Solvent based processing technologies for making tissue/polymer composites
An improved osteoimplant device and method for producing it. Bone particles are mixed with a polymer and a solvent. The mixture is formed into the shape of an osteoimplant and substantially all of the solvent is removed. The osteoimplant may be osteoinductive, osteoconductive, and load-bearing.
1 . A method for producing an osteoimplant device comprising:
mixing bone material, a solvent, and a polymer that is substantially soluble in the solvent;
forming the mixture into the shape of an osteoimplant; and
removing substantially all of the solvent from the osteoimplant.
2 . The method of claim 1 , wherein the bone material is selected from the group consisting of autogenic, allogenic, and xenogenic source bone, and combinations and mixtures thereof.
3 . The method of claim 1 , wherein the bone material is selected from the group consisting of bone powder; bone granules; bone chips; bone shards; bone flakes; products of ground, pulverized, and chipped bone; and combinations and mixtures thereof.
4 . The method of claim 1 , wherein the bone material comprises nondemineralized source bone, fully demineralized source bone, partially demineralized source bone, and combinations and mixtures thereof.
5 . The method of claim 1 , wherein the solvent is selected from the group consisting of alcohols, ketones, ethers, esters, chloride solvents, fluoride solvents, aliphatic hydrocarbons, aromatic hydrocarbons, supercritical liquids, and combinations and mixtures thereof.
6 . The method of claim 5 , wherein the solvent is tetrahydrofuran.
7 . The method of claim 1 , wherein the polymer is a natural, synthetic, or semi-synthetic polymer.
8 . The method of claim 1 , wherein the polymer is substantially bioresorbable.
9 . The method of claim 7 , wherein the natural polymer is selected from the group consisting of fibrin glue, fibrinogen, thrombin, mussel adhesive protein, silk, elastin, collagen, casein, gelatin, albumin, keratin, chitin or chitosan, natural or modified polysaccharides, starches, and combinations and mixtures thereof.
10 . The method of claim 7 , wherein the synthetic polymer is selected from the group consisting of epoxy-based compounds, polyacrylates, polymethacrylates, fluoropolymers, silicone polymers, polyurethanes, polyesters, polyethers, polyolefins, vinyl polymers, polysulfones, polyacetals, polyimides, polyamides, polycarbonates, bisphenol-A based poly(phosphoesters), polyphenylenesulfides, polyamideimides, polyaryletherketones, polyarylethernitriles, aromatic polyhydroxy-ethers, polyphenyleneoxides, amino acid-derived polycarbonates, amino acid-derived polyarylates, polyarylates derived from dicarboxylic acids and amino acid-derived diphenols, anionic polymers derived from L-tyrosine, polyarylate random block copolymers, and combinations and mixtures thereof.
11 . The method of claim 7 , wherein the semi-synthetic polymer is selected from the group consisting of genetically-engineered protein polymers, ethyl cellulose, methyl cellulose, carboxy methyl cellulose, hydroxy ethyl cellulose, sodium carboxymethylcellulose, hydroxy propyl cellulose, cellulose esters, and combinations and mixtures thereof.
12 . The method of claim 8 , wherein the bioresorbable polymer is selected from the group consisting of polylactic acid, polyglycolic acid, polylactic-co-glycolic acid, polyglycolates, polydioxanone, polycaprolactone, polycarbonates, polyorthoesters, polyamino acids, polyanhydrides, polyhydroxybutyrate, polyhydroxyvalyrate, poly(propylene glycol-co-fumaric acid), polyhydroxyalkanoates, polyphosphazenes, poly(alkylcyanoacrylates), polyarylates, amino acid-based polymers, cellulose, celluose derivatives, and combinations and mixtures thereof.
13 . The method of claim 1 , wherein substantially all of the solvent is removed from the osteoimplant by freeze drying.
14 . The method of claim 1 , wherein substantially all of the solvent is removed from the osteoimplant by placing the implant under vacuum.
15 . The method of claim 1 , wherein substantially all of the solvent is removed from the osteoimplant by heating the implant.
16 . The method of claim 1 , wherein substantially all of the solvent is removed from the osteoimplant by drying the osteoimplant in circulating air at room temperature.
17 . The method of claim 1 , further comprising adding a biological agent or additive to the osteoimplant.
18 . The method of claim 17 , wherein the biological agent or additive is selected from the group consisting of antibiotics, growth factors, fibrin, bone morphogenetic factors, bone growth agents, chemotherapeutics, pain killers, bisphosphonates, strontium salt, fluoride salt, magnesium salt, sodium salt, and combinations and mixtures thereof.
19 . The method of claim 1 , further comprising adding a reinforcing component to the osteoimplant.
20 . The method of claim 19 , wherein the reinforcing component is selected from the group consisting of fibers, fibrous webs, woven textiles, nonwoven textiles, mesh, and combinations and mixtures thereof.
21 . The method of claim 1 , wherein mixing additionally comprises mixing a porosity generation agent.
22 . The method of claim 21 , wherein the porosity generation agent is selected from the group consisting of sodium chloride, potassium chloride, other inorganic salts, glucose, sugars, other small molecular weight organic compounds, and combinations and mixtures thereof.
23 . The method of claim 1 , wherein the bone material is treated with a surface treatment agent.
24 . The method of claim 23 , wherein the surface treatment agent chemically or physically binds to the bone material and polymer.
25 . The method of claim 1 , wherein forming the mixture into the shape of an osteoimplant comprises a procedure selected from the group consisting of press-molding, injection molding, extrusion, rolling, solvent-casting, gel-casting, cast-molding, vacuum-forming, sintering, melt-forming, blow-molding, leach molding, leavening, and combinations thereof.
26 . An osteoimplant device produced by the method of claim 1 .
27 . The device of claim 26 , wherein the osteoimplant is in the form of one or more selected from the group consisting of a sheet, plate, dish, cone, pin, screw, tube, tooth, tooth root, bone, bone portion, wedge, wedge portion, cylinder, dowel, intervertebral implant, suture anchor, and combinations thereof.
28 . The device of claim 26 , wherein the bone material is selected from the group consisting of autogenic, allogenic, and xenogenic source bone, and combinations and mixtures thereof.
29 . The device of claim 26 , wherein the bone material is selected from the group consisting of bone powder; bone granules; bone chips; bone shards; bone flakes; products of ground, pulverized, and chipped bone; and combinations and mixtures thereof.
30 . The device of claim 26 , wherein the bone material comprises nondemineralized source bone, fully demineralized source bone, partially demineralized source bone, and combinations and mixtures thereof.
31 . The device of claim 26 , wherein the solvent is selected from the group consisting of alcohols, ketones, ethers, esters, chloride solvents, fluoride solvents, aliphatic hydrocarbons, aromatic hydrocarbons, supercritical liquids, and combinations and mixtures thereof.
32 . The device of claim 31 , wherein the solvent is tetrahydrofuran.
33 . The device of claim 26 , wherein the polymer is a natural, synthetic, or semi-synthetic polymer.
34 . The device of claim 26 , wherein the polymer is substantially bioresorbable.
35 . The device of claim 33 , wherein the natural polymer is selected from the group consisting of fibrin glue, fibrinogen, thrombin, mussel adhesive protein, silk, elastin, collagen, casein, gelatin, albumin, keratin, chitin or chitosan, natural or modified polysaccharides, starches, and combinations and mixtures thereof.
36 . The device of claim 33 , wherein the synthetic polymer is selected from the group consisting of epoxy-based compounds, polyacrylates, polymethacrylates, fluoropolymers, silicone polymers, polyurethanes, polyesters, polyethers, polyolefins, vinyl polymers, polysulfones, polyacetals, polyimides, polyamides, polycarbonates, bisphenol-A based poly(phosphoesters), polyphenylenesulfides, polyamideimides, polyaryletherketones, polyarylethernitriles, aromatic polyhydroxy-ethers, polyphenyleneoxides, amino acid-derived polycarbonates, amino acid-derived polyarylates, polyarylates derived from dicarboxylic acids and amino acid-derived diphenols, anionic polymers derived from L-tyrosine, polyarylate random block copolymers, and combinations and mixtures thereof.
37 . The device of claim 33 , wherein the semi-synthetic polymer is selected from the group consisting of genetically-engineered protein polymers, ethyl cellulose, methyl cellulose, carboxy methyl cellulose, hydroxy ethyl cellulose, sodium carboxymethylcellulose, hydroxy propyl cellulose, cellulose esters, and combinations and mixtures thereof.
38 . The device of claim 34 , wherein the bioresorbable polymer is selected from the group consisting of polylactic acid, polyglycolic acid, polylactic-co-glycolic acid, polyglycolates, polydioxanone, polycaprolactone, polycarbonates, polyorthoesters, polyamino acids, polyanhydrides, polyhydroxybutyrate, polyhydroxyvalyrate, poly(propylene glycol-co-fumaric acid), polyhydroxyalkanoates, polyphosphazenes, poly(alkylcyanoacrylates), polyarylates, amino acid-based polymers, cellulose, celluose derivatives, and combinations and mixtures thereof.
39 . The device of claim 26 , wherein substantially all of the solvent is removed from the osteoimplant by freeze drying.
40 . The device of claim 26 , wherein substantially all of the solvent is removed from the osteoimplant by placing the implant under vacuum.
41 . The device of claim 26 , wherein substantially all of the solvent is removed from the osteoimplant by heating the implant.
42 . The device of claim 26 , wherein substantially all of the solvent is removed from the osteoimplant by drying the osteoimplant in circulating air at room temperature.
43 . The device of claim 26 , further comprising adding a biological agent or additive to the osteoimplant.
44 . The device of claim 43 , wherein the biological agent or additive is selected from the group consisting of antibiotics, growth factors, fibrin, bone morphogenetic factors, bone growth agents, chemotherapeutics, pain killers, bisphosphonates, strontium salt, fluoride salt, magnesium salt, sodium salt, and combinations and mixtures thereof.
45 . The device of claim 26 , further comprising adding a reinforcing component to the osteoimplant.
46 . The device of claim 45 , wherein the reinforcing component is selected from the group consisting of fibers, fibrous webs, woven textiles, nonwoven textiles, mesh, and combinations and mixtures thereof.
47 . The device of claim 26 , wherein mixing additionally comprises mixing a porosity generation agent.
48 . The device of claim 47 , wherein the porosity generation agent is selected from the group consisting of sodium chloride, potassium chloride, other inorganic salts, glucose, sugars, other small molecular weight organic compounds, and combinations and mixtures thereof.
49 . The device of claim 26 , wherein the bone material is treated with a surface treatment agent.
50 . The device of claim 49 , wherein the surface treatment agent chemically or physically binds to the bone material and polymer.
51 . The device of claim 26 , wherein forming the mixture into the shape of an osteoimplant comprises a procedure selected from the group consisting of press-molding, injection molding, extrusion, rolling, solvent-casting, gel-casting, cast-molding, vacuum-forming, sintering, melt-forming, blow-molding, leach molding, leavening, and combinations thereof.