Implants for replacing cartilage, with negatively-charged hydrogel surfaces and flexible matrix reinforcement
A permanent non-resorbable implant allows surgical replacement of cartilage in articulating joints, using a hydrogel material (such as a synthetic polyacrylonitrile polymer) reinforced by a flexible fibrous matrix. Articulating hydrogel surface(s) are chemically treated to provide a negative electrical charge that emulates the negative charge of natural cartilage, and also can be treated with halogenating, cross-linking, or other chemical agents for greater strength. For meniscal-type implants, the reinforcing matrix can extend out from the peripheral rim of the hydrogel, to allow secure anchoring to soft tissue such as a joint capsule. For bone-anchored implants, a porous anchoring layer enables tissue ingrowth, and a non-planer perforated layer can provide a supportive interface between the hard anchoring material and the softer hydrogel material.
1. A surgical implant for replacing cartilage in an articulating mammalian joint, comprising:
an anchoring surface on one side of the implant, configured for attaching the implant to a prepared surface of a bone in the articulating mammalian joint;
a synthetic polymer hydrogel material, on a side of the implant opposite from the anchoring surface, having an exposed smooth and lubricious surface with a negative electrical charge density, adapted for lubricious sliding interactions in mammalian synovial fluid with another bone in the articulating mammalian joint, wherein the smooth and lubricious surface has a negative electrical charge density within a range of about −50 to about −250 millimolar, when measured by sodium equilibration; and,
wherein a flexible fibrous reinforcing matrix is embedded within at least a portion of the hydrogel material.
2. The surgical implant according to claim 1 , wherein the smooth and lubricious surface contains sulfur atoms.
3. The surgical implant according to claim 1 , wherein the smooth and lubricious surface contains sulfonated polyacrylonitrile synthetic polymer.
4. The surgical implant according to claim 1 , wherein the smooth and lubricious surface has been treated with a chemical reagent that creates crosslinking bonds between polymeric molecules.
5. The surgical implant of claim 1 , wherein at least a portion of the anchoring surface comprises a porous material that promotes ingrowth of tissue after surgical implantation.
6. A surgical implant according to claim 1 , wherein the synthetic polymer comprises polyacrylonitrile.
7. A surgical implant for replacing a cartilage segment that covers a hard bone surface in an articulating joint, comprising:
a polymeric hydrogel component, at least a portion of which is reinforced by a flexible fibrous matrix, and having a smooth and lubricious articulating surface having a negative electrical charge;
an anchoring surface on a side of the implant opposite from the smooth and lubricious articulating surface, configured to promote ingrowth of tissue following surgical implantation; and,
a non-planar interface layer having multiple perforations, positioned between the articulating surface and the anchoring surface;
wherein the articulating surface has a negative electrical charge density within a range of about −50 to about −250 millimolar, when measured by sodium equilibration.
8. The surgical implant of claim 7 , wherein the articulating surface has been treated with a chemical reagent that creates crosslinking bonds between polymeric molecules.
9. A surgical implant for replacing a cartilage segment that covers a hard bone surface in an articulating joint, comprising:
a polymeric hydrogel component, at least a portion of which is reinforced by a flexible fibrous matrix, and having a smooth and lubricious articulating surface having a negative electrical charge;
an anchoring surface on a side of the implant opposite from the smooth and lubricious articulating surface, configured to promote ingrowth of tissue following surgical implantation; and,
a non-planar interface layer having multiple perforations, positioned between the articulating surface and the anchoring surface;
wherein the articulating surface contains sulfur atoms.
10. The surgical implant of claim 9 , wherein the articulating surface has been treated with a chemical reagent that creates crosslinking bonds between polymeric molecules.
11. A surgical implant for replacing a cartilage segment that covers a hard bone surface in an articulating joint, comprising:
a polymeric hydrogel component, at least a portion of which is reinforced by a flexible fibrous matrix, and having a smooth and lubricious articulating surface having a negative electrical charge;
an anchoring surface on a side of the implant opposite from the smooth and lubricious articulating surface, configured to promote ingrowth of tissue following surgical implantation; and,
a non-planar interface layer having multiple perforations, positioned between the articulating surface and the anchoring surface;
wherein the articulating surface contains halogen atoms bonded to carbon atoms.