Biomaterial, joint prosthesis using the biomaterial and method of producing the same
The object of the present invention is to provide a joint prosthesis, bearing material and a production method thereof, which suppresses wear in a sliding section and suppresses the production of abrasive powder even during repeated daily operation. To achieve the object, there is provided a biomaterial comprising: a substrate made of metal, alloy or ceramic; and a biocompatible material layer laminated on the substrate, wherein hydroxyl groups are formed on the substrate by surface-treating, while the biocompatible material layer comprises a polymer containing phosphorylcholine groups, the substrate and the biocompatible material layer are bound via a binder layer which is combined with the hydroxyl groups of the substrate and with the biocompatible material layer.
1. A biomaterial comprising:
a substrate made of at least one selected from the group consisting of metal, alloy and ceramic; and
a biocompatible material layer laminated on appropriate sections of the substrate,
wherein:
hydroxyl groups are formed on a surface of the substrate by surface-treating at least one section of the surface, while the biocompatible material layer comprises a polymer containing phosphorylcholine groups,
the substrate and the biocompatible material layer are bound via a binder layer, the binder layer being combined, on the one hand, with the hydroxyl groups of the substrate by graft-polymerization and, on the other hand, with the biocompatible material layer by graft-polymerization respectively,
the binder layer contains an organic compound having carboxyl groups on the one terminal and methacrylic groups or methylene groups on the other terminal, the carboxyl groups on the one terminal are combined with the hydroxyl groups, and
the methacrylic groups or the methylene groups on the other terminal are combined with the polymer containing phosphorylcholine groups by graft-polymerization into the formation of covalent bonds.
2. The biomaterial according to claim 1 , wherein the polymer containing phosphorylcholine groups includes 2-methacryloyloxyethyl phosphorylcholine polymer and a copolymer containing 2-methacryloyloxyethyl phosphorylcholine.
3. The biomaterial according to claim 1 , wherein the substrate made of metal, alloy or ceramic contains a metal oxide or metal component capable of forming hydroxyl groups.
4. The biomaterial according to claim 1 , wherein the substrate is made of titanium metal, or at least one alloy selected from the group consisting of cobalt-chromium alloy, cobalt- chromium -molybdenum alloy, nickel-chromium alloy, stainless steel alloy and titanium alloy, or a ceramic containing at least one substance selected from the group consisting of alumina, zirconia and titania.
5. The biomaterial according to claim 1 , wherein the substrate comprises at least one selected from the group consisting of chromium and titanium,
a surface of chromium or titanium is oxidized by oxygen-plasma treatment to form hydroxyl groups thereon.
6. The biomaterial according to claim 1 , wherein the binder layer is made of at least one selected from the group consisting of 4- methacryloxyethyltrimellitate anhydride, 4-methacryloyloxy ethyl trimellitic acid, methacrylic acid, maleic anhydride and maleic acid.
7. A prosthesis comprising the biomaterial according to claim 1 .
8. A prosthesis comprising the biomaterial according to claim 2 .
9. A prosthesis comprising the biomaterial according to claim 3 .
10. A prosthesis comprising the biomaterial according to claim 4 .
11. A prosthesis comprising the biomaterial according to claim 5 .
12. A prosthesis comprising the biomaterial according to claim 6 .