IP Library Granted Patent US 8,353,967
Granted Patent B2
US 8,353,967 · App. 12/853,793 · Granted Jan 15, 2013

Self-supporting collagen tunnel for guided tissue regeneration and method of using same

Inventors: Jay Malmquist (Portland, OR); David Cheung (Arcadia, CA); William Knox (Newport Beach, CA)
Assignee: Osseous Technologies of America
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Quick Facts
Patent No.
US 8,353,967
App. No.
12/853,793
Granted
Jan 15, 2013
Kind
B2
Abstract

A biocompatible, self-supporting, curved, collagen membrane adapted to be secured by bone tacks or bone screws over exposed bone at a desired bone graft site in the alveolar ridge of a patient such that the membrane defines a space having a predetermined height and width over the exposed bone, in which the membrane maintains its structural integrity for at least 4 months after implantation at the bone graft site and then naturally breaks down and is resorbed by the patient's body, a method of making such a membrane, and a method of using such a membrane for vertical augmentation of the alveolar ridge of the patient.

Claims (32)

1. A method of augmenting a bone in a patient, said method comprising:

surgically exposing bone to be augmented at a desired bone graft site in the patient;

disposing a resorbable self-supporting, curved, collagen membrane over the exposed bone at the desired bone graft site such that said collagen membrane provides a defined space of predetermined height and width adjacent the exposed bone; wherein the membrane retains its structural integrity for a desired time after installation at a bone graft site and then breaks down and is completely resorbed by the patient body;

securing the collagen membrane in position with bone tacks or bone screws; and

packing said defined space with a bone graft material.

2. A method as claimed in claim 1 , wherein said collagen membrane is first trimmed to fit the bone graft site prior to being disposed over the exposed bone.

3. A method as claimed in claim 1 , wherein the membrane retains its structural integrity for at least 4 months after installation at a bone graft site and then breaks down and is resorbed by the patient's body.

4. A method as claimed in claim 1 , wherein the bone to be augmented is the alveolar ridge of the patient.

5. A method as claimed in claim 1 , wherein the membrane is a biocompatible, collagen membrane adapted to be secured to the alveolar ridge of a bone graft patient for containing a bone graft material in a desired configuration and location on the alveolar ridge.

6. A method as claimed in claim 5 , wherein the membrane retains its structural integrity for at least 4 months after installation at a bone graft site and then breaks down and is resorbed by the patient's body.

7. A method as claimed in claim 1 , wherein the membrane has the configuration of an elongated tubular segment.

8. A method as claimed in claim 1 , wherein the membrane is formed of collagen fibers having a native fibrous structure and a fiber length of from 0.2 to 3 millimeters.

9. A method as claimed in claim 8 , wherein said fibers have an average length of about 1.5 millimeters.

10. A method as claimed in claim 1 , wherein said collagen membrane has a tensile strength of approximately 3600 g/mm 2 , a tensile modulus of approximately 95,000 g/mm 2 , pore diameters of less than 50 microns, and a porosity of less than 20%.

11. A method as claimed in claim 1 , wherein said membrane has a radius of curvature a in the range from about 5 to about 10 mm, an overall curved width b in the range from about 10 to about 25 mm, a tunnel width c in the range from about 10 to about 20 mm, a height h in the range from about 3 to about 8 mm and an overall length l in the range from about 10 to about 40 mm.

12. A method as claimed in claim 1 , wherein said membrane is a resorbable collagen membrane produced by the process comprising:

forming a suspension of collagen fibers in an alcohol/water solution;

pouring the suspension into a curved mold cavity of a mold;

subjecting the mold to freezing temperature until the suspension in the mold solidifies;

opening the mold;

subjecting the frozen suspension to freeze drying to produce a membrane;

spraying the freeze-dried membrane with an alcohol/water solution;

thereafter subjecting the membrane to drying; and

heat treating the dried membrane.

13. A method as claimed in claim 12 , wherein said suspension contains from 10 to 60 mg/ml of collagen fibers having a length of 0.2 to 3 mm in a 5 to 25% solution of alcohol in water.

14. A method as claimed in claim 12 , wherein the membrane is sprayed with an alcohol/water solution containing from 40 to 70% alcohol.

15. A method as claimed in claim 12 , wherein perforations are formed in the membrane during casting by extending a plurality of pins through the mold in which the membrane is formed.

16. A method as claimed in claim 12 , wherein the heat treatment is effected at a temperature of from 100 to 140° C. for a period of from 15 minutes to 2 hours.

17. A method as claimed in claim 1 , wherein said membrane takes the form of a bight formed with two legs of unequal length joined by a curved center section.

18. A method as claimed in claim 17 , wherein the two legs are spaced apart a distance of about 8±1 mm.

19. A method as claimed in claim 1 , wherein said membrane takes the form of a circular segment with a circumferential fold forming a peaked structure.

20. A method as claimed in claim 19 , wherein said membrane is provided with at least one projecting tab.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 23, 2018
From: OSSEOUS TECHNOLOGIES OF AMERICA
To: CARDOSO, RONALD
Reel/Frame 045433/0616 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2010
From: MALMQUIST, JAY; CHEUNG, DAVID; KNOX, WILLIAM
To: OSSEOUS TECHNOLOGIES OF AMERICA
Reel/Frame 025060/0931 →
Continuity (3)
Provisional Application 61232587 · Aug 10, 2009
Provisional Application 61329934 · Apr 30, 2010
Related Publication 20110035024A1 · Feb 10, 2011