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Preparation of porous calcium phosphate biomaterials and characterization of.doc

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Preparation of porous calcium phosphate biomaterials and characterization of

 PAGE \* MERGEFORMAT 22 Preparation of porous calcium phosphate biomaterials and characterization of 【Abstract】 Objective To prepare for new bone grew into the porosity, pore size and structure of porous calcium phosphate scaffold for tissue engineering. Methods by wet co-precipitation synthesis of hydroxyapatite (HA) / tricalcium phosphate (TCP) two-phase powder, organic foam Soaking France and the appropriate porogen, respectively, the preparation of porous calcium phosphate ceramics and porous phosphorus Calcium phosphate cement. Using scanning electron microscopy observation of the pore structure of the specimen, measure its porosity, the use of X-ray diffraction analysis of their phase composition. The results of porous calcium phosphate ceramics and calcium phosphate bone cement porosity of 72% and 67%; pore size distribution at about 200μm and 280μm; hole walls there were a large number of aperture number of microns to tens of microns pore ; X-ray diffraction results show that porous calcium phosphate ceramics is composed of HA and β  TCP, bone cement composition of HA, α  TCP and β  TCP. Conclusion Test Preparation of porous calcium phosphate biomaterials for new bone ingrowth with a pore diameter, porosity and good biocompatibility. Keywords: porous calcium phosphate ceramics; bone cement; microporous; biocompatibility Preparation and Characteration of Porous Calcium Phosphate Bioactive Material for Bone Tissue Engineering 【Abstract】 Objective To prepare the adaptive porous calcium phosphate bioactive material. Methods The hydroxyapatite / tricalcium phosphate biphasic powder was synthesized by the wet co  precipitation method. Then polymer sponge immersion method and appropriate progeny were used to prepare porous calcium phosphate (CaP) . The morphology and structure of CaP ceramics and CPC were observed by scanning electronic microscopy (SEM). Their phase composition were analyzed by X  ray diffraction (XRD). Results Th

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