IP Library Granted Patent US 7,041,641
Granted Patent B2
US 7,041,641 · App. 08/822,186 · Granted May 9, 2006

Osteogenic devices and methods of use thereof for repair of endochondral bone and osteochondral defects

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Quick Facts
Patent No.
US 7,041,641
App. No.
08/822,186
Granted
May 9, 2006
Kind
B2
Abstract

Disclosed herein are improved osteogenic devices and methods of use thereof for repair of bone and cartilage defects. The devices and methods promote accelerated formation of repair tissue with enhanced stability using less osteogenic protein than devices in the art. Defects susceptible to repair with the instant invention include, but are not limited to: critical size defects, non-critical size defects, non-union fractures, fractures, osteochondral defects, subchondral defects, and defects resulting from degenerative diseases such as osteochondritis dessicans.

Claims (46)

1. A device for inducing local bone or cartilage formation, comprising:

a bone morphogenetic protein selected from the group consisting of OP1, OP2, OP3, BMP2, BMP3, BMP4, BMP5, BMP6, BMP9, BMP10, BMP11, BMP12, BNP15, BMP16, DPP, Vgl, 60A protein, GDF-1, GDF3, GDF5, GDF6, GDF7, GDF8, GDF9, GDF10 and GDF11, capable of inducing repair of endochondral bone, or cartilage, chondral, or osteochondral defects;

a matrix selected from the group consisting of collagen, apatites, hydroxyapatites, tricalcium phosphate, and admixtures thereof; and

a binding agent selected from the group consisting of cellulosic agents and salts thereof;

wherein said binding agent has a degree of substitution of 0.65–0.90 and a viscosity of about 10–200 cP at a 4% (w/v) concentration of said binding agent.

2. The device of claim 1 , wherein said bone morphogenetic protein is selected from the group consisting of OP1, OP2, BMP2, BMP4, BMP5, and BMP6.

3. The device of claim 1 wherein said bone morphogenetic protein is OP-1.

4. The device of claim 1 wherein said device comprises at least two different bone morphogenetic proteins.

5. The device of claim 1 wherein said claim matrix is collagen.

6. The device of claim 1 wherein said device comprises at least two different matrix materials.

7. The device of claim 1 wherein said binding agent is an alkylcellulose.

8. The device of claim 1 wherein said binding agent is selected from the group consisting of methylcellulose, methylhydroxyethylcellulose, hydroxyethylcellulose, hydroxypropylmethylcellulose, carboxymethylcellulose, sodium carboxymethylcellulose, hydroxyalkylcelluloses, and admixtures thereof.

9. The device of claim 1 wherein said binding agent is carboxymethylcellulose or a sodium salt thereof.

10. The device of claim 1 wherein said device comprises at least two different binding agents.

11. The device of claim 1 further comprising a wetting agent.

12. The device of claim 1 wherein the binding agent to matrix ratio is one part by weight binding agent to 1–10 parts by weight matrix.

13. The device of claim 1 wherein the binding agent to matrix ratio is 1–10 parts by weight binding agent to 1 part by weight matrix.

14. The device of claim 3 , wherein the amount of the OP-1 ranges from approximately 0.125 mg to 10.0 mg.

15. The device of claim 14 , wherein the amount of the OP-1 is approximately 3.5 mg.

16. The device of claim 11 wherein said wetting agent is saline.

17. The device of claim 12 wherein the binding agent to matrix ratio is one part by weight binding agent to 5 parts by weight matrix.

18. The device of claim 12 wherein the binding agent to matrix ratio is one part by weight binding agent to 1–5 parts by weight matrix.

19. The device of claim 13 wherein the binding agent to matrix ratio is fewer than 10 parts by weight binding agent to one part by weight matrix.

20. A device for inducing local bone and cartilage formation comprising a bone morphogenetic protein comprising an amino acid sequence having at least 70% homology with the C-terminal 102–106 amino acids, including the conserved seven cysteine domain, of human OP1;

matrix selected from the group consisting of collagen, apatites, hydroxyapatites, tricalcium phosphate, and admixtures thereof; and

a binding agent selected from the group consisting of cellulosic agents and salts thereof;

wherein said binding agent has a degree of substitution of 0.65–0.90 and a viscosity of about 10–200 cP at a 4% (w/v) concentration of said binding agent; and

wherein said bone morphogenetic protein is capable of inducing repair of endochondral bone when implanted together with a matrix in a mammal.

21. A device for inducing local bone or cartilage formation, comprising at least approximately 1.25 mg of OP-1 and at least approximately 180 mg of carboxymethylcellulose per 1000 mg of collagen matrix, wherein said carboxymethylcellulose has a degree of substitution of 0.65–0.90 and a viscosity of about 10–200 cP at a 4% (w/v) concentration of said carboxymethylcellulose.

22. The device of claim 21 comprising at least approximately 2.5 mg of OP-1 per 1000 mg of collagen matrix.

23. The device of claim 21 or 22 comprising at least approximately 200 mg of carboxymethylcellulose per 1000 mg of collagen matrix.

24. The device of claim 21 or 22 further comprising saline.

25. The device of claim 23 , further comprising saline.

26. A device for inducing local bone or cartilage formation comprising:

OP-1;

collagen matrix; and

carboxymethylcellulose having a degree of substitution of 0.65–0.90 and a viscosity of about 10–200 cP at a 4% (w/v) concentration of said carboxymethylcellulose.

27. A kit for inducing local bone or cartilage formation, the kit comprising:

(a) a first receptacle housing a bone morphogenetic protein selected from the group consisting of OP1, OP2,OP3, BMP2, BMP3, BMP4, BMP5, BMP6, BMP9, BMP10, BMP11, BMP12, BMP15, BMP16, DPP, Vgl, 60A protein, GDF-1, GDF3, GDF5, GDF6, GDF7, GDF8, GDF9, GDF10 and GDF11 and a matrix selected from the group consisting of collagen, apatites, hydroxyapatites, tricalcium phosphates and admixtures thereof, and

(b) a second receptacle housing a binding agent selected from the group consisting of cellulosic agents, and salts thereof,

wherein said binding agent has a degree of substitution of 0.65–0.90 and a viscosity of about 10–200 cP at a 4% (w/v) concentration of said binding agent.

28. The kit of claim 27 further comprising a receptacle adapted to house a wetting agent.

29. A kit for inducing local bone or cartilage formation, the kit comprising:

a first receptacle housing a bone morphogenetic protein selected from the group consisting of OP1, OP2, OP3, BMP2, BMP3, BMP4, BMP5, BMP6, BMP9, BMP10, BMP11, BMP12, BMP15, BMP16, DPP, Vg1, 60A protein, GDF-1, GDF3, GDF5, GDF6, GDF7, GDF8, GDF9, GDF10 and GDF11, a matrix selected from the group consisting of collagen, apatites, hydroxyapatites, tricalcium phosphates, and admixtures thereof, and a binding agent selected from the group consisting of cellulosic agents, and salts thereof,

wherein said binding agent has a degree of substitution of 0.65–0.90 and a viscosity of about 10–200 cP at a 4% (w/v) concentration of said binding agent.

30. The kit of claim 29 , further comprising a second receptacle adapted to house a wetting agent.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2016
From: STRYKER CORPORATION
To: MARIEL THERAPEUTICS, INC.
Reel/Frame 037460/0806 →
LIEN Recorded Jan 8, 2016
From: STRYKER CORPORATION
To: MARIEL THERAPEUTICS, INC.
Reel/Frame 037461/0778 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2014
From: STRYKER CORPORATION
To: MARIEL THERAPEUTICS, INC.
Reel/Frame 033535/0440 →