Method for producing porous β-tricalcium phosphate granules
A porous β-tricalcium phosphate material for bone implantation is provided. The multiple pores in the porous TCP body are separate discrete voids and are not interconnected. The pore size diameter is in the range of 20-500 μm, preferably 50-125 μm. The porous β-TCP material provides a carrier matrix for bioactive agents and can form a moldable putty composition upon the addition of a binder. Preferably, the bioactive agent is encapsulated in a biodegradable agent. The invention provides a kit and an implant device comprising the porous β-TCP, and a bioactive agent and a binder. The invention also provides an implantable prosthetic device comprising a prosthetic implant having a surface region, a porous β-TCP material disposed on the surface region and optionally comprising at least a bioactive agent or a binder. Methods of producing the porous β-TCP material and inducing bone formation are also provided.
1. A method of producing porous β-tricalcium phosphate (β-TCP) granules that have a particle size of 0.1-2 mm, and that comprise a multiplicity of pores having a pore diameter size of 20-500 μm and being single separate voids partitioned by walls and being not interconnected, comprising the steps of:
(a) blending a TCP powder with a pore-forming agent;
(b) adding a granulating solution to form a crumbly mass;
(c) passing the crumbly mass through a sieve to form granules;
(d) vaporizing the pore-forming agent at 700-800° C.; and
(e) sintering the granules to form the porous β-TCP granules.
2. The method of claim 1 , wherein the proportion of the pore-forming agent is 37.5% by weight.
3. The method of claim 1 , wherein the sieve is in the size range of 500-1000 μm or 1000-1700 μm.
4. The method of claim 1 , wherein the granules are sintered at 1000-1200° C. and followed by a slow cooling step to form the porous β-TCP granules.
5. The method of any one of claims 1 to 4 , wherein the pore-forming agent is selected from the group consisting of naphthalene, prepolymers of polyacrylates, prepolymers of polymethacrylates, polymethacrylates, polymethyl methacrylate, copolymers of methyl acrylate and methyl methacrylate, polystyrene, polyethylene glycol, crystalline cellulose, fibrous cellulose, polyurethanes, polyethylenes, nylon resins and acrylic resins.
6. The method of any one of claims 1 to 4 , wherein the granulating solution comprises a compound selected from the group consisting of polyvinyl pyrrolidone, starch, gelatin, polyvinyl alcohol, polyethylene oxide, hydroxyethyl cellulose, polyvinyl butyral and cellulose acetate butyrate.
7. The method of any one of claims 1 to 4 , wherein the porous β-TCP granules are sieved after sintering.
8. The method of claim 1 , wherein the proportion of the pore-forming agent is 10%-50% by weight.
9. The method of claim 1 , wherein the proportion of the pore-forming agent is 30-40% by weight.
10. The method of claim 1 , wherein the pore-forming agent is in bead or resin form.
11. The method of claim 1 , wherein the granulating solution is an aqueous solution.
12. The method of claim 1 , wherein the pore diameter size is 410-460 μm.
13. The method of claim 1 , wherein the pore diameter size is 40-190 μm.
14. The method of claim 1 , wherein the pore diameter size is 20-95 μm.
15. The method of claim 1 , wherein the pore diameter size is 50-125 μm.