IP Library Granted Patent US 7,320,962
Granted Patent B2
US 7,320,962 · App. 10/761,922 · Granted Jan 22, 2008

Hemoactive compositions and methods for their manufacture and use

Assignees: Baxter International Inc.; Baxter Healthcare S.A.
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Quick Facts
Patent No.
US 7,320,962
App. No.
10/761,922
Granted
Jan 22, 2008
Kind
B2
Abstract

Dried hemoactive materials comprise both a cross-linked biologically compatible polymer and a non-cross-linked biologically compatible polymer. The cross-linked polymer is selected to form a hydrogel when exposed to blood. The non-cross-linked polymer is chosen to solubilize relatively rapidly when exposed to blood. The non-cross-linked polymer serves as a binder for holding the materials in desired geometries, such as sheets, pellets, plugs, or the like. Usually, the cross-linked polymer will be present in a particulate or fragmented form. The materials are particularly suitable for hemostasis and drug delivery.

Claims (41)

1. A dried hemoactive material for inhibiting bleeding or delivering an agent, comprising:

a cross-linked biologically compatible polymer which forms a hydrogel when exposed to blood; and

a non-cross-linked biologically compatible polymer which solubilizes when exposed to blood:

wherein the cross-linked polymer is dispersed in a dried matrix of the non-cross-linked polymer.

2. A material as in claim 1 , wherein the cross-linked polymer is a protein selected from the group consisting of gelatin, collagen, albumin, hemoglobin, fibrinogen, fibrin, fibronectin, elastin, keratin, laminin, and casein.

3. A material as in claim 1 , wherein the cross-linked polymer is a carbohydrate or carbohydrate derivative selected from the group consisting of glycosaminglycans, starches, celluloses, hemicelluloses, xylan, agarose, alginate, and chitosan.

4. A material as in claim 1 , wherein the cross-linked polymer is a non-biologic hydrogel-forming polymer or copolymer selected from the group consisting of polyacrylates, polymethacrylates, polyacrylamides, polyvinyl polymers, polylactides-glycolides, polycaprolactones, polyoxyethelenes, and copolymers thereof.

5. A material as in claim 1 , wherein the non-cross-linked biologically compatible polymer is a protein selected from the group consisting of gelatin, collagen, albumin, elastin, and keratin.

6. A material as in claim 1 , wherein the non-cross-linked biologically compatible polymer is a carbohydrate or carbohydrate derivative selected from the group consisting of glycosaminoglycans, alginate, starch, cellulose, and derivatives thereof.

7. A dried hemoactive material for inhibiting bleeding or delivering an agent, comprising:

a non-cross-linked polymer comprising a dry gelatin matrix; and

dry, cross-linked gelatin polymer particles dispersed in the dry non-cross-linked gelatin matrix.

8. A material as in claim 1 or 7 , wherein the cross-linked polymer has a degradation time of at least one day.

9. A material as in claim 1 or 7 , wherein the non-cross-linked polymer solubilizes in 15 minutes or less when exposed to blood.

10. A material as in claim 1 or 7 , wherein the cross-linked polymer is fragmented so that, upon hydration in blood, the polymer will form a gel with a sub-unit size in the range from 0.01 mm to 5 mm.

11. A material as in claim 10 , wherein the cross-linked polymer has an equilibrium swell in the range from 400% to 5,000%.

12. A material as in claim 1 or 7 , in the form of a sheet having a thickness in the range from 1 mm to 75 mm.

13. A material as in claim 12 , wherein the sheet is packed in a sterile pack.

14. A kit comprising:

a sterile pack; a sterile sheet of material as in claim 12 , packaged in the sterile pack; and

instructions for use setting forth a method for inhibiting bleeding by placing the sterilized sheet of material over bleeding tissue.

15. A material as in claim 1 or 7 , wherein the cross-linked polymer is present at from 50 weight % to 95 weight % of the material and the non-cross-linked material is present at from 50 weight % to 1 weight % of the material.

16. A material as in claim 15 , further comprising a plasticizer present at from 1 weight % to 20 weight % of the material.

17. A material as in claim 16 , wherein the plasticizer is present in at least the non-cross-linked polymer.

18. A material as in claim 17 , wherein the plasticizer is selected from the group consisting of polyethylene glycol, sorbitol, and glycerol.

19. A material as in claim 1 or 7 , further comprising an active agent.

20. A material as in claim 19 , wherein the active agent is present in at least the non-cross-linked polymer.

21. A material as in claim 19 , wherein the active agent is present in at least the cross-linked polymer.

22. A material as in claim 19 , wherein the active agent is present in both the non-cross-linked polymer and the cross-linked polymer.

23. A material as in claim 19 , wherein the active agent is selected from the group consisting of antibiotics, anti-neoplastic agents, bacteriostatic agents, bactericidal agents, antiviral agents, anesthetics, anti-inflammatory agents, hormones, anti-angiogenic agents, antibodies, enzymes, enzyme inhibitors, and neurotransmitters.

24. A method for delivering an active agent to a patient, said method comprising:

applying the material of claim 19 to or near a target region of the patient.

25. A material as in claim 19 , wherein the active agent is a hemostatic substance.

26. A method for inhibiting bleeding, said method comprising:

applying the material of claim 25 to a wound site.

27. A material as in claim 25 , wherein the hemostatic substance is a clotting factor.

28. A material as in claim 27 , wherein the clotting factor is thrombin.

29. A method for making a hemoactive material, said method comprising:

dissolving in an aqueous medium a non-cross-linked biologically compatible polymer which solubilizes when exposed to blood;

suspending in said aqueous medium containing the non-cross-linked polymer a cross-linked biologically compatible polymer which forms a hydrogel when exposed to blood; and

drying the resulting aqueous medium containing both polymers to form a solid phase comprising the cross-linked polymer in dry form dispersed in a dry matrix of the non-cross-linked polymer.

Assignments (3)
MERGER Recorded May 13, 2010
From: FUSION MEDICAL TECHNOLOGIES, INC.
To: BAXTER HEALTHCARE CORPORATION
Reel/Frame 024381/0522 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2010
From: BAXTER HEALTHCARE CORPORATION
To: BAXTER INTERNATIONAL INC.; BAXTER HEALTHCARE S.A.
Reel/Frame 024383/0257 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2004
From: REICH, CARY J.; OSAWA, A. EDWARD; TRAN, HELEN
To: BAXTER INTERNATIONAL INC.; BSXTER HEALTHCARE S.A.
Reel/Frame 014778/0816 →
Continuity (7)
Continuation In Part 0955396900 · Apr 21, 2000
Continuation In Part 0933031500 · Jun 10, 1999
Continuation 0903237000 · Feb 27, 1998
Continuation In Part 0890367400 · Jul 31, 1997
Continuation In Part 0870485200 · Aug 27, 1996
Provisional Application 6005043700 · Jun 18, 1997
Related Publication 20040214770A1 · Oct 28, 2004