Mechanically competent scaffold for ligament and tendon regeneration
View Patent ↗A multi-region device for repair, regeneration or reconstruction in articular tissue injury such as torn ligaments and tendons is provided. The device comprises at least one degradable material and biocompatible non-degradable polymeric fiber-based material, in a three-dimensional braided scaffold. The two end sections are designed for attachment of the device at the site of implantation and are designed to allow bone cell ingrowth, and one or more middle regions are designed to allow ligament or tendon cell ingrowth.
1. A device for replacement or regeneration of articular tissue comprising
polymeric fibers degrading at between nine and twelve months following implantation, and
polymeric fibers not degrading following implantation in less than one year,
wherein bundles of the polymeric fibers are braided into a three-dimensional braided scaffold to form two end sections for attachment of the device at a site of implantation and at least one middle section between the end sections, wherein the polymer of the middle section degrades more rapidly or the middle section is more porous than the end sections,
wherein the device has a peak load strength range from 500 to 3200 N, with an initial stiffness range of 200 to 700 N/mm,
wherein the number of fibers per bundle is in the range of 10 to 60 and the number of bundles per braid is in the range of 16 to 64,
wherein the polymeric braid of the middle section of the device has a porosity between 50 and 70%, and pores between 177 μm and 250 μm in diameter, and
wherein the device provides articular tissue function at the site of implantation as tissue integrates into the device.
2. The device of claim 1 for ligament or tendon repair, wherein the end sections are attachable to bone and allow for ingrowth of bony tissue.
3. The device of claim 2 wherein the porosity of the middle section allows in-growth of connective tissue.
4. The device of claim 1 produced by a three-dimensional rotary braiding method or row and column method.
5. The device of claim 1 , wherein the middle section differs from the end sections in size, braiding angle, or porosity.
6. The device of claim 1 wherein between 70 and 90% of the polymeric fibers are degradable in less than one year.
7. The device of claim 1 wherein the degradable polymer fibers are made up of polymers selected from the group consisting of poly(L-lactic acid (PLLA), poly(DL-lactic acid (PLA), poly(DL-lactic-co-glycolic acid) (PLGA), polyorthoesters, polyanhydrides, polyphosphazenes, polycaprolactones, polyhydroxyalkanoates, biodegradable polyurethanes, polyanhydride-co-imides, polypropylene fumarates, polydiaxonane, polysaccharides, collagen, silk, chitosan, and celluloses.
8. The device of claim 1 wherein the non-degradable polymer fibers are made up of polymers selected from the group consisting of polyethylene terephthalate (PET), polyetheretherketone (PEEK), polytetrafluoroethylene (PTFE), polyester, polyethylene, polyamide, polyimide, polyurethane, polybutadiene, polybutylene, and polypropylene.
9. The device of claim 1 , wherein the device is seeded with cells, ingrowth of which is supported by the scaffold.
10. The device of claim 9 wherein the cells are selected from the group consisting of mesenchymal cells, cells generating mesenchymal cells, fibroblasts, pluripotent stem cells, and multipotent stem cells.
11. A method for repairing, regenerating, replacing or reconstructing a damaged tendon or ligament in a patient comprising implanting at a site of a damaged tendon or ligament the device of claim 1 .
12. A kit comprising the device of claim 1 and means for attachment.
13. A method of making the device of claim 1 comprising braiding a three-dimensional scaffold comprising
polymeric fibers degrading at between nine and twelve months following implantation, and
polymeric fibers not degrading following implantation in less than one year,
wherein the polymeric fibers are braided into a three-dimensional braided scaffold to form two end sections for attachment of the device at a site of implantation and at least one middle section between the end sections, wherein the polymer of the middle section degrades more rapidly or the middle section is more porous than the end sections,
wherein the device provides articular tissue function at the site of implantation as tissue integrates into the device.
14. A device for replacement or regeneration of articular tissue comprising
bundles of fibers formed of polymer degrading following implantation,
wherein the bundles of the polymeric fibers are braided into a three-dimensional braided scaffold to form two end sections for attachment of the device at a site of implantation and at least one middle section between the end sections,
wherein the middle section is more porous than the end sections,
wherein the device has a peak load strength range from 500 to 3200 N, with an initial stiffness range of 200 to 700 N/mm, and
wherein the device provides articular tissue function at the site of implantation as tissue integrates into the device.
15. The device of claim 14 wherein the fibers in the bundles are multifilament fibers.