双孔结构70Poly(50乳酸-co- 50甘草酸)/30(60SiO2-40CaQ)生物活性可降解复合材料的合成

Jeong-Cheol Lee, I. Song, Suk-Young Kim, S. Rhee
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摘要

采用气胀法制备了具有双孔结构的70聚(50乳酸-co-50甘草酸)/30(60SiO2-40CaO)复合材料,具有生物活性和可降解性。以正硅酸四乙酯和四水合硝酸钙为原料,在硝酸条件下采用溶胶-凝胶法制备了具有生物活性的60SiO2-40CaO粉体,并在900℃下热处理1 h,以1,1,3,3-六氟-2-丙醇为溶剂,采用溶剂铸造法制备了70聚(50乳酸-co-50甘草酸)/30(60SiO2-40CaO)复合材料。将盘状70聚(50乳酸-co-50甘酸)/30(60SiO2-40CaO)复合材料装入特制的高压气室,然后注入二氧化碳气体,直至最终压力达到20 MPa。加载1天后,二氧化碳气体迅速释放。用FE-SEM观察样品,用x射线衍射仪测定样品的物相,并在模拟体液中测定样品的生物活性。结果表明,释放二氧化碳气体后,聚(50乳酸-co-50甘草酸)基质中形成双孔结构,并观察到60个sio2 - 40cao颗粒在聚(50乳酸-co-50甘草酸)基质中随机分布。在模拟体液中浸泡1周后,复合材料表面形成片状低晶羟基碳酸盐磷灰石。该结果的实际意义是,由于其生物活性和可降解性,它具有作为骨组织工程支架材料的良好潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of a bioactive and degradable 70Poly(50Lactic-co-50Glycoric acid)/30(60SiO2-40CaQ) composite with dual pore structure
The bioactive and degradable 70poly(50lactic-co-50glycoric acid)/30(60SiO2-40CaO) composite, which had a dual pore structure, was synthesized by a gas expansion method. The bioactive 60SiO2-40CaO powders were prepared through a sol-gel method from tetraethyl orthosilicate and calcium nitrate tetrahydrate under nitric acidic condition followed by the heat treatment at 900°C for 1 h. The 70poly(50lactic-co-50glycoric acid)/30(60SiO2-40CaO) composite was then synthesized by a solvent casting method using 1,1,3,3-hexafluoro-2-propanol as a solvent. The disk-shaped 70poly(50lactic-co-50glycoric acid)/30(60SiO2-40CaO) composite was loaded into the custom-made high-pressure gas chamber and then carbon dioxide gas was introduced until achieving a final pressure of 20 MPa. After 1 day of loading, the carbon dioxide gas was released rapidly. The samples were observed by FE-SEM, the phase was evaluated by X-ray diffractometer, and its bioactivity was assessed in simulated body fluid. As a result, double pore structure was developed in the poly(50lactic-co-50glycoric acid) matrix after releasing the carbon dioxide gas and 60SiO2-40CaO particles were observed to place randomly among the poly(50lactic-co-50glycoric acid) matrix. After soaking in simulated body fluid for 1 week, flake-like low crystalline hydroxyl carbonate apatite was formed on the surface of the composite. The practical implication of the results is that it has promising potential for use as a scaffold material for bone tissue engineering due to its bioactivity and degradability.
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