may be used include KF 96A of 6
cSt viscosity, a commercial product from Shin Etsu having a flash
point of 94.degree. C. Preferably, the volatile silicone oils have
a flash point of at least 40.degree. C.
[0209] Non-limiting examples of volatile silicone oils are listed
in Table 1 below.
TABLE-US-00001 TABLE 1 Flash Point Viscosity Compound (.degree. C.)
(cSt) Octyltrimethicone 93 1.2 Hexyltrimethicone 79 1.2
Decamethylcyclopentasiloxane 72 4.2 (cyclopentasiloxane or D5)
Octamethylcyclotetrasiloxane 55 2.5 (cyclotetradimethylsiloxane or
D4) Dodecamethylcyclohexasiloxane (D6) 93 7
Decamethyltetrasiloxane(L4) 63 1.7 KF-96 A from Shin Etsu 94 6 PDMS
(polydimethylsiloxane) DC 200 56 1.5 (1.5 cSt) from Dow Corning
PDMS DC 200 (2 cSt) from Dow Corning 87 2 PDMS DC 200 (5 cSt) from
Dow Corning 134 5 PDMS DC 200 (3St) from Dow Corning 102 3
[0210] Examples of other silicone oils that may be used in the
invention include non-volatile linear polydimethylsiloxanes
(PDMSs), that are liquid at room temperature; polydimethylsiloxanes
comprising alkyl, alkoxy or phenyl groups, which are pendent and/or
at the end of a silicone chain, these groups each containing from 2
to 24 carbon atoms; phenylsilicones, for instance phenyl
trimethicones, phenyl dimethicones, phenyl
trimethylsiloxydiphenylsiloxanes, diphenyl dimethicones, diphenyl
methyldiphenyl trisiloxanes and 2-phenylethyl
trimethylsiloxysilicates.
[0211] Further, a volatile linear silicone oil may be employed in
the compositions of the present invention. Suitable volatile linear
silicone oils include those described in U.S. Pat. No. 6,338,839
and WO03/042221, the contents of which are incorporated herein by
reference. In one embodiment the volatile linear silicone oil is
decamethyltetrasiloxane. In another embodiment, the
decamethyltetrasiloxane is further combined with another solvent
that is more volatile than decamethyltetrasiloxane.
[0212] The volatility of the solvents/oils can be determined using
the evaporation speed as set forth in U.S. Pat. No. 6,338,839.
[0213] According to other preferred embodiments, the composition
may contain one or more non-silicone volatile oils and may be
selected from volatile hydrocarbon oils, alcohols, volatile esters
and volatile ethers. Examples of such volatile non-silicone oils
include, but are not limited to, volatile hydrocarbon oils having
from 8 to 16 carbon atoms and their mixtures and in particular
branched C.sub.8 to C.sub.16 alkanes such as C.sub.8 to C.sub.16
isoalkanes (also known as isoparaffins), isododecane, isodecane,
isohexadecane, and for example, the oils sold under the trade names
of Isopar or Permethyl, the C.sub.8 to C.sub.16 branched esters
such as isohexyl or isodecyl neopentanoate and their mixtures.
Preferably, the volatile non-silicone oils have a flash point of at
least 40.degree. C.
[0214] Non-limiting examples of volatile non-silicone volatile oils
are given in Table 2 below.
TABLE-US-00002 TABLE 2 Compound Flash Point (.degree. C.)
Isododecane 43 Isohexadecane 102 Isodecyl Neopentanoate 118
Propylene glycol n-butyl ether 60 Ethyl 3-ethoxypropionate 58
Propylene glycol methylether acetate 46 Isopar L (isoparaffin
C.sub.11-C.sub.13) 62 Isopar H (isoparaffin C.sub.11-C.sub.12)
56
[0215] Examples of other non-silicone oils which can be used in the
compositions of the present invention include polar oils such as:
[0216] hydrocarbon-based plant oils with a high triglyceride
content consisting of fatty acid esters of glycerol, the fatty
acids of which may have varied chain lengths, these chains possibly
being linear or branched, and saturated or unsaturated; these oils
are especially wheat germ oil, corn oil, sunflower oil, karite
butter, castor oil, sweet almond oil, macadamia oil, apricot oil,
soybean oil, rapeseed oil, cottonseed oil, alfalfa oil, poppy oil,
pumpkin oil, sesame seed oil, marrow oil, avocado oil, hazelnut
oil, grape seed oil, blackcurrant seed oil, evening primrose oil,
millet oil, barley oil, quinoa oil, olive oil, rye oil, safflower
oil, candlenut oil, passion flower oil or musk rose oil; or
caprylic/capric acid triglycerides, for instance those sold by the
company Stearineries Dubois or those sold under the names Miglyol
810, 812 and 818 by the company Dynamit Nobel; [0217] synthetic
oils or esters of formula R.sub.5COOR.sub.6 in which R.sub.5
represents a linear or branched higher fatty acid residue
containing from 1 to 40 carbon atoms, including from 7 to 19 carbon
atoms, and R.sub.6 represents a branched hydrocarbon-based chain
containing from 1 to 40 carbon atoms, including from 3 to 20 carbon
atoms, with R.sub.6+R.sub.7.gtoreq.10, such as, for example,
Purcellin oil (cetostearyl octanoate), isononyl isononanoate,
C.sub.12 to C.sub.15 alkyl benzoate, isopropyl myristate,
2-ethylhexyl palmitate, and octanoates, decanoates or ricinoleates
of alcohols or of polyalcohols; hydroxylated esters, for instance
isostearyl lactate or diisostearyl malate; and pentaerythritol
esters; [0218] synthetic ethers containing from 10 to 40 carbon
atoms; [0219] C.sub.8 to C.sub.26 fatty alcohols, for instance
oleyl alcohol; and [0220] mixtures thereof.
[0221] Preferably, the liquid fatty phase, when present, represents
from 5% to 98.4% of the total weight of the composition, more
preferably from 10% to 80% of the total weight of the composition,
and most preferably from 20% to 75%.
[0222] Film Formers
[0223] The composition of the present invention advantageously also
includes one or more film forming agents. Film forming agents are
known in the art.
[0224] According to preferred embodiments of the present invention,
compositions comprising at least one polyorganosiloxane containing
polymer and at least one silicone film forming agent, preferably an
MK or MQ resin or mixtures thereof, are provided.
[0225] Silicone resin nomenclature is known in the art as "MDTQ"
nomenclature, whereby a silicone resin is described according to
the various monomeric siloxane units which make up the polymer.
[0226] Each letter of "MDTQ" denotes a different type of unit. The
letter M denotes the monofunctional unit
(CH.sub.3).sub.3SiO.sub.1/2. This unit is considered to be
monofunctional because the silicone atom only shares one oxygen
when the unit is part of a polymer. The "M" unit can be represented
by the following structure:
##STR00035##
[0227] At least one of the methyl groups of the M unit may be
replaced by another group, e.g., to give a unit with formula
[R(CH.sub.3).sub.2]SiO.sub.1/2, as represented in the following
structure:
##STR00036##
wherein R is chosen from groups other than methyl groups.
Non-limiting examples of such groups other than methyl groups
include alkyl groups other than methyl groups, alkene groups,
alkyne groups, hydroxyl groups, thiol groups, ester groups, acid
groups, ether groups, wherein the groups other than methyl groups
may be further substituted.
[0228] The symbol D denotes the difunctional unit
(CH.sub.3).sub.2SiO.sub.2/2 wherein two oxygen atoms bonded to the
silicone atom are used for binding to the rest of the polymer. The
"D" unit, which is the major building block of dimethicone oils,
can be represented as:
##STR00037##
[0229] At least one of the methyl groups of the D unit may be
replaced by another group, e.g., to give a unit with formula
[R(CH.sub.3).sub.2]SiO.sub.1/2.
[0230] The symbol T denotes the trifunctional unit,
(CH.sub.3)SiO.sub.3/2 and can be represented as:
##STR00038##
[0231] At least one of the methyl groups of the T unit may be
replaced by another group, e.g., to give a unit with formula
[R(CH.sub.3).sub.2]SiO.sub.1/2.
[0232] Similarly, the symbol Q denotes the tetrafunctional unit,
SiO.sub.4/2 wherein all four oxygens bonded to the silicone atom
are bonded to the rest of the polymer.
[0233] Thus, a vast number of different silicone polymers can be
manufactured. Further, it would be clear to one skilled in the art
that the properties of each of the potential silicone polymers will
vary depending on the type(s) of monomer(s), the type(s) of
substitution(s), the size of the polymeric chain, the degree of
cross linking, and size of any side chain(s).
[0234] Non-limiting examples of silicone polymers include silanes,
siloxanes, siloxysilicates, and silsesquioxanes. A non-limiting
example of such a siloxane is polydimethylsiloxane (PDMS).
Polydimethylsiloxanes are generally composed of long straight
chains of (CH.sub.3).sub.2SiO.sub.2/2 (i.e., D units) and have
viscosities which are dependent on both the size of the polymer and
the presence and nature of any substituent(s) on the polymer. A
non-limiting example of a siloxysilicate is
trimethylsiloxysilicate, which may be represented by the following
formula:
[(CH.sub.3).sub.3--Si--O].sub.x--(SiO.sub.4/2).sub.y
[0235] (i.e, MQ units) wherein x and y may, for example, range from
50 to 80. Silsesquioxanes, on the other hand, may be represented by
the following formula:
(CH.sub.3SiO.sub.3/2)..sub.x
[0236] (i.e., T Units) wherein x may, for example, have a value of
up to several thousand.
[0237] Polymethylsilsesquioxanes are silsesquioxanes that do not
have a substituent replacing the methyl groups. Certain
polymethylsilsesquioxanes have previously been used in hair care
compositions. See, e.g., U.S. Pat. No. 5,246,694, the disclosure of
which is incorporated herein by reference, which discloses a
shampoo composition comprising a surfactant, an aqueous emulsion of
highly viscous silicone in volatile silicone and a cationic polymer
which is a derivative of guar gum. The highly viscous silicone
disclosed therein may be chosen from silicone resins including a
polymethylsilsesquioxane such as Resin MK (also called SiliconHarz
MK) which is available from Wacker, and a siloxysilicate such as
Resin MQ which is available from General Electric and Dow
Corning.
[0238] The Resin MK and Resin MQ silicone resins may form a film
after a volatile carrier has evaporated. The MQ film is generally
hard and brittle at room temperature, while the MK film is
generally continuous and flexible, i.e., not brittle. Depending on
the application, plasticizers may be added to help obtain a more
flexible, thus more comfortable, film.
[0239] In one embodiment, the silicone film former may be a
polymethylsilsesquioxane film former such as Belsil PMS MK, also
referred to as Resin MK, available from Wacker Chemie. This
polymethylsilsesquioxane film former is a polymer comprising
polymerized repeating units of CH.sub.3SiO.sub.3/2 (T units) and
may also contain up to 1% by weight or by mole of units of the
formula (CH.sub.3).sub.2SiO.sub.2/2 (D units). The weight-average
molecular weight of this polymer has been estimated to be 10,000.
It is believed that the polymers are in a "cage" and "ladder"
configuration, as exemplified in the figures below. The majority of
the polymer is in the "ladder" configuration, wherein the ends of
the polymer are capped with ethoxy (CH.sub.3CH.sub.2O) groups. The
ethoxy groups are generally present in an amount of 4.5% by weight
and the mole percent is generally 7% (silicone units). As ethoxy
groups may react with water, a small and variable amount of SiOH
may also be present in the polymer.
##STR00039##
[0240] Another non-limiting example of the at least one
polymethylsilsesquioxane film former suitable for use in the
present invention is KR-220L, which is available from SHIN-ETSU.
This polymethylsilsesquioxane film former is composed of silicone
T-units (i.e., those of formula CH.sub.3SiO.sub.3/2) and has Si--OH
(or silanol) end units. There are no D units in KR-220L.
[0241] Other non-limiting examples of the at least one
polymethylsilsesquioxane film former that may be useful in the
practice of the invention include KR-242A (which is comprised of
methyl T units (98%) and dimethyl D units (2%) and has Si--OH end
units) and KR-251 (which is comprised of methyl T units (88%) and
dimethyl D units (12%) and has Si--OH end units), both of which are
available from SHIN-ETSU.
[0242] Depending on the application, the concentration of the at
least one polymethylsilsesquioxane film former in the presently
claimed composition may vary considerably. One of skill in the art
will be able to determine routinely the amount of the at least one
polymethylsilsesquioxane film former depending on the desired
application.
[0243] In another embodiment, the silicone film former may be
chosen from siloxysilicates. Preferably, the siloxysilicate is
trimethylsiloxysilicate, which may or may not be in powder form.
Trimethylsiloxysilicate (TMS) is commercially available from
General Electric under the tradename SR1000 and from Wacker under
the tradename TMS 803. TMS is also commercially available from Dow
Chemical in a solvent, such as for example, cyclomethicone.
However, according to the present invention, TMS may be used in the
form of 100% active material, that is, not in a solvent.
[0244] Further non-limiting examples of the silicone film formers
include silicone/(meth)acrylate copolymers, such as those as
described in U.S. Pat. Nos. 5,061,481, 5,219,560, and 5,262,087,
the disclosures of which are hereby incorporated by reference.
Still further non-limiting examples of silicone film formers are
non-polar silicone copolymers comprising repeating units of at
least one polar (meth)acrylate unit and vinyl copolymers grafted
with at least one non-polar silicone chain. Non-limiting examples
of such copolymers are acrylates/dimethicone copolymers such as
those commercially available from Shin-Etsu, for example, the
product sold under the tradename KP-545, or acrylates/stearyl
acrylate/dimethicone acrylates copolymers, such as those
commercially available from Shin-Etsu, for example, the product
sold under the tradename KP-561, and acrylates/behenyl
acrylate/dimethicone acrylates copolymer, such as those
commercially available from Shin-Etsu, for example, the product
sold under the tradename KP-562.
[0245] Other non-limiting examples of silicone film formers
suitable for use in the present invention are silicone esters
comprising units of formulae (XIV) and (XV), disclosed in U.S. Pat.
Nos. 6,045,782, 5,334,737, and 4,725,658, the disclosures of which
are hereby incorporated by reference:
R.sub.aR.sup.E.sub.bSiO.sub.[4-(a+b)/2] (XIV); and
R'.sub.xR.sup.E.sub.ySiO.sub.1/2 (XV)
wherein
[0246] R and R', which may be identical or different, are each
chosen from optionally substituted hydrocarbon groups;
[0247] a and b, which may be identical or different, are each a
number ranging from 0 to 3, with the proviso that the sum of a and
b is a number ranging from 1 to 3,
[0248] x and y, which may be identical or different, are each a
number ranging from 0 to 3, with the proviso that the sum of x and
y is a number ranging from 1 to 3;
[0249] R.sup.E, which may be identical or different, are each
chosen from groups comprising at least one carboxylic ester.
[0250] In one embodiment, R.sup.E groups are chosen from groups
comprising at least one ester group formed from the reaction of at
least one acid and at least one alcohol. In another embodiment, the
at least one acid comprises at least two carbon atoms. In another
embodiment, the at least one alcohol comprises at least ten carbon
atoms. Non-limiting examples of the at least one acid include
branched acids such as isostearic acid, and linear acids such as
behenic acid. Non-limiting examples of the at least one alcohol
include monohydric alcohols and polyhydric alcohols, such as
n-propanol and branched etheralkanols such as
(3,3,3-trimethylolpropoxy)propane.
[0251] Further non-limiting examples of the at least one silicone
film former include liquid siloxy silicates and silicone esters
such as those disclosed in U.S. Pat. No. 5,334,737, the disclosure
of which is hereby incorporated by reference, such as diisostearoyl
trimethylolpropane siloxysilicate and dilauroyl trimethylolpropane
siloxy silicate, which are commercially available from General
Electric under the tradenames SF 1318 and SF 1312,
respectively.
[0252] Yet further non-limiting examples of the at least one
silicone film former include polymers comprising a backbone chosen
from vinyl polymers, methacrylic polymers, and acrylic polymers and
at least one chain chosen from pendant siloxane groups and pendant
fluorochemical groups. Non-limiting examples of such polymers
comprise at least one unit derived from at least one A monomer, at
least one unit derived from at least one C monomer, at least one
unit derived from D monomers, and, optionally, at least one unit
derived from at least one B monomer, wherein:
[0253] A, which may be identical or different, are each chosen from
free-radically-polymerizable acrylic esters of at least one alcohol
chosen from 1,1,-dihydroperfluoroalkanols,
omega-hydridofluoroalkanols, fluoroalkylsulfonamido alcohols,
cyclic fluoroalkyl alcohols, and fluoroether alcohols, and analogs
of any of the foregoing at least one alcohols, and
free-radically-polymerizable methacrylic esters of at least one
alcohol chosen from 1,1,-dihydroperfluoroalkanols,
omega-hydridofluoroalkanols, fluoroalkylsulfonamido alcohols,
cyclic fluoroalkyl alcohols, and fluoroether alcohols, and analogs
of any of the foregoing at least one alcohols;
[0254] B, which may be identical or different, are each chosen from
reinforcing monomers which are copolymerizable with at least one A
monomer;
[0255] C, which may be identical or different, are each chosen from
monomers having the formula:
X(Y).sub.nSi(R).sub.3-mZ.sub.m
[0256] wherein
[0257] X is chosen from vinyl groups which are copolymerizable with
at least one A monomer and at least one B monomer,
[0258] Y is chosen from divalent allylene groups, divalent arylene
groups, divalent alkarylene groups, and divalent aralkylene groups,
wherein the groups comprise from 1 to 30 carbon atoms, and further
wherein the groups optionally further comprise at least one group
chosen from ester groups, amide groups, urethane groups, and urea
groups;
[0259] n is zero or 1;
[0260] m is a number ranging from 1 to 3;
[0261] R, which may be identical or different, are each chosen from
hydrogen, C.sub.1-C.sub.4 alkyl groups, aryl groups, and alkoxy
groups; and
[0262] Z, which may be identical or different, are each chosen from
monovalent siloxane polymeric groups; and
[0263] D, which may be identical or different, are each chosen from
free-radically-polymerizable acrylate copolymers and
free-radically-polymerizable methacrylate copolymers. Such polymers
and their manufacture are disclosed in U.S. Pat. Nos. 5,209,924 and
4,972,037, and WO 01/32737, the disclosures of which are hereby
incorporated by reference.
[0264] Other non-limiting examples of the at least one silicone
film former include silicone/acrylate graft terpolymers, for
example, those having the formula:
##STR00040##
[0265] wherein
[0266] a, b, and c are present in a weight ratio of 69.9:0.1:30
respectively,
[0267] R and R.sub.1, which may be identical or different, are each
chosen from hydrogen and C.sub.1-C.sub.6 alkyl groups; and
[0268] m is a number ranging from 100-150.
[0269] In an embodiment, m is chosen to provide a macromer having a
molecular weight ranging from 8,000 to 12,000, such as 10,000. In
another embodiment, m is a number ranging from 124-135, such as
130. Non-limiting examples of these copolymers are described in WO
01/32727 A1, the disclosure of which is hereby incorporated by
reference.
[0270] Still other examples of suitable silicone film formers
include copolymers comprising a backbone chosen from vinyl
backbones, methacrylic backbones, and acrylic polymeric backbones
and further comprising at least one pendant siloxane group.
Non-limiting examples of such polymers are disclosed in U.S. Pat.
Nos. 4,693,935, 4,981,903, 4,981,902, the disclosures of which are
hereby incorporated by reference.
[0271] In an embodiment, the at least one copolymer comprises at
least one A monomer, at least one C monomer, and, optionally at
least one
[0272] B monomer, wherein the at least one A monomer is chosen from
free-radically-polymerizable vinyl monomers,
free-radically-polymerizable methacrylate monomers, and
free-radically-polymerizable acrylate monomers; the at least one B
monomer, if present, is chosen from at least one reinforcing
monomer copolymerizable with the at least one A monomer, and the at
least one C monomer is chosen from monomers having the formula:
X(Y).sub.nSi(R).sub.3-mZ.sub.m
wherein:
[0273] X is chosen from vinyl groups which are copolymerizable with
the at least one A monomer and with the at least one B monomer;
[0274] Y is chosen from divalent groups;
[0275] n is zero or 1;
[0276] m is a number ranging from 1 to 3;
[0277] R, which may be identical or different, are each chosen from
hydrogen, optionally substituted C.sub.1-C.sub.10 alkyl groups,
optionally substituted phenyl groups, and optionally substituted
C.sub.1-C.sub.10 alkoxy groups; and
[0278] Z, which may be identical or different, are each chosen from
monovalent siloxane polymeric groups.
[0279] Non-limiting examples of A monomers include methacrylic acid
esters of C.sub.1-C.sub.12 linear alcohols, methacrylic acid esters
of C.sub.1-C.sub.12 of branched alcohols, styrene monomers, vinyl
esters, vinyl chloride monomers, vinylidene chloride monomers, and
acryloyl monomers.
[0280] Non-limiting examples of B monomers include acrylic monomers
comprising at least one group chosen from hydroxyl, amino, and
ionic groups, and methacrylic monomers comprising at least one
group chosen from hydroxyl, amino, and ionic groups. Non-limiting
examples of ionic groups include quaternary ammonium groups,
carboxylate salts, and sulfonic acid salts.
[0281] The C monomers are the same as those described for the C
monomers in the previous paragraphs.
[0282] Other non-limiting examples of the silicone film-former
include a copolymer chosen from vinyl-silicone graft copolymers
having the following formula and vinyl-silicone block copolymers
having the following formula:
##STR00041##
wherein
[0283] G.sub.5, which may be identical or different, are each
chosen from alkyl groups, aryl groups, aralkyl groups, alkoxy
groups, alkylamino groups, fluoroalkyl groups, hydrogen, and --ZSA
groups, wherein
[0284] A is chosen from vinyl polymeric segments comprising at
least one polymerized free-radically-polymerizable monomer, and
[0285] Z is chosen from divalent C.sub.1-C.sub.10 alkylene groups,
divalent aralkylene groups, divalent arylene groups, and divalent
alkoxylalkylene groups. In an embodiment Z is chosen from methylene
groups and propylene groups.
[0286] G.sub.6, which may be identical or different, are each
chosen from alkyl groups, aryl groups, aralkyl groups, alkoxy
groups, alkylamino groups, fluoroalkyl groups, hydrogen, and --ZSA
groups, as defined above;
[0287] G.sub.2 comprises A;
[0288] G.sub.4 comprises A;
[0289] R.sub.1, which may be identical or different, are each
chosen from alkyl groups, aryl groups, aralkyl groups, alkoxy
groups, alkylamino groups, fluoroalkyl groups, hydrogen, and
hydroxyl. In one embodiment, R.sub.1 is chosen from C.sub.1-C.sub.4
alkyl groups, such as methyl groups, and hydroxyl.
[0290] R.sub.2, which may be identical or different, are each
chosen from divalent C.sub.1-10 alkylene groups, divalent arylene
groups, divalent aralkylene groups, and divalent alkoxyalkylene
groups. In one embodiment, R.sub.2 is chosen from divalent
C.sub.1-C.sub.3 alkylene groups and divalent C.sub.7-C.sub.10
aralkylene groups. In another embodiment, R.sub.2 is chosen from
--CH.sub.2-- groups and divalent 1,3-propylene groups.
[0291] R.sub.3, which may be identical or different, are each
chosen from alkyl groups, aryl groups, aralkyl groups alkoxy
groups, alkylamino groups, fluoroalkyl groups, hydrogen, and
hydroxyl. In one embodiment, R.sub.3 is chosen from C.sub.1-C.sub.4
alkyl groups and hydroxyl. In another embodiment, R.sub.3 is chosen
from methyl groups.
[0292] R.sub.4, which may be identical or different, are each
chosen from divalent C.sub.1-C.sub.10 alkylene groups, divalent
arylene groups, divalent aralkylene groups, and divalent
alkoxyalkylene groups. In one embodiment, R.sub.4 is chosen from
divalent C.sub.1-C.sub.3 alkylene groups and divalent
C.sub.7-C.sub.10 aralkylene groups. In another embodiment, R.sub.4
is chosen from divalent --CH.sub.2-- groups and divalent
1,3-propylene groups.
[0293] x is a number ranging from 0 to 3;
[0294] y is a number greater than or equal to 5. In an embodiment,
y ranges from 10 to 270, and in another embodiment, y ranges from
40 to 270.
[0295] q is a number ranging from 0 to 3;
[0296] Non-limiting examples of these polymers are described in
U.S. Pat. No. 5,468,477, the disclosure of which is hereby
incorporated by reference. A non-limiting example of such polymers
is poly(dimethylsiloxane)-g-poly(isobutyl methacrylate), which is
commercially available from 3M Company under the tradename VS 70
IBM.
[0297] According to preferred embodiments, the silicone film former
is present in the composition in an amount ranging from 0.1% to 30%
by weight relative to the total weight of the composition.
Preferably, the silicone film former is present in an amount
ranging from 0.5% to 20% by weight relative to the total weight of
the composition, and more preferably from 1% to 10%. One of
ordinary skill in the art will recognize that the silicone film
former of the present invention may be commercially available, and
may come from suppliers in the form of a dilute solution. The
amounts of the silicone film former disclosed herein therefore
reflect the weight percent of active material.
[0298] In a preferred embodiment, the polyorganosilxane polymer and
the film forming agent are solid. The composition is prepared by
heating the solids sufficient to combine and form compositions as
described herein. This combination of solid polyorganosilxane
polymer and film forming agent provide beneficial
transfer-resistant, long-wear compositions.
[0299] Organogelator
[0300] According to the invention, the composition comprises at
least one organogelator. An organogelator is defined herein to
include a non-polymeric organic compound whose molecules may be
capable of establishing, between themselves, at least one physical
interaction leading to a self-aggregation of the molecules with
formation of a macromolecular 3-D network which may be responsible
for the gelation of the liquid fatty phase. The network can result
from the formation of a network of fibrils (due to the stacking or
aggregation of organic-gelling molecules), immobilizing the
molecules of the liquid fatty phase. Depending on the nature of the
organogelator, the interconnected fibrils have variable dimensions
which may range up to one micron, or even several microns. These
fibrils may occasionally combine to form strips or columns.
[0301] The term "gelation" means a thickening of the medium which
may result in a gelatinous consistency and even in a solid, rigid
consistency which does not flow under its own weight. The ability
to form this network of fibrils, and thus the gelation, depends on
the nature (or chemical category) of the organogelator, the nature
of the substituents borne by its molecules for a given chemical
category, and the nature of the liquid fatty phase. For example,
this gelation is reversible.
[0302] The physical interactions are diverse but may exclude
co-crystallization. These physical interactions are, for instance,
interactions chosen from self-complementary hydrogen interactions,
.pi. interactions between unsaturated rings, dipolar interactions,
and coordination bonding with organometallic derivatives. The
establishment of these interactions may often be promoted by the
architecture of the molecule, such as by rings, unsaturations, and
the presence of asymmetric carbons. In general, each molecule of an
organogelator can establish several types of physical interaction
with a neighboring molecule. Thus, in one embodiment, the molecules
of the organogelator according to the invention may comprise at
least one group capable of establishing hydrogen bonding, e.g., at
least two groups capable of forming hydrogen bonding; at least one
aromatic ring, e.g., at least two aromatic rings; at least one bond
with ethylenic unsaturation; and/or at least one asymmetric carbon.
The groups capable of forming hydrogen bonding may, for example, be
chosen from hydroxyl, carbonyl, amine, carboxylic acid, amide and
benzyl groups.
[0303] The at least one organogelator of the invention may be
soluble in the liquid fatty phase at room temperature and
atmospheric pressure. They may be solid or liquid at room
temperature and atmospheric pressure.
[0304] Organogelator(s) which can be used in the invention are, for
example, those described in the document "Specialist Surfactants"
edited by D. Robb, 1997, pp. 209-263, chapter 8, by P. Terech, and
the French patent application nos. (FR-A-2796276) 99/09178 and
00/09317 (or FR-A-2811552), the disclosures of which are
incorporated by reference herein. The organogelators described in
these documents are, for example, chosen from: [0305] hydroxylated
carboxylic fatty acids having a linear or branched aliphatic carbon
chain containing, in one embodiment, at least 8 carbon atoms, such
as at least 12 carbon atoms, for instance 12-hydroxystearic acid
and 12-hydroxyoleic acid and salts thereof, such as alkali metal
salts (in particular Li, Na and K salts) and alkaline-earth metal
(for example Mg) salts or esters thereof resulting from
esterification of a mono alcohol or polyol having a linear or
cyclic, saturated or not chain with from 1 to 6 carbon atoms;
[0306] amides of carboxylic acids, such as tricarboxylic acids, for
instance the cyclohexanetricarboxamides (see patent application
FR-A-2796276, the disclosure of which is incorporated by
reference), these amides corresponding, for example, to formula
(III) below; [0307] amino acid amides or esters, for instance
alanine esters and valine amides (such as those described in the
book "Specialist Surfactants"); [0308] N-acylamino acid amides, for
instance the diamides resulting from the action of an N-acylamino
acid with amines containing from 1 to 22 carbon atoms, such as
those disclosed in document WO-93/23008, the disclosure of which is
incorporated by reference, for example, N-acylglutamides in which
the acyl group is a C.sub.8 to C.sub.22 alkyl chain, and
N-laurylglutamic acid dibutylamide, such as the product sold or
made by the company Ajinomoto under the name GP-1; [0309] diamides
having hydrocarbon-based chains each containing from 1 to 22 carbon
atoms, for example, from 6 to 18 carbon atoms, these
hydrocarbon-based chains being optionally substituted with ester,
urea or fluoro groups (see patent application FR 00/09317, the
disclosure of which is incorporated by reference), these diamides
being, for example, those of formula (II) hereafter; and such as
those resulting from the reaction of diaminocyclohexane, for
example, trans-diaminocyclohexane, and of acid chloride; [0310]
steroid amines or amides, such as those from deoxycholic acid,
cholic acid, apocholic acid or lithocholic acid and salts thereof,
for instance
D-17,17-dipropyl-17a-aza-5.alpha.-homoandrostan-3.beta.-ol or
D-17,17-dipropyl-17a-aza-5.alpha.-homoandrostan-3.beta.-ol
17a-oxy;
[0311] compounds containing several aromatic rings (2 or 3), such
as anthryl derivatives comprising at least 2 alkyl chains
containing from 8 to 30 carbon atoms, for instance
2,3-bis(n-decyloxy)anthracene or 2,3-bis(n-decyloxy)anthraquinone,
or comprising a steroid group, for instance cholesteryl
4-(2-anthryloxy)butanoate or cholesteryl
anthraquinone-2-carboxylate and derivatives thereof;
[0312] azobenzene steroids such as those described in the book
"Specialist Surfactants";
[0313] organometallic compounds, for instance mononuclear copper
.beta.-diketonate (the octasubstituted copper complex of
bis(3,4-nonyloxybenzoyl) methanes), binuclear copper
tetracarboxylates or the Zn (II) complexes of trisubstituted
(para-carboxyphenyl)porphyrine;
[0314] surfactants in salt form comprising at least two linear or
branched alkyl chains, such as alkali metal or aluminium alkyl
phosphates comprising two alkyl chains containing from 8 to 30
carbon atoms, for instance the aluminium salt of hexadecyl
phosphate (C.sub.16DP-Al) or bis(2-ethylhexyl)phosphate and alkali
metal (Na) salts thereof, bis(2-ethylhexyl)sulphosuccinate and the
alkali metal (Na) salts thereof; [0315] benzylidene sorbitols or
alditols and derivatives thereof, for instance 1,3:
2,4-di-o-benzylidene-D-sorbitol; [0316] cyclodipeptides which are
cyclic condensates of two amino acids such as those disclosed in
the book "Specialist Surfactants"; [0317] cyclic compounds or
alkylene compounds comprising two urea or urethane groups such as
dialkylurea cyclohexane, having, for example, the formula (IV)
below; [0318] alkylaryl cyclohexanol derivatives in which the alkyl
chain is linear or branched and comprises from 1 to 22 carbon atoms
and the aryl portion is, for example, a phenyl group, these
derivatives being, for instance, 4-tert-butyl-1-phenyl
cyclohexanol; [0319] callixarenes such as those mentioned in the
book "Specialist Surfactants"; [0320] associations of
2,4,6-tri-aminopyrimidine substituted by an alkyl chain and dialkyl
barbituric acid, the alkyl chains of which are linear or branched
and comprise from 1 to 22 carbon atoms; [0321] compounds such as
those described in the document WO-A-01/07007, the disclosure of
which is herein incorporated by reference, and having the following
formula (V):
[0321] Q-O--W--(CHOH).sub.s--W.sup.1--O-Q.sup.1 (V)
[0322] in which W and W.sup.1, which may be identical or different,
are chosen from
[0323] --CH.sub.2--, --CO-- and in which Q and Q.sup.1, which may
be identical or different, are a hydrocarbon-based chain chosen
from saturated or unsaturated linear or branched hydrocarbon-based
chains containing at least 6 carbon atoms, and in which s is an
integer from 2 to 4; such as the compounds in which
W.dbd.W.sup.1=--CH.sub.2-- and s=2 and the compounds in which
W.dbd.W.sup.1=--CO-- and s=4; [0324] gluconamide derivatives such
as those disclosed in the article R. J. H HAFKAMP, Chem. Commun.,
(1997), pages 545-46 and in the article, J. org. Chem, vol 64,
N.sub.o2; 412-26 (1999), the disclosures of which are herein
incorporated by reference and having a formula (VI):
[0324] R.sub.1--NH--CO--[CH(OH)].sub.4--CH.sub.2R.sub.2 (VI)
[0325] in which R.sup.1 is a hydrocarbon-based chain chosen from
saturated or unsaturated linear, branched and cyclic
hydrocarbon-based chains having 1 to 30 carbon atoms; this
hydrocarbon-based chain optionally can comprise at least one hetero
atom such as N, O and S; and for example the compounds in which
R.sub.2=--O--CO--R.sub.3 or --O--R.sub.3 with R.sub.3 chosen from
linear and branched alkyl chains containing 1 to 20 carbon atoms,
C.sub.5-C.sub.8 cycloaliphatic and aromatic chains, C.sub.5-C.sub.8
heterocycles comprising N, O or S atoms, and for example the
compounds in which R.sub.2 is a C.sub.5-C.sub.8 saturated or
unsaturated heterocycles comprising N, O, S atom such as R.sub.2 is
imidazolyl group; and [0326] cyclic ether derivatives of compound
of formula VI, having the formula VI':
##STR00042##
[0327] wherein R.sub.1 and R.sub.2 has the same meaning as defined
in formula (VI). [0328] bis oxalylamides of aminoacides such as
those mentioned in the article M. JOKIC, J. chem. soc., chem.
commun., pages 1723-24 (1995), the disclosure of which is herein
incorporated by reference, and for example having the formula
VII:
[0328] HOCO--CH(R.sub.1)--NH--CO--CO--NH--CH(R.sub.2)--COOH
(VII)
[0329] in which R.sub.1 and R.sub.2 may be identical or different,
are a group chosen from
--CH.sub.2--CH(CH.sub.3).sub.2; --C.sub.6H.sub.5;
--CH.sub.2--C.sub.6H.sub.5; --CH(CH.sub.3).sub.2; [0330] amide and
urea derivatives of lysine ester such as those mentioned in the
article K. HANABUSA, Chemistry Letters, p 1070-71 (2000), the
disclosure of which is herein incorporated by reference, such as
N.sup..epsilon.-lauroyl-N.sup..alpha.-stearyl
aminocarbonyl-L-lysine(ethyl or methyl)ester and derivatives having
a formula:
C.sub.11--H.sub.23--CO--NH--(CH.sub.2).sub.4--CH(COOR.sub.1)--NH-
--CO--R.sub.2;
[0331] in which R.sub.1=--CH.sub.3 or --C.sub.2H.sub.5 and
R.sub.2=--NH--(CH.sub.2).sub.17--CH.sub.3,
--NH--(CH.sub.2).sub.n--CH.sub.3 [0332] derivatives from diamides
benzene dicarboxylic of acides and valine such as those mentioned
in the article K. HANABUSA, Chemistry Letters, 767-8 (1999), the
disclosure of which is herein incorporated by reference, and for
example:
[0333] in which -L-Val- represents:
--NH--CH(CH(CH.sub.3).sub.2)--CO--; [0334] monoalkyloxamides such
as those disclosed by X. LUO, Chem. Commun., 2091-92, (2000), the
disclosure of which is herein incorporated by reference, and for
example having the formula:
[0334] R.sub.1--NH--CO--CO--NH--R.sub.2
[0335] In which R.sub.1 and R.sub.2 which can be identical or
different are a hydrocarbon-based chain chosen from saturated or
unsaturated linear, branched and cyclic hydrocarbon-based chains
having 1 to 30 carbon atoms; [0336] bolaamphiphiles having
1-glucosamide head, such as
N,N'-bis(.beta.-D-glucopyranosyl)alcane-1, n-dicarboxamide, these
compounds being mentioned in the article T. SHIMIZU, J. Am. Chem.
Soc., 119, 2812-18 (1997), the disclosure of which is herein
incorporated by reference, and has the formula VIII:
##STR00043##
[0336] in which n is an integer from 2 to 30, R is --H or
--CO--R.sub.1 in which R.sub.1 is a C.sub.1-C.sub.20 alkyl group,
and for example the compound in which R=--CO--CH.sub.3 [0337]
alkyl-2-ammonium-2-isobutylacetate p-toluene sulfonate such as
those disclosed by K. HANABUSA, Colloid Polym. Sci, 276, 252-59
(1998), the disclosure of which is herein incorporated by
reference, and having the formula XII:
[0337] p-CH.sub.3--C.sub.6H.sub.4--SO.sub.3.sup.-
+H.sub.3N--CH(R.sub.1)--CO--OR.sub.2 (XII)
[0338] in which R.sub.1=--CH.sub.2--CH(CH.sub.3).sub.2;
--CH(CH.sub.3).sub.2; --CH(CH.sub.3)--CH.sub.2--CH.sub.3,
--CH.sub.2--C.sub.6H.sub.5
[0339]
--CH.sub.2--CH.sub.2--CO--O--CH.sub.2--(CH.sub.2).sub.10--CH.sub.3
and R.sub.2=--CH.sub.2--(CH.sub.2).sub.n--CH.sub.3 with n an
integer from 4 to 12.
[0340]
--(CH.sub.2).sub.2--CH(CH.sub.3)--(CH.sub.2).sub.3--CH(CH.sub.3).su-
b.2
[0341] cellobiose fatty esters, such a those mentioned in
WO-A-00/61080, the disclosure of which is herein incorporated by
reference, and WO-A-00/61081, the disclosure of which is herein
incorporated by reference, and having the formula XIII:
##STR00044##
[0342] in which R=--CO--R1 and R1=alkyl or alkylene group with 5 to
12 carbon atoms.
[0343] diamides having the formula XIV or XV
R.sub.2--X--CO--NH--R.sub.1--NH--CO--X--R.sub.2 (XIV) or
R.sub.2--CO--NH--R.sub.1--NH--CO--R.sub.2 (XV)
[0344] in which R.sub.1 is alkylene group chosen from
C.sub.1-C.sub.50 linear, branched and cyclic groups and
C.sub.5-C.sub.8 arylene groups and alkylene groups comprising
C.sub.1-C.sub.4 alkyl group; and in which --X-- represents --O-- or
--NH--; and in which R.sub.2, which may be identical or different
is a C.sub.8-C.sub.60 saturated or unsaturated linear or branched
hydrocarbon-based chain, at least one R.sub.2 comprising optionally
a hydroxyl group or at least one hetero atom such as N, O, S or Si.
[0345] and mixtures thereof.
[0346] In one embodiment, amino acid amides such as N-acylamino
acids and cyclohexane tricarboxamides, and mixtures thereof, are
used.
[0347] Organogelator of Formula (II)
[0348] According to the invention, the organogelator may be a
compound of formula (II) below:
R--CO--NH-A-NH--CO--R'
[0349] in which: [0350] R and R', which may be identical or
different, are chosen from a hydrogen atom and hydrocarbon-based
chains chosen from saturated linear, saturated branched, saturated
cyclic, unsaturated linear, unsaturated branched and unsaturated
cyclic hydrocarbon-based chains containing from 1 to 22 carbon
atoms, for example from 6 to 18 carbon atoms, such as from 10 to 14
carbon atoms, optionally substituted with at least one group chosen
from aryl (--C.sub.6H.sub.5), ester (--COOR'' with R'' being an
alkyl group containing 2 to 12 carbon atoms), amide (--CONHR'' with
R'' being an alkyl group containing from 2 to 12 carbon atoms),
urethane (--OCONHR'' with R'' being an alkyl group containing from
2 to 12 carbon atoms) and urea (--NHCONHR'' with R'' being an alkyl
group containing from 2 to 12 carbon atoms) groups; and/or
optionally containing from 1 to 3 hetero atoms chosen from O, S and
N; and/or optionally substituted with from 1 to 4 halogen atoms, in
particular fluorine atoms, and/or with from 1 to 3 hydroxyl
radicals,
[0351] with the proviso that R and/or R' is other than hydrogen,
and
[0352] A is chosen from saturated and unsaturated, linear, cyclic
and branched hydrocarbon-based chains containing from 1 to 18
carbon atoms, such as from 2 to 12 carbon atoms, and for example
from 4 to 12 carbon atoms, optionally substituted with at least one
group chosen from aryl (--C.sub.6H.sub.5), ester
[0353] (--COOR'' with R'' being an alkyl group containing from 2 to
12 carbon atoms), amide (--CONHR'' with R'' being an alkyl group
containing from 2 to 12 carbon atoms), urethane (--OCONHR'' with
R'' being an alkyl group containing from 2 to 12 carbon atoms) and
urea (--NHCONHR'' with R'' being an alkyl group containing from 2
to 12 carbon atoms) groups; and/or optionally containing from 1 to
3 hetero atoms chosen from O, S and N; and/or optionally
substituted with from 1 to 4 halogen atoms, such as fluorine atoms,
and/or with from 1 to 3 hydroxyl radicals.
[0354] According to formula (II), the expression "unsaturated
hydrocarbon-based chain" means a chain which comprises at least one
C.dbd.C double bond or at least one C.ident.C triple bond, it being
possible for the chain also to be optionally substituted with at
least one group chosen from aryl, ester, amide, urethane and urea
groups; and/or optionally to comprise at least one hetero atom
chosen from O, S and N; and/or optionally to be substituted with at
least one fluorine atom and/or hydroxyl radical. The expression
"hydrocarbon-based chain according to formula (II) comprising an
oxygen, sulphur or nitrogen atom" includes, in particular, a
hydrocarbon-based chain comprising a carbonyl (C.dbd.O), amine
(--NH.sub.2 or --NH--), thiol (--SH), thioether or ether group.
[0355] The compounds, for example, correspond to the formula (II)
in which: [0356] A is chosen from saturated and unsaturated but
non-aromatic, optionally branched hydrocarbon-based rings
containing from 4 to 12 carbon atoms, for example from 5 to 7
carbon atoms, optionally substituted with the substituents
mentioned above and/or optionally comprising at least one hetero
atom and/or optionally substituted with at least one halogen and/or
hydroxyl radical; [0357] R and R', which may be identical or
different, are chosen from a hydrogen atom and hydrocarbon-based
chains chosen from saturated linear, saturated branched, saturated
cyclic, unsaturated linear, unsaturated branched and unsaturated
cyclic hydrocarbon-based chains containing from 10 to 16 carbon
atoms, for example, from 12 to 14 carbon atoms, such as a
saturated, linear hydrocarbon-based chain; or [0358] A is a
saturated hydrocarbon-based chain chosen from linear and branched
saturated hydrocarbon-based chains containing from 2 to 18 carbon
atoms, for example from 3 to 12 carbon atoms, optionally
substituted with the substitutents mentioned above, and/or
optionally comprising at least one hetero atom and/or optionally
substituted with at least one halogen and/or hydroxyl radical;
[0359] R and R', which may be identical or different, are chosen
from a hydrogen atom and a hydrocarbon-based chain chosen from
saturated linear, saturated branched, saturated cyclic, unsaturated
linear, unsaturated branched and unsaturated cyclic
hydrocarbon-based chains, such as saturated, linear,
hydrocarbon-based chains containing from 10 to 20 carbon atoms, for
example, from 11 to 18 carbon atoms;
[0360] or alternatively [0361] A is chosen from aryl and aralkyl
rings containing from 4 to 12 carbon atoms, for instance from 5 to
8 carbon atoms, optionally substituted with the substituents
mentioned above and/or optionally comprising at least one hetero
atom and/or optionally substituted with at least one halogen and/or
hydroxyl radical; [0362] R and R', which may be identical or
different, are chosen from a hydrogen atom and hydrocarbon-based
chains chosen from saturated linear, saturated branched, saturated
cyclic, unsaturated linear, unsaturated branched and unsaturated
cyclic hydrocarbon-based chains, such as a saturated, linear,
hydrocarbon-based chain, containing from 6 to 18 carbon atoms, for
example from 10 to 16 carbon atoms.
[0363] The radical A may be, for example, a divalent radical such
as cyclohexylene, ethylene, propylene, isopropylene, butylene,
isobutylene, pentylene, hexylene, dodecylene, dodecanylene,
benzylene, phenylene, methylphenylene, bis-phenylene or
naphthalene.
[0364] The radicals R and R' may be chosen, independently of each
other, from, for example, pentyl, hexyl, decyl, undecyl, dodecyl,
pentadecyl, hexadecyl, heptadecyl, octadecyl,
3-dodecyloxypropionyl, 3-octadecyloxy-propionyl,
3-dodecyloxypentyl, 3-octadecyloxypentyl and 11-hydroxyheptadecyl
radicals. In one embodiment R and R' are identical.
[0365] When the radical A is cyclic, the radicals R--CO--NH-- and
R'--CO--NH-- may be in an ortho, meta or para position. Moreover,
they may be in a cis or trans position relative to each other. In
one embodiment, the compounds of formula (II) is a mixture of cis
and trans compounds.
[0366] The compounds of formula (II) may be chosen from the
compounds corresponding to one of the following formulae:
##STR00045##
[0367] in which R and R' have the same meanings as above.
[0368] Among the compounds which may be used as organogelators in
the composition of the invention, mention may be made of: [0369]
N,N'-bis(dodecanoyl)-1,2-diaminocyclohexane, in particular in trans
form (compound of formula (II) with R.dbd.R'=n-C.sub.11H.sub.23 and
A=1,2-cyclohexylene divalent radical, also known as
(2-dodecanoylaminocyclohexyl)dodecanamide. This compound is
described in particular in Hanabusa, K; Angew. Chem., 108, 1997,
17, pages 2086-2088, [0370]
N,N'-bis(dodecanoyl)-1,3-diaminocyclohexane, in particular in trans
form (compound of formula (II) with R.dbd.R'=n-C.sub.11H.sub.23 and
A=1,3-cyclohexylene divalent radical, also known as
(3-dodecanoylaminocyclohexyl-dodecanamide), [0371]
N,N'-bis(dodecanoyl)-1,4-diaminocyclohexane, in particular in trans
form (compound of formula (II) with R=n-C.sub.11H.sub.23 and
A=1,4-cyclohexylene divalent radical, also known as
(4-dodecanoylaminocyclohexyl)dodecanamide), [0372]
N,N'-bis(dodecanoyl)-1,2-ethylenediamine (compound of formula (II)
with R.dbd.R'=n-C.sub.11H.sub.23 and A=1,2-ethylene divalent
radical, also known as (2-dodecanoylaminoethyl)dodecanamide),
[0373] N,N'-bis(dodecanoyl)-1-methyl-1,2-ethylenediamine (compound
of formula (II) with R.dbd.R'=n-C.sub.11H.sub.23 and
A=1-methyl-1,2-ethylene divalent radical, also known as
(2-dodecanoylamino-2-methylethyl)dodecanamide), [0374]
N,N'-bis(dodecanoyl)-1,3-diaminopropane (compound of formula (II)
with R.dbd.R'=n-C.sub.11H.sub.23 and A=1,3-propylene divalent
radical, also known as (2-dodecanoylaminopropyl)dodecanamide),
[0375] N,N'-bis(dodecanoyl)-1,12-diaminododecane (compound of
formula (II) with R.dbd.R'=n-C.sub.11H.sub.23 and A=1,12-dodecylene
divalent radical, also known as
(2-dodecanoylaminododecyl)dodecanamide), [0376]
N,N'-bis(dodecanoyl)-3,4-diaminotoluene (compound of formula (II)
with R.dbd.R'=n-C.sub.11H.sub.23 and A=1-methyl-3,4-phenylene
divalent radical, also known as
(2-dodecanoylamino-4-methylphenyl)dodecanamide).
[0377] The compounds of formula (II) can be prepared according to
processes that are well known to those skilled in the art.
[0378] In particular, they may be obtained by reacting a diamine
H.sub.2N-A-NH.sub.2 with an acid chloride RCOCl and/or R'COCl with
R and R' having the above meaning, but other than a hydrogen atom,
in an organic solvent medium which is compatible for carrying out
the reaction (1 mol of acid chloride is used per 1 mol of diamine
if it is desired to obtain a compound of formula (I) containing
only one group R other than a hydrogen atom, or 2 mol of acid
chloride RCOCl and/or R'COCl if it is desired to obtain a compound
of formula (II) with R and R' other than a hydrogen atom). The
reaction is preferably carried out in the presence of a base
capable of neutralizing the formation of the HCl released during
the reaction. The diamide formed is extracted from the reaction
medium according to the conventional extraction techniques that are
well known to those skilled in the art.
[0379] The compounds of formula (II) can be prepared according to
processes that are well known to those skilled in the art and can
be used, alone or as a mixture, in the composition of the
invention.
[0380] Standard preparation of the compounds of formula (II) for
R.dbd.R'
[0381] The diamine and two equivalents of triethylamine are
dissolved in 50 ml of tetrahydrofuran. Two equivalents of acyl
chloride dissolved in THF are added and the reaction mixture is
heated to the reflux point of the tetrahydrofuran, while monitoring
the disappearance of the acyl chloride by infrared spectroscopy
(most typically, two hours). The solution is filtered from the
precipitate, the organic phase is concentrated and a liquid/liquid
extraction is performed on the solid compound obtained. The organic
phase is subsequently dried and then concentrated, and the solid
product obtained is recrystallized.
[0382] Organogelator of formula (III)
##STR00046##
[0383] in which: [0384] R is identical or different and each is
chosen from a hydrogen atom, a saturated linear hydrocarbon-based
chain, and a saturated branched hydrocarbon-based chain, wherein
said hydrocarbon-based chains contain from 1 to 6 carbon atoms, for
example from 1 to 4 carbon atoms; [0385] Y is identical or
different and each is a group chosen from the following groups:
--CO--S--R'; --CO--NHR'; --NH--COR' and --S--COR'; in which R' is
identical or different and each is chosen from: [0386] a hydrogen
atom; [0387] an aryl group; [0388] an aralkyl group, i.e., an aryl
group substituted with a hydrocarbon-based chain chosen from
saturated, linear hydrocarbon-based chains and saturated, branched
hydrocarbon-based chains, wherein the hydrocarbon based chain
contains from 1 to 22 carbon atoms, for example from 10 to 18
carbon atoms; and [0389] a saturated hydrocarbon-based chain chosen
from linear, branched and cyclic hydrocarbon-based chains
containing from 1 to 22 carbon atoms, for example from 10 to 18
carbon atoms, optionally substituted with at least one group chosen
from aryl, ester, amide and urethane groups; and/or optionally
comprising at least one hetero atom chosen from O, S and N; and/or
optionally substituted with at least one fluorine atom and/or
hydroxyl radical.
[0390] R, for example, is chosen from a hydrogen atom.
[0391] Y, for example, is chosen from the groups --CO--NHR' and
--NH--COR'.
[0392] R', for example, is chosen from an aryl group; an aralkyl
group in which the linear or branched alkyl chain contains from
12-16 carbon atoms; and a linear or branched C.sub.11-C.sub.18
alkyl chain.
[0393] In one embodiment, Y is chosen from a group --CO--NHR' in
which R' is chosen from an aryl group substituted with a
C.sub.12-C.sub.16 alkyl chain chosen from linear and branched
C.sub.11-C.sub.16 alkyl chains; or R' is chosen from an
unsubstituted linear C.sub.11-C.sub.18 alkyl chain and an
unsubstituted branched C.sub.11-C.sub.18 alkyl chain.
[0394] The three substitutents represented by Y can be, in the
compounds of formula (III), in cis-cis, cis-trans or trans-trans
conformation relative to each other. In particular, at least one of
these substituents may be placed in an equatorial position on the
cyclohexane ring; for example, all the substituents Y are placed in
an equatorial position. In one embodiment, the compounds of formula
(III) is a mixture of cis-cis, cis-trans and/or trans-trans
compounds.
[0395] Among the compounds of formula (III) which can be used as an
organogelator, alone or as a mixture, in the composition of the
invention, mention may be made of: [0396]
cis-1,3,5-tris(dodecylaminocarbonyl)cyclohexane, [0397]
cis-1,3,5-tris(octadecylaminocarbonyl)cyclohexane, [0398]
cis-1,3,5-tris[N-(3,7-dimethyloctyl)-aminocarbonyl]cyclohexane,
[0399]
trans-1,3,5-trimethyl-1,3,5-tris(dodecylaminocarbonyl)cyclohexane,
and [0400]
trans-1,3,5-trimethyl-1,3,5-tris(octadecylaminocarbonyl)cyclohexan-
e.
[0401] The compounds of formula (III) are well known to those
skilled in the art and can be prepared according to the usual
processes.
[0402] It is also possible to add to the composition an organic
compound as set forth in U.S. Pat. No. 6,156,325, the disclosure of
which is incorporated by reference herein. Such compounds include
urea urethanes having the following formula:
R--O--CO--NH--R'--NH--CO--NH--R''--NH--CO--NH--R'--NH--CO--OR
[0403] wherein R represents C.sub.nH.sub.2n+1-- or
C.sub.mH.sub.2m+1 (C.sub.pH.sub.2pO).sub.r--; n represents an
integer having a value of from 4 to 22; m represents an integer
having a value of from 1 to 18; p represents an integer having a
value of from 2 to 4; and r represents an integer having a value of
from 1 to 10,
[0404] R' represents:
##STR00047##
[0405] and R'' represents:
##STR00048##
[0406] As is evident from the urea urethane formula above, the
alkyl groups and alkyl portions designated for the R variable are
saturated.
[0407] Organogelator of Formula (IV)
[0408] According to the invention the organogelator may be at least
one organogelator of formula (IV);
RNHCONHANHCONHR
[0409] wherein A and R have the same definition as the one provided
above for formula (II), expressed most broadly as:
[0410] R, which may be identical or different, is each chosen from
a hydrogen atom and hydrocarbon-based chains chosen from saturated
linear, saturated branched, saturated cyclic, unsaturated linear,
unsaturated branched and unsaturated cyclic hydrocarbon-based
chains containing from 1 to 22 carbon atoms, for example from 6 to
18 carbon atoms, optionally substituted with at least one group
chosen from aryl (--C.sub.6H.sub.5), ester (--COOR'' with R'' being
an alkyl group containing from 2 to 12 carbon atoms), amide
(--CONHR'' with R'' being an alkyl group containing from 2 to 12
carbon atoms), urethane (--OCONHR'' with R'' being an alkyl group
containing from 2 to 12 carbon atoms) and urea (--NHCONHR'' with
R'' being an alkyl group containing from 2 to 12 carbon atoms)
groups; and/or optionally containing from 1 to 3 hetero atoms
chosen from O, S and N; and/or optionally substituted with from 1
to 4 halogen atoms, in particular fluorine atoms, and/or with from
1 to 3 hydroxyl radicals,
[0411] with the proviso that at least one R is other than hydrogen,
and [0412] A is chosen from saturated and unsaturated, linear,
cyclic and branched hydrocarbon-based chains containing from 1 to
18 carbon atoms, such as from 2 to 12 carbon atoms, optionally
substituted with at least one group chosen from aryl
(--C.sub.6H.sub.5), ester (--COOR'' with R'' being an alkyl group
containing from 2 to 12 carbon atoms), amide (--CONHR'' with R''
being an alkyl group containing from 2 to 12 carbon atoms),
urethane (--OCONHR'' with R'' being an alkyl group containing from
2 to 12 carbon atoms) and urea
[0413] (--NHCONHR'' with R'' being an alkyl group containing from 2
to 12 carbon atoms) groups; and/or optionally containing from 1 to
3 hetero atoms chosen from O, S and N; and/or optionally
substituted with from 1 to 4 halogen atoms, such as fluorine atoms,
and/or with from 1 to 3 hydroxyl radicals.
[0414] In one embodiment, the inventive composition contains from
0.1% to 80% by weight of organogelator. In another embodiment, the
composition contains from 0.5% to 60% by weight of organogelator,
for example, from 1% to 40% or from 2% to 30%, including all values
and ranges there between.
[0415] According to preferred embodiments, cosmetic compositions
comprising at least one polyorganosiloxane containing polymer and
at least one coloring agent are provided. Preferably, such colored
cosmetic compositions are lip compositions (for example, lipstick
or liquid lip colors) or foundations.
[0416] According to this embodiment, the at least one coloring
agent is preferably chosen from pigments, dyes, such as liposoluble
dyes, nacreous pigments, and pearling agents.
[0417] Representative liposoluble dyes which may be used according
to the present invention include Sudan Red, DC Red 17, DC Green 6,
R-carotene, soybean oil, Sudan Brown, DC Yellow 11, DC Violet 2, DC
Orange 5, annatto, and quinoline yellow. The liposoluble dyes, when
present, generally have a concentration ranging up to 20% by weight
of the total weight of the composition, such as from 0.0001% to
6%.
[0418] The nacreous pigments which may be used according to the
present invention may be chosen from white nacreous pigments such
as mica coated with titanium or with bismuth oxychloride, colored
nacreous pigments such as titanium mica with iron oxides, titanium
mica with ferric blue or chromium oxide, titanium mica with an
organic pigment chosen from those mentioned above, and nacreous
pigments based on bismuth oxychloride. The nacreous pigments, if
present, be present in the composition in a concentration ranging
up to 50% by weight of the total weight of the composition, such as
from 0.1% to 20%, preferably from 0.1% to 15%.
[0419] The pigments, which may be used according to the present
invention, may be chosen from white, colored, inorganic, organic,
polymeric, nonpolymeric, coated and uncoated pigments.
Representative examples of mineral pigments include titanium
dioxide, optionally surface-treated, zirconium oxide, zinc oxide,
cerium oxide, iron oxides, chromium oxides, manganese violet,
ultramarine blue, chromium hydrate, and ferric blue. Representative
examples of organic pigments include carbon black, pigments of D
& C type, and lakes based on cochineal carmine, barium,
strontium, calcium, and aluminum.
[0420] If present, the pigments may be present in the composition
in a concentration ranging up to 50% by weight of the total weight
of the composition, such as from 0.5% to 40%, and further such as
from 2% to 30%. In the case of certain products, the pigments,
including nacreous pigments, may, for example, represent up to 50%
by weight of the composition.
[0421] According to preferred embodiments of the present invention,
the compositions comprising at least one polyorganosiloxane
containing polymer are anhydrous. By "anhydrous," it is meant that
the composition contains substantially no water (that is, less than
about 0.1% by weight of the composition of water).
[0422] According to other preferred embodiments, the compositions
comprising at least one polyorganosiloxane containing polymer
further comprise water. In this embodiment, water is preferably
present in an amount ranging from about 0.1 to about 70%,
preferably from about 0.5 to 50%, and more preferably from about 1
to about 30% relative to the total weight of the composition.
Preferably, such water-containing cosmetic compositions are lip
compositions (for example, lipstick or liquid lip colors),
foundations or mascaras, and are emulsions or dispersions.
[0423] Additional Additives
[0424] The composition of the invention can also comprise any
additive usually used in the field under consideration. For
example, dispersants such as poly(12-hydroxystearic acid),
antioxidants, essential oils, preserving agents, fragrances, waxes,
liposoluble polymers that are dispersible in the medium, fillers,
neutralizing agents, cosmetic and dermatological active agents such
as, for example, emollients, moisturizers, vitamins, essential
fatty acids, sunscreens, and mixtures thereof can be added. Further
examples of suitable additional components can be found in the
references which have been incorporated by reference in this
application, including but not limited to the applications from
which this application claims priority. Still further examples of
such additional ingredients may be found in the International
Cosmetic Ingredient Dictionary and Handbook (9.sup.th ed.
2002).
[0425] A person skilled in the art will take care to select the
optional additional additives and/or the amount thereof such that
the advantageous properties of the composition according to the
invention are not, or are not substantially, adversely affected by
the envisaged addition.
[0426] These substances may be selected variously by the person
skilled in the art in order to prepare a composition which has the
desired properties, for example, consistency or texture.
[0427] These additives may be present in the composition in a
proportion from 0% to 20% (such as from 0.01% to 20%) relative to
the total weight of the composition and further such as from 0.01%
to 10% (if present).
[0428] Non-limiting examples of such additional components
include:
[0429] Active Agents
[0430] The composition of the present invention advantageously
contains at least one cosmetic active agent and/or at least one
dermatological active agent, i.e., an agent having a beneficial
effect on the skin, lips or body growths and/or at least one
coloring agent.
[0431] Gelling Agent
[0432] The composition of the invention may also contain at least
one agent useful for gelling a liquid fatty phase. The gelling
agent increases the liquid fatty phase viscosity and leads to a
solid or flowable composition when introduced in said fatty phase.
The gelling agent does not encompass waxes, in the sense that it is
not waxy.
[0433] The at least one gelling agent may be chosen from gelling
agents in polymeric form and gelling agents in mineral form.
[0434] In one embodiment, the at least one gelling agent is not
soluble in an aqueous phase or in water.
[0435] The gelling agent according to the present invention is
preferably selected from the group consisting of agents that gel
via chemical reticulation and agents that gel via physical
reticulation.
[0436] Gelling Agents that Gel Via Chemical Reticulation
[0437] According to one embodiment, crosslinked elastomeric
polyorganosiloxanes of three-dimensional structure are preferred.
These elastomeric silicones can bear hydrophile groups, such as
polyoxyethylene or copoly(oxyethylene/oxypropylene).
[0438] As elastomeric polyorganosiloxanes which can be used in the
invention, mention may be made of the crosslinked elastomeric
polyorganosiloxanes described in application EP-A-0,295,886, the
disclosure of which is incorporated herein by reference. According
to that application, they are obtained by addition reaction and
crosslinking, in the presence of a platinum-type catalyst, of at
least:
[0439] (a) a polyorganosiloxane having at least two C.sub.2 to
C.sub.6 lower alkenyl groups per molecule; and
[0440] (b) a polyorganosiloxane having at least two hydrogen atoms
linked to a silicon atom per molecule. It is also possible to use
the polyorganosiloxanes described in U.S. Pat. No. 5,266,321, the
disclosure of which is incorporated by reference herein. According
to that patent, they are chosen in particular from:
[0441] i) polyorganosiloxanes comprising R.sub.2SiO and
RSiO.sub.1.5 units and optionally R.sub.3SiO.sub.0.5 and/or
SiO.sub.2 units in which the radicals R, independently of each
other, are chosen from a hydrogen, an alkyl such as methyl, ethyl
or propyl, an aryl such as phenyl or tolyl, an unsaturated
aliphatic group such as vinyl, the weight ratio of the units
R.sub.2SiO to the units RSiO.sub.1.5 ranging from 1/1 to 30/1;
[0442] ii) polyorganosiloxanes which are insoluble and swellable in
silicone oil, obtained by addition of an
polyorganohydrogenosiloxane (1) and of a polyorganosiloxane (2)
having unsaturated aliphatic groups such that the amount of
hydrogen or of unsaturated aliphatic groups in (1) and (2)
respectively ranges from 1 to 20 mol % when the polyorganosiloxane
is non-cyclic and from 1 to 50 mol % when the polyorganosiloxane is
cyclic. Optionally, these polyorganosiloxanes can comprise from 1
to 40 oxyalkylene groups, such as oxypropylene and/or oxyethylene
groups.
[0443] As examples of elastomeric polyorganosiloxanes which can be
used according to the invention, mention may be made of those sold
or made under the names KSG6 from Shin-Etsu, Trefil E-505C or
Trefil E-506C from Dow-Corning, Gransil from Grant Industries
(SR-CYC, SR DMF10, SR-DC556) or those marketed in the form of
preconstituted gels (KSG15, KSG17, KSG16, KSG18, KSG21 from
Shin-Etsu, Gransil SR 5CYC gel, Gransil SR DMF 10 gel, Gransil SR
DC556 gel, SF 1204 and JK 113 from General Electric or emulsifying
elastomers such as those sold under the names of KSG-210, KSG-30,
KSG-31, KSG-32, KSG-33, KSG-40, KSG 41, KSG-42, KSG-43 and KSG-44
from Shin-Etsu. A mixture of these commercial products may also be
used.
[0444] Gelling Agents that Gel Via Physical Reticulation
[0445] Gelling agents that gel via physical reticulation, in
particular via molecular muddling, hydrogen interactions, sequences
incompatibility or dipolar interactions, as well as liposoluble
polymers having liquid crystal groups, are preferred.
[0446] Gelling agents that gel via molecular muddling are polymers
having high molecular weights, preferably higher than 500 000, such
as silicone gums.
[0447] The silicone gum can correspond to the formula:
##STR00049##
[0448] in which:
[0449] R.sub.7, R.sub.9, R.sub.11 and R.sub.12 are identical or
different, and each is chosen from alkyl radicals comprising from 1
to 6 carbon atoms,
[0450] R.sub.9 and R.sub.10 are identical or different, and each is
chosen from alkyl radicals comprising from 1 to 6 carbon atoms and
aryl radicals,
[0451] X is chosen from alkyl radicals comprising from 1 to 6
carbon atoms, a hydroxyl radical and a vinyl radical,
[0452] n and p are chosen so as to give the silicone gum a
viscosity of greater than 100 000 mPas, such as greater than 500
000 mPas.
[0453] In general, n and p can each take values ranging from 0 to 5
000, such as from 0 to 3 000.
[0454] Among the silicone gums which can be used according to the
invention, mention may be made of those for which:
[0455] the substituents R.sub.7 to R.sub.12 and X represent a
methyl group, p=0 and n=2 700, such as the product sold or made
under the name SE30 by the company General Electric,
[0456] the substituents R.sub.7 to R.sub.12 and X represent a
methyl group, p=0 and n=2 300, such as the product sold or made
under the name AK 500 000 by the company Wacker,
[0457] the substituents R.sub.7 to R.sub.12 represent a methyl
group, the substituent X represents a hydroxyl group, p=0 and n=2
700, as a 13% solution in cyclopentasiloxane, such as the product
sold or made under the name Q2-1401 by the company Dow Corning,
[0458] the substituents R.sub.7 to R.sub.12 represent a methyl
group, the substituent X represents a hydroxyl group, p=0 and n=2
700, as a 13% solution in polydimethylsiloxane, such as the product
sold or made under the name Q2-1403 by the company Dow Corning,
and
[0459] the substituents R.sub.7, R.sub.8, R.sub.11, R.sub.12 and X
represent a methyl group and the substituents R.sub.9 and R.sub.10
represent an aryl group, such that the molecular weight of the gum
is about 600 000, for instance the product sold or made under the
name 761 by the company Rhone-Poulenc (Rhodia Chimie).
[0460] In preferred embodiments, the silicone gum correspond to the
following formula:
##STR00050##
[0461] In this formula the terminal Si's can also be other than
methyl and may be represented with substitutions on the repeating
Si such that the R group is an alkyl of 1 to 6 carbon atoms, which
may be linear, branched and/or functionalized selected from methyl,
ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, amyl, hexyl,
vinyl, allyl, cyclohexyl, phenyl, fluoroalkyl, and mixtures
thereof. The silicone gums employed in the present invention may be
terminated by triorganosilyl groups of the formula R'.sub.3 where
R' is a radical of monovalent hydrocarbons containing from 1 to 6
carbon atoms, hydroxyl groups, alkoxyl groups and mixtures thereof.
The silicone gums used in the invention have an affinity with the
structuring polymer and/or with the silicone gum, and the liquid
fatty phase, the polymer and the silicone gum form a
physiologically acceptable medium.
[0462] A particularly preferred fluid diorganopolysiloxane polymer
is poly(dimethylsiloxane), herein referred to as PDMS. Also useful
is a mixture of silicone gums such as the commercially available DC
1503 which is a blend of dimethicone and dimethiconol. Other useful
silicone gums are DC 1428 fluid (Dow Corning) and those silicone
gums described in U.S. Pat. No. 4,574,082, the contents of which
are incorporated herein by reference.
[0463] In certain embodiments of the present invention, crystalline
silicone compounds are included in the compositions.
[0464] A crystalline silicone compound is a compound comprising
silicone in its molecule, which is solid at room temperature, and
has a crystalline character. This compound or class of compounds is
compatible with the liquid fatty phase and the structuring
agent.
[0465] The crystalline silicone compounds belong to a class of
alkyl siloxane waxes corresponding to the formulae below:
##STR00051## [(CH.sub.3).sub.3SiO].sub.2(CH.sub.3)SiR
(CH.sub.3).sub.3SiO[(CH.sub.3).sub.2SiO].sub.x(RCH.sub.3SiO).sub.ySi(CH.-
sub.3).sub.3
[0466] This could also be written as
R.sub.3SiO[(CH.sub.3).sub.2SiO].sub.x(RCH.sub.3SiO).sub.ySiR.sub.3
where R is an alkyl chain. x may be 0. The substituent R may be as
low as 1 or as high as 50 or more as long as this silicone compound
crystallizes at room temperature.
[0467] Examples of crystalline silicone compounds include, but are
not limited to, C20-24 Alkyl Methicone, C24-28 Alkyl Dimethicone,
C20-24 Alkyl Dimethicone, C24-28 Alkyl Dimethicone commercially
available from Archimica Fine Chemicals, Gainesville, Fla. under
the designation of SilCare 41M40, SilCare 41M50, SilCare 41M70 and
SilCare 41M80. Stearyl Dimethicone available as SilCare 41M65 from
Archimica or as DC-2503 from Dow-Corning, Midland, Mich. Similarly,
stearoxytrimethylsilane sold as SilCare 1M71 or DC-580 may be used
in an embodiment of this invention. Furthermore, similar
crystalline compounds are available from Degussa Care Specialties,
Hopewell, Va. under the designation ABIL Wax 9810, 9800, or 2440,
or Wacker-Chemie GmbH, Burghausen, Germany, under the designation
BelSil SDM 5055, or OSi Specialties, Greenwich, Conn. under the
designation Silsoft. Other crystalline silicone compounds include
C30-45 Alkyl Methicone available from Dow Corning as AMS-C30 Wax,
as well as GE's SF1642, or SF-1632 available from General Electric,
Fairfield, Conn.
[0468] Gelling agents that gel the liquid fatty phase via hydrogen
interactions are preferably chosen in the group consisting of:
[0469] amino silicones polymers having triazinyl groups or
pyrimidinyl groups bound to amino groups of amino silicones as
described in patent application EP 0 751 170, the disclosure of
which is incorporated herein by reference,
[0470] non-silicone polyamides, ends of which bear ester or
triamides functions, such as compounds described in patents and
patent applications U.S. Pat. No. 5,783,657, U.S. Pat. No.
6,268,466, WO 01/95871, WO 00/40216, US 2002/0035237, and EP 1 068
856, the disclosure of which are incorporated herein by
reference,
[0471] polyurethanes, such as compounds described in patent
applications DE 10022247 and FR 2 814 365, the disclosure of which
are incorporated herein by reference, and
[0472] vinyl and/or (meth)acrylic polymers bearing lateral groups
that can create mutual hydrogen interactions, such as compounds
described in patent application WO 93/01797, the disclosure of
which is incorporated herein by reference.
[0473] Gelling agents that gel the liquid fatty phase via sequences
incompatibility are preferably selected from the group consisting
of:
[0474] block (di ou tri blocks) copolymers, such as
polystyrene-silicone, or polyethylene-silicone, described in
patents U.S. Pat. No. 6,225,390, U.S. Pat. No. 6,160,054, U.S. Pat.
No. 6,174,968 and U.S. Pat. No. 6,225,390, the disclosures of which
are incorporated herein by reference,
[0475] block or grafted copolymers comprising a silicone sequence
and another sequence or graft that is polyvinyl or
poly(meth)acrylic, such as those described in patents U.S. Pat. No.
5,468,477 et U.S. Pat. No. 5,725,882, the disclosures of which are
incorporated herein by reference.
[0476] polymers or copolymers resulting from the polymerization or
copolymerization of an ethylenic monomer, comprising one or more
ethylenic, preferably conjugated, bonds (or dienes),
[0477] polymers or copolymers resulting from the polymerization or
copolymerization of an ethylenic monomer, in particular use may be
made of vinyl, acrylic or methacrylic copolymers which may be block
copolymers, such as diblock or triblock copolymers, or even
multiblock or starburst or radial copolymers. The at least one
ethylenic gelling agent may comprise, for example, a styrene block
(S), an alkylstyrene block (AS), an ethylene/butylene block (EB),
an ethylene/propylene block (EP), a butadiene block (B), an
isoprene block (I), an acrylate block (A), a methacrylate block
(MA) or a combination of these blocks.
[0478] In one embodiment, a copolymer comprising at least one
styrene block is used as gelling agent or ethylenic rheological
agent. A triblock copolymer and in particular those of the
polystyrene/polyisoprene or polystyrene/polybutadiene type, such as
those sold or made under the name "Luvitol HSB" by BASF and those
of the polystyrene/copoly(ethylene-propylene) type or alternatively
of the polystyrene/copoly(ethylene/butylene) type, such as those
sold or made under the brand name "Kraton" by Shell Chemical Co. or
Gelled Permethyl 99A by Penreco, may be used. Styrene-methacrylate
copolymers can also be used.
[0479] As ethylenical gelling agent which can be used in the
composition of the invention, mention may be made, for example, of
Kraton (G1650 (SEBS), Kraton G1651 (SEBS), Kraton G1652 (SEBS),
Kraton G1657X (SEBS), Kraton G1701X (SEP), Kraton G1702X (SEP),
Kraton G1726X (SEB), Kraton G1750X (EP) multiarm, Kraton G1765X
(EP) multiarm, Kraton D-1101 (SBS), Kraton D-1102 (SBS), Kraton
D-1107 (SIS), Gelled Permethyl 99A-750, Gelled Permethyl 99A-753-58
(mixture of starburst block polymer and triblock polymer), Gelled
Permethyl 99A-753-59 (mixture of starburst block polymer and
triblock polymer), Versagel 5970 and Versagel 5960 from Penreco
(mixture of starburst polymer and triblock polymer in isododecane),
and OS 129880, OS 129881 and OS 84383 from Lubrizol
(styrene-methacrylate copolymer).
[0480] Di or triblocks such as
polystyrene-copoly(ethylene/propylene) or
polystyrene-copoly(ethylene/butylene) such as those described in
patent applications WO 98/38981 and US 2002/0055562, the
disclosures of which are hereby incorporated by reference, are also
included in the present invention.
[0481] Gelling agents that gel via dipolar interactions are
preferably chosen from compounds describes in documents WO 01/30886
et U.S. Pat. No. 6,228,967, the disclosures of which are
incorporated herein by reference. Ionized groups of said compounds,
for example zwitterionic groups, create said dipolar
interactions.
[0482] Gelling agents such as liposoluble polymers having liquid
crystal groups are also preferred according to the present
invention, especially liposoluble polymers whose backbone is
silicone, vinyl and/or (meth)acrylic and that possess des lateral
liquid crystal groups, in particular compounds described in patent
application FR 2 816 503, the disclosure of which is incorporated
herein by reference.
[0483] In another embodiment, the at least one gelling agent may be
in mineral form with particle sizes that cause little or no light
scattering. Thus, it may be possible to obtain a translucent or
even transparent composition.
[0484] As modified clays which can be used, mention may be made of
hectorites modified with an ammonium chloride of a C.sub.10 to
C.sub.22 fatty acid, such as hectorite modified with
distearyldimethylammonium chloride, also known as quatermium-18
bentonite, such as the products sold or made under the names
Bentone 34 by the company Rheox, Claytone XL, Claytone 34 and
Claytone 40 sold or made by the company Southern Clay, the modified
clays known under the name quaternium-18 benzalkonium bentonites
and sold or made under the names Claytone HT, Claytone GR and
Claytone PS by the company Southern Clay, the clays modified with
stearyldimethylbenzoylammonium chloride, known as steralkonium
bentonites, such as the products sold or made under the names
Claytone APA and Claytone AF by the company Southern Clay, and
Baragel 24 sold or made by the company Rheox.
[0485] As other mineral gelling agents, which can be used in the
invention, mention may be made of silica, such as fumed silica. The
fumed silica may have a particle size, which may be nanometric to
micrometric, for example ranging from about 5 nm to 200 nm.
[0486] The fumed silicas may be obtained by high-temperature
hydrolysis of a volatile silicon compound in a hydrogen-oxygen
flame, producing a finely divided silica. This process makes it
possible to obtain hydrophilic silicas that have a large number of
silanol groups at their surface. Such hydrophilic silicas are sold
or made, for example, under the names "Aerosil 130.RTM.", "Aerosil
200.RTM.", "Aerosil 255.RTM.", "Aerosil 300.RTM." and "Aerosil
380.RTM." by the company Degussa, and "CAB-O-SIL HS-5.RTM.",
"CAB-.beta.-SIL EH-5.RTM.", "CAB-O-SIL LM-130.RTM.", "CAB-O-SIL
MS-55.RTM." and "CAB-O-SIL M-5.RTM." by the company Cabot.
[0487] It is thus possible to chemically modify the surface of the
hydrophilic silica by chemical reaction, producing a reduction in
the number of silanol groups. The silanol groups can be replaced,
for example, with hydrophobic groups: this then gives a hydrophobic
silica. The hydrophobic groups may be:
[0488] trimethylsiloxyl groups, which are obtained in particular by
treating fumed silica in the presence of hexamethyldisilazane.
Silicas thus treated are known as "silica silylate" according to
the CTFA (6th edition, 1995). They are sold or made, for example,
under the references "Aerosil R812.RTM." by the company Degussa and
"CAB-O-SIL TS-530.RTM." by the company Cabot;
[0489] dimethylsilyloxyl or polydimethylsiloxane groups, which are
obtained in particular by treating fumed silica in the presence of
polydimethylsiloxane or dimethyldichlorosilane. Silicas thus
treated are known as "silica dimethyl silylate" according to the
CTFA (6th edition, 1995). They are sold or made, for example, under
the references "Aerosil R972.RTM." and "Aerosil R974.RTM." by the
company Degussa, and "CAB-O-SIL TS-610.RTM." and "CAB-O-SIL
TS-720.RTM." by the company Cabot;
[0490] groups derived from reacting fumed silica with silane
alkoxides or siloxanes. These treated silicas are, for example, the
products sold or made under the reference "Aerosil R805.RTM." by
the company Degussa.
[0491] According to the invention, hydrophobic silica, such as
fumed silica, may be used as lipophilic gelling agent. The use of
fumed silica makes it possible to obtain a translucent or even
transparent composition, in particular in the form of a stick,
which does not exude, in the absence of opacifying particles such
as waxes, fillers and pigments (including nacres).
[0492] The at least one liposoluble gelling agent can allow the
exudation of the composition to be limited and can allow its
stability to be increased, while at the same time conserving the
composition's glossy appearance, which is not possible with waxes
such as those used conventionally in cosmetics and dermatology.
These gelling agents can be used, for example, at concentrations of
from 0.05% to 35% relative to the total weight of the composition,
for example from 0.5% to 20% or from 1% to 10%.
[0493] In addition, short chain esters may be included in the
compositions of the present invention.
[0494] According to the invention, the esters may either be
monoesters, diesters or polyesters. These esters may be linear,
branched or cyclic, saturated or unsaturated. These esters should
preferably be branched and saturated. They may also be aliphatic or
aromatic.
[0495] These esters may have from 6 to 25 carbon atoms and
particularly from 14 to 22 carbon atoms. They may be chosen amongst
acid esters having from 2 to 18 carbon atoms, and particularly
amongst alcohol esters having from 2 to 20 carbon atoms or amongst
polyols having from 2 to 8 carbon atoms or their mixtures, on
condition that the number of carbon atoms is higher than 10, so
that the ester is not volatile and penetrates the skin.
[0496] Particularly, these esters are hydrocarbon-based esters
which correspond to the following formula RCOOR' where R represents
a residue of fatty acid having from 1 to 29 carbon atoms, and R'
represents a hydrocarbon-based chain containing from 2 to 30 carbon
atoms, on condition that the number of carbon atoms in R' is higher
than 10, so that the ester is not volatile and penetrates the
skin.
[0497] The ester may be chosen among a non-limitative list
including the following:
[0498] Neopentanoic acid esters such as isodecyl neopentanoate,
isotridecyl neopentanoate, isostearyl neopentanoate, octyldocecyl
neopentanoate,
[0499] Isononanoic acid esters such as isononyl isononanoate, octyl
isononanoate, isodecyl isononanoate, isotridecyl isononanoate,
isostearyl isononanoate, ethylhexyl isononanoate,
[0500] Isopropylic alcohol esters, such as isopropyl myristate,
isopropyl palmitate, isopropyl stearate or isostearate, isopropyl
laurate, diisopropyl adipate,
[0501] Alkyl or polyalkyl octanoates, decanoates or ricinoleates,
such as cetyl octanoate, tridecyl octanoate,
[0502] Polyalkylene glycol esters, such as polyethylene glycol
diheptanoate, hexanoate-2-diethyl propylene glycol and their
mixtures,
[0503] Benzoate alkyls particularly benzoate alkyls having from 12
to 15 carbon atoms,
[0504] Hydroxylated esters such as isotearyl lactate and
diisostearyl malate, and
[0505] Pentaerythritol esters.
[0506] Examples of short chain esters also include purcellin oil
(cetostearyl octanoate), ethylhexyl ethylhexanoate, dicapryl ester,
2-ethylhexyl palmitate, 2-ethyl-palmitate and isostearyl
isostearate.
[0507] The isononyl isononanoate and diisostearyl malate are
particularly suited for the embodiment of this invention.
[0508] This or these hydrocarbon-based ester(s) may be used in the
composition at a percentage of 5 to 90%, notably of 10 to 60%,
particularly of 20 to 50% by weight of the total weight of the
composition.
[0509] The mass ratio between the short chain ester, if present,
and the polyorganosiloxane containing polymer is preferably between
1/4 and 2/1, more preferably between 1/3 and 1/1.
[0510] Additional ingredients which offer similar cosmetic
properties as the short chain esters are short chain ethers which
may be represented as
J-O--K
[0511] where J and K are identical or different and represent a
linear or branched alkyl radical from 1 to 40 carbon atoms,
preferably from 7 to 19 carbon atoms, possibly including one or
more double bonds. An example of such an ether includes dicapryl
ether.
[0512] Waxes
[0513] The composition can optionally contain one or more waxes to
improve the structuring in stick form, although this rigid form can
be obtained in the absence of wax. For the purposes of the present
invention, a wax is a lipophilic fatty compound that is solid at
room temperature (25.degree. C.) and atmospheric pressure (760
mmHg, i.e. 101 KPa), which undergoes a reversible solid/liquid
change of state, having a melting point of greater than 40.degree.
C. and further such as greater than 55.degree. C. and which may be
up to 200.degree. C., and having an anisotropic crystal
organization in the solid state. The size of the crystals is such
that the crystals diffract and/or scatter light, giving the
composition a cloudy, more or less opaque appearance. By bringing
the wax to its melting point, it is possible to make it miscible
with oils and to form a microscopically homogeneous mixture, but on
returning the temperature of the mixture to room temperature,
recrystallization of the wax in the oils of the mixture is
obtained. It is this recrystallization in the mixture which is
responsible for the reduction in the gloss of the mixture. Thus,
the composition advantageously contains little or no wax, and in
particular less than 5% wax.
[0514] For the purposes of the invention, the waxes are those
generally used in cosmetics and dermatology; they are, for example,
of natural origin, for instance beeswax, carnauba wax, candelilla
wax, ouricury wax, Japan wax, cork fiber wax, sugar cane wax,
paraffin wax, lignite wax, microcrystalline waxes, lanolin wax,
montan wax, ozokerites and hydrogenated oils such as hydrogenated
jojoba oil as well as waxes of synthetic origin, for instance
polyethylene waxes derived from the polymerization of ethylene,
waxes obtained by Fischer-Tropsch synthesis, fatty acid esters and
glycerides that are solid at 40.degree. C., for example, at above
55.degree. C., silicone waxes such as alkyl- and
alkoxy-poly(di)methylsiloxanes and/or poly(di)methyl-siloxane
esters that are solid at 40.degree. C., for example, at above
55.degree. C.
[0515] According to the invention, the melting point values
correspond to the melting peak measured by the "Differential
Scanning calorimetry" method with a temperature rise of 5 or
10.degree. C./min.
[0516] Liposoluble or Dispersible Polymers
[0517] The composition of the invention also can contain at least
one polymer that is liposoluble or dispersible in the medium, other
than the polyorganosiloxane containing polymer, and may have
film-forming properties and may have, for example, an average
molecular weight of from 500 to 1,000,000, such as from 1,000 to
500,000, and for example, further such as from 5,000 to 100,000,
and even further such as from 5,000 to 20,000. This at least one
liposoluble polymer may contribute towards increasing the viscosity
and/or improving the staying power of the film. The at least one
liposoluble polymer can have a softening point of not more than
30.degree. C.
[0518] As examples of liposoluble polymers which can be used in the
invention, mention may be made of: polyalkylenes, in particular
polybutene, poly(meth)acrylates, alkylcelluloses with a linear or
branched, saturated or unsaturated C.sub.1 to C.sub.8 alkyl
radical, such as ethylcellulose and propylcellulose, silicone
polymers that are compatible with the fatty phase, as well as
vinylpyrrolidone (VP) copolymers, and mixtures thereof.
[0519] Vinylpyrrolidone copolymers, copolymers of a C.sub.2 to
C.sub.30, such as C.sub.3 to C.sub.22 alkene, and combinations
thereof, can be used. As examples of VP copolymers which can be
used in the invention, mention may be made of VP/vinyl acetate,
VP/ethyl methacrylate, butylated polyvinylpyrrolidone (PVP),
VP/ethyl methacrylate/methacrylic acid, VP/eicosene, VP/hexadecene,
VP/triacontene, VP/styrene or VP/acrylic acid/lauryl methacrylate
copolymer.
[0520] Not only for the staying power properties but also for the
feel and consistency properties of the film, the PVP/hexadecene
copolymer having an average molecular weight of from 7,000 to 7,500
or alternatively the PVP/eicosene copolymer having an average
molecular weight of from 8,000 to 9,000 can be used.
[0521] The liposoluble or dispersible polymers in the composition
of the invention can be also used in an amount of from 0.01% to 20%
(as active material) relative to the total weight of the
composition, such as, for example, from 1% to 10%, if they are
present.
[0522] Emollients
[0523] Emollients and/or humectants that may be used in the
compositions of the invention include glycerin, propylene glycol,
and emollients and other similar ingredients disclosed in the
International Cosmetic Ingredient Dictionary and Handbook Vol. 4
(9.sup.th ed. 2002), more particularly the emollients disclosed on
pages 2930-2936. The disclosure of the International Cosmetic
Ingredient Dictionary and Handbook Vol. 4, pages 2930-2936, is
hereby incorporated by reference.
[0524] Surfactants
[0525] The compositions of the invention may further include
formulation aids which are usually employed in the field of
application envisaged. The formulation aids used in the present
invention can be, but are not limited to, surfactants. Useful
surfactants include, but are not limited to, organic and
organosilicone emulsifiers for water-in-oil systems. Examples of
organic emulsifiers include any ethoxylated surfactants known in
the art such as Polysorbate-20, Laureth-7, Laureth-4, Sepigel.RTM.
305 available from SEPPIC and other similar ingredients disclosed
in the International Cosmetic Ingredient Dictionary and Handbook
Vol. 4 (9.sup.th ed. 2002), more particularly the emulsifiers
disclosed on pages 2962-2971. The disclosure of the International
Cosmetic Ingredient Dictionary and Handbook Vol. 4, pages
2962-2971, is hereby incorporated by reference. Examples of
organosilicone emulsifiers include cetyl dimethicone
copolyol-polyglyceryl-4-isostearate-hexylaurate (ABIL.RTM. WE 09)
available from Goldschmidt Chemical Corporation, Cetyl Dimethicone
Copolyol (ABIL.RTM. EM 90), (ABIL.RTM. EM 97), Laurylmethicone
Copolyol (5200), Cyclomethicone (and) Dimethicone Copolyol (DC 5225
C and DC 3225 C) available from GE Silicones, Cyclopentasiloxane
& Dimethicone Copolyol (GE SF 1528) or any other formulation
aids known by one of skill in the art.
[0526] Plasticizers
[0527] Plasticizers may also be added to the compositions to
improve the flexibility and cosmetic properties of the resulting
formulation. Plasticizers are materials which soften synthetic
polymers. They are frequently required to avoid brittleness and
cracking of film formers. One skilled in the art may routinely vary
the amount of plasticizer desired based on the properties desired
and the application envisaged. Plasticizers useful in the practice
of the invention include lecithin, polysorbates, dimethicone
copolyol, glycols, citrate esters, glycerin, dimethicone, and other
similar ingredients disclosed in the International Cosmetic
Ingredient Dictionary and Handbook Vol. 4 (9.sup.th ed. 2002), more
particularly the plasticizers disclosed on page 2927. The
disclosure of the International Cosmetic Ingredient Dictionary and
Handbook Vol. 4, page 2927, is hereby incorporated by
reference.
[0528] Sunscreens
[0529] In one embodiment, the composition may contain sunscreens.
In certain embodiments, the combination of the
polysiloxane-containing polymer when combined with one or more
sunscreens improves, quite significantly, the overall SPF value of
the composition relative to a composition without the
polysiloxane-containing polymer.
[0530] Sunscreens may be inorganic nanoparticles or organic
compounds. In one embodiment the nanoparticles are inorganic
compounds composed essentially of metal oxides. Suitable metal
oxides comprise one or more of iron oxide, aluminum oxide,
zirconium oxide, vanadium oxide, niobium oxide, tantalum oxide,
chromium oxide, molybdenum oxide, tungsten oxide, cobalt oxide,
nickel oxide, cerium cupric oxide, zinc oxide, tin oxide, antimony
oxide titanium dioxide and mixtures thereof, among others. In yet
another embodiment titanium dioxide and zinc oxide are used.
Without being limited to theory, in most cases the metal oxide
nanoparticles provide a sun protection benefit by diffracting the
ultraviolet light. The elemental size of 1 nanoparticle is
typically from less than 1 .mu.m in size, including from about 100
nm to about 500 nm, including about 200 nm to about 350 nm.
[0531] Sunscreens according to this invention which are chemical
absorbers actually absorb harmful ultraviolet radiation. It is well
known that chemical absorbers are classified, depending on the type
of radiation they protect against, as either UV-A or UV-B
absorbers. UV-A absorbers generally absorb radiation in the 320 to
400 nm region of the ultraviolet spectrum. UV-A absorbers include
anthranilates, benzophenones, and dibenzoyl methanes. UV-B
absorbers generally absorb radiation in the 280 to 320 nm region of
the ultraviolet spectrum. UV-B absorbers include p-aminobenzoic
acid derivatives, camphor derivatives, cinnamates, and
salicylates.
[0532] Classifying the chemical absorbers generally as UV-A or UV-B
absorbers is accepted within the industry. However, a more precise
classification is one based upon the chemical properties of the
sunscreens. There are eight major classifications of sunscreen
chemical properties which are discussed at length in
"Sunscreens--Development, Evaluation and Regulatory Aspects," by N.
Shaath et al., 2nd. Edition, pages 269-273, Marcel Dekker, Inc.
(1997). This discussion, in its entirety, is incorporated by
reference herein.
[0533] The sunscreens which may be formulated according to the
present invention typically comprise chemical absorbers, but may
also comprise physical blockers. Exemplary sunscreens which may be
formulated into the compositions of the present invention are
chemical absorbers such as p-aminobenzoic acid derivatives,
anthranilates, benzophenones, camphor derivatives, cinnamic
derivatives, dibenzoyl methanes, diphenylacrylate derivatives,
salicylic derivatives, triazine derivatives, benzimidazole
compounds, bis-benzoazolyl derivatives, methylene
bis-(hydroxyphenylbenzotriazole) compounds, the sunscreen polymers
and silicones, or mixtures thereof. These are variously described
in U.S. Pat. Nos. 2,463,264, 4,367,390, 5,166,355 and 5,237,071 and
in EP-0,863,145, EP-0,517,104, EP-0,570,838, EP-0,796,851,
EP-0,775,698, EP-0,878,469, EP-0,933,376, EP-0,893,119,
EP-0,669,323, GB-2,303,549, DE-1,972,184 and WO-93/04665, also
expressly incorporated by reference.
[0534] A wide variety of sunscreens is described in U.S. Pat. No.
5,087,445, issued to Haffey et al. on Feb. 11, 1992; U.S. Pat. No.
5,073,372, issued to Turner et al. on Dec. 17, 1991; and Chapter
VIII of Cosmetics and Science and Technology by Segarin et al.,
pages 189 et seq. (1957), all of which are incorporated herein by
reference in their entirety.
[0535] Non-limiting examples of sunscreens which may be formulated
into the compositions of the instant invention include those
selected from among: aminobenzoic acid, amyldimethyl PABA,
cinoxate, diethanolamine p-methoxycinnamate, digalloyl trioleate,
dioxybenzone, 2-ethoxyethyl p-methoxycinnamate, ethyl
4-bis(hydroxypropyl)aminobenzoate,
2-ethylhexyl-2-cyano-3,3-diphenylacrylate, ethylhexyl
p-methoxycinnamate, 2-ethylhexyl salicylate, glyceryl
aminobenzoate, homomethyl salicylate, homosalate,
3-imidazol-4-ylacrylic acid and ethyl ester, methyl anthranilate,
octyldimethyl PABA, 2-phenylbenzimidazole-5-sulfonic acid and
salts, red petrolatum, sulisobenzone, titanium dioxide,
triethanolamine salicylate, N,N,N-trimethyl-4-(2-oxoborn-3-ylidene
methyl)anillinium methyl sulfate, and mixtures thereof.
[0536] Sunscreens active in the UV-A and/or UV-B range can also
include:
[0537] p-aminobenzoic acid,
[0538] oxyethylene (25 mol) p-aminobenzoate,
[0539] 2-ethylhexyl p-dimethylaminobenzoate,
[0540] ethyl N-oxypropylene p-aminobenzoate,
[0541] glycerol p-aminobenzoate,
[0542] 4-isopropylbenzyl salicylate,
[0543] 2-ethylhexyl 4-methoxycinnamate,
[0544] methyl diisopropylcinnamate,
[0545] isoamyl 4-methoxycinnamate,
[0546] diethanolamine 4-methoxycinnamate,
[0547] 3-(4'-trimethylammunium)-benzyliden-bornan-2-one
methylsulfate,
[0548] 2-hydroxy-4-methoxybenzophenone,
[0549] 2-hydroxy-4-methoxybenzophenone-5-sulfonate,
[0550] 2,4-dihydroxybenzophenone,
[0551] 2,2',4,4'-tetrahydroxybenzophenone,
[0552] 2,2'-dihydroxy-4,4'dimethoxybenzophenone,
[0553] 2-hydroxy-4-n-octoxybenzophenone,
[0554] 2-hydroxy-4-methoxy-4'-methoxybenzophenone,
[0555] -(2-oxoborn-3-ylidene)-tolyl-4-sulfonic acid and soluble
salts thereof,
[0556] 3-(4'-sulfo)benzyliden-bornan-2-one and soluble salts
thereof,
[0557] 3-(4'methylbenzylidene)-d,l-camphor,
[0558] 3-benzylidene-d,l-camphor,
[0559] benzene 1,4-di(3-methylidene-10-camphosulfonic) acid and
salts thereof (the product Mexoryl SX described in U.S. Pat. No.
4,585,597 issued to Lange et al. on Apr. 29, 1986, hereby
incorporated by reference),
[0560] urocanic acid,
[0561]
2,4,6-tris[p-(2'-ethylhexyl-1'-oxycarbonyl)-anilino]-1,3,5-triazine-
,
[0562]
2-[(p-(tertiobutylamido)anilino]-4,6-bis-[(p-(2'-ethylhexyl-V-oxyca-
rbonyl)anilino]-1,3,5-triazine,
[0563]
2,4-bis{[4-(2-ethyl-hexyloxy)]-2-hydroxyl-phenyl}-6-(4-methoxy-phen-
yl)-1,3,5-triazine ("TINOSORB S" marketed by Ciba),
[0564] the polymer of N-(2 et
4)-[(2-oxoborn-3-yliden)methyl]benzyl]-acrylamide,
[0565] 1,4-bisbenzimidazolyl-phenylen-3,3',5,5'-tetrasulfonic acid
and salts thereof,
[0566] the benzalmalonate-substituted polyorganosiloxanes,
[0567] the benzotriazole-substituted polyorganosiloxanes
(Drometrizole Trisiloxane),
[0568] dispersed
2,2'-methylene-bis-[6-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)-
phenol] such as that marketed under the trademark MIXXIM BB/100 by
Fairmount Chemical, or micronized in dispersed form thereof such as
that marketed under the trademark TINOSORB M by Ciba-Geigy, and
[0569] solubilized
2,2'-methylene-bis-[6-(2H-benzotriazol-2-yl)-4-(methyl)phenol] such
as that marketed under the trademark MIXXIM BB/200 by Fairmount
Chemical.
[0570] Typically, combinations of one of more of these sunscreens
are used.
[0571] The dibenzoyl methane derivatives other than avobenzone are
described, for example, in FR-2,326,405, FR-2,440,933 and
EP-0,114,607, hereby expressly incorporated by reference.
[0572] Other dibenzoyl methane sunscreens other than avobenzone
include (whether singly or in any combination): [0573]
2-methyldibenzoylmethane [0574] 4-methyldibenzoylmethane [0575]
4-isopropyldibenzoylmethane [0576] 4-tert.-butyldibenzoylmethane
[0577] 2,4-dimethyldibenzoylmethane [0578]
2,5-dimethyldibenzoylmethane [0579]
4,4'-diisopropyldibenzoylmethane [0580]
4,4'-dimethoxydibenzoylmethane [0581]
2-methyl-5-isopropyl-4'-methoxydibenzoylmethane [0582]
2-methyl-5-tert.-butyl-4'-methoxydibenzoylmethane [0583]
2,4-dimethyl-4'-methoxydibenzoylmethane [0584]
2,6-dimethyl-4-tert.-butyl-4'-methoxydibenzoylmethane
[0585] Additional sunscreens that can be used are described in
pages 2954-2955 of the International Cosmetic Ingredient Dictionary
and Handbook (9.sup.th ed. 2002).
[0586] The sunscreens are generally present in the compositions
according to the invention in proportions ranging from 0.1 to 30%
by weight with respect to the total weight of the composition and
preferably ranging from 0.2 to 15% by weight with respect to the
total weight of the composition. Compositions of the invention
preferably have a SPF of 30 and above, including 35, 40, 45,
etc.
[0587] Fillers
[0588] According to the present invention, the compositions may
further comprise at least one filler. As used herein, the term
"filler" means any particle that is solid at room temperature and
atmospheric pressure, used alone or in combination, which does not
react chemically with the various ingredients of the emulsion and
which is insoluble in these ingredients, even when these
ingredients are raised to a temperature above room temperature and
in particular to their softening point or their melting point. In
an embodiment, the at least one filler has a melting point at least
greater than 1700.degree. C., for example, greater than
2000.degree. C. In an embodiment, the at least one filler may have
an apparent diameter ranging from 0.01 .mu.m to 150 .mu.m, such as
from 0.5 .mu.m to 120 .mu.m, for example from 1 .mu.m to 80 .mu.m.
An apparent diameter corresponds to the diameter of the circle into
which the elementary particle fits along its shortest dimension
(thickness for leaflets). Further, the at least one filler may be
absorbent, i.e., capable in particular of absorbing the oils of the
composition and also the biological substances secreted by the
skin, may be surface-treated, e.g., to make it lipophilic, and/or
may be porous so as to absorb the sweat and/or sebum secreted by
the skin.
[0589] The at least one filler may be chosen from inorganic and
organic fillers, and may have any shape such as lamellar, spherical
and/or oblong. Non-limiting examples of the at least one inert
filler include talc, mica, silica, kaolin, polyimide powders (such
as Nylon.RTM. powder, and such as the product sold by Atochem as
Orgasol.RTM.), poly-.beta.-alanine powders, polyethylene powders,
acrylic polymer powders (such as polymethyl methacrylate (PMMA)
powder, for instance the product sold by Wacker as Covabead LH-85
(particle size 10-12 .mu.m) and the acrylic acid copolymer powder
sold by Dow Corning as Polytrap.RTM.), polytetrafluoroethylene
(Teflon.RTM.) powders, lauroyllysine, boron nitride, silica,
kaolin, starch, starch derivatives, hollow polymer microspheres
(such as those hollow polymer microspheres formed from
polyvinylidene chloride and acrylonitrile, for instance the product
sold by Nobel Industrie as Expancel.RTM.), and polymerized silicone
microspheres (such as those polymerized silicone microspheres sold
by Toshiba as Tospearl.RTM.), precipitated calcium carbonate,
magnesium carbonate and hydrocarbonate, hydroxyapatite, ceramic
microcapsules, polyester particles and coated elastomers such as
products sold under the denomination KSP (KSP100, KSP 200, KSP 300)
sold by Shin Etsu and/or those described in U.S. Pat. No.
5,538,793, the disclosure of which is hereby incorporated by
reference.
[0590] The composition according to the invention can be in the
form of a tinted or non tinted dermatological composition or a care
composition for keratin materials such as the skin, the lips and/or
superficial body growths, in the form of an antisun composition or
make-up-removing product in stick form. It can be used in
particular as a care base for the skin, superficial body growths or
the lips (lip balms, for protecting the lips against cold and/or
sunlight and/or the wind, or care cream for the skin, the nails or
the hair). As defined herein, a deodorant product is personal
hygiene product and does not relate to care, make-up or treatment
of keratin materials, including keratinous fibers.
[0591] The composition of the invention may also be in the form of
a colored make-up product for the skin, in particular a foundation,
optionally having care or treating properties, a blusher, a face
powder, an eye shadow, a concealer product, an eyeliner, a make-up
product for the body; a make-up product for the lips such as a
lipstick, optionally having care or treating properties; a make-up
product for superficial body growths such as the nails or the
eyelashes, in particular in the form of a mascara cake, or for the
eyebrows and the hair, in particular in the form of a pencil.
[0592] Needless to say, the composition of the invention should be
cosmetically or dermatologically acceptable, i.e., it should
contain a non-toxic physiologically acceptable medium and should be
able to be applied to the skin, superficial body growths or the
lips of human beings. For the purposes of the invention, the
expression "cosmetically acceptable" means a composition of
pleasant appearance, odor, feel and/or taste.
[0593] According to preferred embodiments of the present invention,
methods of treating, caring for and/or making up keratinous
material such as skin, lips, hair and mucous membranes by applying
compositions of the present invention to the keratinous material in
an amount sufficient to treat, care for and/or make up the
keratinous material are provided.
[0594] According to other preferred embodiments, methods of
covering or hiding defects associated with keratinous material such
as imperfections or discolorations by applying compositions of the
present invention to the keratinous material in an amount
sufficient to cover or hide such defects are provided.
[0595] According to yet other preferred embodiments, methods of
enhancing the appearance of keratinous material by applying
compositions of the present invention to the keratinous material in
an amount sufficient to enhance the appearance of the keratinous
material are provided.
[0596] In accordance with the three preceding preferred
embodiments, the compositions of the present invention comprising
at least one polyorganosiloxane containing polymer, preferably a
polysilicone-polyamide copolymer, are applied topically to the
desired area of the skin in an amount sufficient to treat, care for
and/or make up the keratinous material, to cover or hide defects
associated with keratinous material, skin imperfections or
discolorations, or to enhance the appearance of keratinous
material. The compositions may be applied to the desired area as
needed, preferably once or twice daily, more preferably once daily
and then preferably allowed to dry before subjecting to contact
such as with clothing or other objects. The composition is
preferably applied to the desired area that is dry or has been
dried prior to application. Most preferably, the composition
further comprises at least one film forming agent, at least one
volatile oil, or a mixture thereof and/or pigments.
[0597] According to a preferred embodiment of the present
invention, compositions having improved cosmetic properties such
as, for example, improved long wear, transfer resistance or
waterproof properties are provided. The improved properties may
also be chosen from improved flexibility, wearability, drying time
or retention as well as reduced tackiness or migration over
time.
[0598] The present invention also envisages kits and/or prepackaged
materials suitable for consumer use containing one or more
compositions according to the description herein. The packaging and
application device for any subject of the invention may be chosen
and manufactured by persons skilled in the art on the basis of
their general knowledge, and adapted according to the nature of the
composition to be packaged. Indeed, the type of device to be used
can be in particular linked to the consistency of the composition,
in particular to its viscosity; it can also depend on the nature of
the constituents present in the composition, such as the presence
of volatile compounds.
[0599] Unless otherwise indicated, all numbers expressing
quantities of ingredients, reaction conditions, and so forth used
in the specification and claims are to be understood as being
modified in all instances by the term "about." Accordingly, unless
indicated to the contrary, the numerical parameters set forth in
the following specification and attached claims are approximations
that may vary depending upon the desired properties sought to be
obtained by the present invention.
[0600] Notwithstanding that the numerical ranges and parameters
setting forth the broad scope of the invention are approximations,
the numerical values set forth in the specific examples are
reported as precisely as possible. Any numerical value, however,
inherently contain certain errors necessarily resulting from the
standard deviation found in their respective measurements. The
following examples are intended to illustrate the invention without
limiting the scope as a result. The percentages are given on a
weight basis.
Example 1
Foundation
TABLE-US-00003 [0601] Phase Ingredient Name % w/w A
Cyclopentasiloxane and Dimethicone Copolyol.sup.1 8.00
Polyglyceryl-4-isostearate and Hexyl Laurate and 3.50 Cetyl
PEG/PPG-10/1 Dimethicone.sup.2 Treated Pigments 9.90 B1 Volatile
Oil 16.10 Siloxane based polyamide.sup.3 1.00 Silicone
Acrylates.sup.4 12.00 B2 Fillers 6.00 B3 Preservative 0.40
Disteardimonium Hectorite 0.60 Propylene Carbonate 0.20 C Water
40.00 Magnesium Sulfate 1.00 Preservatives 0.70 Non-ionic
emulsifier 0.50 100.00 .sup.1Dow Corning DC5225C .sup.2ABIL WE 09
.sup.3Dow Corning DC2-9179 (DP = 100) .sup.4KP545
[0602] Phase A ingredients were mixed well and ground with a
Silverson homogenizer at a speed of 6000 rpm. Separately the phase
B1 ingredients were heated to 80 to 85.degree. C. with stirring for
10-15 minutes or until dissolution of the siloxane based polyamide.
Phase A and B1 were then combined in the main beaker and mixed well
at 70 to 75.degree. C. Phase B2 was added to the main beaker and
was mixed well or until uniform. In a separate side beaker, phase C
was heated to 70 to 75.degree. C. Emulsification was carried out by
adding phase C to main beaker with the use of a homogenizer at
medium/high speed. The batch was cooled to room temperature with a
paddle stirring.
[0603] This composition exhibited good wear, excellent
transfer-resistance after drying, good water resistance and felt
cushiony.
Example 2
Foundation
TABLE-US-00004 [0604] Phase Ingredient Name % w/w A
Cyclopentasiloxane and Dimethicone Copolyol.sup.1 8.00
Polyglyceryl-4-isostearate and Hexyl Laurate and 3.50 Cetyl
PEG/PPG-10/1 Dimethicone.sup.2 Pigments 9.90 B1 Volatile Oil 26.10
Siloxane based polyamide.sup.3 3.00 B2 Fillers 6.00 B3 Preservative
0.40 Disteardimonium Hectorite 0.60 Propylene Carbonate 0.20 C
Water 40.00 Magnesium Sulfate 1.00 Preservatives 0.70 Non ionic
emulsifier 0.50 100.00 .sup.1Dow Corning DC5225C .sup.2ABIL WE 09
.sup.3Dow Corning DC2-8179 (DP = 100)
[0605] Phase A ingredients were mixed well and ground with a
Silverson homogenizer at a speed of 6000 rpm. Separately the phase
B1 ingredients were heated to 80 to 85.degree. C. with stirring for
10-15 minutes or until dissolution of the siloxane based polyamide.
Phase A and B1 were then combined in the main beaker and mixed well
at 70 to 75.degree. C. Phase B2 was added to the main beaker and
was mixed well or until uniform. Disteardimonium Hectorite was
added to the main beaker and dispersed well before adding the rest
of phase B3 ingredients. In a separate side beaker, phase C was
heated to 70 to 75.degree. C. Emulsification was carried out by
adding phase C to the main beaker with the use of a homogenizer at
medium/high speed. The batch was cooled to room temperature with a
paddle stirring.
[0606] This composition exhibited good transfer-resistance after
drying, good water resistance and felt cushiony.
Example 3
Foundation
TABLE-US-00005 [0607] Phase Ingredient Name % w/w A
Cyclopentasiloxane and Dimethicone Copolyol.sup.1 8.00
Polyglyceryl-4-isostearate and Hexyl Laurate and 3.50 Cetyl
PEG/PPG-10/1 Dimethicone.sup.2 Treated Pigments 9.90 B1 Volatile
Oil 26.10 Siloxane based polyamide.sup.3 2.00
TiO.sub.2/Silicone-Acrylates.sup.4 12.00 B2 Fillers 6.00 B3
Preservative 0.40 Disteardimonium Hectorite 1.00 Propylene
Carbonate 0.30 C Water 40.00 Magnesium Sulfate 1.00 Preservatives
0.70 Laureth-4 0.50 100.00 .sup.1Dow Corning DC5225C .sup.2ABIL WE
09 .sup.3Dow Corning DC2-8179 (DP = 100) .sup.4SPD-T1S: Silicone
acrylate treated TiO.sub.2
[0608] Phase A ingredients were mixed well and ground with a
Silverson homogenizer at a speed of 6000 rpm. Separately the phase
B1 ingredients were heated to 80 to 85.degree. C. with stirring for
10-15 minutes or until dissolution of the siloxane based polyamide.
Phase A and B1 were then combined in the main beaker and mixed well
at 70 to 75.degree. C. Phase B2 was added to the main beaker and
was mixed well or until uniform. Disteardimonium Hectorite was
added to the main beaker and dispersed well before adding the rest
of phase B3 ingredients. In a separate side beaker, phase C was
heated to 70 to 75.degree. C. Emulsification was carried out by
adding phase C to the main beaker with the use of a homogenizer at
medium/high speed. The batch was cooled to room temperature with a
paddle stirring.
[0609] This composition exhibited good transfer-resistance after
drying, good water resistance and felt cushiony.
Example 4
Foundation
TABLE-US-00006 [0610] Phase Ingredient Name % w/w A Oil Soluble
Sunscreen 4.00 Cyclopentasiloxane and Dimethicone Copolyol.sup.1
8.00 Treated Pigments 9.90 B Volatile Oil 26.10 Siloxane based
polyamide.sup.2 3.00 Polyglyceryl-4-isostearate and Hexyl Laurate
and 3.50 Cetyl PEG/PPG-10/1 Dimethicone.sup.3 Preservative 0.20 C
Fillers 6.04 D Water 42.16 Magnesium Sulfate 1.00 Preservatives
0.30 Laureth-4 0.50 E Water 1.00 Preservative 0.30 100.00 .sup.1Dow
Corning DC5225C .sup.2Dow Corning DC2-9179 (DP = 100) .sup.3ABIL WE
09
[0611] Phase A ingredients were mixed well and ground with a
Silverson homogenizer at a speed of 6000 rpm. Separately the phase
B ingredients were heated to 80 to 85.degree. C. with stirring for
10-15 minutes or until dissolution of siloxane polyamide. Phase A
and B were then combined in the main beaker and mixed well at 60 to
65.degree. C. Phase C ingredients (powders) were added to the main
beaker and were mixed until uniform. Phase D was heated to 65 to
70.degree. C. in a separate side beaker. Emulsification was carried
out by adding phase D to main beaker with the use of a homogenizer
at medium/high speed. Cool the batch to 40 to 45.degree. C., then
add phase E slowly with good mixing. The batch was then cooled to
room temperature with a paddle stirring.
[0612] This composition had good wear, exhibited transfer
resistance and water resistance while feeling cushion
Example 5
Foundation
TABLE-US-00007 [0613] Phase Ingredient Name % w/w A Oil Soluble
Sunscreen 4.00 Cyclopentasiloxane and Dimethicone Copolyol.sup.1
8.00 Cyclopentasiloxane and Diphenyl Dimethicone.sup.2 8.00 Treated
Pigments 10.00 B1 Volatile Oil 18.00 Siloxane based polyamide.sup.3
3.00 Polyglyceryl-4-isostearate and Hexyl Laurate and 3.50 Cetyl
PEG/PPG-10/1 Dimethicone.sup.4 Preservative 0.20 Fillers 6.04 D
Water 42.16 Emollient 10.00 Magnesium Sulfate 1.00 Preservatives
0.30 Laureth-4 0.50 E Water 1.00 Preservative 0.30 100.00 .sup.1Dow
Corning DC5225C .sup.2Mirasil C-DPDM .sup.3Dow Corning DC 2-9179
(DP = 100) .sup.4ABIL WE 09
[0614] Phase A ingredients were mixed well and ground with a
Silverson homogenizer at a speed of 6000 rpm. Separately the phase
B ingredients were heated to 80 to 85.degree. C. with stirring for
10-15 minutes or until dissolution of siloxane polyamide. Phase A
and B were then combined in the main beaker and mixed well at 60 to
65.degree. C. Phase C ingredients (powders) were added to the main
beaker and were mixed until uniform. Phase D was heated to 65 to
70.degree. C. in a separate side beaker. Emulsification was carried
out by adding phase D to main beaker with the use of a homogenizer
at medium/high speed. Cool the batch to 40 to 45.degree. C., then
add phase E slowly with good mixing. The batch was then cooled to
room temperature with a paddle stirring.
[0615] This composition exhibited good wear, transfer resistance
and water resistance
Example 6
Lipstick
TABLE-US-00008 [0616] Ingredient Name Trade name % w/w Dimethicone
20cst DC200 20cs (Dow Corning) 39.04 Polyglyceryl-2-diisostearate
Dermol DGDIS 40.00 Pigments 0.96 Polyamidodimethylsiloxane.sup.1
DC2-8179 15.0 Diisostearyl malate Schercemol DSIM Qsp 100 .sup.1Dow
Corning DC 2-9179 (DP = 115)
[0617] The ingredients are added together in a beaker, heated to
about 80-85.degree. C. while mixing. Once homogeneous, the mixture
is milled at 60 to 65.degree. C. until well dispersed. Once
dispersed, the mixture was discharged from the mill, transferred to
a mixing kettle and heated to 90-95.degree. C. The mill was rinsed
with diisostearyl malate for 10-15 minutes and the contents
transferred to the mixing kettle. The mixture was mixed until
uniform and then poured into molds.
[0618] This composition was supple and elastic.
Example 7
Lipstick
TABLE-US-00009 [0619] Phase Ingredient Name Trade name % w/w A
Dimethicone 20cst DC200 20cs (Dow 20.0 Corning) A
Polyglyceryl-2-diisostearate Dermol DGDIS 20.5 A Diisostearyl
malate Schercemol DSIM 6.0 A Phenyltrimethicone Belsil PDM 1000
20.0 A Phenyltrimethicone DC 556 10.0 B
Polyamidodimethylsiloxane.sup.1 DC2-8179 20.0 C Pigments 1.5 C
Fillers 2.0 .sup.1Dow Corning DC 2-9179 (DP = 15)
[0620] Phase A ingredients were added one by one in a mixing kettle
heated to 90-95.degree. C. and mixed until homogeneous. Phase B was
added and mixed until homogeneous at 90-95.degree. C. Phase C was
added and mixed well. The resulting mixture is poured into molds
and allowed to cool to form sticks.
[0621] This composition was supple and elastic.
Example 8
Lip Gloss
TABLE-US-00010 [0622] Ingredient Trade Name % w/w Film Former SA-70
from 3M 20.0 Polyamidodimethylsiloxane.sup.1 DC2-8179 8.0
Phenyltrimethicone DC 556 65.1 Pigments 6.9 .sup.1Dow Corning DC
2-9179 (DP = 15)
[0623] This composition was supple and elastic.
[0624] The film forming polymer is introduced under agitation with
a magnetic stirrer after the rest of the formula has been heated.
The gloss is introduced into a container and applied using a sponge
type applicator.
[0625] The composition exhibits better wear when compared with one
not containing a film forming polymer.
Examples 9-20
[0626] The preparation procedures for the following examples are as
such:
[0627] Composition without Pigments:
[0628] Mix Phase A until uniform and heat to 110.degree. C.;
[0629] When the temperature of the oil bath reaches 110.degree. C.,
add phase B with agitation until melted and the phase is
uniform;
[0630] Mix the mass and let cool to 90.degree.-95.degree. C.;
[0631] Pour the bulk into lipstick molds.
[0632] Composition with Pigments:
[0633] Charge a portion of Phase A (the oil phase) into a Disconti
Mill;
[0634] Heat to about 65.degree. C. to 70.degree. C.;
[0635] Add the pigments (Phase C). Mill for 40-45 minutes at
65.degree. C. to 70.degree. C. Check the dispersion for the absence
of clumps. This forms the color phase;
[0636] Melt the wax and polymer structuring agent (Phase B) by
heating to 105.degree. C.-110.degree. C. in a melting kettle;
[0637] Discharge the color phase from the mill
[0638] Rinse the mill with the remaining oil phase for 20-30
minutes;
[0639] Complete the color phase with the rinse residual;
[0640] Add the color phase into the melting kettle and heat to
103.degree. C.-105.degree. C.;
[0641] Mix for 20-30 minutes until homogeneous;
[0642] Let cool to 90.degree. C.-95.degree. C. and pour the bulk
into lipstick molds.
Example 9
Lip Composition
TABLE-US-00011 [0643] Ingredient INCI Name Ingredient Trade Name %
w/w Phase A Hydrogenated Polyisobutene Polysynlane V 10.00
Polygyceryl-2 Diisostearate Dermol DGDIS 10.00 Diisostearyl Malate
Schercemol DISM 16.00 Phenyltrimethicone DC 556 10.00 Isononyl
isononanoate Wickenol 151 19.95 Dimethicone and DC 1503 Fluid 10.00
Dimethiconol Phase B Polyamidodimethylsiloxane Example 3 of 16.00
U.S. Pat. No. 5,981,680 Phase C Pigments Pigments 3.05 Mica Mica
Micro C-3000 2.00 Silica MSS-500/3H 1.00 Mica and Titanium Dioxide
Timiron Super Silver 2.00
Example 10
Lip Composition
TABLE-US-00012 [0644] % Ingredient INCI Name Ingredient Trade Name
w/w Phase A Polyglyceryl-2 diisostearate Dermol DGDIS 31.00
Dimethicone Dow Corning 200, 5 cSt 14.89 Dimethicone and DC 1403
5.00 dimethiconol C12-15 Alkyl Benzoate Finsolv TN .TM. 9.00
Isododecyl neopentanoate DUB VCI 10 10.00 Phase B C30-45 alkyl
dimethicone SF-1642 10.00 Polyamidodimethylsiloxane Example 3 of
15.00 U.S. Pat. No. 5,981,680 Phase C Pigments 5.11
Example 11
Lip Balm
TABLE-US-00013 [0645] % Ingredient INCI Name Ingredient Trade Name
w/w Phase A Polyglyceryl-2 diisostearate Dermol DGDIS 43.0
Dimethicone Dow Corning 200, 5 cSt 30.0 C12-15 Alkyl Benzoate
Finsolv TN .TM. 9.0 Dimethicone DC 1428 Fluid 4.0 Phase B Stearyl
Dimethicone DC 2503 Cosmetic Wax 4.0 Polyamidodimethylsiloxane
Example 3 of 10.0 U.S. Pat. No. 5,981,680
[0646] The composition is hydrating, offers good shine, is
comfortable to wear and has a silky feel.
Example 12
Thick Pasty Lipstick
TABLE-US-00014 [0647] Ingredient INCI Name Ingredient Trade Name %
w/w Phase A Hydrogenated Polyisobutene Polysynlane V 10.00
Polygyceryl-2 Diisostearate Dermol DGDIS 10.00 Diisostearyl Malate
Schercemol DISM 16.00 Phenyltrimethicone DC 556 10.00 Isononyl
isononanoate Wickenol 151 19.95 Dimethicone and DC 593 Fluid 10.00
Trimethylsiloxy silicate Phase B Polyamidopolysiloxane Example 3
according to 16.00 U.S. Pat. No. 5,981,680 Phase C Pigments
Pigments 3.05 Mica Mica Micro C-3000 2.00 Silica MSS-500/3H 1.00
Mica and Titanium Dioxide Timiron Super Silver 2.00
Example 13
Lip Balm
TABLE-US-00015 [0648] % Ingredient INCI Name Ingredient Trade Name
w/w Phase A Polyglyceryl-2 diisostearate Dermol DGDIS 47.0
Dimethicone Dow Corning 200, 5 cSt 30.0 C12-15 Alkyl Benzoate
Finsolv TN .TM. 9.0 Phase B Stearyl Dimethicone DC 2503 Cosmetic
Wax 4.0 Polyamidodimethylsiloxane Example 3 according to 10.00 U.S.
Pat. No. 5,981,680
[0649] This composition provided moisturizing, shine, comfort and a
silky feel.
Example 14
Lipstick
TABLE-US-00016 [0650] % Ingredient INCI Name Ingredient Trade Name
w/w Phase A Polyglyceryl-2 diisostearate Dermol DGDIS 36.00
Dimethicone Dow Corning 200, 5 cSt 14.89 C12-15 Alkyl Benzoate
Finsolv TN .TM. 9.00 Isododecyl neopentanoate DUB VCI 10 10.00
Phase B C30-45 alkyl dimethicone SF-1642 10.00
Polyamidodimethylsiloxane Example 3 according to 15.00 U.S. Pat.
No. 5,981,680 Phase C Pigments 5.11
[0651] This composition provided long wear, shine, comfort and a
silky feel.
Example 15
Lipstick
TABLE-US-00017 [0652] % Ingredient INCI Name Ingredient Trade Name
w/w Phase A Polyglyceryl-2 diisostearate Dermol DGDIS 47.0
Dimethicone Dow Corning 200, 5 cSt 30.0 C12-15 Alkyl Benzoate
Finnsolv TN 9.0 Phase B Stearyl Dimethicone DC 2503 Cosmetic Wax
4.0 Polyamidodimethylsiloxane Example 3 according to 10.00 U.S.
Pat. No. 5,981,680
[0653] The composition exhibited good hydration properties with
good skin feel.
Example 16
Lipstick
TABLE-US-00018 [0654] % Ingredient INCI Name Ingredient Trade Name
w/w Phase A Polyglyceryl-2 diisostearate Dermol DGDIS 36.00
Dimethicone Dow Corning 200, 5 cSt 14.89 C12-15 Alkyl Benzoate
Finnsolv TN 9.00 Isododecyl neopentanoate DUB VCI 10 10.00 Phase B
C30-45 alkyl dimethicone SF-1642 10.00 Polyamidodimethylsiloxane
Example 3 according to 15.00 U.S. Pat. No. 5,981,680 Phase C
Pigments 5.11
[0655] The composition was non tacky, with a silky skin feel and
good wear.
Example 17
Lipstick
TABLE-US-00019 [0656] Ingredient INCI Name Ingredient Trade Name %
w/w Phase A Hydrogenated Polyisobutene Polysynlane V 10.00
Polyglyceryl-2 diisostearate Dermol DGDIS 10.00 Diisostearoyl
malate Schercemol DISM 16.00 Phenyltrimethicone DC 556 10.00
Isononyl isononanoate Wickenol 151 19.95 Dimethicone and trimethyl-
DC 593 Fluid 10.00 Siloxysilicate Phase B Polyamidodimethylsiloxane
Example 3 according to 16.00 U.S. Pat. No. 5,981,680 Phase C
Pigments 3.05 Fillers 5.00
[0657] The composition was glossy, non tacky with a silky feel and
good wear.
Examples 18, 19 & 20
Lipsticks
TABLE-US-00020 [0658] Ex. 18 Ex. 19 Ex. 20 (% (% (% Phase
Ingredient Name Trade Name w/w) w/w) w/w) A Dimethicone DC 200 20
cST 40.00 40.00 39.04 Polyglygeryl-2 Dermol DGDIS 50.00 50.00 40.00
Diisostearate Diisostearyl malate Schercemol -- -- 5.00 DISM B
Polyamidodimethyl- DP* = 100 16.00 -- -- siloxane Example 3
according to U.S. Pat. No. 5,981,680 Polyamidodimethyl- DP8 = 100
-- 10.00 16.00 siloxane prepared per U.S. Pat. No. 5,981,680 C
Pigments -- -- 0.96 DP* = Degree of polymerization
[0659] The compositions exhibited good hydration with excellent
skin feel.
[0660] The sticks of lipstick obtained had a diameter of 8.1 mm and
a hardness of 135.+-.2 gf measured using a "cheese wire".
[0661] The stability of the compositions was tested using the test
described herein. The composition was found to have good stability
in that there was no exudation at room temperature (25.degree. C.)
and 47.degree. C. for 1 month.
Example 21
Lipstick
TABLE-US-00021 [0662] silicone polyamide (polymerization degree 45)
20% phenyl trimethicone 66.3% (DC 556 .RTM. DOW CORNING)
hydrophobic silica (Aerosil R972) 5% pigments qsp 100%
[0663] Procedure
[0664] Silica gel: the gel was prepared, with stirring in a Rayneri
stirrer at 60.degree. C., using a hotplate, by introducing 5 g
silica portionwise into 53 g DC 556.
[0665] Ground pigmentary material: the pigments were mixed with
13.3 g DC 556 heated to 60.degree. C.; the mixture was ground three
times in a three-roll mill.
[0666] The silicone polyamide was solubilized (or dissolved) at
100.degree. C.-110.degree. C. in the ground pigmentary material,
followed by addition of the Silica gel. The whole mixture was mixed
using a deflocculating turbomixer (Raynerie) and left stirring for
1H 30 min. The product obtained was then cast in molds for
lipsticks in stick form.
[0667] The sticks of lipstick obtained had a diameter of 8.1 mm and
a hardness of 135.+-.2 gf measured using a "cheese wire".
[0668] The stability of the compositions was tested using the test
described herein. The composition was found to have good stability
in that there was no exudation at room temperature (25.degree. C.)
and 47.degree. C. for 1 month.
[0669] It is observed that a similar composition containing no
silica only shows a hardness of 100.+-.2 gf. This lipstick is easy
to apply, non greasy and shiny. It does not exude.
Example 22
Foundation
[0670] In phase A, ingredients are mixed well and ground with a
Silverson homogenizer at a speed of 6000 rpm.
[0671] Separately the phase B1 ingredients are heated to 80 to
85.degree. C. with stirring for 10-15 minutes or until dissolution
of the siloxane-polyamide.
[0672] Phase A and B1 are then combined in the main beaker and
mixed well at 70 to 75.degree. C.
[0673] Phase B2 is added to the main beaker and is mixed until
uniform.
[0674] Disteardimonium Hectorite is added to the main beaker and
dispersed well before adding rest of phase B3 ingredients.
[0675] Phase C is heated to 70 to 75.degree. C. in a separate side
beaker. Emulsification is carried out by adding phase C to main
beaker and homogenizing at medium/high speed.
[0676] The batch is cooled to room temperature with a paddle
stirrer.
TABLE-US-00022 PHASE INCI Name % w/w A Cyclopentasiloxane (and)
dimethicone copolyol 8.0 Polyglyceryl-4 isostearate (and) hexyl
laurate (and) 3.5 cetyl PEG/PPG-10/1 dimethicone Treated pigments
9.9 B1 Cyclopentasiloxane 26.1 Silicone polyamide 3.0 B2
Polytrap/cyclopentasiloxane 1.0 MMA* Crosspolymer 4.0 Nylon-12 1.0
B3 Preservative 0.4 Disteardimonium Hectorite 0.6 Propylene
Carbonate 0.2 C Water 40.0 Magnesium Sulfate 1.0 Preservatives 0.7
Non ionic emulsifier 0.5 TOTAL 100.00 *MMA =
methyl-methacrylate
[0677] The foundation provides a smooth application with excellent
slip and cushion, and excellent transfer-resistance after drying.
It further shows a very good water resistance.
Example 23
Foundation
[0678] The composition is prepared as described in example 21.
TABLE-US-00023 PHASE INCI Name % w/w A Cyclopentasiloxane (and)
dimethicone copolyol 8.0 Polyglyceryl-4 isostearate (and) hexyl
laurate (and) 3.5 cetyl PEG/PPG-10/1 dimethicone Treated pigments
9.9 B1 Volatile oil 16.1 Silicone polyamide 1.0 Silicone-Acrylates
12.0 B2 Polytrap/cyclopentasiloxane 1.0 MMA* Crosspolymer 4.0
Nylon-12 1.0 B3 Preservative 0.4 Disteardimonium Hectorite 0.6
Propylene Carbonate 0.2 C Water 40.0 Magnesium Sulfate 1.0
Preservatives 0.2 Non ionic emulsifier 0.5 TOTAL 100.00 *MMA =
methyl-methacrylate
[0679] The foundation provides a good application with cushion,
good transfer-resistance after drying. The deposit shows very good
water resistance.
Example 24
Lip Gloss
TABLE-US-00024 [0680] Ingredient Trade Name % w/w Film Former SA-70
from 3M 20.0 Polyamidodimethylsiloxane.sup.1 DC2-8179 8.0
Phenyltrimethicone DC 556 65.1 Pigments 6.9 .sup.1Dow Corning DC
2-9179 (DP = 15)
[0681] This composition was supple and elastic.
[0682] The film forming polymer is introduced under agitation with
a magnetic stirrer after the rest of the formula has been heated.
The gloss is introduced into a container and applied using a sponge
type applicator.
[0683] The composition exhibits better wear when compared with one
not containing a film-forming polymer.
Example 25
Foundation
[0684] In phase A, ingredients are mixed well and ground with a
Silverson homogenizer at a speed of 6000 rpm.
[0685] Separately the phase B1 ingredients are heated to 80 to
85.degree. C. with stirring for 10-15 minutes or until dissolution
of the siloxane-polyamide.
[0686] Phase A and B1 are then combined in the main beaker and
mixed well at 70 to 75.degree. C.
[0687] Phase B2 is added to the main beaker and is mixed until
uniform.
[0688] Disteardimonium Hectorite is added to the main beaker and
dispersed well before adding rest of phase B3 ingredients.
[0689] Phase C is heated to 70 to 75.degree. C. in a separate side
beaker. Emulsification is carried out by adding phase C to main
beaker and homogenizing at medium/high speed.
[0690] The batch is cooled to room temperature with a paddle
stirrer.
TABLE-US-00025 PHASE INCI Name % w/w A Cyclopentasiloxane (and)
dimethicone copolyol 8.0 Polyglyceryl-4 isostearate (and) hexyl
laurate (and) 3.5 cetyl PEG/PPG-10/1 dimethicone Treated pigments
9.9 B1 Cyclopentasiloxane 16.1 Polysiloxane/Polyamide 1.0
Silicone-Acrylates 12.0 B2 Fillers 6.0 B3 Preservative 0.4
Disteardimonium Hectorite 0.6 Propylene Carbonate 0.2 C Water Qsp
100 Magnesium Sulfate 1.0 Preservative 0.7 Non ionic emulsifier 0.5
TOTAL 100.00
Example 26
Foundation
[0691] The composition is prepared according to the same procedure
as described in example 25.
TABLE-US-00026 Phase Ingredient Name % w/w A Cyclopentasiloxane and
Dimethicone Copolyol 8.00 Polyglyceryl-4-isostearate and Hexyl
Laurate and Cetyl 3.50 PEG/PPG-10/1 Dimethicone2 Treated Pigments
9.90 B1 Volatile Oil 26.10 Siloxane based polyamide 2.00
TiO.sub.2/Silicone-Acrylates 12.00 B2 Fillers 6.00 B3 Preservative
0.40 Disteardimonium Hectorite 1.00 Propylene Carbonate 0.30 C
Water qsp Magnesium Sulfate 1.00 Preservatives 0.70 Laureth-4 0.50
100.00
Example 27
Foundation
TABLE-US-00027 [0692] Phase Trade Name INCI Name % w/w A1 PERMETHYL
99A ISODODECANE 26.80 DC 2-8179 GELLANT - NYLON-611/ 0.50 BATCH #
18841-9 DIMETHICONE COPOLYMER (DP = 100) A2 SR-1000 TRIMETHYL- 5.00
SILOXYSILICATE ISOLAN GI 34 POLYGLYCERYL-4 2.00 ISOSTEARATE ABIL EM
90 CETYL PEG/PPG-10/1 0.50 DIMETHICONE BELSIL DMC 6038 BIS-PEG-15
METHYL 1.00 ETHER DIMETHICONE ITT-Titanium Dioxide ITT-Titanium
Dioxide 10.00 ITT-Iron Oxide - Yellow ITT-Iron Oxides 1.25 ITT-Iron
Oxide - Red ITT-Iron Oxides (and) Iron 0.50 Oxides ITT-Iron Oxide -
Black ITT-Iron Oxides (and) Iron 0.25 Oxides B1 SUNSPHERE H 51
SILICA 3.00 MSS-500W SILICA 3.00 KSP-100 VINYL 1.00 DIMETHICONE/
METHICONE SILSESQUIOXANE CROSSPOLYMER B2 Butylparaben Butylparaben
0.20 Betone 38V Disteardimonium Hectorite 1.40 Propylene Carbonate
Propylene Carbonate 0.70 C Water Water 40.00 SODIUM CHLORIDE SODIUM
CHLORIDE 1.00 HYDROLITE-5 PENTYLENE GLYCOL 0.50 SODIUM SODIUM 0.20
DEHYDROACETATE DEHYDROACETATE MONOHYDRATE Methylparaben
Methylparaben 0.20 BRIJ 30 Laureth-4 0.50 Phenoxyethanol
Phenoxyethanol 0.50 Total: 100.00
[0693] Preparation Procedure:
1. Heat Al at 85 to 90.degree. C. for 15 minutes or until DC2-8179
is dissolved. Cool to room temperature. 2. Mix phase A ingredients,
grinding with Silverson at 6000 to 7000 rpm for 30 to 40 minutes.
3. Add phase B1 ingredients, one at a time, mix well with Silverson
at about 6000 rpm. 4. Add Butylparaben and Disteardimonium
Hectorite, mixing with Silverson at 6000 rpm until good dispersion
is obtained, then add propylene carbonate, mix at 6000 to 7000 rpm
for 10 to 15 minutes. 5. Removed the main beaker from Silverson and
transfer to Homogenizer. Warm the contents to 25 to 30.degree. C.
6. In separate beaker, heat phase C to 40 to 45.degree. C. After it
is uniform, cool to 25 to 30.degree. C. 7. Add phase C slowly to
the main beaker at 25 to 30.degree. C. to form an emulsion.
Homogenize at 30% for 5 minutes.
Example 28
Foundation
TABLE-US-00028 [0694] Phase Trade Name INCI Name % w/w A1 PERMETHYL
99A ISODODECANE 28.50 DC 2-8179 GELLANT - NYLON-611/ 1.00
DIMETHICONE BATCH # 18841-9 COPOLYMER (DP = 100) PERMETHYL 101A
ISOHEXADECANE 2.00 A2 SR-1000 TRIMETHYL- 6.00 SILOXYSILICATE ISOLAN
GI 34 POLYGLYCERYL-4 2.00 ISOSTEARATE ABIL EM 90 CETYL PEG/PPG-10/1
0.50 DIMETHICONE BELSIL DMC 6038 BIS-PEG-15 METHYL 1.00 ETHER
DIMETHICONE ITT-Titanium Dioxide ITT-Titanium Dioxide 10.05
ITT-Iron Oxide - Yellow ITT-Iron Oxides 1.25 ITT-Iron Oxide - Red
ITT-Iron Oxides (and) Iron 0.45 Oxides ITT-Iron Oxide - Black
ITT-Iron Oxides (and) Iron 0.25 Oxides B1 SUNSPHERE H 51 SILICA
3.00 MSS-500W SILICA 3.00 KSP-100 VINYL DIMETHICONE/ 1.00 METHICONE
SILSESQUIOXANE CROSSPOLYMER B2 Butylparaben Butylparaben 0.20
Betone 38V Disteardimonium Hectorite 1.40 Propylene Carbonate
Propylene Carbonate 0.70 C Water Water 35.00 SODIUM CHLORIDE SODIUM
CHLORIDE 1.00 HYDROLITE-5 PENTYLENE GLYCOL 0.50 SODIUM SODIUM 0.20
DEHYDROACETATE DEHYDROACETATE MONOHYDRATE Methylparaben
Methylparaben 0.20 BRIJ 30 Laureth-4 0.50 Phenoxyethanol
Phenoxyethanol 0.30 Total: 100.00
[0695] Preparation Procedure:
1. Heat Al at 85 to 90.degree. C. for 15 minutes or until DC2-8179
is dissolved. Cool to room temperature. 2. Mix phase A ingredients,
grinding with Silverson at 6000 to 7000 rpm for 30 to 40 minutes.
3. Add phase B1 ingredients, one at a time, mix well with Silverson
at about 6000 rpm. 4. Add Butylparaben and Disteardimonium
Hectorite, mixing with Silverson at 6000 rpm until good dispersion
is obtained, then add propylene carbonate, mix at 6000 to 7000 rpm
for 10 to 15 minutes. 5. Removed the main beaker from Silverson and
transfer to Homogenizer. Warm the contents to 25 to 30.degree. C.
6. In separate beaker, heat phase C to 40 to 45.degree. C. After it
is uniform, cool to 25 to 30.degree. C. 7. Add phase C slowly to
the main beaker at 25 to 30.degree. C. to form an emulsion.
Homogenize at 30% for 5 minutes.
Example 29
Foundation
TABLE-US-00029 [0696] Phase Trade Name INCI Name % w/w A1 PERMETHYL
99A ISODODECANE 26.00 DC2-8179 PS/PA (DP-100) 0.50 A2 SR-1000
TRIMETHYL 6.00 SILOXYSILICATE ISOLAN GI 34 POLYGLYCERYL-4 1.50
ISOSTEARATE ABIL EM 90 CETYL PEG/PPG-10/1 1.00 DIMETHICONE BELSIL
DMC 6038 BIS-PEG-15 METHYL 0.80 ETHER DIMETHICONE ITT-Titanium
Dioxide ITT-Titanium Dioxide 10.00 ITT-Iron Oxide - Yellow ITT-Iron
Oxides 1.25 ITT-Iron Oxide - Red ITT-Iron Oxides (and) Iron 0.50
Oxides ITT-Iron Oxide - Black ITT-Iron Oxides (and) Iron 0.25
Oxides B1 SUNSPHERE H 51 SILICA 3.00 MSS-500W SILICA 3.00 KSP-100
VINYL DIMETHICONE/ 1.00 METHICONE SILSESQUIOXANE CROSSPOLYMER B2
Butylparaben Butylparaben 0.20 Betone 38V Disteardimonium Hectorite
1.40 Propylene Carbonate Propylene Carbonate 0.70 C Water Water
40.00 SODIUM CHLORIDE SODIUM CHLORIDE 1.00 HYDROLITE-5 PENTYLENE
GLYCOL 0.50 SODIUM SODIUM 0.20 DEHYDROACETATE DEHYDROACETATE
MONOHYDRATE Methylparaben Methylparaben 0.20 BRIJ 30 Laureth-4 0.50
Phenoxyethanol Phenoxyethanol 0.50 Total: 100.00
[0697] Preparation Procedure:
1. Heat Al at 85 to 90.degree. C. for 15 minutes or until PS/PA is
dissolved. Cool to room temperature. 2. Mix phase A ingredients,
grinding with Silverson at 6000 to 7000 rpm for 30 to 40 minutes.
3. Add phase B1 ingredients, one at a time, mix well with Silverson
at about 6000 rpm. 4. Add Butylparaben and Disteardimonium
Hectorite, mixing with Silverson at 6000 rpm until good dispersion
is obtained, then add propylene carbonate, mix at 6000 to 7000 rpm
for 10 to 15 minutes. 5. Removed the main beaker from Silverson and
transfer to Homogenizer. Warm the contents to 25 to 30.degree. C.
6. In separate beaker, heat phase C to 40 to 45.degree. C. After it
is uniform, cool to 25 to 30.degree. C. 7. Add phase C slowly to
the main beaker at 25 to 30.degree. C. to form an emulsion.
Homogenize at 30% for 5 minutes.
Example 30
Foundation
TABLE-US-00030 [0698] Phase Trade Name INCI Name % w/w A1 PERMETHYL
99A ISODODECANE 27.30 DC2-8179 PS/PA (DP-100) 0.50 A2 SR-1000
TRIMETHYL- 5.00 SILOXYSILICATE ISOLAN GI 34 POLYGLYCERYL-4 2.00
ISOSTEARATE BELSIL DMC 6038 BIS-PEG-15 METHYL 1.00 ETHER
DIMETHICONE ITT-Titanium Dioxide ITT-Titanium Dioxide 10.00
ITT-Iron Oxide - Yellow ITT-Iron Oxides 1.25 ITT-Iron Oxide - Red
ITT-Iron Oxides (and) Iron 0.50 Oxides ITT-Iron Oxide - Black
ITT-Iron Oxides (and) Iron 0.25 Oxides B1 SUNSPHERE H 51 SILICA
3.00 MSS-500W SILICA 3.00 KSP-100 VINYL DIMETHICONE/ 1.00 METHICONE
SILSESQUIOXANE CROSSPOLYMER B2 Butylparaben Butylparaben 0.20
Betone 38V Disteardimonium Hectorite 1.40 Propylene Carbonate
Propylene Carbonate 0.70 C Water Water 40.00 SODIUM CHLORIDE SODIUM
CHLORIDE 1.00 HYDROLITE-5 PENTYLENE GLYCOL 0.50 SODIUM SODIUM 0.20
DEHYDROACETATE DEHYDROACETATE MONOHYDRATE Methylparaben
Methylparaben 0.20 BRIJ 30 Laureth-4 0.50 Phenoxyethanol
Phenoxyethanol 0.50 Total: 100.00
[0699] Preparation Procedure:
1. Heat Al at 85 to 90.degree. C. for 15 minutes or until PS/PA is
dissolved. Cool to room temperature. 2. Mix phase A ingredients,
grinding with Silverson at 6000 to 7000 rpm for 30 to 40 minutes.
3. Add phase B1 ingredients, one at a time, mix well with Silverson
at about 6000 rpm. 4. Add Butylparaben and Disteardimonium
Hectorite, mixing with Silverson at 6000 rpm until good dispersion
is obtained, then add propylene carbonate, mix at 6000 to 7000 rpm
for 10 to 15 minutes. 5. Removed the main beaker from Silverson and
transfer to Homogenizer. Warm the contents to 25 to 30.degree. C.
6. In separate beaker, heat phase C to 40 to 45.degree. C. After it
is uniform, cool to 25 to 30.degree. C. 7. Add phase C slowly to
the main beaker at 25 to 30.degree. C. to form an emulsion.
Homogenize at 30% for 5 minutes.
Example 31
Foundation
TABLE-US-00031 [0700] Phase Trade Name INCI Name % w/w A1 PERMETHYL
99A ISODODECANE 26.80 DC 2-8179 GELLANT - NYLON-611/ 0.50
DIMETHICONE BATCH # 18841-9 COPOLYMER (DP-100) A2 SR-1000
TRIMETHYL- 5.00 SILOXYSILICATE ISOLAN GI 34 POLYGLYCERYL-4 2.00
ISOSTEARATE ABIL EM 90 CETYL PEG/PPG-10/1 0.50 DIMETHICONE BELSIL
DMC 6038 BIS-PEG-15 METHYL 1.00 ETHER DIMETHICONE ITT-Titanium
Dioxide ITT-Titanium Dioxide 10.00 ITT-Iron Oxide - Yellow ITT-Iron
Oxides 1.25 ITT-Iron Oxide - Red ITT-Iron Oxides (and) Iron 0.50
Oxides ITT-Iron Oxide - Black ITT-Iron Oxides (and) Iron 0.25
Oxides B1 SUNSPHERE H 51 SILICA 3.00 MSS-500W SILICA 3.00 KSP-100
VINYL DIMETHICONE/ 1.00 METHICONE SILSESQUIOXANE CROSSPOLYMER B2
Butylparaben Butylparaben 0.20 Betone 38V Disteardimonium Hectorite
1.40 Propylene Carbonate Propylene Carbonate 0.70 C Water Water
40.00 SODIUM CHLORIDE SODIUM CHLORIDE 1.00 HYDROLITE-5 PENTYLENE
GLYCOL 0.50 SODIUM SODIUM 0.20 DEHYDROACETATE DEHYDROACETATE
MONOHYDRATE Methylparaben Methylparaben 0.20 BRIJ 30 Laureth-4 0.50
Phenoxyethanol Phenoxyethanol 0.50 Total: 100.00
[0701] Preparation Procedure:
1. Heat A1 at 85 to 90.degree. C. for 15 minutes or until DC2-8179
is dissolved. Cool to room temperature. 2. Mix phase A ingredients,
grinding with Silverson at 6000 to 7000 rpm for 30 to 40 minutes.
3. Add phase B1 ingredients, one at a time, mix well with Silverson
at about 6000 rpm. 4. Add Butylparaben and Disteardimonium
Hectorite, mixing with Silverson at 6000 rpm until good dispersion
is obtained, then add propylene carbonate, mix at 6000 to 7000 rpm
for 10 to 15 minutes. 5. Removed the main beaker from Silverson and
transfer to Homogenizer. Warm the contents to 25 to 30.degree. C.
6. In separate beaker, heat phase C to 40 to 45.degree. C. After it
is uniform, cool to 25 to 30.degree. C. 7. Add phase C slowly to
the main beaker at 25 to 30.degree. C. to form an emulsion.
Homogenize at 30% for 5 minutes.
Example 32
Foundation
TABLE-US-00032 [0702] Phase Trade Name INCI Name % w/w A1 PERMETHYL
99A ISODODECANE 25.20 DC 2-8179 GELLANT - NYLON-611/ 0.50
DIMETHICONE BATCH # 18841-9 COPOLYMER (DP-100) PERMETHYL 101A
ISOHEXADECANE 2.00 A2 SR-1000 TRIMETHYL- 6.00 SILOXYSILICATE ISOLAN
GI 34 POLYGLYCERYL-4 2.00 ISOSTEARATE ABIL EM 90 CETYL PEG/PPG-10/1
0.50 DIMETHICONE BELSIL DMC 6038 BIS-PEG-15 METHYL 0.80 ETHER
DIMETHICONE X-22-8238 Isododecane (60%) (and) 3.50 ACRYLATES/
DIMETHICONE COPOLYMER ITT-Titanium Dioxide ITT-Titanium Dioxide
10.34 ITT-Iron Oxide - Yellow ITT-Iron Oxides 1.10 ITT-Iron Oxide -
Red ITT-Iron Oxides (and) Iron 0.36 Oxides ITT-Iron Oxide - Black
ITT-Iron Oxides (and) Iron 0.20 Oxides A3 SUNSPHERE H 51 SILICA
3.00 MSS-500W SILICA 2.00 ORGASOL 2002 Nylon-12 1.00 KSP-100 VINYL
DIMETHICONE/ 1.00 METHICONE SILSESQUIOXANE CROSSPOLYMER A4
Butylparaben Butylparaben 0.20 Betone 38V Disteardimonium Hectorite
1.65 Propylene Carbonate Propylene Carbonate 0.85 B Water Water
35.00 SODIUM CHLORIDE SODIUM CHLORIDE 1.00 HYDROLITE-5 PENTYLENE
GLYCOL 0.50 SODIUM SODIUM 0.20 DEHYDROACETATE DEHYDROACETATE
MONOHYDRATE Methylparaben Methylparaben 0.20 BRIJ 30 Laureth-4 0.50
Phenoxyethanol Phenoxyethanol 0.40 Total: 100.00
[0703] Preparation Procedure:
1. Heat Al at 85 to 90.degree. C. for 15 minutes or until DC2-8179
is dissolved. Cool to room temperature. 2. Add phase A2
ingredients, grinding with Silverson at 6000 to 7000 rpm for 60
minutes. 3. Add phase A3 ingredients, one at a time, mix well with
Silverson at about 6000 rpm. 4. Add Butylparaben and
Disteardimonium Hectorite, mixing with Silverson at 6000 rpm until
good dispersion is obtained, then add propylene carbonate, mix at
6000 to 7000 rpm for 10 to 15 minutes. 5. Removed the main beaker
from Silverson and transfer to Homogenizer. 6. In separate beaker,
heat phase B to 50 to 55.degree. C. After it is uniform, cool to 25
to 30.degree. C. 7. Add phase B slowly to the main beaker at 25 to
30.degree. C. to form an emulsion. Homogenize at 30% for 5
minutes.
Examples 33 and 34
Lipsticks
TABLE-US-00033 [0704] Phase Trade Name INCI Name Ex. 33 Ex. 34 A
PERMETHYL 99A ISODODECANE 27.19 17.19 DC 200 1.5 cst dimethicone
10.00 SR 1000 trimethylsyloxysilicate 22.00 22.00 DC 2-8179
NYLON-611/ 7.50 7.50 GELLANT - DIMETHICONE BATCH # 18841-9
COPOLYMER (DP-100) Bentone gel ISD V DISTEARDIMONIUM 30.00 30.00
HECTORITE/ isododecane THIXCIN R trihydroxystearin 0.50 0.50
Liquapar oil isopropylparaben, 0.20 0.20 isobutylparaben B Black
Iron Oxide Iron Oxides 0.24 0.24 FDC red 21 Al Lake red 21 Lake
1.83 1.83 DC Red 7 W Red 7 Lake 0.24 0.24 Yellow Iron Oxide Iron
Oxides 0.97 0.97 Red Iron Oxide Iron Oxides 1.83 1.83 MSS-500/3H
silica 1.00 1.00 Aerosil R 972 Silica simethyl silylate 0.50 0.50 C
Flamenco mica and titanium 3.00 3.00 Superpearl 120C dioxide mica M
mica 3.00 3.00 total= 100.00 100.00
[0705] Preparation Procedure: [0706] 1. Combine Phase A ingredients
in a beaker, then transfer the beaker to a 90.degree. C. oil bath
and mix with a propeller mixer until uniform. [0707] 2. Combine
Phase B ingredients together into Phase A, then transfer the
mixture to a Disconti Ball Mill and mill the mixture for about 40
minutes. [0708] 3. Transfer the mixture into a beaker, then add
Phase C ingredients and mix with a propeller mixer at room
temperature until uniform. [0709] 4. Transfer the resulting fluid
to individual packages.
Examples 34 and 35
Gelled Makeup
TABLE-US-00034 [0710] Phase Material Ex. 35 Ex. 36 Ingredient name
A Dow Corning PS/PA 7.00 7.00 Nylon-611/Dimethicone Copolymer
copolymer (DC 2-8179 lot 18841-9) Dow Corning PS/PA
Nylon-611/Dimethicone Copolymer copolymer (DC 2-8178) KSP-100 8.00
8.00 Vinyl dimethicone/methicone sissesquioxane crosspolymer
GP1/Inin 4% Dibutyl Lauryl glutamide/Isononyl isononanoate GP1 0.20
1.00 Dibutyl lauryl glutamide Dimethicone Copolyol Bis-PEG-15
Methyl Ether Dimethicone Dimethicone Copolyol Shin-Etsu KF-6105,
Polyglycerin modified silicone w/lauryl group Emerest 2452
Polyglycerol-3-diisostearate Isononyl isononanoate 51.30 50.50 DC
200 @ 10 cst 2.00 2.00 Dimethicone B SNI TA 46R 7.66 7.66 Talc,
Hydrogenated C12-18 Triglyceride, Methicone NAI treated Red
C33-8075- 0.42 0.42 Red Iron oxide, Disodium Stearoyl 10 Glutimate,
Aluminum hydroxide NAI treated Yellow C33- 0.72 0.72 Iron Oxide
yellow, Disodium Stearoyl 8073-10 Glutimate, Aluminum hydroxide NAI
treated blue C43-1810- 0.40 0.40 Ultramarine Blue, Disodium
Stearoyl 10 Glutimate, Aluminum hydroxide NAI treated TiO2
C47-051-10 6.00 6.00 TiO2, Disodium Stearoyl Glutimate, Aluminum
hydroxide TiO2 STT 65-S 5.00 5.00 Ultrafine TiO2, Isopropyl
titanium triisostearate MMA cross polymer 11.30 11.30 Ganzpearl
GMX-0610 Total 100.00 100.00
[0711] Heat phase A components to 135.degree. C. Cover and mix
until ingredients are dissolved. Once phase A is dissolved, add
74275 (KSP-100). Cool to 96-98.degree. C. In a quart mason jar
using an Osterizer blender, blend the dry phase B ([Si tr. Talc],
[NAI tr red I.O.], [NAI tr. Yellow I.O.], [NAI tr. U. Blue], [NAI
tr. T102], [U.F. Ultrafine TiO2], [Luxsil], [Mica PHN]), powders).
Blend for 1.5 minutes, scrape the sides, then blend for an
additional 1.5 minutes. Note: the volume in the jar must be approx
1/3 full, usually approx. 100 g for adequate powder mixing. Once
the batch has cooled to 96-98.degree. C. add phase B. Blend with
enough agitation to disperse pigment, but avoid aerating batch. For
5 to 10 minutes. Decrease agitation to deair batch. A vacuum may be
used. Drop the batch at 90-95.degree. C. into pans.
* * * * *