Osteoinductive putties and methods of making and using such putties
The present disclosure relates to osteoinductive putties and other implantable compositions for repair of bone defects and other medical uses. Specifically, the technology pertains to carriers for use in implantable compositions, such as osteoinductive putties. The osteoinductive putties are made entirely from donor tissue such as demineralized bone matrix, and the putties have excellent physical properties. The present disclosure relates to osteoinductive putties, carriers, compositions, implants, kits, methods of making and methods of using any of the foregoing.
1. A carrier for use in an implantable composition comprising a mixture of thermally denatured collagen fragments,
wherein said mixture of thermally denatured collagen fragments has a sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) profile, and said SDS-PAGE profile comprises a region between about 29 kDa and about 97 kDa,
wherein said region is without prominent, intense, or discernable bands as compared to a Type-I collagen reference material, wherein
said SDS-PAGE profile was obtained on standard 12 lane 8-16% gradient pre-made gels through analysis at constant voltage of 100 V for 2.5 h, transferred to nitrocellulose filter and stained with 0.1% ponceau red to confirm protein transfer and mark the position of molecular weight markers; and
wherein said carrier is not a gelatin, does not have a measurable Bloom strength and wherein said SDS-PAGE profile also has a band between about 15 kDa and about 20 kDa; and
wherein said carrier is made from demineralized bone matrix (DBM).
2. The carrier of claim 1 , wherein said SDS-PAGE profile is substantially the same as shown in Lane C of any of FIG. 2A, 2B, 2C , or 2 D.
3. An osteoinductive putty comprising an osteoinductive substance, and the carrier of claim 1 in an amount of from about 27 to about 38 percent, wherein the putty is extrudable, moldable, resistant to irrigation, and exhibits cohesiveness in solution at 37° C. for at least about 60 seconds; and wherein said osteoinductive substance is demineralized bone matrix (DBM).
4. The osteoinductive putty of claim 3 , wherein the putty is adapted for packing into a bone defect.
5. The osteoinductive putty of claim 3 , wherein the putty remains extrudable after extended storage in a sealed package.
6. A method of making the carrier of claim 1 comprising: providing a collagen source comprising demineralized bone matrix (DBM); combining the collagen source with a denaturing solution other than water or saline to create a collagen source mixture; and heating the collagen source mixture to a temperature greater than 100° C.
7. The method of claim 6 wherein the denaturing solution comprises 0.05 N HCl and the temperature is about 120° C., and the collagen source mixture is heated for about 90 minutes.
8. An osteoinductive putty comprising an osteoinductive substance, the carrier of claim 1 in an amount of from about 27 to about 38 percent, and a liquid medium; and a package, wherein the osteoinductive substance and carrier are sealed in the package, and wherein the putty is ready to use (RTU) upon removal from the package; and wherein said osteoinductive substance is demineralized bone matrix (DBM).
9. A method of treating a subject in need of treatment for a bone defect, the method comprising: implanting the osteoinductive putty of claim 8 into a bone defect.