WO1995022997A1 - Scar treatment sheeting and method of manufacture - Google Patents

Scar treatment sheeting and method of manufacture Download PDF

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Publication number
WO1995022997A1
WO1995022997A1 PCT/US1995/002147 US9502147W WO9522997A1 WO 1995022997 A1 WO1995022997 A1 WO 1995022997A1 US 9502147 W US9502147 W US 9502147W WO 9522997 A1 WO9522997 A1 WO 9522997A1
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Prior art keywords
article
layer
useful shapes
polydimethylsiloxane
polymer network
Prior art date
Application number
PCT/US1995/002147
Other languages
French (fr)
Inventor
Mark E. Dillon
Original Assignee
Bio Med Sciences, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to AU18801/95A priority Critical patent/AU1880195A/en
Application filed by Bio Med Sciences, Inc. filed Critical Bio Med Sciences, Inc.
Priority to DE69532990T priority patent/DE69532990T2/en
Priority to DK95911065T priority patent/DK0746341T3/en
Priority to JP52241395A priority patent/JP3739394B2/en
Priority to EP95911065A priority patent/EP0746341B1/en
Publication of WO1995022997A1 publication Critical patent/WO1995022997A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/225Mixtures of macromolecular compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like

Definitions

  • the present invention relates to the treatment of dermatologic scars, and more particularly
  • Silicone chemistry has evolved since the early 1900' s into a wide variety of systems used for industrial as well as medical applications.
  • Medical grade silicones are usually based on thermoset dimethyl systems, whereby the molecular formula may be represented as follows:
  • a crosslinking agent is used to create bonds between the hydrogen atoms on the methyl groups of adjacent molecules.
  • These silicone formulations are often supplied as a two (2) part system, wherein one part contains a catalyst for vulcanization and the other part contains the base resin and crosslinking agent.
  • the crosslink density may be adjusted to achieve desired bulk or surface qualities of the vulcanized elastomer. Physical strength and durability tend to increase, while softness and coefficient of friction decrease with higher crosslink densities. Materials with a high crosslink density are relatively slick and tough, but have poor compliancy or
  • densities give a soft gel with a more adhesive or "tacky" surface. These materials are more drapable, although they are inherently weak and tend to fragment easily with low levels of stress.
  • This invention relates to the treatment of dermatologic scars associated with traumatic or surgical injuries by using silicone elastomer materials.
  • scar formation may be excessive, resulting in raised, textured or colored surfaces.
  • Scars can not only be disfiguring, but also limit range of motion and functionality. Historically, the application of pressure to an affected area of the body has been used to minimize these effects,
  • Garments made of an elastic textile are used to achieve such pressure. This method of treatment eventually became a standard of care in many medical institutions, particularly burn treatment centers.
  • Silastic ® (Dow Corning Corporation) consists of a soft polydimethylsiloxane (“PDMS”) gel material of approximately 0.125 inch (0.32 cm) in
  • the low modulus of elasticity is beneficial by providing surface tack, thus promoting skin contact on difficult anatomical areas or during movement.
  • the PDMS composition is inherently weak, however, and endures only several days in practice before breaking apart because of mechanical
  • the above mentioned product uses a reinforcing scrim embedded into the body of the material to improve durability. This macroscopic mesh complicates the manufacturing process and may cause skin irritation if exposed during use.
  • the second type of commercial product such as
  • Sil-K ® (Degania Silicone, Ltd.), consists of a relatively stiff silicone elastomer of approximately 0.03 inches (0.08 cm) in thickness. The increased modulus of elasticity provides for increased
  • the material is relatively non-adherent, so adhesive tape is typically used to maintain the position of the material on the body. Although this material may last for the duration of treatment, it does not conform well to anatomical areas and does not provide a high level of patient comfort. This compromises patient compliancy and may limit the efficacy of the treatment.
  • Moisture Vapor Transmission The rate at which water vapor Rate permeates through a material calculated gravimetrically and expressed in units of g/m 2 /day.
  • the test conditions are 50% relative humidity, 98°F (37oC), with an air flow of 650 cubic feet per minute over the specimen.
  • Tensile Strength The load required to break a test specimen divided by the cross-sectional area of the specimen.
  • Interpenetrating polymer networks are defined as a blend of two or more polymers where each material forms a continuous network, each network interpenetrating the other (Sperling, 1981).
  • An IPN is therefore a type of polymer/polymer composite.
  • a true IPN comprises
  • an IPN with a modulus of elasticity and surface chemistry substantially comprised of PDMS may be produced while also possessing the strength and durability of PTFE.
  • the resultant material is semipermeable in that it allows moisture vapor transmission while preventing liquid water break-through.
  • This technology has provided skin-like bandages and dressing materials for woundcare applications such as burn treatment (Dillon et al., 1992, FDA 510[k] approval no. K912032).
  • IPN of PDMS and PTFE may be used as the basis of an
  • the subject of this invention allows the opposing properties of strength and softness in silicones elastomers to be simultaneously achieved; e.g. durability may be combined with drapability and surface tack. Furthermore, by causing one side of the structure to have a greater silicone content than the other, disparate surface properties may be imparted to each surface.
  • the subject of the present invention represents an improvement over prior art in that the product:
  • Fig. 1 is a view in cross section of a sheet constructed in accordance with this invention
  • Fig. 2 is a view in top plan of a face mask constructed in accordance with this invention.
  • Fig. 3 is a view in top plan of a sheet which includes holes adapted for applying treatment to the webbed spaces between fingers or toes;
  • Fig. 4 shows a sheet which has perforations to facilitate the transfer of body heat through the sheet to thereby promote patient comfort
  • Fig. 5 shows a view in section of a "finger cot" for application to the digits of the hand or other anatomical protrusions.
  • IPN film of PDMS and PTFE was produced in the form of a continuous roll 12 inches (30 cm) wide according to the methods described in U.S. Patent number 4,945,125, the disclosures of which are
  • a second blend of PDMS materials was prepared as follows:
  • a casting process was used to apply a 0.01 inch (0.025 cm) surface coating of the above PDMS
  • the casting process involved passing the substrate through a reservoir of liquid PDMS prepolymer and using a
  • FIG. 1 shows a sectional view of the construction of this example, with IPN layer 11 and PDMS coating 12.
  • a paper release liner H.P. Smith Company
  • IPN film of PDMS and PTFE was produced in the form of a continuous roll 12 inches (30 cm) wide using the PDMS blend of Table V according to the methods previously described. Approximately 1.3 g of PTFE (Tetratec Corporation) was used per linear foot of IPN film produced. The final IPN was measured to have a thickness of 0.002 inches (0.05 cm).
  • a second blend of PDMS materials were prepared as follows:
  • MDX4-4515, Q7-2213, Q7-2167, Q7-2168, Q7-2174, Q7-2245, Q7-4840, and Q7-4850 are suitable substitutes.
  • various thicknesses of IPN films and silicone coatings may be useful.
  • the range of suitable IPN thickness is between 0.0005 inch (12.5 microns) and 0.02 inch (0.05 cm), and that for the PDMS is between 0.005 inch (0.0125 cm) and 0.25 inch (0.64 cm).
  • An important consideration is that the final construction is not so thin as to have a tendency to wrinkle or otherwise be difficult to handle.
  • the steps of creating a layered article may be reversed or even consolidated into one process.
  • the invention may be converted into sheets or rolls for final use.
  • Other embodiments include face-mask designs as shown in top plan view in Figure 2 which shows a face mask 21 with cut openings 22 which accommodate the features of the face.
  • An additional embodiment is shown in top plan view in Figure 3, wherein a sheet 31 includes holes 32 cut as to apply treatment to the web-spaces between fingers and toes.
  • a sheet 41 has perforations 42 to facilitate the transfer of body heat through the sheet 41, thereby promoting patient comfort.
  • invention is a "finger cot" for application to the digits of the hand or other anatomical protrusions.
  • Figure 5 shows a sectional view of this embodiment and shows a mandrill 51 covered by an inventive article 52.
  • This configuration may be achieved by: (1) conforming - -or forming ⁇ a PTFE/PDMS IPN article around the end of a suitable mandrill, (2) dipping the mandrill in a reservoir of uncured polysiloxane, (3) removing the mandrill from the reservoir, (4) allowing the residual surface coating of polysiloxane to vulcanize, (5) removing the polysiloxane coated IPN article by peeling it off of the mandrill as it is turned in-side-out, and (6) (optionally) rolling the mouth of the shaped article outward and back to facilitate application by rolling the mouth of the product back down over the anatomical protrusion.

Abstract

Elastomeric sheeting materials are described which are formed from the process of creating a membrane comprising a semi-interpenetrating polymer network ('IPN') of polytetrafluoroethylene ('PTFE') and polydimethylsiloxane ('PDMS') by causing a matrix of PDMS to be formed in situ with a matrix of PTFE (11) and causing surface of substantially pure PDMS to be formed on at least one side thereof (12), allowing PDMS compositions to vulcanize. The product of the process is suitable for the treatment of dermatologic scars.

Description

SCAR TREATMENT SHEETING AND METHOD OF MANUFACTURE
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to the treatment of dermatologic scars, and more particularly
concerns scar treatment sheeting and other articles, and a method of manufacture thereof.
2. Description of the Prior Art
Silicone chemistry has evolved since the early 1900' s into a wide variety of systems used for industrial as well as medical applications. Medical grade silicones are usually based on thermoset dimethyl systems, whereby the molecular formula may be represented as follows:
Figure imgf000004_0001
A crosslinking agent is used to create bonds between the hydrogen atoms on the methyl groups of adjacent molecules. These silicone formulations are often supplied as a two (2) part system, wherein one part contains a catalyst for vulcanization and the other part contains the base resin and crosslinking agent. By varying the amount of crosslinking agent, the crosslink density may be adjusted to achieve desired bulk or surface qualities of the vulcanized elastomer. Physical strength and durability tend to increase, while softness and coefficient of friction decrease with higher crosslink densities. Materials with a high crosslink density are relatively slick and tough, but have poor compliancy or
"drapability". Silicones with low crosslink
densities give a soft gel with a more adhesive or "tacky" surface. These materials are more drapable, although they are inherently weak and tend to fragment easily with low levels of stress.
A number of U.S. Patents and other publications relate to the field of the invention, and are as follows: U.S. PATENT DOCUMENTS
4,832,009 5/23/89 Dillon
4,945,125 7/31/90 Dillon et al.
5,066,683 11/19/91 Dillon et al.
5,157,058 10/20/92 Dillon et al.
OTHER PUBLICATIONS
Sperling, Interpenetrating Polymer Networks and
Related Materials, Plenum Press, New York, 1981, pp. 1-5.
Dillon, ME, Okunski, WJ, "Silon* Non-Adherent Film Dressings on Autograft and Donor Sites", Wounds, 1992, vol. 4, no. 5:203-207.
Dillon, ME, "Silicone and Poly(tetrafluoroethylene) Interpenetrating Polymer Networks: Brief History,
Summary of Recent Developments, and Discussion of Applications", Interpenetrating Polymer Networks, Klempner et al. ed, ACS Books, New York, NY, 1991, pp. 393-404.
Perkins, et. al., "Silicone Gel: A New Treatment for
Burn Scars and Contractures", Burns. 1982, 9, pp. 201.
Quinn, KJ, "Silicone Gel in Scar Treatment", Burns . 1987, 13, pp. 33-40.
This invention relates to the treatment of dermatologic scars associated with traumatic or surgical injuries by using silicone elastomer materials. In many cases, scar formation may be excessive, resulting in raised, textured or colored surfaces. Scars can not only be disfiguring, but also limit range of motion and functionality. Historically, the application of pressure to an affected area of the body has been used to minimize these effects,
particularly regarding hypertrophic and keloidal scars. Garments made of an elastic textile are used to achieve such pressure. This method of treatment eventually became a standard of care in many medical institutions, particularly burn treatment centers.
An Australian research group reported using silicone gel under pressure garments to evenly apply pressure in anatomic depressions, over areas of flexure, and during ambulation (Perkins et al., 1982). Quinn (1987) later found that the efficacy of silicone for scar modification was unrelated to pressure, in that the silicone material itself had a beneficial effect on the cosmetic appearance and elasticity of scars. The exact biological mechanism of this effect is not well understood.
In recent years, two (2) general types of silicone sheeting products have gained commercial acceptance in the marketplace for scar modification applications. One of the first types, Silastic® (Dow Corning Corporation) consists of a soft polydimethylsiloxane ("PDMS") gel material of approximately 0.125 inch (0.32 cm) in
thickness. The low modulus of elasticity is beneficial by providing surface tack, thus promoting skin contact on difficult anatomical areas or during movement. The PDMS composition is inherently weak, however, and endures only several days in practice before breaking apart because of mechanical
agitation. The above mentioned product uses a reinforcing scrim embedded into the body of the material to improve durability. This macroscopic mesh complicates the manufacturing process and may cause skin irritation if exposed during use.
Although durability is increased, these products still disintegrate from normal wear and tear within a matter of weeks. This is a limiting factor in the cost effectiveness of the product in that the treatment may last for several months, thus
requiring numerous repurchases. Together, the scrim and thickness of the product compromise drapability and comfort features.
The second type of commercial product, such as
Sil-K® (Degania Silicone, Ltd.), consists of a relatively stiff silicone elastomer of approximately 0.03 inches (0.08 cm) in thickness. The increased modulus of elasticity provides for increased
physical strength and durability, and the lack of a reinforcing scrim simplifies the manufacturing process. The material is relatively non-adherent, so adhesive tape is typically used to maintain the position of the material on the body. Although this material may last for the duration of treatment, it does not conform well to anatomical areas and does not provide a high level of patient comfort. This compromises patient compliancy and may limit the efficacy of the treatment.
Both types of products are relatively occlusive and impermeable to moisture vapor, which further detracts from patient comfort. There are other silicone-based scar treatment materials which have been commercialized, each generally falling into one of the two categories above. Some of the important properties of the above two examples of commercial products are listed in Table VII.
Definitions
Moisture Vapor Transmission The rate at which water vapor Rate permeates through a material calculated gravimetrically and expressed in units of g/m2/day. The test conditions are 50% relative humidity, 98°F (37ºC), with an air flow of 650 cubic feet per minute over the specimen. Tensile Strength The load required to break a test specimen divided by the cross-sectional area of the specimen.
Modulus of Elasticity The tensile strength of a
material at break divided by the elongation at break.
Coefficient of Friction The force, measured in pounds, required to initiate the slide of a 1 inch square (6.45 cm2) by 0.5 inch (1.27 cm) thick piece of high density polyethylene over a test specimen on a horizontal surface.
Drapability The distance the edge of a
length of material bends when extended one inch beyond the surface of a ridged support with a corner radius of less than 1/16th inch. SUMMARY OF THE INVENTION
Interpenetrating polymer networks are defined as a blend of two or more polymers where each material forms a continuous network, each network interpenetrating the other (Sperling, 1981). An IPN is therefore a type of polymer/polymer composite. A true IPN comprises
polymeric ingredients which are independently
crosslinked. Systems wherein only one component is crosslinked are called semi-IPNs or pseudo-IPNs, such as an IPN of a linear thermoplastic polymer and a thermoset elastomer. For the purposes of this discussion, the terms IPN, semi-IPN, and pseudo-IPN shall be used
interchangeably.
Because of the nature of composite materials, synergistic effects may be gained by carefully
engineering the morphology and chemistry of the polymers in an IPN. My previous patents on this subject
demonstrate increased strength may be gained without sacrificing other important properties, such as
breathability. By using PDMS and polytetrafluoroethylene ("PTFE"), an IPN with a modulus of elasticity and surface chemistry substantially comprised of PDMS may be produced while also possessing the strength and durability of PTFE. The resultant material is semipermeable in that it allows moisture vapor transmission while preventing liquid water break-through. This technology has provided skin-like bandages and dressing materials for woundcare applications such as burn treatment (Dillon et al., 1992, FDA 510[k] approval no. K912032).
I have unexpectedly discovered that an IPN of PDMS and PTFE may be used as the basis of an
elastomeric sheet useful for scar treatment
applications. The subject of this invention allows the opposing properties of strength and softness in silicones elastomers to be simultaneously achieved; e.g. durability may be combined with drapability and surface tack. Furthermore, by causing one side of the structure to have a greater silicone content than the other, disparate surface properties may be imparted to each surface. The subject of the present invention represents an improvement over prior art in that the product:
1. is soft and compliant,
2. is strong and durable,
3. has a thinner profile,
4. has disparate surface properties on each side,
5. is moisture vapor permeable, and
6. has greater comfort features. The manufacturing process lends itself to large-scale production in that continuous rolls of material may be made in virtually unlimited lengths. This provides for rapid and cost effective
conversion into die-cut shapes or self-wound rolls.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a view in cross section of a sheet constructed in accordance with this invention;
Fig. 2 is a view in top plan of a face mask constructed in accordance with this invention;
Fig. 3 is a view in top plan of a sheet which includes holes adapted for applying treatment to the webbed spaces between fingers or toes;
Fig. 4 shows a sheet which has perforations to facilitate the transfer of body heat through the sheet to thereby promote patient comfort; and
Fig. 5 shows a view in section of a "finger cot" for application to the digits of the hand or other anatomical protrusions.
DETAILED DESCRIPTION OF THE DRAWINGS
Several embodiments of this invention are shown in the following illustrative examples and are not intended to be limiting. The following two-part silicone compositions were used in each example:
Figure imgf000013_0001
EXAMPLE 1
The following blend of PDMS materials was prepared using trichloroethane as a processing aid:
Figure imgf000014_0001
An IPN film of PDMS and PTFE was produced in the form of a continuous roll 12 inches (30 cm) wide according to the methods described in U.S. Patent number 4,945,125, the disclosures of which are
incorporated herein by reference. Approximately 0.9 g of PTFE (Tetratec Corporation) was used per linear foot of IPN film produced. The IPN film was measured to have a thickness of 0.001 inches (0.0025 cm). The properties of this material are given in Table VII.
A second blend of PDMS materials was prepared as follows:
Figure imgf000015_0001
A casting process was used to apply a 0.01 inch (0.025 cm) surface coating of the above PDMS
composition to one side of the IPN film. The casting process involved passing the substrate through a reservoir of liquid PDMS prepolymer and using a
doctoring roll to meter off a controlled amount of liquid as to leave a precise thickness of PDMS on the surface of the IPN substrate. Numerous other methods of achieving such a coating will be apparent to those skilled in the art. The coated material was passed through a tunnel style oven as to initiate the curing process, then post cured in a closed oven for 3 hours at 158 ºF (70ºC) to achieve full vulcanization. Figure 1 shows a sectional view of the construction of this example, with IPN layer 11 and PDMS coating 12. For comparative purposes, the same process was used to create 0.01 inch (0.025 cm) sheet of the same PDMS material without the bottom layer of IPN film. A paper release liner (H.P. Smith Company) was used as a temporary substrate from which the PDMS sheet was later removed. Some of the important physical
characteristics of each material produced by this example are given in Table VII. EXAMPLE 2
The following blend of PDMS materials was
produced:
Figure imgf000017_0001
An IPN film of PDMS and PTFE was produced in the form of a continuous roll 12 inches (30 cm) wide using the PDMS blend of Table V according to the methods previously described. Approximately 1.3 g of PTFE (Tetratec Corporation) was used per linear foot of IPN film produced. The final IPN was measured to have a thickness of 0.002 inches (0.05 cm).
A second blend of PDMS materials were prepared as follows:
Figure imgf000018_0001
The process outlined above was used to apply a a 0.036 inch (0.091 cm) surface coating of the above PDMS blend to one side of the IPN film. As with the previous example, the material was passed through tunnel style oven as to initiate the curing process, then post-cured in a closed oven for 3 hours at 158°F (70° C). Again the same process was used to create 0.03 inch (0.075 cm) sheet of the same PDMS material without the bottom layer of IPN film. Some of the important physical characteristics of the materials produced by this example are given in Table VII.
The above samples are preferred embodiments of this invention. Other formulations and constructions will be apparent to those skilled in the art. For example, there are many other silicone compositions that would be suitable for the subject of this invention, either in combination or in blends. Dow Corning Silastic® grades
MDX4-4515, Q7-2213, Q7-2167, Q7-2168, Q7-2174, Q7-2245, Q7-4840, and Q7-4850 are suitable substitutes. Furthermore, various thicknesses of IPN films and silicone coatings may be useful. The range of suitable IPN thickness is between 0.0005 inch (12.5 microns) and 0.02 inch (0.05 cm), and that for the PDMS is between 0.005 inch (0.0125 cm) and 0.25 inch (0.64 cm). An important consideration is that the final construction is not so thin as to have a tendency to wrinkle or otherwise be difficult to handle. The steps of creating a layered article may be reversed or even consolidated into one process.
In addition to various compositions, there are numerous shapes and sizes useful for the subject of this invention. For example, the invention may be converted into sheets or rolls for final use. Other embodiments include face-mask designs as shown in top plan view in Figure 2 which shows a face mask 21 with cut openings 22 which accommodate the features of the face. An additional embodiment is shown in top plan view in Figure 3, wherein a sheet 31 includes holes 32 cut as to apply treatment to the web-spaces between fingers and toes. Yet another embodiment is shown in Figure 4 where a sheet 41 has perforations 42 to facilitate the transfer of body heat through the sheet 41, thereby promoting patient comfort.
A particularly novel configuration of this
invention is a "finger cot" for application to the digits of the hand or other anatomical protrusions.
Figure 5 shows a sectional view of this embodiment and shows a mandrill 51 covered by an inventive article 52. This configuration may be achieved by: (1) conforming - -or forming╌ a PTFE/PDMS IPN article around the end of a suitable mandrill, (2) dipping the mandrill in a reservoir of uncured polysiloxane, (3) removing the mandrill from the reservoir, (4) allowing the residual surface coating of polysiloxane to vulcanize, (5) removing the polysiloxane coated IPN article by peeling it off of the mandrill as it is turned in-side-out, and (6) (optionally) rolling the mouth of the shaped article outward and back to facilitate application by rolling the mouth of the product back down over the anatomical protrusion.
Figure imgf000022_0001

Claims

1. A composite article suitable for the treatment of dermatologic scars comprising
a first layer of a crosslinked elastomer, and a second layer of a membranous film.
2. The article of Claim 1,
wherein the membranous film is a semi-interpenetrating polymer network of
polydimethylsiloxane and polytetrafluoroethylene.
3. The article of Claim 1,
wherein the crosslinked elastomer is
polydimethylsiloxane.
4. The article of Claim 1,
wherein each layer has surface characteristics that are disparate from the other layer.
5. The article of Claim 1,
with a moisture vapor transmission rate of at least 51.9 g/m2/day.
6. The article of Claim 1,
with a drapability of at least 0.88 inches.
7. The article of Claim 1,
with a modulus of elasticity of less than or equal to 38.1 lbs/in2.
8. The article of Claim 2,
wherein each layer has surface characteristics that are disparate from the other layer.
9. The article of Claim 2,
with a moisture vapor transmission rate of at least 51.9 g/m2/day.
10. The article of Claim 2,
with a drapability of at least 0.88 inches.
11. The article of Claim 2,
with a modulus of elasticity of less than or equal to 38.1 lbs/in2.
12. The article of Claim 3,
wherein each layer has surface characteristics that are disparate from the other layer.
13. The article of Claim 3,
with a moisture vapor transmission rate of at least 51.9 g/m2/day.
14. The article of Claim 3,
with a drapability of at least 0.88 inches.
15. The article of Claim 3,
with a modulus of elasticity of less than or equal to 38.1 lbs/in2.
16. The article of Claim 3,
wherein the layer of polydimethylsiloxane is 0.01 inches thick.
17. The article of Claim 3,
wherein the layer of polydimethylsiloxane is 0.03 inches thick.
18. The article of Claim 2,
wherein the semi-interpenetrating polymer network is 0.001 inches thick.
19. The article of Claim 2,
wherein the semi-interpenetrating polymer network is 0.002 inches thick.
20. A process which comprises the steps of
(1) forming a membranous film,
(2) causing a surface of substantially pure polysiloxane to be formed on at least one side thereof to form a composite structure, and
(3) converting said structure into useful shapes suitable for application to anatomical areas of the body.
21. The process of Claim 20, including
applying said useful shapes to dermatologic scars.
22. The process of Claim 20,
wherein the membranous film is an
interpenetrating polymer network of polysiloxane and polytetrafluoroethylene.
23. The process of Claim 21,
wherein the useful shapes have holes to
accommodate fingers, toes or other anatomical protrusions.
24. The process of Claim 21,
wherein the useful shapes are configured in a face-mask fashion.
25. The process of Claim 21,
wherein the useful shapes have perforations to promote heat transfer from the body.
26. The process of Claim 21,
wherein the useful shapes are configured in the fashion of a finger cot.
27. A composite article suitable for the treatment of dermatologic scars comprising
a first layer of a crosslinked elastomer, and a second layer of a membranous film,
the membraneous film being a semi-interpenetrating polymer network of
polydimethylsiloxane and polytetrafluoroethylene, the crosslinked elastomer being
polydimethylsiloxane,
wherein each layer has surface characteristics that are disparate from the other layer,
the layer of polydimethylsiloxane being 0.01 inches thick, and
the semi-interpenetrating polymer network being 0.001 inches thick.
28. A process which comprises the steps of (1) forming a membranous film,
(2) causing a surface of substantially pure polysiloxane to be formed on at least one side thereof to form a composite structure, and
(3) converting said structure into useful shapes suitable for application to anatomical areas of the body,
said membranous film being an interpenetrating polymer network of polysiloxane and
polytetrafluoroethylene,
said useful shapes have holes to accommodate fingers, toes or other anatomical protrusions, and said useful shapes having perforations so as to promote heat transfer from the body.
29. The process of claim 28,
wherein the useful shapes are configured in the fashion of a finger cot.
PCT/US1995/002147 1994-02-23 1995-02-23 Scar treatment sheeting and method of manufacture WO1995022997A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
AU18801/95A AU1880195A (en) 1994-02-23 1995-02-21 Scar treatment sheeting and method of manufacture
DE69532990T DE69532990T2 (en) 1994-02-23 1995-02-23 A COMPOSITE OBJECT FOR THE TREATMENT OF DERMATOLOGIC SCALES, A METHOD FOR THE PRODUCTION OF THE SUBJECT AND THE USE THEREOF
DK95911065T DK0746341T3 (en) 1994-02-23 1995-02-23 Composite article for the treatment of dermatological scars, a method of making such composite article and its use
JP52241395A JP3739394B2 (en) 1994-02-23 1995-02-23 Scar treatment sheet and method for producing the same
EP95911065A EP0746341B1 (en) 1994-02-23 1995-02-23 A composite article for treating dermatologic scars, a process of forming such composite article and the use of it

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US08/200,152 1994-02-23
US08/200,152 US5656279A (en) 1994-02-23 1994-02-23 Semi-interpenetrating polymer network scar treatment sheeting, process of manufacture and useful articles thereof

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EP0874609A1 (en) * 1995-11-13 1998-11-04 Bio Med Sciences, Inc. Therapeutic medical garments for scars and process
EP0874609A4 (en) * 1995-11-13 2000-01-19 Bio Medical Sciences Inc Therapeutic medical garments for scars and process
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CA2183993A1 (en) 1995-08-31
US5980923A (en) 1999-11-09
DK0746341T3 (en) 2004-09-06
DE69532990D1 (en) 2004-06-09
EP0746341A1 (en) 1996-12-11
EP0746341A4 (en) 1998-02-25
US5656279A (en) 1997-08-12
JPH10501431A (en) 1998-02-10
AU1880195A (en) 1995-09-11
JP3739394B2 (en) 2006-01-25
EP0746341B1 (en) 2004-05-06
DE69532990T2 (en) 2009-09-17

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