U.S. patent application number 11/198567 was filed with the patent office on 2006-01-26 for antimicrobial material for implanting in bones.
This patent application is currently assigned to Bio-Gate Bioinnovative Materials GmbH. Invention is credited to Thorsten Bechert, Peter Steinruecke.
Application Number | 20060018943 11/198567 |
Document ID | / |
Family ID | 7654674 |
Filed Date | 2006-01-26 |
United States Patent
Application |
20060018943 |
Kind Code |
A1 |
Bechert; Thorsten ; et
al. |
January 26, 2006 |
Antimicrobial material for implanting in bones
Abstract
The invention relates to an antimicrobial material for
implanting in bones and for coating or producing an implant or an
implantable medical device, whereby particles formed from an
antimicrobial material are remotely dispersed inside a matrix
material that forms a matrix when hardened. In order to improve the
compatibility of the antimicrobial material, the invention provides
that the metal is formed from aggregates of primary particles
having an average particle size ranging from 10 to 100 nm.
Inventors: |
Bechert; Thorsten;
(Forchheim, DE) ; Steinruecke; Peter; (Erlangen,
DE) |
Correspondence
Address: |
PEARNE & GORDON LLP
1801 EAST 9TH STREET
SUITE 1200
CLEVELAND
OH
44114-3108
US
|
Assignee: |
Bio-Gate Bioinnovative Materials
GmbH
Nurnberg
DE
|
Family ID: |
7654674 |
Appl. No.: |
11/198567 |
Filed: |
August 5, 2005 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
10363120 |
Apr 28, 2003 |
|
|
|
PCT/DE01/03210 |
Aug 28, 2001 |
|
|
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11198567 |
Aug 5, 2005 |
|
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Current U.S.
Class: |
424/422 ;
424/618; 424/649 |
Current CPC
Class: |
A61L 31/10 20130101;
A61L 29/085 20130101; A61L 24/0015 20130101; A61L 2300/104
20130101; A61L 27/34 20130101; A61L 27/54 20130101; A61L 27/34
20130101; A61L 29/085 20130101; A61L 31/10 20130101; A61L 2300/624
20130101; A61L 2300/102 20130101; A61L 31/128 20130101; A61L 27/446
20130101; C08L 33/06 20130101; C08L 33/06 20130101; C08L 33/00
20130101; C08L 33/06 20130101; A61L 2430/02 20130101; A61L 31/16
20130101; A61L 29/16 20130101; A61L 2300/404 20130101; A61L 27/34
20130101; A61L 2300/606 20130101; A61L 29/126 20130101 |
Class at
Publication: |
424/422 ;
424/618; 424/649 |
International
Class: |
A61K 33/24 20060101
A61K033/24; A61K 33/38 20060101 A61K033/38; A61F 13/00 20060101
A61F013/00 |
Foreign Application Data
Date |
Code |
Application Number |
Aug 31, 2000 |
DE |
100 43 151.8 |
Claims
1. An antimicrobial powder comprising discrete aggregates formed
from an antimicrobial metal, wherein the aggregates are highly
porous and are formed of primary particles connected together by
necks, the primary particles having an average size between 10 and
100 nm.
2. The antimicrobial powder as in claim 1, wherein the aggregates
have an average aggregate size of from 1 to 20 .mu.m.
3. The antimicrobial powder as in claim 2, wherein the aggregates
have an average aggregate size of from 10 to 20 .mu.m.
4. The antimicrobial powder as in claim 1, 2, or 3, wherein the
aggregates have a surface area of from 3 to 6 m.sup.2 per gram.
5. The antimicrobial powder as in claim 1, 2, or 3, wherein the
aggregates have a porosity of up to 95%.
6. The antimicrobial powder as in claim 1, wherein the aggregates
are produced by inert gas vaporization and condensation.
7. The antimicrobial metal powder of claim 6, wherein the
aggregates are produced under a pressure of from 10 to 100 mbar of
inert gas.
8. The antimicrobial powder as in claim 1, wherein the metal is
formed from one or more of the following components: Ag, Au, Pt,
Pd, Ir, Sn, Cu, Sb, Zn.
9. The antimicrobial powder as in claim 1, wherein the metal has an
essentially undisordered lattice structure.
10. The antimicrobial powder as in claim 1, 2, or 3, wherein said
primary particles have a generally spherical shape.
11. An antimicrobial material including a matrix material made of a
polymer and containing the antimicrobial powder according to one of
claims 1, 2 or 3.
12. The antimicrobial material of claim 11, wherein the polymer
comprises an acrylic ester and/or a methacrylic ester.
Description
[0001] This application is a continuation of U.S. application Ser.
No. 10/363,120, filed Apr. 28, 2003, which application is a
national stage application under 35 USC .sctn. 371 and claims
benefit under 35 USC .sctn. 119(a) of International Application No.
PCT/DE01/03210 having an International filing date of Aug. 28,
2001, which claims benefit of DE 100 43 151.8 filed on Aug. 31,
2000.
[0002] The invention relates to an antimicrobial material for
implanting in bones, for coating or producing implants or an
implantable device corresponding to the preamble of claim 1. It
further relates to a process for producing such a material.
[0003] EP 0 190 504 discloses an antimicrobial composition which
contains 5 to 10% by weight of silver. In addition, to improve the
antimicrobial properties, a hydratable or a hydrated oxide is
added.
[0004] DE 31 10 681 C2 describes a material for bone implants. The
material is produced from a polymer to which silver phosphate is
added as antimicrobial agent.
[0005] WO 81/02667 discloses an antimicrobial surgical implant.
Metallic silver is added to the implant as antimicrobial agent.
[0006] The generic WO 82/01990 describes a bone cement based on
polymethylmethacrylate as main component, to which 5% by volume of
a silver salt is added as antimicrobial agent.
[0007] U.S. Pat. No. 5,837,275 discloses an antimicrobial material
which contains, inter alia, silver particles with a particle size
of less than 200 nm. The silver lattice has lattice disorders and
defects in order to facilitate release of silver ions.
[0008] WO 84/01721 discloses a material provided with silver
sulfate or silver acetate. This material releases a concentration
of more than 1 .mu.M silver ions in a surrounding fluid within 24
hours.
[0009] DE 32 288 849 A1 describes a material with a coating made of
silver. Elemental carbon or titanium is added to the material. The
addition is intended to facilitate increased release of silver ions
into the surroundings.
[0010] U.S. Pat. No. 4,849,233 discloses a bone cement to which
about 10% by weight of elemental silver plus titanium oxide or
tantalum oxide are added. The bone cement is distinguished by a
high rate of release of silver ions.
[0011] The antimicrobial activity of the materials disclosed in the
prior art has been detected using the so-called measurement of
zones of inhibition. Measurement of zones of inhibition is
described, for example, in Raad I. et al., J. Infec. Dis. 173
(1996). This entails the material to be tested being embedded in a
nutrient medium, e.g. agar. A zone of inhibition forms around the
material because of the release of metal ions with antimicrobial
activity. The formation and the size of such a zone of inhibition
has been regarded in the prior art as indicating the antimicrobial
activity of the material. The materials known in the prior art have
in some cases the disadvantage that they release a sufficiently
high concentration of silver ions for only a relatively short time.
Their antimicrobial activity is restricted to this time. In order
to counteract this disadvantage, relatively large amounts of metals
with antimicrobial activity are added in the prior art. This in
turn leads to unwanted cytotoxic effects in vivo.
[0012] It is an object of the invention to eliminate the
disadvantages of the prior art. It is intended in particular to
indicate an antimicrobial material which has improved properties
and which can be produced as easily and inexpensively as possible.
The tolerability of the material by the patient should be maximal.
It is additionally intended to indicate a process for producing the
antimicrobial material.
[0013] This object is achieved by the features of claims 1 and 14.
Expedient embodiments are evident from the features of claims 2 to
13 and 15 to 27.
[0014] The invention provides for the metal to be formed from
aggregates of primary particles having an average particle size
between 10 and 100 nm.
[0015] The primary particles in the aggregates of the invention can
still be identified on the basis of their external shape. The
primary particles are bound together essentially by necks formed
during sintering. The aggregates form a highly porous framework
structure. The matrix material may, depending on the particular
embodiment, be essentially bioinert.
[0016] The proposed material is distinguished by an excellent
antimicrobial activity. A sufficiently high concentration of silver
ions is made available on the surface of the material. Moreover the
rate of diffusion of silver ions into the surrounding tissue is
particularly low. This means that the antimicrobial activity
remains confined to the surface of the material. It is possible
with the material of the invention to produce, for example, bone
cements, implants or else implantable devices such as catheters,
with improved antimicrobial properties. No unwanted cytotoxic
effects occur. The antimicrobial effect of the material is
particularly long-lasting. The pharmacological stress on the
patient is less.
[0017] In an advantageous embodiment, the aggregates have an
average particle size of from 1 to 20 .mu.m, preferably 10 to 20
.mu.m. The surface area of the aggregates is expediently from 3 to
6 m.sup.2/g. They may have a porosity of up to 95%. The porosity is
expediently between 70 and 95%. The aforementioned features
contribute to a uniform and cytotoxically unobjectionable delivery
of silver ions on the surface of the material.
[0018] The aggregates can be produced by inert gas vaporization and
condensation, preferably under a pressure of from 10 to 100 mbar of
inert gas. The metal may be formed from one or more of the
following components: Ag, Au, Pt, Pd, Ir, Sn, Cu, Sb, Zn. The metal
expediently has an essentially undisordered lattice structure. This
avoids undesirably high release of silver ions into the surrounding
tissue.
[0019] According to a particularly advantageous embodiment feature,
the metal content is not more than 2% by weight, preferably 0.01 to
2% by weight, based on the weight of the matrix material. Silver is
expediently used as metal. The proposed addition of metal is
relatively small. The material can be produced inexpensively.
[0020] It has further proved to be expedient for the aggregates to
be completely infiltrated with the matrix material. It is
advantageous for the aggregates to be homogeneously dispersed or
distributed in the matrix material. These features contribute to
the amount of silver ions released always being the same at all
sites on the surface of the material.
[0021] The matrix material may be a polymer preferably formed from
a plurality of components. The polymer may essentially comprise
acrylic esters and/or methacrylic esters. However, other matrix
materials used in the prior art for producing bone cements are also
suitable as matrix material.
[0022] The proposed antimicrobial material is suitable for
producing or else for coating implants or an implantable medical
device, e.g. a catheter or intratracheal tubes. It is possible in
particular to use the proposed antimicrobial material to coat or
produce hip joint implants, heart valves, stents, knee joint
implants, dental fillings, contact lenses or intraocular lenses,
produced, for example, from titanium or ceramic.
[0023] In addition, a process for producing the material according
to the invention is proposed, having the following steps: [0024] a)
vaporization and condensation of metal under inert gas atmosphere,
where the pressure of the inert gas and the vaporization
temperature are adjusted so that aggregates consisting of primary
particles having an average particle size of from 10 to 100 nm are
formed, and [0025] b) mixing of the aggregates with a curable
matrix material.
[0026] The proposed process is relatively easy to carry out. It is
possible thereby to produce the antimicrobial material in uniform
quality and relatively inexpensively.
[0027] According to one embodiment feature, the aggregates are
classified after step a). It is expedient for a particle size
fraction of the aggregates in the range from 1 to 20 .mu.m
preferably 10 to 20 .mu.m to be mixed with the matrix material,
which is preferably in the liquid state. The particle size fraction
can be stirred into the matrix material.
[0028] It has proved to be expedient to use an inert gas which
comprises as an essential component at least one of the following
gases: argon, krypton, xenon, helium.
[0029] Reference is made to the preceding statements concerning
further advantageous embodiments. The features described there can
also be applied analogously in the process.
[0030] Exemplary embodiments of the invention are described in
detail below with reference to the drawing.
[0031] These show
[0032] FIG. 1 bacterial proliferation on bone cements, comparing
silver powders of the prior art and the silver powder of the
invention,
[0033] FIG. 2 a scanning electron micrograph of a silver
aggregate,
[0034] FIG. 3 the dependence of the cytotoxicity of a bone cement
as a function of the silver content and
[0035] FIG. 4 a zone of inhibition test for various bone
cements.
[0036] The results shown in FIG. 1 were obtained by the method
disclosed in DE 197 51 581 A1. This method is further described in
Bechert, Thorsten et al., Nature Medicine, Vol. 6, No. 8 (September
2000). The disclosure of both the aforementioned documents is
incorporated herein by reference.
[0037] Initially in each case 8 parallel samples (A-H) are made
from the same batch of bone cement. The samples are normally
cylindrical in shape. They have a length of about 1 cm and a
diameter of from 2 to 5 mm. Subsequently, 200 .mu.l of a
bacteria-containing solution are introduced into each well of a
microtiter plate. The samples are incubated at 37.degree. C. for
one hour. The samples are then removed and washed three times with
physiological buffers. The samples are then placed in the wells of
a microtiter plate which are filled with a minimal medium. 200
.mu.l of minimal medium are introduced into each well. The samples
are incubated at 37.degree. C. for 24 hours. The samples are then
removed and discarded. 50 .mu.l of a complete medium (trypticase
soya) are added to each well of the microtiter plate. The turbidity
of the solution is then measured at 30-minute intervals over a
period of 48 hours. The solution is kept at a temperature of
37.degree. C. during this. The turbidity is measured by means of a
suitable reader using light of a wavelength of 578 nm. A turbidity
indicates that bacteria have been released from the surface of the
sample into the surroundings.
[0038] FIG. 1 shows a comparison of a bone cement to which various
contents of conventional silver powder supplied by Chempur (columns
2-6) have been added with a second bone cement to which comparable
amounts of silver aggregates of the invention have been added
(columns 7 to 11).
[0039] 2.0% by weight of silver have been added to the samples of
columns 2 and 7, 1.0% by weight of silver to the samples of columns
3 and 8, 0.5% by weight of silver to the samples of columns 4 and
9, 0.1% by weight of silver to the samples of columns 5 and 10 and
0.05% by weight of silver to the samples of columns 6 and 11.
Column 12 shows the results of samples without added silver
(control).
[0040] It is evident that addition of only 1.0% by weight of silver
aggregates of the invention results in an excellent antimicrobial
activity. When conventional silver powders are used, no reliable
antimicrobial activity is achieved even on addition of 2.0% by
weight.
[0041] FIG. 2 shows a scanning electron micrograph of the silver
aggregate of the invention. The silver aggregate consists
essentially of spherical primary particles with an average particle
size of about 20 nm. The primary particles are essentially
connected together by necks formed during sintering. They form a
highly porous structure. The silver aggregate shown here has a size
of about 10 .mu.m.
[0042] FIG. 3 shows the results of the cytotoxic effect of the bone
cements of the invention. The method used here was the test of
Greil et al. (Infection, Vol. 27, 1999, Suppl. 1, pp. 34-37). This
entails a tetrazole dye (MTT) being converted into an intensely
colored formazan by a vital cell line showing respiratory activity
(MRC-5 cells or by phytohemagglutinin-stimulated lymphocytes). The
extent of the coloration achieved in a predefined time period is a
measure of the vitality of the cells. The test is carried out in
accordance with the ISO guideline. For this purpose, initially
samples are incubated extracts of the bone cement with culture
medium at 37.degree. C. for 24 hours. The samples are incubated in
the formazan assay together with the cells for a period of 72
hours. The cytotoxicity is defined as the relative percentage loss
of respiratory activity through formazan formation as a consequence
of addition of the extract.
[0043] Extracts obtained in accordance with the ISO guideline from
PVC in independent experiments served as positive control.
Cytotoxicity levels of greater than or equal to 30% are regarded as
cytotoxic effects. The controls used were extracts of PE (negative
control) and PVC (positive control).
[0044] FIG. 3a shows the result of an extract diluted 1:10 for
positive control with lymphocytes. The cytotoxicity in this case is
100%.
[0045] FIG. 3b shows the result of the positive control with MRC-5
cells. The cytotoxicity in this case is 60%.
[0046] FIG. 3c shows the result using a bone cement of the
invention with addition of 1.0% by weight of silver aggregate. The
cytotoxicity in this case was only 8.4% for lymphocytes and 4.8%
for MRC-5 cells (FIG. 3d).
[0047] FIG. 4 shows the results of a measurement of the zone of
inhibition with bone cements of the invention compared with
conventional bone cements. The sample composition was as follows:
[0048] sample a: bone cement with 0.05% by weight of silver
aggregates, [0049] sample b: bone cement with 0.1% by weight of
silver aggregates, [0050] sample c: bone cement with 0.5% by weight
of silver aggregates, [0051] sample d: bone cement with 2.0% by
weight of silver aggregates, [0052] sample e: bone cement with 5.0%
by weight of silver aggregates, [0053] sample f: conventional
gentamycin-containing bone cement (Merck "Palacos") [0054] sample
g, h: conventional bone cements without additions (Merck
"Palacos").
[0055] Samples a to h had, in order to carry out the measurement of
the zones of inhibition, been embedded in a Muller-Hinton agar
which had been incubated with coagulase-negative staphylococci as
test microbe for 24 hours. No zone of inhibition is evident with
the bone cements containing silver aggregates. By contrast, the
conventional gentamycin-containing bone cement shows a clear zone
of inhibition. The bone cements of the invention thus release only
a small concentration of silver ions into the surroundings.
* * * * *