Biocompatible surgical implant

• US 5,630,842 A
• Filed: 01/26/1994
• Issued: 05/20/1997
• Est. Priority Date: 07/27/1992
• Status: Expired due to Term

• Current Assignee: Angiotech Pharmaceuticals Incorporated
• Original Assignee: Haemacure Biotech, Inc.
• Inventors: Brodniewicz, Teresa
• Primary Examiner(s): MERRIAM, ANDREW EDWIN
• Application Number:
  US08/186,590
• Time in Patent Office: 1,210 Days
• Field of Search: 424/423, 424/424, 523/113, 514/1, 514/21, 623/8, 623/11, 623/15, 623/14, 530/382
• US Class Current: 623/8
• CPC Class Codes: A61F 2/02 Prostheses implantable into the body closure means for urethra or rectum or for artificial body openings therefor A61F2/0004
• CPC Class Codes: A61F 2/12 Mammary prostheses and implants
• CPC Class Codes: A61F 2310/00377 Fibrin
• CPC Class Codes: A61L 27/225 Fibrin; Fibrinogen
• CPC Class Codes: A61L 27/36 containing ingredients of undetermined constitution or reaction products thereof , e.g. transplant tissue, natural bone, extracellular matrix isolated natural compounds, e.g. collagen A61L27/24

Abstract

The invention provides a biocompatible surgical implant particularly useful for breast or testicular reconstruction or augmentation comprising a stabilized fibrin semisolid, optionally sealed in a shaped shell. Preferred starting material for production of the implant is whole plasma from autologous or homologous donation, concentrated with respect to fibrinogen.

Claims

1. A surgical prosthesis for soft tissue reconstruction or augmentation in a mammal comprising a resorption-resistant semisolid fibrin coagulate consisting essentially of insoluble fibrin polymer strands stabilized against biodegradation and sealed in a biocompatible, resorption-resistant plastic shell, wherein the semisolid fibrin coagulate is produced from a fibrinogen solution consisting essentially of fibrinogen, thrombin, and factor XIII in amounts sufficient to substantially convert the fibrinogen to insoluble fibrin polymer.

2. The prosthesis of claim 1, wherein the semisolid fibrin coagulate is produced from a plasma fraction consisting essentially of fibrinogen, thrombin, and factor XIII in amounts sufficient to substantially convert the fibrinogen to insoluble fibrin polymer.

3. The prosthesis of claim 1, wherein the fibrinogen solution further includes a cocrosslinking agent.

4. The surgical prosthesis of claim 2, wherein the plasma fraction further includes a cocrosslinking agent.

5. The surgical prosthesis of claim 1, wherein the fibrinogen solution contains from about 1 to 1000 IU thrombin per about 2 to 150 mg fibrinogen, and about 0.01 to 250 units factor XIII per about 1 gm fibrinogen.

6. The surgical prosthesis of claim 2, wherein the plasma fraction contains from about 1 to 1000 IU thrombin per about 2 to 150 mg fibrinogen, and about 0.01 to 250 units factor XIII per about 1 gm fibrinogen.

7. The surgical prosthesis of claim 3, wherein the cocrosslinking agent is calcium chloride present in the fibrinogen solution in a concentration of about 0.001 to about 50 mM.

8. The surgical prosthesis of claim 4, wherein the cocrosslinking agent is calcium chloride present in the plasma fraction in a concentration of about 0.001 to about 50 mM.

9. The surgical prosthesis of claim 4, wherein the plasma fraction is substantially free of biologically active proteolytic enzymes.

10. The surgical prosthesis of claim 9, wherein the coagulate is stabilized by treatment with a crosslinking agent.

11. The surgical prosthesis of claim 2, stabilized against biodegradation by substantial removal of plasma components deleterious to the stability of the product from the plasma fraction;

deactivation of proteolytic enzymes present; and

crosslinkage of the fibrin polymer.

12. The surgical prosthesis of claim 2, wherein the plasma is autologous or homologous to the mammal.

13. The surgical prosthesis of claim 6, wherein the plasma is autologous or homologous to the mammal.

14. The surgical prosthesis of claim 1, wherein the prosthesis is a breast or testicle prosthesis.

15. The surgical prosthesis of claim 2, wherein the prosthesis is a breast or testicle prosthesis.

16. The surgical prosthesis of claim 2, wherein the prosthesis is a breast prosthesis and wherein the plasma is autologous to the mammal.

17. The prosthesis of claim 1, implanted in the soft tissue of a mammal.

18. A method for soft tissue anaplasty in a mammal comprising surgically implanting the prosthesis of claim 1 in the mammal.

19. A method for soft tissue anaplasty in a mammal comprising surgically implanting the prosthesis of claim 2 in the mammal.

20. A method for soft tissue anaplasty in a mammal, comprising surgically implanting the prosthesis of claim 15 in the mammal.

21. A method for mammaplasty in a mammal, comprising surgically implanting the prosthesis of claim 16 in the breast of the mammal.

22. The surgical prosthesis of claim 1, having a deformability corresponding to a Precision Penetrometer reading of about 180.

23. The surgical prosthesis of claim 2, having a deformability corresponding to a Precision Penetrometer reading of about 180.