GB2094809A - Stoma seal adhesive - Google Patents
Stoma seal adhesive Download PDFInfo
- Publication number
- GB2094809A GB2094809A GB8207447A GB8207447A GB2094809A GB 2094809 A GB2094809 A GB 2094809A GB 8207447 A GB8207447 A GB 8207447A GB 8207447 A GB8207447 A GB 8207447A GB 2094809 A GB2094809 A GB 2094809A
- Authority
- GB
- United Kingdom
- Prior art keywords
- composition
- weight
- pressure
- adhesive
- moisture absorbing
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J105/00—Adhesives based on polysaccharides or on their derivatives, not provided for in groups C09J101/00 or C09J103/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L24/00—Surgical adhesives or cements; Adhesives for colostomy devices
- A61L24/04—Surgical adhesives or cements; Adhesives for colostomy devices containing macromolecular materials
- A61L24/043—Mixtures of macromolecular materials
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L2400/00—Materials characterised by their function or physical properties
- A61L2400/14—Adhesives for ostomy devices
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/54—Inorganic substances
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Surgery (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Materials For Medical Uses (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
A pressure-sensitive adhesive composition having the capacity to absorb from about 15 to about 40% of its own weight in water comprises; (a) from about 30 to about 80 parts by weight of a pressure-sensitive adhesive component selected from the group consisting of natural rubber, silicone rubber, acrylonitrile rubber, polyurethane rubber, polyisobutylene and acrylic polymers; (b) from about 30 to about 80 parts by weight of a moisture absorbing component selected from the group consisting of karaya gum, locust bean gum, sodium acrylates, polyvinylalcohol, powdered pectin, gelatin, carboxymethylcellulose, high molecular weight carbowax, and carboxypolymethylene; and (c) from about 2% to about 20% by weight based on the total weight of said adhesive composition of silica. The invention also includes a pressure-sensitive surgical sheet material comprising a thin pliable substrate bearing on at least one surface thereof a composition as defined above.
Description
SPECIFICATION
Stoma seal adhesive
BACKGROUND OF THE INVENTION 1. Field of the Invention
This invention relates to pressure-sensitive adhesives having the capacity to absorb moisture and therefore adhere to moist body surfaces for a prolonged period of time. More particularly, this invention relates to an improvement in such adhesives which affords them a combination of high plasticity and "wet-stick" adhesion at acceptable levels of moisture absorption over prolonged periods of time, which renders the adhesive particularly suitable for such applications as stoma seal adhesives.This invention also relates to surgical sheet materials such as adhesive tapes and to adhesive bandages and dressings, including plasters that are particularly suitable for use in connection with ostomy appliances as weil as for coverings for cuts, abrasions and the like, which comprise a flexible backing member, one of whose major surfaces has adhered thereto a coating of a pressure-sensitive adhesive of the present invention.
Various types of pressure-sensitive adhesives have been proposed and utilized as the adhesive component in adhesive bandages, adhesive tapes and the like. Acrylate polymers, polyolefinic polymers and compounded systems based on natural or synthetic rubbber polymers have all been tried or utilized as pressure-sensitive adhesives with varying degrees of success.
A pressure-sensitive adhesive must have certain characteristics to be useful. It must be sufficiently tacky, i.e., have sufficient "grab" or quick-stick," to adhere quickly to the surface to which it is to be adhered. It must also continue to adhere to that surface over extended periods of time. A pressure-sensitive adhesive composition should also have sufficient internal strength to prevent splitting and leaving particles of adhesive on a surface to which an article coated with the adhesive has been adhered when the article is removed. Where the pressure-sensitive adhesive is designed for application to the skin, the problems of adherence are substantially increased.Although the initial tack or stick may be good, adherence over an extended period of time for many pressure-sensitive adhesives requires relatively high shear adhesion to withstand movement of the underlying skin. Also, the adhesive must be tailored to accommodate the nature of the underlying skin surface, as where perspiration and other surface changes may occur. The problem is further complicated by the fact that any pressure-sensitive adhesive designed for application to the skin must release from the skin sufficiently readily to permit removal without skin damage. Where the adhesive is too strongly adhered to the skin and has substantial internal strength, small particles of the upper layer of skin are removed with the adhesive with resulting irritation to the skin.As a result, although many pressure-sensitive adhesives are available for various commerical uses, relatively few have been found which are suitable for articles for skin applications, particularly in that many of those having desirable, high shear adhesion, have an undesirably high resistance to removal, or peel adhesion. This problem is further complicated when the adhesive is intended in such applications as those involving ostomy appliances, where it is required to maintain adhesion for prolonged periods of time while in contact with body fluids, and at the same time to prevent leakage of such fluids therethrough.
A colostomy is the surgical creation of a new opening for the colon on the surface of the body, while an ileostomy is the surgical creation of an opening for the ileum. In an ileostomy the entire colon, the rectum, and sometimes a small portion of the ileum, is removed. In a colostomy the rectum, and sometimes a portion of the colon, is removed.
Both ileostomy and colostomy ooperations involve the creation of an artifical opening (stoma) in the abdomen to which the distal end of the healthy intestine is attached. Generally, the stoma is placed low on the abdomen and to one side. A related enterostomy for which the stoma seal adhesive of the present invention might be useful is the urinary diversion. It involves the formation of a permanent fistula through which the ureter may discharge it contents.
As a result of the ostomy procedure, means must be provided for conveniently and hygenically collecting human waste material from the resulting stoma. While there are many such ostomy applications, a common problem experienced with them, as indicated above, is the establishment and maintenance of both good skin adhesion and an adequate seal to prevent waste material coming in contact with the patient's skin. This requires, inter alia, an adhesive material that has good adhesion to both dry and wet skin, adequate moisture absorptivity and sufficient elastic modulus or plasticity to prevent either inadvertent detachment from wet skin or inordinate difficulty or discomfort to the user when the device is intentionally removed.
2. Description of the Prior Art
U.S. Patent No. 3,339,546, issued September 5, 1967, to Chen, discloses an adhesive composition, that is a blend of a water soluble or swellable hydrocolloid admixed with a water insoluble viscous gum-like elastomer binder, that has been found useful for ostomy appliances.
U.S. Patent No. 3,925, 271, issued Decesuber 9, 1975, to Balinth, discloses an uncured pressure-sensitive adhesive that does not have moisture absorbing properties comprising an uncured elastomer, a tackifier and at least 14% by weight of silica. The silica is disclosed to provide the adhesive composition with improved tack and holding power at moderately high temperatures, particularly when in contact with metal surfaces. The adhesive is said to be particularly suited to be used on tapes for joining and sealing together sections of metal ventilating ducts, and the electrical insulation of fractional horsepower electical motors. This patent also refers to U.S.Patent No. 2,909,278 as disclosing the inclusion of small amount of silica in a pressure-sensitive adhesive composition comprising an elastomer and a tackifier in order to improve the aging characteristics of pressure-sensitive adhesive tape.
U.K. Patent Application Publication GB 2038661A filed November20, 1978 as Application
No. 7845281 and published July 3O, 1980, entitled "Surgical Sealant Composition", is concerned with providing material for effecting a seal around a surgically created stoma. The adhesive sealing composition of the invention described and claimed in this British application comprises 100 parts by weight of a non-biodegradable, tacky polymeric binding agent-such as polyisoprene, polyurethane, silicone or polyisobutylene-preferably polyisobutylene, Vistanex LM/MS by Esso Chemicals being particularly preferred; from 1 2 to 25 parts by weight of an inert reinforcing filler--the only disclosed examples of suitable material being precipitated or fume silica, a particularly preferred example being Aerosil 200V, a form of fume silica sold by
Degussa; and from 5 to 1 50 parts by weight of a water-activated adhesive thickenor-the only disclosed suitable example being a polyacrylamide, preferably that sold by Cyanamid as "Cyanomer P250".
Another recent patent that addresses the problem of providing adequate sealing for ostomy devices and contains a discussion of the prior art at columns 2 and 3 is U.S. Patent h!lo.
4,231,369, issued November 4, 1980, to Sorensen et al. That patent is directed to the use, as ostomy sealing means, of a shaped, gel-like composition comprising a selected cross-linked elastomer, a hydrocolloid dispersed therein, and a hydrocarbon tackifier.
SUMMARY OF THE INVENTION
We have discovered, quite unexpectedly, that the addition of from about 2 to about 20 % by weight, based on the total weight of the adhesive composition, of silica to a blend o from about 30 to about 80 parts by weight of a pressure-sensitive adhesive component that is a gum-like substance and from about 30 to about 80 parts by weight of a moisture absorbing component that is a water soluble or swellable synthetic hydrocarbon or natural hydrocolloid provides significantly improved plasticity to the resulting adhesive composition while maintaining good "wet-stick" and "dry-stick" characteristics, thereby providing a highly desirable adhesive for stoma seal and similar uses.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
In general, the pressure-senstive adhesive compositions of this invention comprise a pressuresensitive adhesive component selected from the natural and synthetic gum-like substances, including natural and synthetic elastomers, a moisture absorbing component selected from the synthetic carbohydrate and natural water swellable and water soluble hydrocolloids, and silica.
Each of the pressure-sensitive adhesive component and the moisture absorbing component is present in the composition of the invention in an amount of from about 30 to about o0 parts by weight, preferably from about 40 to about 60 parts by weight, while the silica is present in an amount of from about 2 to about 20 weight percent, preferably from about 5 to about 1 2 weight percent, based on the total weight of the adhesive composition.
Generally the silica should be of a sufficiently small particle size to provide a surface area of at least 1 30 square meters per gram. Particles having an ultimate particle size of less than 0.03 microns are desirable, while those havin an ultimate particle size in the range of 0.020 to 0.030 microns are preferred.
As used herein, the term silica is meant to describe a material having a composition which comprises SiO2 as the major component, usually greater than 80%. It is recognized in the art that silica, however obtained, whether from fumed silica, precipitated silica or natural mined silica, will contain various amounts of other metal oxides such as magnesium oxide, together with some water of crystallization, varying amounts of which can be driven off upon ignition.
The presence of these impurities does not alter the properties imparted to the adhesive composition in any observable way. However, to insure uniformity of product, the commercially available silica Hi-Sil 233 manufactured by PPG, Pittsburgh, Pennsylvania, is preferred.
Suiable natural and synthetic gum-like substances which may be used singly or in admixture as the pressure-sensitive adhesive component in the adhesive compositions of this invention include natural rubber, silicone rubber, acrylonitrile rubber, polyurethane rubber, pol'/iso- butylene, acrylic polymers and other like substances. Particularly preferred are the polyisobutyk enes (such as those supplied commercially by Exxon as Vistanex L100 and Vistanex LM-MH) and acrylic polymers (such as Acrylate QR667 from Rohm a Hays). The gum-like substance acts as a binder for the hydrocolloid particles and, in addition, renders the final bonding composition elastic and pliable.
Suitable synthetic carbohydrate and natural water swellable or soluble hydrocolloids for use, singly or in admixture, as the moisture absorbing component include karaya gum, locust bean gum, sodium acrylates, polyvinyl-alcohol, powdered pectin, gelatin, carboxymethylcellulose, high molecular weight carbowax, carboxypolymethylene and other like substances.
If desired, the pressure-sensitive adhesive compositions of the present invention can include from 0 to about 10% by weight of the usual modifiers, fillers, extenders, tackifiers, antioxidants, stabilizers, plasticizers, and other such ingredients known in the art for inclusion in such compositions. Thus, for example, plasticizers or solvents, such as mineral oil or petrolatum may be added to improve adhesive characteristics and/or to provide the desired consistency.
Particularly when the gum-like substance comprises a polyisobutylene, a low molecular weight polybutene (such as Vistac 300 from Exxon) may be included as a tackifier. The extenders can include finely divided clays, bentonites, carbonates such as calcium carbonates, diatomaceous earth, starches or other inert ingredients normally used in adhesive compositions. Antioxidants and stabilizers can be utilized at levels of from about 0.2% to about 3% by weight-of the total composition, preferably from about 1% to about 2%.Suitable antioxidants and stabilizers include butyl zimate; 2,6,ditert.-butyl-4 methyl phenol, sold under the trademark lonol by Shell
Chemical Company; 2,5-di(tertamyl)-hydroquione, sold under the trademark Santowar A by
Monsanto Chemical Company; a mixture of alkylated diphenylamines sold under the trademark
Agerite Stalite by Vanderbilt Chemical Company, and the like. These stabilizers and antioxidants give improved shelf life characteristics and prevent degradation of the pressure-sensitive adhesive compositions of the present invention.
It has further been found that to obtain pressure-sensitive adhesive compositions with the desired characteristics, it is necessary for such compositions to have a Williams plasticity measurement of from about 2 mm to about 4 mm, preferably about 2.3 mm to about 2.7 mm.
If the Williams plasticity is below 2 mm, the adhesive compositions will be too soft and exhibit undesirable flow, and have an undesirably high tendency to leave particles of adhesive adhered to the skin upon removal. If the Williams plasticity is above 4 mm, the adhesive compositions will be too hard and exhibit poor tackiness.
In addition to the use of the adhesive compositions of this invention by themselves, very satisfactory surgical sheet materials are obtained when a thin, pliable substrate has coated on one side thereof a layer of an adhesive bonding composition of this invention. Suitable substrates which may be employed in the practice of this invention include various papers, woven and non-woven fabrics, such as cellulose acetate cloth, polymeric films prepared from such materials as polyethylene polymers, polypropylene, copolymers of vinylidene chloride, fluorohalocarbon film, condensation products of ethylene glycol and terephthalic acid, polyamide films and other like flexible sheet materials.
In the preparation of pressure-sensitive surgical sheet materials for application to the skin, such as pressure-sensitive adhesive tapes, adhesive bandages, surgical drapes, and the like, the pressure-sensitive adhesive compositions of the present invention are coated onto a flexible backing material in accordance with known techniques, such as calendering, extrusion, deposition using organic media, and the like.
The film or other substrate which may be employed in the practice of this invention may have a thickness of from 0.0005 inch to 0.05 inch, more preferably from 0.0005 to 0.002 inch. The adhesive composition is applied to a surface of the film in sufficient amount to afford adequate adhesion in use.
EXAMPLES
Specific embodiments of the present invention are illustrated by the following examples. It will be understood, however, that the present invention is not confined to the specific limitations set forth in the individual examples, but rather to the scope of the appended claims.
Example 1
A pressure-sensitive adhesive composition was prepared on a two roll laboratory mill at a temperature of about 240OF as follows: 510 grams of polyisobutylene were mixed for 10 minutes. Next, 300 grams of carboxymethylcellulose, 200 grams of karaya gum and 100 grams of silica were blended as dry powders and slowly sprinkled onto the mill over about 10 minutes and mixing continued for an additional 1 5 minutes. 90 grams of liquid polybutene were then slowly poured onto the adhesive and milled until uniform in appearance.
The adhesive composition was then pressed into 4 inch square wafers, 60 mils thick, and tested for wet stick, moisture absorption and adhesive properties.
Example 2-8
Following the procedure of Example 1, pressure-sensitive adhesive compositions illustrative of the present invention were prepared, having the compositions shown in the following table:
Example No. 2 3 4 5 6 7 8
Elastomer
Polyisobutylene 530 200 - - 600 510 510
Acrylate copolymer - 400 600 600 - -
Polybutene 70 - - - - 90 70
Hydrocolloid Carboxymethylcellulose 180 350 350 - 300 300 300 300aya Gum - 150 150 - 200 200
Gelatin 175 - - 100 - - 100
Pectin 175 - - 100 - - 100
Silica 70 100 100 100 100 100 100
As v:ll be apparent to those skilled in the art, and as indicated above, many modifications and variations of the foregoing detailed description are possible within the spirit and scope of the present invention.
Having thus described our invention, what we desire to secure by Letters Patent is defined in the appended claims.
Claims (11)
1. A pressure-sensitive adhesive compositions having the capacity to absorb from about 1 5 to about 40% of its own weight in water comprising:
(a) from about 30 to about 80 parts by weight of a pressure-sensitive adhesive component selected from the group consisting of natural rubber, silicone rubber, acrylonitrile rubber, polyurethane rubber, polyisobutylene and acrylic polymers;
(b) from about 30 to about 80 parts by weight of a moisture absorbing component selected from the group consisting of karaya gum, locust bean gum, sodium acrylate, polyvinylalcohol, powdered pectin, gelatin, carboxymethylcellulose, high molecular weight carbowax, and carboxypolymelthylene; and
(c) from about 2% to about 20% by weight based on the total weight of said adhesive compositions of silica.
2. The composition of claim 1 wherein the silica is present in an amount of from about 4 to about 12% by weight.
3. The composition of claiml wherein the adhesive component is selected from polyisobutylene and acrylic polymers.
4. The composition of claim 1 wherein the moisture absorbing component is selected from carboxymethylecellulose, karaya gum, pectin and gelatin.
5. The composition of claim 1 which comprises from about 40 to about 60 parts by weight of each of said adhesive component and said moisture absorbing component.
6. The composition of claim 5 wherein the adhesive component is polyisobutylene and the moisture absorbing component comprises carboxymethylcellulose and karaya gum.
7. The composition of claim 5 wherein the adhesive component is a blend of polyisobutylene and an acrylate copolymer and the moisture absorbing component comprises carboxymethylcellulose, gelatin and pectin.
8. The composition of claim 6 further comprising polybutene.
9. A pressure-sensitive surgical sheet material comprising a thin pliable substrate bearing on at least one surface thereof the composition of any of claims 1 to 8.
10. A composition as claimed in claim 1 substantially as described in respect of any of the foregoing Examples 1-8.
11. A sheet material as claimed in claim 9 bearing the composition of claim 10.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24419481A | 1981-03-16 | 1981-03-16 |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2094809A true GB2094809A (en) | 1982-09-22 |
GB2094809B GB2094809B (en) | 1985-01-09 |
Family
ID=22921745
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8207447A Expired GB2094809B (en) | 1981-03-16 | 1982-03-15 | Stoma seal adhesive |
Country Status (15)
Country | Link |
---|---|
JP (1) | JPS57168970A (en) |
AT (1) | AT392796B (en) |
AU (1) | AU554204B2 (en) |
BR (1) | BR8201392A (en) |
CA (1) | CA1187231A (en) |
DE (1) | DE3209374A1 (en) |
ES (1) | ES510450A0 (en) |
FR (1) | FR2501707B1 (en) |
GB (1) | GB2094809B (en) |
GR (1) | GR76361B (en) |
IN (1) | IN155486B (en) |
IT (1) | IT1148136B (en) |
MX (2) | MX173767B (en) |
PH (1) | PH16755A (en) |
ZA (1) | ZA821730B (en) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0126312A1 (en) * | 1983-04-21 | 1984-11-28 | Avery International Corporation | Reduced build-up pressure-sensitive adhesives |
GB2198441A (en) * | 1986-12-04 | 1988-06-15 | Smith & Nephew Ass | Pressure sensitive adhesives |
EP0379933A2 (en) * | 1989-01-20 | 1990-08-01 | LTS Lohmann Therapie-Systeme GmbH & Co. KG | Surface treatment system containing an antineoplastic agent, particularly 5-fluor uracil |
EP0421454A2 (en) * | 1989-10-06 | 1991-04-10 | LTS Lohmann Therapie-Systeme GmbH & Co. KG | Dressing containing estrogen |
WO1998010801A1 (en) * | 1996-09-16 | 1998-03-19 | Laboratoires D'hygiene Et De Dietetique | Novel hydrophile adhesive mass |
WO1998047977A1 (en) * | 1997-04-21 | 1998-10-29 | Scapa Group Plc | Masking material for lacquered surfaces |
EP0880973A2 (en) * | 1997-05-30 | 1998-12-02 | Bristol-Myers Squibb Company | Adhesive composition or structure |
EP0936223A1 (en) * | 1998-02-11 | 1999-08-18 | Bayer Ag | Modified superabsorbant based on polyacrylonitrile emulsions |
WO2007036338A2 (en) * | 2005-09-27 | 2007-04-05 | Inatec Gmbh | Method and device for applying adhesive threads and points to a substrate, web of material comprising a fleece and a layer composed of adhesive threads, and products made therefrom |
GB2432120A (en) * | 2005-11-09 | 2007-05-16 | Welland Medical Ltd | A support for an ostomy device with silicone adhesive |
WO2010018108A1 (en) * | 2008-08-15 | 2010-02-18 | Tesa Se | Pressure-sensitive adhesive |
CN111883697A (en) * | 2020-07-17 | 2020-11-03 | 东莞华誉精密技术有限公司 | Multi-station pressing process for battery cover |
WO2023242542A1 (en) * | 2022-06-17 | 2023-12-21 | Welland Medical Limited | Adhesive composition for ostomy bag |
CN117942420A (en) * | 2024-03-26 | 2024-04-30 | 上海威高医疗技术发展有限公司 | Degradable in-vivo pressure-sensitive adhesive with acellular matrix material as base material and preparation method thereof |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3344691A1 (en) * | 1983-12-10 | 1985-06-20 | Bayer Ag, 5090 Leverkusen | ACTIVE GAS EXHAUST SYSTEMS |
DE3346100A1 (en) * | 1983-12-21 | 1985-07-04 | Beiersdorf Ag, 2000 Hamburg | RESIDUE-FREE RE-DETACHABLE ADHESIVE SURFACES |
IE65163B1 (en) * | 1987-06-29 | 1995-10-04 | Squibb & Sons Inc | Process for preparing a wound dressing comprising a hydrophilic acrylic adhesive layer |
US4831070A (en) * | 1987-11-02 | 1989-05-16 | Dow Corning Corporation | Moldable elastomeric pressure sensitive adhesives |
JPH01197585A (en) * | 1988-02-02 | 1989-08-09 | Kinugawa Rubber Ind Co Ltd | Adhesive |
US5190818A (en) * | 1990-04-20 | 1993-03-02 | Toppan Moore Co., Ltd. | Adhesive composition for temporary adhesive bonding of paper sheets |
NZ248977A (en) | 1992-11-09 | 1995-06-27 | Squibb & Sons Inc | Pressure-sensitive adhesive comprising a polyurethane having excess hydroxyl functionality; medical articles comprising a layer of such adhesive |
DE10114382A1 (en) * | 2001-03-23 | 2002-09-26 | Beiersdorf Ag | Moisture-absorbing material used for plasters, medical fixings, wound coverings and bandages comprises adhesive matrix of silicon, gel former and optionally silicone resin |
WO2016173600A1 (en) * | 2015-04-30 | 2016-11-03 | Coloplast A/S | Adhesive composition |
CN108096628A (en) * | 2018-01-04 | 2018-06-01 | 武汉市思泰利医疗器械发展有限公司 | A kind of special paste of stoma and preparation method thereof |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3980084A (en) * | 1974-01-09 | 1976-09-14 | Hydro Optics, Inc. | Ostomy gasket |
JPS511585A (en) * | 1974-06-26 | 1976-01-08 | Honey Kasei Kk | Kinzoku gomuno setsuchakuhoho |
US3906951A (en) * | 1974-08-05 | 1975-09-23 | Squibb & Sons Inc | Stomal device including means to prolong attachment of flange |
DE2531085C2 (en) * | 1975-07-11 | 1984-09-13 | Bischof & Klein Verpackungswerke, 4540 Lengerich | Extrudable adhesive |
JPS5232084A (en) * | 1975-09-05 | 1977-03-10 | Honny Chem Ind Co Ltd | Process for bonding a metal to rubber |
GB1586182A (en) * | 1977-03-04 | 1981-03-18 | Rhodes J | Adhesive compositions suitable for application to the skin and surgical products incorporating same |
CA1124154A (en) * | 1977-07-05 | 1982-05-25 | John A. Hill | Ostomy appliance |
JPS5476632A (en) * | 1977-11-30 | 1979-06-19 | Nitto Electric Ind Co Ltd | Self-bonding adhesive composition |
US4356819A (en) * | 1979-03-21 | 1982-11-02 | Advance Tapes (U.K) Limited | Article of manufacture having adhesive properties |
FR2479002A1 (en) * | 1980-04-01 | 1981-10-02 | Biotrol Sa Lab | Adhesive contg. pressure sensitive adhesive and a hydro-colloid - plus an aluminium silicate used medically, esp. in stoma |
-
1982
- 1982-02-12 IN IN167/CAL/82A patent/IN155486B/en unknown
- 1982-03-04 GR GR67484A patent/GR76361B/el unknown
- 1982-03-12 FR FR8204174A patent/FR2501707B1/en not_active Expired
- 1982-03-12 IT IT47976/82A patent/IT1148136B/en active
- 1982-03-15 ZA ZA821730A patent/ZA821730B/en unknown
- 1982-03-15 CA CA000398375A patent/CA1187231A/en not_active Expired
- 1982-03-15 ES ES510450A patent/ES510450A0/en active Granted
- 1982-03-15 BR BR8201392A patent/BR8201392A/en not_active IP Right Cessation
- 1982-03-15 GB GB8207447A patent/GB2094809B/en not_active Expired
- 1982-03-15 JP JP57039590A patent/JPS57168970A/en active Granted
- 1982-03-15 AT AT1022/82A patent/AT392796B/en not_active IP Right Cessation
- 1982-03-15 DE DE19823209374 patent/DE3209374A1/en not_active Withdrawn
- 1982-03-15 PH PH26992A patent/PH16755A/en unknown
- 1982-03-16 MX MX016193A patent/MX173767B/en unknown
- 1982-03-16 MX MX191832A patent/MX161551A/en unknown
- 1982-03-16 AU AU81543/82A patent/AU554204B2/en not_active Ceased
Cited By (31)
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WO1998010801A1 (en) * | 1996-09-16 | 1998-03-19 | Laboratoires D'hygiene Et De Dietetique | Novel hydrophile adhesive mass |
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US8323730B2 (en) | 2005-09-27 | 2012-12-04 | Illinois Tools Works, Inc. | Method and device for applying adhesive therads and points to a substrate, web of material comprising a fleece and a layer composed of adhesive threads, and products made therefrom |
WO2007036338A2 (en) * | 2005-09-27 | 2007-04-05 | Inatec Gmbh | Method and device for applying adhesive threads and points to a substrate, web of material comprising a fleece and a layer composed of adhesive threads, and products made therefrom |
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CN102159661B (en) * | 2008-08-15 | 2014-07-02 | 德莎欧洲公司 | Pressure-sensitive adhesive |
CN111883697A (en) * | 2020-07-17 | 2020-11-03 | 东莞华誉精密技术有限公司 | Multi-station pressing process for battery cover |
WO2023242542A1 (en) * | 2022-06-17 | 2023-12-21 | Welland Medical Limited | Adhesive composition for ostomy bag |
GB2621307A (en) * | 2022-06-17 | 2024-02-14 | Welland Medical Ltd | Adhesive composition for ostomy bag |
CN117942420A (en) * | 2024-03-26 | 2024-04-30 | 上海威高医疗技术发展有限公司 | Degradable in-vivo pressure-sensitive adhesive with acellular matrix material as base material and preparation method thereof |
CN117942420B (en) * | 2024-03-26 | 2024-06-18 | 上海威高医疗技术发展有限公司 | Degradable in-vivo pressure-sensitive adhesive with acellular matrix material as base material and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0216786B2 (en) | 1990-04-18 |
MX173767B (en) | 1994-03-28 |
AT392796B (en) | 1991-06-10 |
FR2501707B1 (en) | 1987-01-02 |
AU554204B2 (en) | 1986-08-14 |
JPS57168970A (en) | 1982-10-18 |
ES8305815A1 (en) | 1983-04-16 |
ATA102282A (en) | 1990-11-15 |
BR8201392A (en) | 1983-02-01 |
ZA821730B (en) | 1983-10-26 |
IT1148136B (en) | 1986-11-26 |
MX161551A (en) | 1990-10-31 |
IT8247976A0 (en) | 1982-03-12 |
FR2501707A1 (en) | 1982-09-17 |
DE3209374A1 (en) | 1982-11-25 |
GR76361B (en) | 1984-08-06 |
ES510450A0 (en) | 1983-04-16 |
IN155486B (en) | 1985-02-09 |
PH16755A (en) | 1984-02-15 |
CA1187231A (en) | 1985-05-14 |
AU8154382A (en) | 1982-09-23 |
GB2094809B (en) | 1985-01-09 |
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Legal Events
Date | Code | Title | Description |
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PE20 | Patent expired after termination of 20 years |
Effective date: 20020314 |