Composite bone graft material
A bone graft material comprising about 50-90% quickly bioresorbable porogen particles and about 10-50% of a calcium phosphate compound or salt matrix material. A bioactive substance may be included in the matrix material, the porogen particles, or both. Commercial packages containing the bone graft materials and methods for repairing bone therewith are also claimed.
1 . A bone graft material having a calcium matrix component and porogen particles, present in a porogen particle-to-matrix material ratio of 1:1 to about 9:1.
2 . The bone graft material according to claim 1 , wherein said calcium matrix component comprises calcium sodium phosphate, tricalcium phosphate, dicalcium phosphate dihydrate, calcium hydroxyapatite, or a combination thereof.
3 . The bone graft material according to claim 1 , wherein said calcium matrix component further comprises at least one plasticizing agent, at least one bioactive agent, or a combination thereof.
4 . The bone graft material according to claim 1 , wherein said porogen particles comprise at least one biocompatible, biodegradable substance.
5 . The bone graft material according to claim 4 , wherein said biocompatible, biodegradable substance is osteoinductive demineralized bone matrix (DBM) or an osteoinductive DBM substitute.
6 . The bone graft material according to claim 5 , wherein said DBM is human or bovine DBM and said DBM substitute is osteoinductive-factor-supplemented demineralized mollusk nacre.
7 . The bone graft material according to claim 4 , wherein said biocompatible, biodegradable substance is a biocompatible, biodegradable polymer.
8 . The bone graft material according to claim 7 , wherein said biocompatible, biodegradable polymer is a biocompatible, biodegradable polyester, polyanhydride, tyrosine-derived polycarbonate, polyorthoester, or polymer blend containing at least one such polymer.
9 . The bone graft material according to claim 7 , wherein said biocompatible, biodegradable polymer is a biocompatible, biodegradable polyester.
10 . The bone graft material according to claim 9 , wherein said biocompatible, biodegradable polyester is a biocompatible, biodegradable polyhydroxyalkanoate.
11 . The bone graft material according to claim 10 , wherein said biocompatible, biodegradable polyhydroxyalkanoate is formed from hydroxyl-carboxylic acid monomers independently containing about 2 to about 6 carbon atoms, from lactone forms thereof, or from a combination thereof.
12 . The bone graft material according to claim 11 , wherein the average size of said carboxylic acid monomers is about 2 to about 4 carbon atoms.
13 . The bone graft material according to claim 7 , wherein said biocompatible, biodegradable polymer has a weight average molecular weight of about 2,000 to about 100,000.
14 . The bone graft material according to claim 7 , wherein said biocompatible, biodegradable polymer has a weight average molecular weight of about 20,000 to about 80,000.
15 . The bone graft material according to claim 7 , wherein said biocompatible, biodegradable polymer has a weight average molecular weight of about 50,000 to about 55,000.
16 . The bone graft material according to claim 1 , wherein said porogen particles comprise at least one bioactive agent.
17 . The bone graft material according to claim 1 , wherein said porogen particles comprise at least substantially regular polyhedral, lenticular, ovate, or spherical particles, or a combination thereof.
18 . The bone graft material according to claim 1 , wherein said porogen particles collectively have at least one average axial, transverse, or lateral dimension that is about 100 to about 500 microns.
19 . The bone graft material according to claim 1 , wherein said porogen particles collectively have at least one average axial, transverse, or lateral dimension that is about 120 to about 425 microns.
20 . The bone graft material according to claim 1 , wherein said porogen particles collectively have at least one average axial, transverse, or lateral dimension that is about 120 to about 350 microns.
21 . The bone graft material according to claim 1 , wherein each of the average axial, transverse, and lateral dimensions of the porogen particles is independently about 100 to about 500 microns.
22 . The bone graft material according to claim 1 , wherein each of the average axial, transverse, and lateral dimensions of the porogen particles is independently about 120 to about 425 microns.
23 . The bone graft material according to claim 1 , wherein each of the average axial, transverse, and lateral dimensions of the porogen particles is independently about 120 to about 350 microns.
24 . The bone graft material according to claim 1 , wherein said porogen particles have a ratio of average width to average length that is from about 5:1 to about 1:5.
25 . The bone graft material according to claim 1 , wherein said porogen particles have a ratio of average width to average length that is from about 2:1 to about 1:2.
26 . The bone graft material according to claim 1 , wherein said porogen particles have a ratio of average width to average length that is about 1:1.
27 . The bone graft material according to claim 1 , wherein said porogen particles make up about 50% to about 90% by volume of the bone graft material.
28 . The bone graft material according to claim 1 , wherein said porogen particles make up about 75% to about 90% by volume of the bone graft material.
29 . The bone graft material according to claim 1 , wherein said porogen particles make up about 80% to about 90% by volume of the bone graft material.
30 . The bone graft material according to claim 1 , wherein said porogen particles make up more than 80% to about 90% by volume of the bone graft material.
31 . The bone graft material according to claim 1 , wherein said porogen particles are solid particles.
32 . The bone graft material according to claim 1 , wherein said porogen particles are capable of being biodegraded in vivo in about 10 minutes to about 7 days, or wherein said porogen particles are DBM or DBM substitute porogen particles that are capable of being biodegraded in vivo in about 10 minutes to about 8 weeks, or said porogen particles comprise a combination of these porogen particles.
33 . The bone graft material according to claim 1 , wherein said porogen particles are hollow or laminar particles.
34 . The bone graft material according to claim 33 , wherein at least one wall or layer of said porogen particles is capable of being biodegraded in about 10 minutes to about 7 days, or wherein at least one wall or layer of said porogen particles is DBM or a DBM substitute wall or layer that is capable of being biodegraded in vivo in about 10 minutes to about 8 weeks, or said porogen particles comprise a combination of these hollow or laminar particles.
35 . The bone graft material according to of claim 1 , wherein said material is provided in the form of a paste, injectible solution or slurry, dry powder, or dry solid.
36 . The bone graft material according to claim 1 , wherein said material is provided in the form of a paste, injectible solution or slurry that has been hydrated by application of a neat solution or biological fluid to a dry bone graft material according to claim 1 .
37 . A commercial package containing a bone graft material according to claim 1 and instructions for use thereof in repairing bone.
38 . A method for repairing bone comprising:
providing a bone graft material according to claim 1 , and
administering said bone graft material to a living bone tissue surface in need thereof.
39 . The method according to claim 38 , said method further comprising permitting said material to remain at an in vivo site in which it is placed, for a sufficient time to permit the porogen particles thereof to be biodegraded in vivo.
40 . The bone graft material according to claim 1 , wherein said porogen particles include a plurality of first porogen particles comprising osteoinductive DBM or osteoinductive DBM substitute, and a plurality of second porogen particles comprising a biocompatible, biodegradable polymer or polymers.
41 . The bone graft material according to of claim 30 , wherein said material is provided in the form of a paste, injectible solution or slurry, dry powder, or dry solid.
42 . The bone graft material according to claim 30 , wherein said material is provided in the form of a paste, injectible solution or slurry that has been hydrated by application of a neat solution or biological fluid to a dry bone graft material according to claim 30 .
43 . A commercial package containing a bone graft material according to claim 30 and instructions for use thereof in repairing bone.
44 . A method for repairing bone comprising:
providing a bone graft material according to claim 30 , and
administering said bone graft material to a living bone tissue surface in need thereof.