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Preparation of hybrid biomaterials for bone tissue engineering

机译:用于骨组织工程的混合生物材料的制备

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Tissue engineering has evolved from the use of biomaterials for bone substitution that fulfill the clinical demands of biocompatibility, biodegradability, non-immunogeneity, structural strength and porosity. Porous scaffolds have been developed in many forms and materials, but few reached the need of adequate physical, biological and mechanical properties. In the present paper we report the preparation of hybrid porous polyvinyl alcohol (PVA)/bioactive glass through the sol-gel route, using partially and fully hydrolyzed polyvinyl alcohol, and perform structural characterization. Hybrids containing PVA and bioactive glass with composition 58SiO2-33CaO-9P2O5 were synthesized by foaming a mixture of polymer solution and bioactive glass sol-gel precursor solution. Sol-gel solution was prepared from mixing tetraethoxysilane (TEOS), triethylphosphate (TEP), and calcium chloride as chemical precursors. The hybrid composites obtained after aging and drying at low temperature were chemically and morphologically characterized through infrared spectroscopy and scanning electron microscopy. The degree of hydrolysis of PVA, concentration of PVA solution and different PVA-bioglass composition ratios affect the synthesis procedure. Synthesis parameters must be very well combined in order to allow foaming and gelation. The hybrid scaffolds obtained exhibited macroporous structure with pore size varying from 50 to 600 μm.
机译:组织工程学已经从使用生物材料进行骨替代发展而来,满足了生物相容性,生物降解性,非免疫原性,结构强度和孔隙度的临床需求。多孔支架已经以多种形式和材料被开发,但是很少有人达到足够的物理,生物学和机械性能的需要。在本文中,我们报告了使用部分和完全水解的聚乙烯醇通过溶胶-凝胶法制备混合多孔聚乙烯醇(PVA)/生物活性玻璃的方法,并进行了结构表征。通过使聚合物溶液和生物活性玻璃溶胶-凝胶前体溶液的混合物发泡,合成了含有PVA和生物活性玻璃的杂物,其成分为58SiO2-33CaO-9P2O5。溶胶-凝胶溶液是通过混合四乙氧基硅烷(TEOS),磷酸三乙酯(TEP)和氯化钙作为化学前体制备的。通过红外光谱和扫描电子显微镜对低温老化和干燥后获得的杂化复合材料进行化学和形态表征。 PVA的水解程度,PVA溶液的浓度和不同的PVA-生物玻璃组成比会影响合成过程。合成参数必须很好地结合起来才能发泡和凝胶化。获得的杂种支架表现出大孔结构,其孔径在50至600μm之间变化。

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