U.S. patent number 3,618,609 [Application Number 04/887,523] was granted by the patent office on 1971-11-09 for braided absorbent material.
This patent grant is currently assigned to American Cyanamid Company. Invention is credited to Arthur Glick, Sol Singerman.
United States Patent |
3,618,609 |
Glick , et al. |
November 9, 1971 |
BRAIDED ABSORBENT MATERIAL
Abstract
A process is provided for removing body fluids from an area
under surgery which comprises contacting the fluid with a brush
comprising a core of continuous monofilament hydrophilic fibers,
each of said fibers having a denier between about 1.5 and 10
surrounded by a braided sheath of multifilament yarn, said yarn
having a denier in the range of about 100 to about 2,400.
Inventors: |
Glick; Arthur (Danbury, CT),
Singerman; Sol (Norwalk, CT) |
Assignee: |
American Cyanamid Company
(Stamford, CT)
|
Family
ID: |
25391335 |
Appl.
No.: |
04/887,523 |
Filed: |
December 23, 1969 |
Current U.S.
Class: |
604/1; 15/160;
15/207.2 |
Current CPC
Class: |
A61F
9/007 (20130101) |
Current International
Class: |
A61F
9/007 (20060101); A61f 013/00 () |
Field of
Search: |
;128/267,269,285,296,357
;15/159-160,171,206 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
Primary Examiner: Rosenbaum; Charles F.
Claims
What is claimed is:
1. A lint-free brush useful for absorbing body fluids comprising a
core formed from continuous monofilament, hydrophilic fibers, each
of said fibers having a denier between about 1.5 and about 10, and
a braided sheath surrounding said core comprised of multifilament
yarn, said yarn having a denier in the range of from about 100 to
about 2,400.
2. The brush of claim 1 wherein the fibers are produced from
viscose rayon.
3. The brush of claim 1 wherein the fibers of the sheath are fused
to each other along at least a part of the length of the brush to
provide a rigid section to serve as a brush handle.
Description
This invention relates to a capillary brush for use in surgery to
absorb fluids. More particularly, the present invention relates to
a lint-free capillary brush which is useful for removing body
fluids especially during surgery in such sensitive areas as the
eye.
Fluids, including blood, which tend to accumulate in areas
undergoing surgery, interfere with efficient performance of the
surgical technique, and must be removed in a manner so as not to
injure the patient. There are available at the present time a wide
variety of methods and surgical instruments employed to remove
fluids from the situs of operation. It is common practice to employ
absorbent sponges which are contacted with the fluid. When the
sponge is saturated, it is replaced with a fresh sponge. In most
instances, the use of a sponge or other soft absorbent material is
preferred over mechanical means for removing fluid to materially
reduce the probability of lacerations and/or hematoma of exposed
organs. Sponges or apparatus having sponge material thereon are
most commonly employed in operations where relatively large
incisions are made. In operations where small incisions are made
and the operation is confined to a relatively small area of the
body, such as in eye operations, it is preferred to employ
absorbent materials which are softer and less abrasive than sponges
to further reduce the probability of damage to the area of the body
being treated. Cotton swabs are widely used in operations where the
fluid accumulation is not excessive and where the operation is
confined to a small area. However, certain disadvantages are
associated with the use of cotton even through it is highly
absorbent. Thus, cotton swabs are comprised of small fibers and
when they become saturated with liquid and are removed, lint is
usually left behind. When lint is allowed to remain, the healing
process is inhibited and infection may result. Thus, the lint must
be continually removed as, for example, with warm saline washes
during and after completion of the operation. This extends the time
needed to complete surgery and together with the additional
cleaning steps, increases the probability of injury to the patient.
It, therefore, would be highly desirable to provide a means for
removing liquid during surgery which will not cause injury to the
patient and which does not leave a lint residue after being removed
from the surgical area.
It is an object of the present invention to provide means which
overcome the disadvantages described above.
It is a further object of the present invention to provide an
article adapted to remove fluid from the situs of surgical
operations which does not leave a lint residue after being
removed.
It is a further object of the present invention to provide means
for removing fluid from the situs of the surgical operation without
causing damage to the area being originally treated. Further
objects of this invention will become evident in view of the
following detailed discussion.
In accordance with the present invention, there is provided an
absorbent lint-free surgical brush adapted to remove fluid from the
area of surgical operation. The brush comprises a core of highly
absorbent monofilament fibers surrounded by a braided sheath
prepared of the same or different fibers. The core is comprised of
low twist, relatively high denier, hydrophilic monofilament fibers
which may be formed as tightly packed separate parallel fibers or
they may be twisted, woven or braided. The sheath is made of
multifilament yarns comprised of monofilaments whose individual
denier is the same or lower than the core fibers by braiding the
yarn around the fibers of the core. The sheath can be made of
either hydrophobic or hydrophilic polymeric materials, and can be
treated along a portion of its length to increase its rigidity.
The capillary brush of this invention is employed to remove fluids
from the area of surgical operations by contacting the fluid in the
surgical area with the exposed cross section of the core. The
hydrophilic filaments in the core carry the fluid away from the
surgical area through a portion of the length of the brush by
absorption and capillary action. The portion of the brush in
contact with the surgical area is extremely soft and flexible so
that the probability of lacerations or hematoma is thereby reduced.
The brush can be of any length to facilitate placing it in, and
removing it from, the surgical area. Since all parts of the brush
are made of long, continuous monofilaments, no lint is associated
therewith, thereby eliminating the necessity of additional washing
steps during the operation to remove lint and reducing the
probability of injury of the patient.
The core of the brush can be made of any hydrophilic polymeric
material which can be formed into continuous monofilament fibers.
To form the core, it is necessary to employ monofilament fibers
having an individual denier between about 1.5 and about 10 in order
to provide the desired softness and flexibility and to provide a
relatively high rate of removal of fluid from the surgical area
through absorption and capillary action. The fibers in the core are
compacted so that a relatively large number of fibers are confined
in a given area. Generally, the core should contain more than about
750 fibers and preferably, more than about 1,000 fibers, so that
the liquid is removed from the situs of surgery at a relatively
rapid rate.
The sheath is prepared by braiding multifilament yarn composed of
continuous monofilaments around the core. The multifilament yarn
may be spun from any hydrophilic or hydrophobic polymer such as the
cellulosics, polyethylene, polypropylene, the vinyl polymers such
as polyvinyl-chloride, or the like. Standard braiding equipment can
be employed for this purpose. The sheath can be conveniently formed
by braiding yarns having a denier of from about 100 to about 2,400
around the core. Preferably, the braid should be formed employing
from about 8 to about 24 carriers and should contain about 40 to
about 60 picks per inch. Although the braided sheath can have a
total denier greater or less than the total denier of the core, it
is considered preferable to employ a braided sheath exhibiting a
total denier higher than that of the core. Generally, the weight
ratio of the sleeve to the core can vary from about 0.25:1 to about
3:1. Preferably, the weight ratio ranges from about 1.5:1 to about
3:1.
The capillary brush of this invention can have a diameter of any
size suitable to permit entry thereof into the surgical area.
Generally, the diameter of the brush varies between about 0.008 and
0.25 inch. The capillary brush is especially suitable for removing
the humor which accumulates during eye operations.
In a further aspect of the present invention, the sheath is braided
from thermoplastic filaments and can be rigidified along at least a
portion of its length, by heating to fuse and shrink the filaments
in the sheath. After being heat-treated, the sheath can function as
a handle for placing the end of the brush into the surgical area.
The heat treatment can be accomplished by rolling the outer surface
of the sheath across a hot plate which is heated to a temperature
which fuses or shrinks the sheath, without causing damage thereto.
During the heat treatment, care should be taken so that the core is
not heated to a sufficiently high temperature to effect shrinkage
or fusion of the core fibers.
Suitable polymeric materials which can be employed to form the core
are hydrophilic polymers such as viscose rayon, acetates,
polyamides and the like. These polymeric materials are commercially
available as continuous multifilament yarns of the desired
denier.
As stated above, the filaments employed to form the sheath can be
either hydrophilic or hydrophobic. When it is desired to employ
hydrophilic materials to increase the absorbency of the brush, any
of the hydrophilic materials employed for the core can be used. On
the other hand, it may be desired to form the sheath from a
hydrophobic material to maintain the outer sheath surface dry and
thereby promote convenient handling of the brush. Suitable
hydrophobic materials are polyethylene, polypropylene, poly(vinyl
chloride), polyesters and the like.
The invention is described below with reference to the attached
drawings.
FIG. 1 is an isometric view of a brush formed by a core of
monofilaments surrounded by a braided sheath.
FIG. 2 is the brush construction of FIG. 1 in which a portion of
the sheath has been heat-treated to form the rigid handle.
Referring now to FIG. 1, the capillary brush is comprised of a
braided sheath 1 prepared from polymeric multifilament yarns which
are either hydrophilic or hydrophobic and a core 2 prepared from
monofilament fibers of hydrophilic polymer. In use, the exposed end
3 of core 2 is contacted with the fluid, the removal of which is
desired. The liquid is passed by absorbency and capillary action
from the end 3 into the body of the core 2 away from the surgical
area.
Referring now to FIG. 2, the carrier brush is comprised of a sheath
having a flexible braided portion 4 and a rigid heat-fused portion
5 and a core 2 comprised of untwisted or low-twist fibers. The end
3 of the core 2 is contacted with the fluid in the manner described
above with reference to the brush in FIG. 1.
The following examples illustrate the present invention and are not
intended to limit the same.
EXAMPLES 1- 3
Method of Making Absorbent Brush
Viscose rayon was wound onto braider bobbins to form the braided
sheath. The wound bobbins were placed on braiding carriers (carry
bobbins) which braid around the core material that travels through
the center of the braider.
The following table sets forth the construction of three different
brushes, all formed with cores comprising viscose rayon
monofilaments, in terms of the type of braider (carrier capacity),
number of carriers employed for the braided sheath, denier of the
yarn/carrier, total denier of the core: ##SPC1##
In a similar manner, smaller sized brushes are prepared by using
yarns of lower denier with a smaller capacity braider, e.g., an 8
carrier braider.
EXAMPLE 4
Method of Preparing Absorbent Brush with Fused Sheath
An absorbent brush with a fused sheath was prepared employing the
procedure described in example 1 except that 150-denier
multifilament polyethylene yarn was substituted for the viscose
rayon yarn. Fusion of the sheath yarn was achieved by rolling the
cut brush across a hot plate maintained at about 175.degree. C.
until the sheath noticeably shrank and fused.
EXAMPLES 5- 9
Employing the procedure set forth in example 1, absorbent brushes
were prepared as summarized in table II below: ##SPC2##
These brushes were successfully employed to remove body fluids
during surgical procedures without causing lacerations and/or
hematoma of exposed organs.
* * * * *