CA2449436A1 - Compositions and methods for reducing blood and fluid loss from open wounds - Google Patents

Compositions and methods for reducing blood and fluid loss from open wounds Download PDF

Info

Publication number
CA2449436A1
CA2449436A1 CA002449436A CA2449436A CA2449436A1 CA 2449436 A1 CA2449436 A1 CA 2449436A1 CA 002449436 A CA002449436 A CA 002449436A CA 2449436 A CA2449436 A CA 2449436A CA 2449436 A1 CA2449436 A1 CA 2449436A1
Authority
CA
Canada
Prior art keywords
composition
polyacrylic acid
structural formula
kit
group
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
Application number
CA002449436A
Other languages
French (fr)
Other versions
CA2449436C (en
Inventor
Millard Marsden Mershon
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
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
Application filed by Individual filed Critical Individual
Publication of CA2449436A1 publication Critical patent/CA2449436A1/en
Application granted granted Critical
Publication of CA2449436C publication Critical patent/CA2449436C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

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
    • A61L26/00Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0061Use of materials characterised by their function or physical properties
    • A61L26/008Hydrogels or hydrocolloids
    • 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
    • A61L26/00Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0009Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form containing macromolecular materials
    • A61L26/0052Mixtures of macromolecular compounds
    • 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
    • A61L2400/00Materials characterised by their function or physical properties
    • A61L2400/04Materials for stopping bleeding

Abstract

The invention described herein relates to methods for reducing and/or stopping bleeding or fluid loss from open wound, denuded tissue, or burned skin, comprising the step of applying to the open wound, denuded tissue or burned skin a gel-fonning composition comprising at least one of the following compositions: a polyacry1ic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000; a polyacrylic acid and a desiccated water soluble organic or inorganic base; polyacrylic acid and a desiccated poorly soluble basic salt, and a polyvinyl alcohol having the structural formula of [CH2=CHOH]n, where n is between 15,000 and 150,000. When the gel-forming composition is applied to the open wound, denuded tissue, or burned skin, its ions react therein in the presence of water from blood or body fluid therein to form an aqueous gel or mucilage having sufficient viscosity and adhesiveness to cover and adhere to the open wound, denuded tissue, or burned skin so that bleeding or fluid loss is thereby reduced and/or stopped.

Claims (25)

1. A method for reducing bleeding or fluid loss from open wound, denuded tissue, or burned skin, comprising the step of applying to the open wound, denuded tissue or burned skin a gel-forming composition comprising at least one of the compositions selected from the group consisting of (a) a polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, (b) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a dessicated water soluble organic or inorganic base, (c) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a dessicated basic salt and (d) a polyvinyl alcohol having the structural formula of [CH2=CHOH]n, where n is between 10,000 and 70,000, (e) wherein when the gel-forming composition is applied to the open wound, denuded tissue, or burned skin, it reacts with water of blood or body fluid therein to form an aqueous gel or mucilage having sufficient viscosity and adhesiveness to cover and adhere to the open wound, denuded tissue, or burned skin so that bleeding or fluid loss is thereby reduced.
2. The method of claim 1, wherein the polyacrylic acid is a carboxypolymethylene.
3. The method of claim 1, wherein the polyacrylic acid is designated as a NF
or USP Carbopol or Noveon product.
4. The method of claim 1, wherein the polyacrylic acid comprises strands that are cross-linked by divalent ions.
5. The method of claim 1, wherein in composition (b) the polyacrylic acid and the anhydrous water soluble organic or inorganic base are admixed to form a water mucilage or gel with a viscosity that increases with pH in the range between about 4 and about 8.
6. The method of claim 1, wherein in composition (c) the desiccated basic salt is selected from the group consisting of calcium hydroxide, calcium carbonate, calcium sulfate, magnesium hydroxide, and neoprene grade magnesium oxide.
7. The method of claim 1, wherein in composition (c) the desiccated basic salt provide divalent cations that ionically crosslink polymer strands and increase mucilage viscosities to greater degree than monovalent cations.
8. The method of claim 7, wherein the divalent cations are selected from the group consisting of Ca++ and Mg++.
9. The method of claim 1, wherein the composition further comprises (a) at least one calcium salt with a readily metabolized anion, and (b) a desiccated vasoconstrictive drug.
10. The method of claim 9, wherein the calcium salt is soluble and has a metabolizable anion.
11. The method of claim 9, wherein the anhydrous vasoconstrictive drug is L
epinephrine tartrate.
12. The method of claim 1, which comprises the further step of applying. to the open wound, denuded tissue or burned skin therapeutic substances incorporated as anhydrous soluble drugs that become dissolved in water from the tissue and diffuse into the tissues from the mucilage to serve as (a) antimicrobial agents, (b) anti-inflammation agents (c) agents that resist apoptosis, or (d) agents that preserve cellular functions.
12. The method of claim 12, wherein the antimicrobial agents are selected from the group consisting of antibiotics and sulfonamides.
13. The method of claim 12, wherein the anti-inflammation agents, the agents that resist apoptosis, and the agents that preserve cellular functions are selected from the group consisting of antioxidants and nutrients.
14. The method of claim 1, wherein the gelling composition further protects the open wound, denuded tissue or burned skin from loss of body substances selected from the group consisting of water, blood, plasma, serum, proteins, electrolytes and nutrients.
15. The method of claim 1, wherein the gelling composition provides a barrier to protect the open wound, denuded tissue or burned skin from access by and further damage by substances selected from the group consisting of oxygen, dirt, foreign protein antigens, foreign organisms, pathogens and saprophytes.
16. The method of claim 1, wherein the gelling composition provides a protective shield that limits development of fibroblastic tissue and supports epithelialization.
17. The method of claim 1, wherein the gelling composition provides a barrier to protect the open wound, denuded tissue or burned skin from access by and further damage by chemical warfare agents, biological warfare agents, and/or noxious industrial substances.
18. The method of claim 1, wherein the gelling composition further comprises one or more of the substances selected from the group consisting of decontaminating reagents, detoxifiers, camouflage pigment, pH indicators, agents capable of detecting the presence of toxic or infectious agents.
19. The method of claim 1, which comprises the further step of applying pressure to the site.
20. The method of claim 1, wherein the composition is present on or in a woven or non-woven fabric.
21. The method of claim 1, which comprises the further step of adding water to the outside surface of the gelling composition during gelling or after gelling occurs.
22. The method of claim 1, wherein the composition is in the form of an anhydrous powder.
23. The method of claim 1, wherein the composition is suspended in a desiccated hydrophilic liquid.
The method of claim 1, wherein the polyvinyl alcohol is Vinol 205.
24. The method of claim 1, wherein the gelling composition comprises (a) a polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, (b) a non-corrosive alkaline salt capable of neutralizing acidic sites of the polyacrylic acid, and (c) an anhydrous hydrophilic liquid, in which the polyacrylic acid and the alkaline salt are suspended and which permits the polyacrylic acid to form a gel in the presence of water, and (d) optionally, one or more of an antibiotic, blot-clotting enzymes, decontaminating reagents, detoxifiers, camouflage pigment, pH indicators, vasoconstrictive agents, agents capable of detecting the presence of toxic or infectious compounds, starch, sodium borate, calcium hydroxide, calcium gluconate, magnesium oxide and borax.
25. The method of claim 25, wherein the anhydrous hydrophilic liquid is selected from the group consisting of polyoxyalkylene glycol and nitrile silicone fluid.
27. A method for reducing skin exposure and penetration by chemical agents selected from the group consisting of o-chlorobenzalmalononitrile, sesquimustard, CN, VX, CS-2, and EA3580, comprising the step of coating skin with a composition comprising (a) at least one of the compositions selected from the group consisting of (i) a polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, (ii) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a desiccated water soluble organic or inorganic base, (iii) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a desiccated basic salt, and (iv) a polyvinyl alcohol having the structural formula of [CH2=CHOH]n, where n is between 15,000 and 150,000, (b) at least one compound capable of resisting penetration of chemical warfare agents selected from the group consisting of o-chlorobenzalmalononitrile, sesquimustard, CN, VX, CS-2 and EA3580, and (j) optionally, one or more of an antibiotic, blot-clotting enzymes, decontaminating reagents, detoxifiers, camouflage pigment, pH indicators, vasoconstrictive agents, agents capable of detecting the presence of toxic or infectious compounds, starch, sodium borate, calcium hydroxide, calcium gluconate, magnesium oxide, and borax..
28. The method of claim 27, wherein when the composition comprises one of (i), (ii) or (iii), the composition further includes an anhydrous hydrophilic media, in which the polyacrylic acid and the alkaline salt are suspended and which permits the polyacrylic acid to form a gel in the presence of water.
29. The method of claim 27, wherein the polyacrylic acid is a carboxypolymethylene.
30. The method of claim 27, wherein the polyacrylic acid is a Carbopol.
31. The method of claim 27, wherein the polyacrylic acid comprises strands that are cross-linked.
32. The method of claim 27, wherein in composition (ii) the polyacrylic acid and the anhydrous water soluble organic or inorganic base are admixed to form a water mucilage or gel with a viscosity that increases with pH in the range between about 4 and about 8.
33. The method of claim 27, wherein in composition (iii) the desiccated basic salt is selected from the group consisting of calcium hydroxide, calcium carbonate, calcium sulfate, magnesium hydroxide, and neoprene grade magnesium oxide.
34. The method of claim 27, wherein in composition (iii) the desiccated basic salt provides divalent cations that ionically crosslink polymer strands and increases mucilage viscosity to greater degree than monovalent cations.
34. .The method of claim 33, wherein the divalent cations are selected from the group consisting of Ca++ and Mg++.

35. A skin and soft tissue adhesive composition comprising at least one of the gel-forming compositions selected from the group consisting of (a) a polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, (b) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a desiccated water soluble organic or inorganic base, (c) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a dessicated poorly soluble basic salt, and (d) a polyvinyl alcohol having the structural formula of [CH2=CHOH]n, where n is between 15,000 and 150,000, and (e) optionally, one or more of an antibiotic, blot-clotting enzymes, decontaminating reagents, detoxifiers, camouflage pigment, pH indicators, vasoconstrictive agents, agents capable of detecting the presence of toxic or infectious compounds, starch, sodium borate, calcium hydroxide, calcium gluconate, magnesium oxide, and borax, wherein when the composition contacts water or a polar solvent the at least one gel-forming compositions react with the water or polar solvent to form an adhesive gel that adheres to skin and soft tissue.
36. The adhesive composition of claim 35, wherein the polyacrylic acid is a carboxypolymethylene.
37. The adhesive composition of claim 35, wherein the polyacrylic acid is a Carbopol.
38. The adhesive composition of claim 35, wherein the polyacrylic acid comprises strands that are cross-linked.

39. The adhesive composition of claim 35, wherein in composition (b) the polyacrylic acid and the anhydrous water soluble organic or inorganic base are admixed to form a water mucilage or gel with a viscosity that increases with pH
in the range between about 4 and about 8.
40. The adhesive composition of claim 35, wherein in composition (c) the anhydrous basic salt is selected from the group consisting of calcium hydroxide, calcium carbonate, calcium sulfate, magnesium hydroxide, and neoprene grade magnesium oxide.
41. The adhesive composition of claim 35, wherein in composition (c) the desiccated basic salt provides divalent cations that ionically cross-link polymer strands and increase mucilage viscosities to greater degree than monovalent cations.
42. The adhesive composition of claim 41, wherein the divalent cations are selected from the group consisting of Ca++ and Mg++.
43. A method for forming an artificial scab on an open wound, denuded tissue, or burned skin, comprising the step of applying to the open wound, denuded tissue or burned skin a gel-forming composition comprising at least one of the compositions selected from the group consisting of (a) a polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, (b) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a dessicated water soluble organic or inorganic base, (c) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a dessicated basic salt, and (d) a polyvinyl alcohol having the structural formula of [CH2=CHOH]n, where n is between 10,000 and 70,000, wherein when the gel-forming composition is applied to the open wound, denuded tissue, or burned skin, it reacts with water of blood or body fluid therein to form an aqueous gel or mucilage having sufficient viscosity and adhesiveness to cover and adhere to the open wound, denuded tissue, or burned skin so that bleeding or fluid loss is thereby reduced, and an artificial scab is thereby formed.
44. A kit for reducing blood or fluid loss from open wounds, denuded tissue or burned skin in a mammal, comprising, packaged in association, (i) a gel-forming composition comprising at least one of the compositions selected from the group consisting of (a) a polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, (b) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a desiccated water soluble organic or inorganic base, (c) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a desiccated poorly soluble basic salt, and (d) a polyvinyl alcohol having the structural formula of [CH2=CHOH]n, where n is between 15,000 and 150,000, (ii) optionally, one or more of an antibiotic, blot-clotting enzymes, decontaminating reagents, detoxifiers, camouflage pigment, pH indicators, vasoconstrictive agents, agents capable of detecting the presence of toxic or infectious compounds, starch, sodium borate, calcium hydroxide, calcium gluconate, magnesium oxide, and borax, wherein upon application of the composition to the site of the open wounds, denuded tissue or burned skin, component (i) reacts with water present in blood or other bodily fluid exposed in the site to form a gel that adheres to the site and reduces loss of blood or bodily fluid, and (ii) a dispenser for applying the composition to open wounds, denuded tissue or burned skin.
45. The kit of claim 44, wherein the dispenser is a non-woven fabric, a woven fabric, a tube, a bandage impregnated with the composition, or a container having at least one opening through which the composition may be dispensed.
46. The kit of claim 44, wherein the polyacrylic acid is a carboxypolymethylene.
47. The kit of claim 44, wherein the polyacrylic acid is a Carbopol.
48. The kit of claim 44, wherein the polyacrylic acid comprises strands that are cross-linked.
49. The kit of claim 44, wherein in composition (b) the polyacrylic acid and the desiccated water soluble organic or inorganic base are admixed to form a water mucilage or gel with a viscosity that increases with pH in the range between about 4 and about 8.
50. The kit of claim 44, wherein in composition (c) the anhydrous basic salt is selected from the group consisting of calcium hydroxide, calcium carbonate, calcium sulfate, magnesium hydroxide, and neoprene grade magnesium oxide.
51. The kit of claim 44, wherein in composition (c) the anhydrous basic salt provide divalent cations that ionically crosslink polymer strands and increase mucilage viscosities to greater degree than monovalent cations.
52. The kit of claim 51, wherein the divalent cations are selected from the group consisting of Ca++ and Mg++.

53. A kit for reducing skin exposure and penetration by chemical agents selected from the group consisting of o-chlorobenzalmalononitrile, sesquimustard, CN, VX, CS-2, and EA3580, comprising, packaged in association, (i) a gel-forming composition comprising at least one of the compositions selected from the group consisting of (a) a polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, (b) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a desiccated water soluble organic or inorganic base, (c) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a desiccated poorly soluble basic salt, (d) a polyvinyl alcohol having the structural formula of [CH2=CHOH]n, where n is between 15,000 and 150,000, at least one compound capable of resisting penetration of o-chlorobenzalmalononitrile, sesquimustard, CN, VX, CS-2 and EA3580, and (e) optionally, one or more of an antibiotic, blot-clotting enzymes, decontaminating reagents, detoxifiers, camouflage pigment, pH
indicators, vasoconstrictive agents, agents capable of detecting the presence of toxic or infectious compounds, starch, sodium borate, calcium hydroxide, calcium gluconate, magnesium oxide, and borax;
and (ii) a dispenser for applying the composition to skin.
54. The kit of claim 53, wherein the dispenser is a non-woven fabric, a woven fabric, a tube, a bandage impregnated with the composition, or a container having an opening through which the composition may be dispensed.
55. The kit of claim 53, wherein the polyacrylic acid is a carboxypolymethylene.

56. The kit of claim 53, wherein the polyacrylic acid is a Carbopol.
57. The kit of claim 53, wherein the polyacrylic acid comprises strands that are cross-linked.
58. The kit of claim 53, wherein in composition (b) the polyacrylic acid and the anhydrous water soluble organic, or inorganic base are admixed to form a water mucilage or gel with a viscosity that increases with pH in the range between about 4 and about 8.
59. The kit of claim 53, wherein in composition (c) the desiccated basic salt is selected from the group consisting of calcium hydroxide, calcium carbonate, calcium sulfate, magnesium hydroxide, and neoprene grade magnesium oxide.
60. The kit of claim 53, wherein in composition (c) the desiccated basic salt provide divalent cations that ionically crosslink polymer strands and increase mucilage viscosities to greater degree than monovalent cations.
61. The kit of claim 60, wherein the divalent cations are selected from the group consisting of Ca++ and Mg++.
62. A kit for forming an artificial scab on open wounds, denuded tissue or burned skin in a mammal, comprising, packaged in association, (i) a gel-forming composition comprising at least one of the compositions selected from the group consisting of (e) a polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, (f) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a desiccated water soluble organic or inorganic base, (g) a composition comprising polyacrylic acid having the structural formula [CH2=CHCO2H]n, where n is between 10,000 and 70,000, and a desiccated poorly soluble basic salt, and (h) a polyvinyl alcohol having the structural formula of [CH2=CHOH]n, where n is between 15,000 and 150,000, (ii) optionally, one or more of an antibiotic, blot-clotting enzymes, decontaminating reagents, detoxifiers, camouflage pigment, pH indicators, vasoconstrictive agents, agents capable of detecting the presence of toxic or infectious compounds, starch, sodium borate, calcium hydroxide, calcium gluconate, magnesium oxide, and borax, wherein upon application of the composition to the site of the open wounds, denuded tissue or burned skin, component (i) reacts with water present in blood or other bodily fluid exposed in the site to form a gel that adheres to the site and reduces loss of blood or bodily fluid, and forms an artificial scab, and (ii) a dispenser for applying the composition to open wounds, denuded tissue or burned skin.
63. The kit of claim 62, wherein the dispenser is a non-woven fabric, a woven fabric, a tube, a bandage impregnated with the composition, or a container having at least one opening through which the composition may be dispensed.
64. The kit of claim 62, wherein the polyacrylic acid is a carboxypolymethylene.
65. The kit of claim 62, wherein the polyacrylic acid is a Carbopol.
66. The kit of claim 62, wherein the polyacrylic acid comprises strands that are cross-linked.
67. The kit of claim 62, wherein in composition (b) the polyacrylic acid and the desiccated water soluble organic or inorganic base are admixed to form a water mucilage or gel with a viscosity that increases with pH in the range between about 4 and about 8.
68. The kit of claim 62, wherein in composition (c) the anhydrous basic salt is selected from the group consisting of calcium hydroxide, calcium carbonate, calcium sulfate, magnesium hydroxide, and neoprene grade magnesium oxide.
69. The kit of claim 62, wherein in composition (c) the anhydrous basic salt provide divalent cations that ionically crosslink polymer strands and increase mucilage viscosities to greater degree than monovalent cations.
70. The kit of claim 69, wherein the divalent cations are selected from the group consisting of Ca++ and Mg++.
CA2449436A 2001-06-22 2002-06-20 Compositions and methods for reducing blood and fluid loss from open wounds Expired - Fee Related CA2449436C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US30038401P 2001-06-22 2001-06-22
US60/300,384 2001-06-22
PCT/US2002/019554 WO2003000155A2 (en) 2001-06-22 2002-06-20 Compositions and methods for reducing blood and fluid loss from open wounds

Publications (2)

Publication Number Publication Date
CA2449436A1 true CA2449436A1 (en) 2003-01-03
CA2449436C CA2449436C (en) 2012-05-01

Family

ID=23158880

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2449436A Expired - Fee Related CA2449436C (en) 2001-06-22 2002-06-20 Compositions and methods for reducing blood and fluid loss from open wounds

Country Status (6)

Country Link
US (1) US7303759B2 (en)
EP (1) EP1408902A4 (en)
AU (1) AU2002350088A1 (en)
CA (1) CA2449436C (en)
IL (2) IL159156A0 (en)
WO (1) WO2003000155A2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015089626A1 (en) * 2013-12-16 2015-06-25 The University Of British Columbia Self-fueled particles for propulsion through flowing aqueous fluids

Families Citing this family (66)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10204819A1 (en) * 2002-01-31 2003-08-14 Aesculap Ag & Co Kg Hemostatic agents and their provision for medicine
US20060216267A1 (en) * 2002-08-20 2006-09-28 Kovacs Stephen G Hydrophobic elastomeric polymer chemistry device for inhibiting the growth of onychomycosis and urushiol-induced allergic contact dermatitis
US7074425B2 (en) * 2002-09-26 2006-07-11 Bonewax, Llc Hemostatic compositions and methods
ITMI20030414A1 (en) * 2003-03-06 2004-09-07 Biofarm S R L Ora Biofarmitalia S P A BUFFER WITH GEL LAYER WITH COSMETIC OR THERAPEUTIC ACTIVITY.
US7955616B2 (en) * 2003-09-23 2011-06-07 Orthocon, Inc. Absorbable implants and methods for their use in hemostasis and in the treatment of osseous defects
EP2462957B1 (en) * 2003-09-23 2019-04-24 Abyrx, Inc. Absorbable implants and methods for their use in hemostasis and in the treatment of osseous defects
CN1856283A (en) * 2003-09-23 2006-11-01 奥斯治疗有限公司 Bioabsorbable putty-like hemostatic implants
US7455248B2 (en) * 2004-03-17 2008-11-25 Genzyme Corporation Powder delivery device
US20060178609A1 (en) 2005-02-09 2006-08-10 Z-Medica, Llc Devices and methods for the delivery of molecular sieve materials for the formation of blood clots
JP2008531498A (en) 2005-02-15 2008-08-14 バージニア コモンウェルス ユニバーシティ Mineral technology (MT) for emergency hemostasis and treatment of acute wounds and chronic ulcers
CN101267831B (en) 2005-04-25 2013-04-24 麻省理工学院 Compositions and methods for promoting hemostasis and other physiological activities
US20070129630A1 (en) * 2005-12-07 2007-06-07 Shimko Daniel A Imaging method, device and system
US20070135706A1 (en) * 2005-12-13 2007-06-14 Shimko Daniel A Debridement method, device and kit
WO2008018892A2 (en) * 2005-12-22 2008-02-14 Pluromed, Inc. Methods and kits for treating lacerations and puncture wounds using inverse thermosensitive polymers
CN101472620A (en) * 2006-04-25 2009-07-01 麻省理工学院 Compositions and methods for affecting movement of contaminants, bodily fluids or other entities, and/or affecting other physiological conditions
US8938898B2 (en) 2006-04-27 2015-01-27 Z-Medica, Llc Devices for the identification of medical products
US7968114B2 (en) 2006-05-26 2011-06-28 Z-Medica Corporation Clay-based hemostatic agents and devices for the delivery thereof
US7604819B2 (en) 2006-05-26 2009-10-20 Z-Medica Corporation Clay-based hemostatic agents and devices for the delivery thereof
US8202532B2 (en) 2006-05-26 2012-06-19 Z-Medica Corporation Clay-based hemostatic agents and devices for the delivery thereof
US20080014251A1 (en) * 2006-07-14 2008-01-17 Advanced Vascular Dynamics Hemostatic compound and its use
US7622533B2 (en) * 2006-08-04 2009-11-24 Nerites Corporation Biomimetic compounds and synthetic methods therefor
WO2008127287A2 (en) * 2006-10-11 2008-10-23 Biolife, L.L.C. Materials and methods for wound treatment
GB2447012B (en) * 2007-02-21 2011-03-16 Pharmacure Health Care Ab Composition for combating epistaxis
US7823761B2 (en) * 2007-05-16 2010-11-02 The Invention Science Fund I, Llc Maneuverable surgical stapler
US7832611B2 (en) * 2007-05-16 2010-11-16 The Invention Science Fund I, Llc Steerable surgical stapler
US20080287987A1 (en) * 2007-05-16 2008-11-20 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Dispensing system for tissue sealants
US7922064B2 (en) * 2007-05-16 2011-04-12 The Invention Science Fund, I, LLC Surgical fastening device with cutter
US7810691B2 (en) * 2007-05-16 2010-10-12 The Invention Science Fund I, Llc Gentle touch surgical stapler
US7798385B2 (en) 2007-05-16 2010-09-21 The Invention Science Fund I, Llc Surgical stapling instrument with chemical sealant
US8485411B2 (en) * 2007-05-16 2013-07-16 The Invention Science Fund I, Llc Gentle touch surgical stapler
US8771725B2 (en) * 2007-10-12 2014-07-08 Chesson Laboratory Associates, Inc. Poly(urea-urethane) compositions useful as topical medicaments and methods of using the same
US20090112243A1 (en) * 2007-10-25 2009-04-30 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Surgical cutter with dispensing system for tissue sealants
US20090112256A1 (en) * 2007-10-30 2009-04-30 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Suturing device with tissue sealant dispenser
US20110054375A1 (en) * 2007-11-27 2011-03-03 Hans Smola Dressing comprising polyacrylate particles and use thereof
US20090143816A1 (en) * 2007-11-30 2009-06-04 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Grasper with surgical sealant dispenser
GB2460815A (en) * 2008-04-04 2009-12-16 Kays Medical A sterilisable gel formulation comprising calcium gluconate
US20090275904A1 (en) * 2008-05-02 2009-11-05 Sardesai Neil Rajendra Sheet assemblies with releasable medicaments
US8999297B2 (en) * 2008-07-11 2015-04-07 Inter-Med, Inc. Hemostatic agent
WO2010068509A1 (en) * 2008-11-25 2010-06-17 Biolife, L.L.C. Hemostatic wound dressings
WO2010102283A2 (en) * 2009-03-06 2010-09-10 Jack Mentkow Hemostatic agent composition, delivery system and method
US20100226873A1 (en) * 2009-03-06 2010-09-09 Biolife, L.L.C. Hemostatic Composition with Magnetite
US8110208B1 (en) 2009-03-30 2012-02-07 Biolife, L.L.C. Hemostatic compositions for arresting blood flow from an open wound or surgical site
US9439941B2 (en) 2009-12-14 2016-09-13 The University Of Hong Kong Nano cancer barrier device (NCBD) to immobilize and inhibit the division of metastic cancer stem cells
US8409628B2 (en) 2010-02-04 2013-04-02 Penguin IP Holdings, Inc. Methods and compositions for oxygenation of skin to treat skin disorders
US20110200683A1 (en) * 2010-02-16 2011-08-18 Piper Medical, Inc Hydrogen peroxide solution producing first aid substance, packaging, and treatment
US8900601B2 (en) 2010-03-31 2014-12-02 Jennifer Bartels Permeable mixtures, methods and compositions for the skin
US9119605B2 (en) 2010-05-06 2015-09-01 Zimmer, Inc. Synthetic polymer adhesives and methods for making, using and delivering the same
US8858969B2 (en) 2010-09-22 2014-10-14 Z-Medica, Llc Hemostatic compositions, devices, and methods
EP2637707A4 (en) 2010-11-09 2014-10-01 Kensey Nash Corp Adhesive compounds and methods use for hernia repair
GB201104175D0 (en) * 2011-03-11 2011-04-27 Medtrade Products Ltd Haemostatic material
PL395069A1 (en) * 2011-05-31 2012-12-03 Warszawski Uniwersytet Medyczny An analgesic pharmaceutical composition for oral administration
US10022083B2 (en) 2011-06-02 2018-07-17 Abdulmohsen E. A. H. Al-Terki Multiple oral and nasal surgical procedures method and kit
US8387798B1 (en) 2012-04-27 2013-03-05 Abdulmohsen E. A. H. Al-Terki Mutiple oral and nasal surgical procedures method and kit
US20130202675A1 (en) 2012-02-03 2013-08-08 Dynasil Biomedical Corporation Systems and methods for the fabrication of tissue patches
US9220646B2 (en) * 2012-03-30 2015-12-29 Kimberly-Clark Worldwide, Inc. Absorbent articles with improved stain decolorization
KR101945031B1 (en) 2012-06-22 2019-02-01 지-메디카 엘엘씨 Hemostatic devices
EP2968651B1 (en) * 2013-03-15 2020-10-21 Cook Medical Technologies LLC Adhesive medical products and methods for treating gastrointestinal lesions
US11931227B2 (en) * 2013-03-15 2024-03-19 Cook Medical Technologies Llc Bimodal treatment methods and compositions for gastrointestinal lesions with active bleeding
US9540548B1 (en) 2015-08-07 2017-01-10 Xcede Technologies, Inc. Adhesive compositions and related methods
AU2016307447A1 (en) 2015-08-07 2018-02-22 Xcede Technologies, Inc. Adhesive compositions and related methods
US9833538B2 (en) 2015-08-07 2017-12-05 Xcede Technologies, Inc. Adhesive compositions and related methods
IL247786B (en) 2016-09-12 2019-08-29 Plotkin Alexander Wound covering with haemostatic action and the method of its creation
KR102387327B1 (en) * 2017-04-28 2022-04-15 쿡 메디컬 테크놀러지스 엘엘씨 Bimodal treatment method and composition for gastrointestinal lesions with vigorous bleeding
US11452798B2 (en) 2017-09-27 2022-09-27 Cook Medical Technologies Llc Crosslinking submucosal injectate system
US20210106717A1 (en) * 2019-10-10 2021-04-15 Cook Medical Technologies Llc Bonded powders for the treatment of bodily lesions
US20230330297A1 (en) * 2022-04-15 2023-10-19 Waldir Teixeira Renó Homeostatic single layer dressing

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1249458B (en) * 1960-10-14 1967-09-07 Mmisterul Industnei Petrolului si Chimiei Bukarest Film-forming skin protection agent
US4215106A (en) * 1978-04-07 1980-07-29 Annenkova Valentina M Local hemostatic
DE3224382A1 (en) * 1982-06-30 1984-01-12 Beiersdorf Ag, 2000 Hamburg HYDROGEL-BASED FABRIC MATERIAL AND METHOD FOR THE PRODUCTION THEREOF
US4732755A (en) * 1983-01-17 1988-03-22 University Of Health Sciences/The Chicago Medical School Skin burn treatment
US4822349A (en) 1984-04-25 1989-04-18 Hursey Francis X Method of treating wounds
JPS6270318A (en) * 1985-09-25 1987-03-31 Nippon Kayaku Co Ltd Hemostatic and wound-protecting agent
JPS63220876A (en) * 1987-03-10 1988-09-14 日本曹達株式会社 Wound protecting agent
US5457093A (en) * 1987-09-18 1995-10-10 Ethicon, Inc. Gel formulations containing growth factors
US4920158A (en) * 1989-10-11 1990-04-24 Medipro Sciences Limited Hydrogel-forming wound dressing or skin coating material
CA2073254A1 (en) * 1990-11-09 1992-05-10 Mitsuji Akazawa Procaterol-containing preparation for application to the skin
US5260066A (en) * 1992-01-16 1993-11-09 Srchem Incorporated Cryogel bandage containing therapeutic agent
US5459177A (en) * 1993-03-09 1995-10-17 Sun Medical Co., Ltd. Adhesive for soft tissue and kit thereof
US5858350A (en) 1993-12-01 1999-01-12 Marine Polymer Technologies Methods and compositions for poly-β-1→4-N-acetylglucosamine cell therapy system
US5578661A (en) * 1994-03-31 1996-11-26 Nepera, Inc. Gel forming system for use as wound dressings
US6133326A (en) 1994-08-31 2000-10-17 Pfizer Inc Compositions and methods for decreasing sebum production
US5891074A (en) * 1996-08-22 1999-04-06 Avitar, Inc. Pressure wound dressing
US6706690B2 (en) * 1999-06-10 2004-03-16 Baxter Healthcare Corporation Hemoactive compositions and methods for their manufacture and use
CA2244017A1 (en) 1998-07-28 2000-01-28 Stephane Tetreault Moisture-curable adhesive suture strip
US6211296B1 (en) * 1998-11-05 2001-04-03 The B. F. Goodrich Company Hydrogels containing substances
US6060461A (en) 1999-02-08 2000-05-09 Drake; James Franklin Topically applied clotting material
US6531500B2 (en) * 1999-07-23 2003-03-11 Alwyn Company, Inc. Methods for treatment of inflammatory diseases
IL133473A0 (en) * 1999-12-12 2001-04-30 Avenir R & B Medical Technolog Bactericidal haemostatic preparations for local use and the methods of their production and conservation
US6187347B1 (en) 2000-02-09 2001-02-13 Ecosafe, Llc. Composition for arresting the flow of blood and method
US6399092B1 (en) * 2000-12-27 2002-06-04 Healthpoint, Ltd. Anhydrous, hydrophilic absorbent wound dressing (tube) with antimicrobials or other pharmaceutically active agents

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015089626A1 (en) * 2013-12-16 2015-06-25 The University Of British Columbia Self-fueled particles for propulsion through flowing aqueous fluids
US10238598B2 (en) 2013-12-16 2019-03-26 The University Of British Columbia Self-fueled particles for propulsion through flowing aqueous fluids
US11266596B2 (en) 2013-12-16 2022-03-08 The University Of British Columbia Self-fueled particles for propulsion through flowing aqueous fluids

Also Published As

Publication number Publication date
IL159156A (en) 2010-11-30
CA2449436C (en) 2012-05-01
EP1408902A4 (en) 2008-02-13
WO2003000155A3 (en) 2003-07-03
EP1408902A2 (en) 2004-04-21
WO2003000155A2 (en) 2003-01-03
IL159156A0 (en) 2004-06-01
US20030008011A1 (en) 2003-01-09
AU2002350088A1 (en) 2003-01-08
US7303759B2 (en) 2007-12-04

Similar Documents

Publication Publication Date Title
CA2449436A1 (en) Compositions and methods for reducing blood and fluid loss from open wounds
KR100909233B1 (en) Wound coating preparations
US11937922B2 (en) pH-triggered diagnostic wound dressing
US11931477B2 (en) PH-triggered therapeutical wound dressing
EP1345636B1 (en) Anhydrous, hydrophilic absorbent wound dressing
DE69910210T2 (en) IMPLANTABLE MEDICAL DEVICE WITH ANTI-INFECTIOUS AND CONCEPTUAL PROPERTIES
KR101506933B1 (en) Improvements relating to skin dressings
DE3787573D1 (en) BIOADHAESIVE, EXTRUDED FILM FOR INTRA-ORAL ACTIVE SUBSTANCE DELIVERY AND METHOD.
WO2001001994A1 (en) Water resistant film-forming antimicrobial skin-preparation
CA2130015A1 (en) Preparation of a skin surface for a surgical procedure
AU2005304389A1 (en) Systems and methods for treating warts
JP2011500123A (en) System for providing a method for applying a skin sealant containing a phase change visual indication component
US7867510B2 (en) Material having antimicrobial activity when wet
CA2811045C (en) Hydrogel sheet for wound bed preparation
KR20080018360A (en) A wound-healing dressing patch with hydrogel layer containing chitosan
US7745686B2 (en) Catamenial device
WO2004112851A1 (en) Hydrogel compositions comprising enzymes
US20040151688A1 (en) Adhesive treatment for epistaxis
JP2007513693A (en) Methods and compositions for the treatment of skin wounds
US20090320856A1 (en) Sealant Applicator and Method
US20040142020A1 (en) Anhydrous, hydrophilic absorbent wound dressing
US20110104303A1 (en) Material having antimicrobial activity when wet
US20080248135A1 (en) Combination Therapy for Otitis with Antiseptic and pH Adjustment
AU1635200A (en) Silver-based pharmaceutical compositions
WO2005072665A1 (en) Cooling composition

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed

Effective date: 20150622