CA1151041A - Wound dressing - Google Patents
Wound dressingInfo
- Publication number
- CA1151041A CA1151041A CA000359667A CA359667A CA1151041A CA 1151041 A CA1151041 A CA 1151041A CA 000359667 A CA000359667 A CA 000359667A CA 359667 A CA359667 A CA 359667A CA 1151041 A CA1151041 A CA 1151041A
- Authority
- CA
- Canada
- Prior art keywords
- layer
- dressing
- weight
- foam
- curative
- 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.)
- Expired
Links
Classifications
-
- 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
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
- A61L15/225—Mixtures of macromolecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/02—Adhesive plasters or dressings
- A61F13/0203—Adhesive plasters or dressings having a fluid handling member
- A61F13/0206—Adhesive plasters or dressings having a fluid handling member the fluid handling member being absorbent fibrous layer, e.g. woven or nonwoven absorbent pad, island dressings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/02—Adhesive plasters or dressings
- A61F13/0203—Adhesive plasters or dressings having a fluid handling member
- A61F13/0213—Adhesive plasters or dressings having a fluid handling member the fluid handling member being a layer of hydrocoloid, gel forming material
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/02—Adhesive plasters or dressings
- A61F13/0203—Adhesive plasters or dressings having a fluid handling member
- A61F13/0226—Adhesive plasters or dressings having a fluid handling member characterised by the support layer
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/02—Adhesive plasters or dressings
- A61F13/0246—Adhesive plasters or dressings characterised by the skin adhering layer
-
- 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
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/18—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing inorganic materials
-
- 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
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/46—Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
Abstract
Abstract WOUND DRESSING A multi-layered dressing including a layer of curative and absorbant material which contacts the wound, an intermediate layer of deodorizing material, and an air and gas permeable outer flexible layer which secures the dressing to the body.
Description
~lSiO~
XFll WOUND DRESSING
This invention is directed to a multi-layered bandage useful in the treatemnt of open wounds such as decubitis ulcers. A problem with treating certain wounds, particularly ulcerated sores, is to meet the conflicting requirements of providing a comfortable covering which protects the wound and substantially doedorizes any escaping gas without impeding the passage of such gas away from the wound area.
The multi-layered bandage of this invention includes at least a layer of curative and absorbant material which contacts the wound, a layer of deodorizing material, and an outer flexible layer that secures the bandage to the body.
Figure 1 is an exploded view of a multi-layered bandage of this invention.
Figure 2 is a perspective view of the bandage of Figure 1 applied to a wound.
Figure 3 is an enlarged view of an alternate layer B.
Figure 4 is an enlarged view of another alternate layer B.
Figure 5 is an enlarged view of still another alternate layer B.
Figure 6 is an exploded view of another embodiment of the multi-layered bandage of this invention.
This invention is directed to a multi-layered bandage or dressing. The dressing includes a layer of curative and absorbant material which contacts the wound, a layer of deodorizing material, and an outer flexible layer that secures the bandage to the body.
.~.
~1510~1 XFll The layer of curative and absorbant material is shown in the Figures as layer B. Layer B may be formed entirely as a homogeneous cohesive mass 11 as shown in Figures 1 and 2, layer B may be formed as a homogeneous cohesive mass 11 having a backing film 12 as shown in Figure 3, layer B may be formed as homogeneous mass 11 having as the backing an intermediate layer of semi-open cell polymeric foam 13 and an optional outer polymeric film 14 as shown in Figure 4, or layer B may be formed as a curative and absorbant foam lS which may have an optional backing film 16 as shown in Figure 5.
The layer B has a plurality of apertures 20 extending through the curative and absorbant homogeneous mass or foam material and any of the optional backings that may be present. The apertures may be in a regular pattern or randomly placed. The ratio between the surface area of layer B and the apertures can vary from about
XFll WOUND DRESSING
This invention is directed to a multi-layered bandage useful in the treatemnt of open wounds such as decubitis ulcers. A problem with treating certain wounds, particularly ulcerated sores, is to meet the conflicting requirements of providing a comfortable covering which protects the wound and substantially doedorizes any escaping gas without impeding the passage of such gas away from the wound area.
The multi-layered bandage of this invention includes at least a layer of curative and absorbant material which contacts the wound, a layer of deodorizing material, and an outer flexible layer that secures the bandage to the body.
Figure 1 is an exploded view of a multi-layered bandage of this invention.
Figure 2 is a perspective view of the bandage of Figure 1 applied to a wound.
Figure 3 is an enlarged view of an alternate layer B.
Figure 4 is an enlarged view of another alternate layer B.
Figure 5 is an enlarged view of still another alternate layer B.
Figure 6 is an exploded view of another embodiment of the multi-layered bandage of this invention.
This invention is directed to a multi-layered bandage or dressing. The dressing includes a layer of curative and absorbant material which contacts the wound, a layer of deodorizing material, and an outer flexible layer that secures the bandage to the body.
.~.
~1510~1 XFll The layer of curative and absorbant material is shown in the Figures as layer B. Layer B may be formed entirely as a homogeneous cohesive mass 11 as shown in Figures 1 and 2, layer B may be formed as a homogeneous cohesive mass 11 having a backing film 12 as shown in Figure 3, layer B may be formed as homogeneous mass 11 having as the backing an intermediate layer of semi-open cell polymeric foam 13 and an optional outer polymeric film 14 as shown in Figure 4, or layer B may be formed as a curative and absorbant foam lS which may have an optional backing film 16 as shown in Figure 5.
The layer B has a plurality of apertures 20 extending through the curative and absorbant homogeneous mass or foam material and any of the optional backings that may be present. The apertures may be in a regular pattern or randomly placed. The ratio between the surface area of layer B and the apertures can vary from about
2~ 1:2 to 2:1, with about 1:1 being preferred. The apertures can be punched through layer B or may be formed by a molding operation. The particular shape and dimensions of layer B are not critical.
The rectangular shape shown in the drawings is 2~ preferred though it may be desirable in treating wounds a~ various body locations such as the elbow or heel to have a circular shape. The layer B
may vary in thickness from about 1 to about 4 mm.
and the apertures may have a diameter of from about 2 to about 4 mm.
~1510~
XFll The homogeneous cohesive mass 11 comprises a blend of one or more water soluble or swellable hydro-colloids and a natural or synthetic viscous substance which acts as a binder for the hydrocolloids. The hydrocolloids are present at from about 30% to about 70% by weight of the mass. Suitable hydrocolloids include pectin, gelatin, karaya gum, guar gum, locust bean gum, and sodium carboxymethylcellulose provided that at least about 20% by weight of the mass is one or more curative hydrocolloid substances such as pectin, gelatin and karaya gum. Suitable viscous sub-stances include natural rubber, silicone rubber, acryl-onitrile rubber, polyurethane rubber, and polyisobutyl-enes and such binder is also present at from about 30~ to about 70% by weight of the cohesive mass.
Other substances such as a plasticizer, antioxidant, or a pharmaceutically active substance such as an antibacterial agent can be included within the mass at up to about 5% by weight and a cohesive strengthening agent, for example, fibrous cotton, finely divided wood cellulose or microcrystalline cellulose can be included within the mass at up to about 10% by weight. Preferably, the homogeneous cohesive mass 11 comprises about 20% by weight of pectin, about 20% by weight of gelatin, about 20% by weight of sodium carboxymethylcellulose, and about 40% by weight of polyisobutylene.
The backing film 12 as shown in Figure 3 is secured to the surface of the homogeneous cohesive mass 11 which does not contact the wound. The film 12 is a thin sheet of polymeric material such as polyethylene, polypropylene, polyvinylchloride, etc.
As shown in Figure 4, the cohesive mass 11 may have a layer of semi-open cell polymeric foam 13 secured to the surface which does not contact the wound. This foam can be prepared from various elastomer materials such as polyester or polyether polyurethane foams, styrene-butadiene foams, or certain rubbex-based foams. The preferred material is a flexible polyurethane foam having from about 50 to about 100 cells per linear inch.
By semi-open cell it is meant that the percentage of open or ruptured cells is from about 30 to about 70%. An outer polymeric film 14 from a pliable elastomer material such as flexible polyurethane, polyacrylate, polyethylene, etc., may be secured to the foam. Alternatively instead of film 14 the top surface of foam 13 can be sealed by flaming or scorching.
The curative and absorbant homogeneous cohesive mass 11 may be prepared as taught by Ch-en in United States Patents 3,339,546 and 3,972,328 or Chen et al. in United States Patent 4,192,785.
For example, the hydrocolloids and any optional ingredients, preferably in finely divided fvrm, are blended and the mixture is slowly added to the viscous substance in a kneader mixer until a homogeneous mass is formed. The backing film 12 ~1510~1 X~ll or the semi-open cell foam 13 and film 14 may then be secured and the apertures 20 punched there through. Alternatively, the homogeneous mixture of hydrocolloids and binder before setting may be molded to form the apertures 20.
The layer B of curative and absorbant material may also be a foam 15 as shown in Figure 5. This foam can be prepared by hot air drying or lyophilizing a foamed aqueous colloidal dispersion of or more hydrocolloids such as pectin, gelatin, karaya gum, guar gum, locust bean gum, and sodium carboxymethylcellulose provided that at least about 20~ by weight of the hydrocolloid dispersion is one or more curative hydrocolloid substances such as pectin, gelatin and karaya gum. Such foams are described in various patents such as United States Patents 2,465,357, 2,558,395 and 3,767,784. Preferably the foam is prepared from a mixture of gelatin, pectin and sodium carboxymethylcellulose. This preferred foam contains from about 10% to about 50% by weight of pectin and sodium carboxymethylcellulose and from about 20% to about 80% by weight of gelatin and is prepared by dry blending the hydrocolloids, adding the blend to water with agitation so as to form a colloidal dispersion having a solids content of from about 1% to about 20% by weight, foaming the colloidal dispersion so that its volume ~510~1 XFll increases from about 10~ to about 60~, freezing and then freeze drying.
An optional film backing 16 of various polymeric materials such as polyethylene, poly-propylene, polyvinylchloride, etc., can besecured to the surface of foam 15 which does not contact the wound.
The layer of deodorizing material is shown as layer D in Figures 1, 2 and 6. This deodorizing layer is formed of an air-permeable woven or non-woven material carrying or impregnated with a deodorizing substance. One type of suitable material is a sheet of foamed non-woven synthetic - polymeric material, for example, polyurethane, having a large number of activated carbon particles distributed over one of its major surfaces.
Preferably, the carbon particles are bound to the top surface, i.e., that furthest away from layer B, and the surface which contacts layer B is coated with a layer adhesive. Such a material is commercially available under the tradename Bondina. Another type of suitable deodorizing material is a layer of carbon cloth such as that disclosed by Bailey et al. in British Patent 1,301,101.
As shown in Figure 6, an intervening layer C may be included within the dressinq between deodorizing layer D and curative and absorbant layer B. This intervening layer C is an air-permeable but liquid-impermeable material such llSlO~L
XFll _ 7 _ as a non-woven fabric and it serves to prevent any liquid discharge which passes through layer B from escaping further. However, any gaseous discharge from the wound passes through layer C to layer D
where it is deodorized. Layer C can be coated with a microporous pressure sensitive adhesive on one or both sides.
The outer layer of the wound dressing is shown as layer E in Figures 1, 2 and 6. This layer is a flexible breathable adhesive tape which allows air and gas to pass therethrough. This layer compri-ses a porous non-woven fibrous or polymeric backing having a coating of a microporous pressure sensitive adhesive on its bottom surface. Layer E extends in size beyond the periphery of layers B, D and C so that it holds the dressing together. During shipping a piece of silicon release paper is attached across the bottom of layer B and the extending portion of layer E.
Examples of suitable materials for layer E are disclo-sed by Copeland in United States Patent 3,121,021 and Hodgson in United States Patent 3,645,835. It is also possible to replace the adhesive coating ~aught by Copeland with a hydrocolloid containing pressure sensi-tive adhesive such as that taught by Chen in the above noted patents. The layer E allows any gas which has been deodorized by layer D to pass to the atmosphere.
Layer E also secures the dressing to the patient and provides overall protection of the wound.
llS10~
X~l;
The dressing of this invention is employed by placing the proper sized piece over the wound so that layer B contacts the wound. Optionally, the wound can be packed under the dressing with the hydrocolloid containing adhesive mass disclosed by Chen in United States Patent 3,339,546, the hydrocolloid powder disclosed by Steinhardt in United States Patent 3,029,187, karaya gum, or other healing material. This packing is represented as A in Figure 2. The dressing is changed on a periodic bases and.the wound is kept covered until the healing is complete.
The rectangular shape shown in the drawings is 2~ preferred though it may be desirable in treating wounds a~ various body locations such as the elbow or heel to have a circular shape. The layer B
may vary in thickness from about 1 to about 4 mm.
and the apertures may have a diameter of from about 2 to about 4 mm.
~1510~
XFll The homogeneous cohesive mass 11 comprises a blend of one or more water soluble or swellable hydro-colloids and a natural or synthetic viscous substance which acts as a binder for the hydrocolloids. The hydrocolloids are present at from about 30% to about 70% by weight of the mass. Suitable hydrocolloids include pectin, gelatin, karaya gum, guar gum, locust bean gum, and sodium carboxymethylcellulose provided that at least about 20% by weight of the mass is one or more curative hydrocolloid substances such as pectin, gelatin and karaya gum. Suitable viscous sub-stances include natural rubber, silicone rubber, acryl-onitrile rubber, polyurethane rubber, and polyisobutyl-enes and such binder is also present at from about 30~ to about 70% by weight of the cohesive mass.
Other substances such as a plasticizer, antioxidant, or a pharmaceutically active substance such as an antibacterial agent can be included within the mass at up to about 5% by weight and a cohesive strengthening agent, for example, fibrous cotton, finely divided wood cellulose or microcrystalline cellulose can be included within the mass at up to about 10% by weight. Preferably, the homogeneous cohesive mass 11 comprises about 20% by weight of pectin, about 20% by weight of gelatin, about 20% by weight of sodium carboxymethylcellulose, and about 40% by weight of polyisobutylene.
The backing film 12 as shown in Figure 3 is secured to the surface of the homogeneous cohesive mass 11 which does not contact the wound. The film 12 is a thin sheet of polymeric material such as polyethylene, polypropylene, polyvinylchloride, etc.
As shown in Figure 4, the cohesive mass 11 may have a layer of semi-open cell polymeric foam 13 secured to the surface which does not contact the wound. This foam can be prepared from various elastomer materials such as polyester or polyether polyurethane foams, styrene-butadiene foams, or certain rubbex-based foams. The preferred material is a flexible polyurethane foam having from about 50 to about 100 cells per linear inch.
By semi-open cell it is meant that the percentage of open or ruptured cells is from about 30 to about 70%. An outer polymeric film 14 from a pliable elastomer material such as flexible polyurethane, polyacrylate, polyethylene, etc., may be secured to the foam. Alternatively instead of film 14 the top surface of foam 13 can be sealed by flaming or scorching.
The curative and absorbant homogeneous cohesive mass 11 may be prepared as taught by Ch-en in United States Patents 3,339,546 and 3,972,328 or Chen et al. in United States Patent 4,192,785.
For example, the hydrocolloids and any optional ingredients, preferably in finely divided fvrm, are blended and the mixture is slowly added to the viscous substance in a kneader mixer until a homogeneous mass is formed. The backing film 12 ~1510~1 X~ll or the semi-open cell foam 13 and film 14 may then be secured and the apertures 20 punched there through. Alternatively, the homogeneous mixture of hydrocolloids and binder before setting may be molded to form the apertures 20.
The layer B of curative and absorbant material may also be a foam 15 as shown in Figure 5. This foam can be prepared by hot air drying or lyophilizing a foamed aqueous colloidal dispersion of or more hydrocolloids such as pectin, gelatin, karaya gum, guar gum, locust bean gum, and sodium carboxymethylcellulose provided that at least about 20~ by weight of the hydrocolloid dispersion is one or more curative hydrocolloid substances such as pectin, gelatin and karaya gum. Such foams are described in various patents such as United States Patents 2,465,357, 2,558,395 and 3,767,784. Preferably the foam is prepared from a mixture of gelatin, pectin and sodium carboxymethylcellulose. This preferred foam contains from about 10% to about 50% by weight of pectin and sodium carboxymethylcellulose and from about 20% to about 80% by weight of gelatin and is prepared by dry blending the hydrocolloids, adding the blend to water with agitation so as to form a colloidal dispersion having a solids content of from about 1% to about 20% by weight, foaming the colloidal dispersion so that its volume ~510~1 XFll increases from about 10~ to about 60~, freezing and then freeze drying.
An optional film backing 16 of various polymeric materials such as polyethylene, poly-propylene, polyvinylchloride, etc., can besecured to the surface of foam 15 which does not contact the wound.
The layer of deodorizing material is shown as layer D in Figures 1, 2 and 6. This deodorizing layer is formed of an air-permeable woven or non-woven material carrying or impregnated with a deodorizing substance. One type of suitable material is a sheet of foamed non-woven synthetic - polymeric material, for example, polyurethane, having a large number of activated carbon particles distributed over one of its major surfaces.
Preferably, the carbon particles are bound to the top surface, i.e., that furthest away from layer B, and the surface which contacts layer B is coated with a layer adhesive. Such a material is commercially available under the tradename Bondina. Another type of suitable deodorizing material is a layer of carbon cloth such as that disclosed by Bailey et al. in British Patent 1,301,101.
As shown in Figure 6, an intervening layer C may be included within the dressinq between deodorizing layer D and curative and absorbant layer B. This intervening layer C is an air-permeable but liquid-impermeable material such llSlO~L
XFll _ 7 _ as a non-woven fabric and it serves to prevent any liquid discharge which passes through layer B from escaping further. However, any gaseous discharge from the wound passes through layer C to layer D
where it is deodorized. Layer C can be coated with a microporous pressure sensitive adhesive on one or both sides.
The outer layer of the wound dressing is shown as layer E in Figures 1, 2 and 6. This layer is a flexible breathable adhesive tape which allows air and gas to pass therethrough. This layer compri-ses a porous non-woven fibrous or polymeric backing having a coating of a microporous pressure sensitive adhesive on its bottom surface. Layer E extends in size beyond the periphery of layers B, D and C so that it holds the dressing together. During shipping a piece of silicon release paper is attached across the bottom of layer B and the extending portion of layer E.
Examples of suitable materials for layer E are disclo-sed by Copeland in United States Patent 3,121,021 and Hodgson in United States Patent 3,645,835. It is also possible to replace the adhesive coating ~aught by Copeland with a hydrocolloid containing pressure sensi-tive adhesive such as that taught by Chen in the above noted patents. The layer E allows any gas which has been deodorized by layer D to pass to the atmosphere.
Layer E also secures the dressing to the patient and provides overall protection of the wound.
llS10~
X~l;
The dressing of this invention is employed by placing the proper sized piece over the wound so that layer B contacts the wound. Optionally, the wound can be packed under the dressing with the hydrocolloid containing adhesive mass disclosed by Chen in United States Patent 3,339,546, the hydrocolloid powder disclosed by Steinhardt in United States Patent 3,029,187, karaya gum, or other healing material. This packing is represented as A in Figure 2. The dressing is changed on a periodic bases and.the wound is kept covered until the healing is complete.
Claims (13)
1. A wound dressing comprising a layer of curative and absorbant material which contacts the wound and has a series of apertures therethrough, a layer of air-permeable deodorizing material, and an outer flexible air-permeable layer having an adhesive coating which secures the dressing to the body.
2. The dressing of Claim 1 wherein said layer of curative and absorbant material is a homogeneous mass of from about 30% to about 70% by weight of one or more hydrocolloids selected from the group consisting of pectin, gelatin, karaya gum, guar gum, locust bean gum, and sodium carboxymethylcellulose provided that at least about 20% by weight of said mass is one or more curative hydrocolloids selected from the group consisting of gelatin, pectin and karaya gum and from about 30% to about 70% by weight of a viscous binder selected from the group consisting of natural rubber, silicone rubber, acrylonitrile rubber, polyurethane rubber and polyisobutylenes.
3. The dressing of Claim 2 wherein said homogeneous mass has a thin flexible polymeric film attached to the surface which does not contact the wound and said apertures extend through said homo-geneous mass and said film.
4. The dressing of Claim 2 wherein said homogeneous mass has a layer of semi-open cell polymeric foam secured to the surface which does not contact the wound and said apertures extend through said homogeneous mass and said polymeric foam.
5. The dressing of Claim 4 wherein said semi-open cell foam has a thin polymeric film secured to its top surface and said apertures extend through said homogeneous mass, said polymeric foam, and said film.
6. The dressing of Claim 2 wherein said homo-geneous mass is about 20% by weight of gelatin, about 20% by weight of pectin, about 20% by weight of sodium carboxymethylcellulose, and about 40%
by weight of polyisobutylene.
by weight of polyisobutylene.
7. The dressing of Claim 1 wherein said layer of curative and absorbant material is a foam of one or more hydrocolloids selected from the group consist-ing of pectin, gelatin, karaya gum, locust bean gum, guar gum and sodium carboxymethylcellulose provided that the foam contains at least about 20% by weight of one or more curative hydrocolloids selected from the group consisting of gelatin, pectin and karaya gum.
8. The dressing of Claim 7 wherein said foam contains from about I0% to about 50% by weight of pectin, from about 10% to about 50% by weight of sodium carboxymethylcellulose, and from about 20% to about 80% by weight of gelatin.
9. The dressing of Claim 7 wherein a thin poly-meric film is secured to said foam and said apertures extend through saic foam and film.
10. The dressing of Claim 1 wherein a layer of air-permeable liquid-impermeable non-woven fabric is included within the dressing between said curative and absorbant layer and said layer of deodorizing material.
11. The dressing of Claim 1 wherein said layer of deodorizing material is a foamed non-woven synthetic material having a large number of activated carbon particles distributed over one of its major surfaces.
12. The dressing of Claim 1 wherein said layer of deodorizing material is carbon cloth.
13. The dressing of Claim 1 wherein said outer layer is a porous non-woven fibrous backing having a coating of microporous pressure sensitive adhesive.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7931164 | 1979-09-07 | ||
GB7931164 | 1979-09-07 | ||
GB8012994 | 1980-04-21 | ||
GB8012994 | 1980-04-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1151041A true CA1151041A (en) | 1983-08-02 |
Family
ID=26272799
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000359667A Expired CA1151041A (en) | 1979-09-07 | 1980-09-05 | Wound dressing |
Country Status (8)
Country | Link |
---|---|
US (1) | US4341207A (en) |
EP (1) | EP0026572B1 (en) |
CA (1) | CA1151041A (en) |
DE (1) | DE3065372D1 (en) |
DK (1) | DK155917C (en) |
IE (1) | IE50352B1 (en) |
IL (1) | IL60976A (en) |
NO (1) | NO802603L (en) |
Families Citing this family (100)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4292972A (en) * | 1980-07-09 | 1981-10-06 | E. R. Squibb & Sons, Inc. | Lyophilized hydrocolloio foam |
US4995382A (en) * | 1981-02-13 | 1991-02-26 | Smith And Nephew Associated Companies Limited | Wound dressing, manufacture and use |
US4753231A (en) * | 1981-02-13 | 1988-06-28 | Smith & Nephew Associated Companies P.L.C. | Adhesive wound dressing |
US4499896A (en) * | 1982-03-30 | 1985-02-19 | Minnesota Mining And Manufacturing Co. | Reservoir wound dressing |
NZ203706A (en) * | 1982-04-22 | 1986-03-14 | Squibb & Sons Inc | Occlusive multi-layer wound dressing and hydrocolloidal granules for wound treatment |
DE3464326D1 (en) * | 1983-04-06 | 1987-07-30 | Smith & Nephew Ass | Dressing |
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-
1980
- 1980-08-15 DE DE8080302824T patent/DE3065372D1/en not_active Expired
- 1980-08-15 EP EP80302824A patent/EP0026572B1/en not_active Expired
- 1980-08-25 US US06/180,717 patent/US4341207A/en not_active Expired - Lifetime
- 1980-09-03 NO NO802603A patent/NO802603L/en unknown
- 1980-09-03 IE IE1850/80A patent/IE50352B1/en unknown
- 1980-09-05 CA CA000359667A patent/CA1151041A/en not_active Expired
- 1980-09-05 IL IL60976A patent/IL60976A/en unknown
- 1980-09-05 DK DK379780A patent/DK155917C/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
EP0026572B1 (en) | 1983-10-19 |
DE3065372D1 (en) | 1983-11-24 |
IL60976A0 (en) | 1980-11-30 |
EP0026572A1 (en) | 1981-04-08 |
DK379780A (en) | 1981-03-08 |
IE801850L (en) | 1981-03-07 |
US4341207A (en) | 1982-07-27 |
DK155917B (en) | 1989-06-05 |
IE50352B1 (en) | 1986-04-02 |
DK155917C (en) | 1989-11-13 |
NO802603L (en) | 1981-03-09 |
IL60976A (en) | 1983-09-30 |
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