Modified demineralized cortical bone fibers
Methods for making surgical implants (or grafts) for the repair of bone defects, and more particularly, surgical implants that include demineralized bone fibers, are disclosed. Also disclosed are methods for increasing the wettability and ensuring uniform density of such implants. The surgical implants have a wettability time of less than 5 minutes and a residual moisture content of less than 6% by weight, and they remain cohesive and retain their shape upon complete rehydration.
1. A method for producing an implant from modified demineralized cortical bone fibers, said method comprising the steps of:
contacting the demineralized cortical bone fibers with a salt solution prior to lyophilizing; and
shaping a mass of demineralized cortical bone fibers to form an implant having a desired shape; and
lyophilizing the implant to produce a lyophilized implant that has a residual moisture content of less than about 6% by weight, based on the total weight of the implant, and a complete rehydration time of less than about 30 minutes, and wherein said lyophilized implant remains cohesive and retains its shape upon complete hydration.
2. The method of claim 1 , wherein the implant has a wettability time of less than about 5 minutes and a complete rehydration time of less than about 30 minutes.
3. The method of claim 1 , further comprising contacting the demineralized cortical bone fibers with a chemical solution, which may or may not be combined with the salt solution prior to shaping and is selected from: a biocompatible polar molecule, a buffer solution, and combinations thereof.
4. The method of claim 3 , wherein the chemical solution is a buffered saline solution.
5. The method of claim 1 , further comprising the step of curing the implant at a temperature of from about 20° C. to about 50° C. for a period of up to about 48 hours by one or more techniques selected from air drying, heat drying and applying energy to the implant, said curing step being performed prior to said lyophilizing step.
6. The method of claim 1 , further comprising the step of crosslinking at least a portion of the implant by one or more techniques selected from: exposing the implant to energy, chemical crosslinking and heating, said crosslinking step being performed prior to said lyophilizing step.
7. The method of claim 6 , wherein said crosslinking step is performed by exposing the implant to energy and the energy is selected from ultraviolet light or microwave energy.
8. The method of claim 1 , wherein the step of shaping comprises:
providing to an implant forming container a solution comprising demineralized cortical bone fibers and a liquid;
separating the liquid from the demineralized cortical bone fibers; and
removing the liquid from the container.
9. The method of claim 8 , wherein the step of shaping further comprises agitating the solution in the implant forming container to homogenously distribute the demineralized cortical bone fibers in the liquid.
10. The method of claim 9 , wherein the implant forming container is a press mold comprising a reservoir for holding the solution therein and a plunger which is reciprocatingly movable in and out of the reservoir, wherein the step of separating is performed by pressing the plunger into the reservoir, thereby compressing the demineralized cortical bone fibers and causing the liquid to separate from the demineralized cortical bone fibers by either flowing through a filter at an end of the reservoir that is opposite the plunger, or by flowing through a plurality of perforations provided in the plunger.
11. A method for producing an implant from modified demineralized cortical bone fibers, said method comprising the steps of:
contacting the demineralized cortical bone fibers with a salt solution prior to lyophilizing;
shaping a mass of demineralized cortical bone fibers to form an implant having a desired shape;
curing the implant at a temperature of from about 20° C. to about 50° C. for a period of up to about 48 hours by one or more techniques selected from air drying, heat drying and applying energy to the implant, said curing step being performed prior to said lyophilizing step; and
lyophilizing the implant to produce a lyophilized implant that has a residual moisture content of less than about 6% by weight, based on the total weight of the implant, and a complete rehydration time of less than about 30 minutes, and wherein said lyophilized implant remains cohesive and retains its shape upon complete hydration.
12. The method of claim 11 , wherein the step of shaping comprises:
providing to an implant forming container a solution comprising demineralized cortical bone fibers and a liquid;
separating the liquid from the demineralized cortical bone fibers; and
removing the liquid from the container.
13. The method of claim 12 , wherein the implant forming container is a press mold comprising a reservoir for holding the solution therein and a plunger which is reciprocatingly movable in and out of the reservoir, wherein the step of separating is performed by pressing the plunger into the reservoir, thereby compressing the demineralized cortical bone fibers and causing the liquid to separate from the demineralized cortical bone fibers by either flowing through a filter at an end of the reservoir that is opposite the plunger, or by flowing through a plurality of perforations provided in the plunger.
14. The method of claim 11 , further comprising the step of contacting the demineralized cortical bone fibers with a chemical solution, either prior to or after they are shaped to form the implant.
15. The method of claim 14 , wherein the chemical solution is selected from: a biocompatible polar molecule, a salt solution, a buffer solution and combinations thereof.
16. The method of claim 11 , further comprising the step of crosslinking at least a portion of the implant by one or more techniques selected from: exposing the implant to energy, chemical crosslinking and heating, said crosslinking step being performed prior to said lyophilizing step.