Biostaples suitable for wrist, hand and other ligament replacements or repairs
The disclosure describes implantable medical products, that include dry or partially hydrated biocompatible biostaples suitable for ligament repairs or replacements comprising collagen fibers that may be configured to expand in situ after implantation to frictionally engage a bone tunnel wall or bone sleeve to thereby affix the construct in the bone tunnel.
1. A system for fabricating medical biostaples formed of biocompatible fibers, comprising:
a mold holding at least one bundle of collagen fibers therein;
a liquid bath comprising gelatin; and
a vacuum system configured to cause the gelatin to infiltrate the collagen fibers.
2. The system of claim 1 , wherein the gelatin comprises nordihydroguaiaretic acid (NDGA) treated gelatin.
3. The system of claim 1 , wherein the liquid bath comprises about 5% to about 30% gelatin.
4. The system of claim 1 , wherein the at least one bundle of collagen fibers comprises about 2 to about 400 elongate collagen fibers.
5. The system of claim 1 , wherein the at least one bundle of collagen fibers comprises about 10 to about 200 elongate collagen fibers.
6. A mold for fabricating biostaples, comprising:
a mold body having a plurality of pairs of substantially vertical mold tunnels spaced apart across a crown mold channel for forming staple legs on opposing sides of a crown portion of a bundle of collagen fibers; and
a holder comprising a thread that cooperates with the mold body to insert the bundle of collagen fibers into at least one pair of the mold tunnels.
7. A method of making a medical construct, comprising:
forming a plurality of collagen fibers into a staple shape having a crown portion and two outwardly extending leg portions;
processing the plurality of collagen fibers to retain the staple shape, thereby providing staple shaped collagen fibers; and
dehydrating the staple shaped collagen fibers to a desired dry or partially hydrated state to form dry or partially hydrated staple shaped collagen fibers, thereby providing the medical construct.
8. A method according to claim 7 , wherein the forming step comprises:
arranging the plurality of collagen fibers into a bundle of elongate fibers;
grasping a medial portion of the bundle of elongate fibers with a thread;
pulling the thread out of a channel of a fiber holder; then
pulling the bundle of elongate fibers through the channel of the fiber holder in response to the pulling of the thread to fold the bundle of elongate fibers and cause opposing end portions of the bundle of elongate fibers to travel together; then
inserting the thread serially through first and second spaced apart mold tunnels; and then
pulling the folded bundle of elongate fibers through the first and second spaced apart mold tunnels in response to the inserting step.
9. A method according to claim 7 , wherein the collagen fibers comprise NDGA polymerized collagen fibers.
10. The method of claim 7 , further comprising enclosing the dry or partially hydrated shaped collagen fibers in a sterile package.
11. The method of claim 7 , wherein the plurality of collagen fibers comprises about 2 to about 400 elongate collagen fibers.
12. The method of claim 11 , wherein at least a majority of the elongate collagen fibers have a length sufficient to extend across the crown portion and each of the leg portions.
13. The method of claim 12 , wherein the plurality of collagen fibers comprises about 10 to about 200 elongate collagen fibers.
14. The method of claim 11 , wherein at least a majority of the elongate collagen fibers are substantially parallel to each other over at least a major portion of the staple shape of the medical construct.
15. The method of claim 7 , wherein the medical construct is an implant for a collateral ligament for the hand or wrist.
16. The method of claim 7 , wherein the medical construct is an implant for a medial ulnar collateral ligament.
17. The method of claim 7 , wherein the medical construct is an implant for a scapholunate ligament.
18. The method of claim 7 , wherein the medical construct comprises a thin film of polylactic acid (PLA).
19. The method of claim 7 , wherein each of the leg portions have a length of about 5 mm to about 10 mm, and wherein the crown portion is shorter than each of the leg portions.
20. The method of claim 7 , wherein each of the leg portions has a beveled end.