Method for making a light energized tissue adhesive

• US 6,780,840 B1
• Filed: 10/09/2001
• Issued: 08/24/2004
• Est. Priority Date: 10/09/2001
• Status: Expired due to Term

• Current Assignee: Conversion Energy Enterprises
• Original Assignee: Tissue Adhesive Technologies, Inc.
• Inventors: Soltz, Michael A., Soltz, Robert, Soltz, Barbara A., DeVore, Dale P., DeVore, Braden P.
• Primary Examiner(s): Tate, Christopher R.
• Assistant Examiner(s): AUDET, MAURY A
• Application Number:
  US09/973,263
• Time in Patent Office: 1,050 Days
• Field of Search: 514/2, 522/68, 530/356, 424/78.03, 128/898, 525/54.1, 606/214
• US Class Current: 530/356
• CPC Class Codes: A61B 17/00491 Surgical glue applicators surgical adhesives A61L24/00; two-component delivery syringes A61M5/19
• CPC Class Codes: A61B 2017/0007 Pyrometers
• CPC Class Codes: A61B 2017/00084 Temperature
• CPC Class Codes: A61B 2017/005 hardenable using external energy source, e.g. laser, ultrasound
• CPC Class Codes: A61B 2017/00508 using laser
• CPC Class Codes: A61B 2017/00517 using laser
• CPC Class Codes: A61L 24/102 Collagen

Abstract

Consistent with the present invention, tissue adhesive compositions and an associated laser exposure system are provided for bonding or sealing biological tissues. The compositions are comprised of chemically derivatized soluble collagen which is formulated to concentrations ranging from 300 mg/ml (30%) to 800 mg/ml (80%) collagen protein. In particular, Type I collagen, for example, is first prepared by extraction from bovine or porcine hide and purified. The collagen preparations are then chemically derivatized with sulfhydryl reagents to improve cohesive strength and with secondary derivatizing agents, such as carboxyl groups, to improve the adhesive strength of the solder to the tissue. The compositions are then formed into viscous solutions, gels or solid films, which when exposed to energy generated from an infrared laser, for example, undergo thermally induced phase transitions. Solid or semi-solid protein compositions become less viscous enabling the high concentration protein to penetrate the interstices of treated biological tissue or to fill voids in tissue. As thermal energy is released into the surrounding environment, the protein compositions again become solid or semi-solid, adhering to the treated tissue or tissue space.

Claims

1. A method of making a tissue adhesive, comprising the steps of:

heating a solution including collagen derivatized with a COO⁻

functional group to thereby gelatinize said derivatized collagen;

adding derivatized collagen to said solution, said derivatized collagen being derivatized with a COO⁻

functional group; and

repeating said heating and adding steps until the derivatized collagen concentration in said solution is from 300 mg/ml (30%) up to 800 mg/ml (80%), said added derivatized collagen in said solution being gelatinized after said repeated heating steps.

2. A method in accordance with claim 1, further comprising the step of extracting said collagen from a tissue source prior to said derivatizing step.

3. A method in accordance with claim 2, wherein said tissue source includes an animal tissue.

4. A method in accordance with claim 1, wherein said collagen is further derivatized with 4-mercapto-1,8-naphthalic anhydride.

5. A method in accordance with claim 1, wherein said collagen is derivatized with glutaric anhydride.

6. A method in accordance with claim 1, wherein said collagen is derivatized with an SH-functional group.

7. A method in accordance with claim 1, further comprising a step of adding a pH altering material to said to thereby adjust a pH of said solution to be within a range of 6.8-7.8.

8. A method in accordance with claim 1, further comprising the step of deaerating said solution.

9. A method in accordance with claim 7, wherein said pH altering material includes NaOH.

10. A method in accordance with claim 8, further comprising the step of:

adding a material to said solution, said material being selected from the group of collagen fibrils, collagen fibers and collagen fiber bundles.

11. A method in accordance with claim 1, further comprising the step of solidifying said solution.

12. A method in accordance with claim 11, further comprising the step of sectioning said solidified solution into strips.

13. A method in accordance with claim 1, wherein said added collagen is dried collagen.

14. A method in accordance with claim 1, wherein said added collagen is lyophilized.