Method for forming impregnated synthetic vascular grafts

• US 4,842,575 A
• Filed: 08/05/1988
• Issued: 06/27/1989
• Est. Priority Date: 01/30/1984
• Status: Expired due to Term

• Current Assignee: Maquet Cardiovascular LLC (Getinge AB)
• Original Assignee: Meadox Medicals, Inc. (Boston Scientific Corporation)
• Inventors: Schankereli, Kemal, Hoffman, Harmon Jr.
• Primary Examiner(s): NOT, DEFINED
• Assistant Examiner(s): NOT, DEFINED
• Application Number:
  US07/228,613
• Time in Patent Office: 326 Days
• Field of Search: 623/1, 623/66, 426/657, 427/2, 128/DIG. 8, 527/200, 527/201, 600/36, 106/124, 106/125, 424/95, 514/801
• US Class Current: 600/36
• CPC Class Codes: A61F 2/06 Blood vessels
• CPC Class Codes: A61F 2002/065 Y-shaped blood vessels
• CPC Class Codes: A61L 27/34 Macromolecular materials
• CPC Class Codes: A61L 27/502 Plasticizers
• CPC Class Codes: A61L 27/507 for artificial blood vessels apparatus for applying cells on a blood vessel prosthesis A61F2/062
• CPC Class Codes: C08L 89/06 derived from leather or skin , e.g. gelatin
• CPC Class Codes: Y10S 128/08 Collagen
• CPC Class Codes: Y10S 623/921 Blood vessel

Abstract

A collagen impregnated synthetic vascular graft including a synthetic vascular graft substrate and cross-linked collagen fibril is formed by depositing an aqueous slurry of collagen fibrils in the lumen of the graft and massaging to insure intimate mixing of the fibrils into the porous structure of the substrate. After massaging, the collagen is dried and cross-linked. Repeated applications and massaging and drying further reduce porosity of the graft.

Claims

1. A process for preparing a blood-tight collagen-impregnated synthetic vascular graft, comprising:

providing a porous tubular flexible synthetic graft substrate;

placing an aqueous slurry of water-insoluble collagen fibrils and plasticizer onto at least the inner surface of the substrate;

massaging the substrate to insure intimate mixing of the collagen fibrils into the porous structure of the substrate;

drying the collagen;

cross-linking the collagen by exposure to formaldehyde vapor; and

vacuum drying to remove excess formaldehyde.

5. The process of claim 1, wherein the slurry is applied and massaged through the substrate at least three times and dried between applications.

2. A collagen fibril slurry for forming a blood-tight synthetic vascular graft comprising about 0.5 to 5.0 percent collagen fibril, 4.0 to 12.0 percent of a biologically compatible plasticizer and the balance water.

3. The slurry of claim 2, wherein the collagen fibrils are obtained by acid digestion of bovine skin.

4. The slurry of claim 2, wherein the plasticizer is selected from the group consisting of sorbitol and glycerine.

6. A process for preparing a blood-type collagen-impregnated synthetic vascular graft, comprising:

providing a porous tubular flexible synthetic graft substrate;

placing a aqueous slurry of water-insoluble collagen fibrils and plasticizer onto the inner surface of the substrate;

massaging the substrate to mature intimate mixing of the collagen fibrils into the porous structure of the substrate;

drying the collagen;

cross-linking the collagen by exposure to a biocompatible cross-linking agent; and

vacuum drying to remove excess cross-linking agent.

7. The process of claim 6, wherein the substrate has a porosity of less than about 3,000 ml/min.-cm² (purified water at 120 mm Hg);

8. The process of claim 6, wherein the cross-linking agent is formaldehyde vapor.

9. The process of claim 7, wherein the cross-linking agent is formaldehyde vapor.

10. The process of claim 6, wherein the slurry is applied in at least three applications and dried between each application.

11. The process of claim 7, wherein the slurry is applied in at least three applications and dried between each application.

12. The process of claim 6, wherein the aqueous slurry contains between about 0.5 to 5.0 weight percent water-insoluble collagen fibrils.

13. The process of claim 7, wherein the aqueous slurry contains between about 0.5 to 5.0 weight percent water-insoluble collagen fibrils.

14. The process of claim 12, wherein the platicizer is present in an amount between about 4 to 12 weight percent.

15. The process of claim 13, wherein the plasticizer is present in an amount between about 4 to 12 weight percent.