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In vitro and Mechanical Properties of Bioactive- Glass/polymer Composites

机译:生物活性玻璃/聚合物复合材料的体外和力学性能

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摘要

Polymer/bioactive glass composites are getting more interest nowadays in bone tissue engineering and orthopedic applications where polymers are used as matrix material and bioactive glasses are used as either filler material or as coating. The idea of combining bioactive glasses with biodegradable polymers is to develop composites that takes an advantages of osteoconductive properties of bioactive glasses and their strengthening effect on polymer matrices. Such composites are expected to have superior mechanical properties than the neat unreinforced polymer and to improve structural integrity and flexibility over brittle glasses for eventual load-bearing applications.The thesis is based on composites consisting of PLA 70/30 as matrix polymer and bio-active glass as a filler material prepared by twin-screw extrusion method. The polymer matrix was combined with different weight percent of silicate and phosphate based bioactive glasses. Fourier Transform Infrared Spectroscopy (FTIR) was used to analyze the surface and structural changes in the composites upon immersion in the buffer solution. Mass change, water uptake measurement and FTIR indicates that with increasing the filling content the water absorption was increased. The changes were more drastic with the phosphate based composites compared to the silicate one. Ca release profile was analyzed by Atomic Absorption Spectroscopy (AAS) and was found to increase with immersion time. The mechanical properties of all investigated glasses were found to first decrease, as expected upon degradation of the composite. However, the bending strength increased after two weeks of immersion was unexpected, especially since the shear strength was not found to greatly change over the course of the test, and calls for more in-depth analysis. Finally, molecular weight of the polymer was found to decrease upon immersion up to two weeks and remained stable for longer immersion time in silicate based composite while in case of phosphate based composites, molecular weight was found to increase drastically after two weeks of immersion, raising the question of the impact of P release on the cross linking of the polymer chains. Overall a 30 weight % of glass within the composite was found to be optimum to maintain high mechanical properties, ductility, while providing significant Ca release, promising indication of the bioactivity.
机译:如今,聚合物/生物活性玻璃复合材料在骨组织工程和骨科应用中越来越受到关注,其中聚合物被用作基质材料,而生物活性玻璃被用作填充材料或涂层。将生物活性玻璃与可生物降解的聚合物结合在一起的想法是开发一种复合材料,该复合材料具有生物活性玻璃的骨传导特性及其对聚合物基质的增强作用的优点。预期这种复合材料比纯净的非增强聚合物具有更好的机械性能,并且比脆性玻璃具有更好的结构完整性和柔韧性,从而最终可用于承重应用。本文基于由PLA 70/30作为基质聚合物和生物活性成分的复合材料通过双螺杆挤出法制备的玻璃作为填充材料。将聚合物基质与不同重量百分比的基于硅酸盐和磷酸盐的生物活性玻璃组合。傅里叶变换红外光谱(FTIR)用于分析复合材料在浸入缓冲溶液中后的表面和结构变化。质量变化,吸水率测量和FTIR表明,随着填充量的增加,吸水率增加。与硅酸盐相比,磷酸盐基复合材料的变化更为剧烈。通过原子吸收光谱法(AAS)分析了Ca的释放曲线,并发现其随浸入时间的增加而增加。发现所有被研究的玻璃的机械性能首先下降,这是复合材料降解所期望的。但是,浸泡两周后抗弯强度增加是出乎意料的,特别是因为未发现在整个测试过程中抗剪强度发生很大变化,因此需要进行更深入的分析。最后,发现该聚合物的分子量在浸入至两周后会降低,并且在硅酸盐基复合物中的浸入时间较长时保持稳定,而在磷酸盐基复合材料的情况下,浸入两周后分子量会急剧增加,从而升高P释放对聚合物链交联的影响的问题。总的来说,发现复合物中30重量%的玻璃是最佳的,以维持高机械性能,延展性,同时提供显着的Ca释放,有望证明其具有生物活性。

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    Ghimire Srijana;

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  • 年度 2016
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