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首页> 外文期刊>Acta biomaterialia >In vivo degradation of calcium phosphate cement incorporated into biodegradable microspheres.
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In vivo degradation of calcium phosphate cement incorporated into biodegradable microspheres.

机译:掺入可生物降解微球的磷酸钙水泥的体内降解。

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摘要

In this study we have investigated the influence of the mechanism of microsphere degradation or erosion on the in vivo degradation of microsphere/calcium phosphate cement composites (microsphere CPCs) used in tissue engineering. Microspheres composed of poly(lactic-co-glycolic acid) (PLGA), gelatin and poly(trimethylene carbonate) (PTMC) were used as the model and the resulting microsphere CPCs were implanted subcutaneously for 4, 8 or 12weeks in the back of New Zealand white rabbits. Besides degradation, the soft tissue response to these formulations was evaluated. After retrieval, specimens were analyzed by physicochemical characterization and histological analysis. The results showed that all microsphere CPCs exhibited microsphere degradation after 12weeks of subcutaneous implantation, which was accompanied by decreasing compression strength. The PLGA microspheres exhibited bulk erosion simultaneously throughout the whole composite, whereas the gelatin type B microspheres were degradated from the outside to the center of the composite. High molecular weight PTMC microspheres exhibited surface erosion resulting in decreasing microsphere size. Furthermore, all composites showed a similar tissue response, with decreasing capsule thickness over time and a persistent moderate inflammatory response at the implant interface. In conclusion, microsphere CPCs can be used to generate porous scaffolds in an in vivo environment after degradation of microspheres by various degradation/erosion mechanisms.
机译:在这项研究中,我们研究了微球降解或侵蚀机制对组织工程中使用的微球/磷酸钙水泥复合材料(微球CPC)的体内降解的影响。将由聚乳酸-乙醇酸(PLGA),明胶和聚碳酸三亚甲基酯(PTMC)组成的微球作为模型,并将所得微球CPC皮下植入New Back的第4、8或12周。新西兰白兔。除了降解之外,还评估了软组织对这些制剂的反应。取回后,通过理化特征和组织学分析对标本进行分析。结果表明,皮下植入12周后,所有微球CPC均表现出微球降解,并伴有压缩强度降低。 PLGA微球在整个复合材料中同时表现出整体侵蚀,而明胶B型微球则从复合材料的外部降解到中心。高分子量PTMC微球表现出表面侵蚀,从而导致微球尺寸减小。此外,所有复合材料均表现出相似的组织反应,随着时间的推移胶囊厚度逐渐减小,并且植入物界面持续出现中度炎症反应。总之,在通过各种降解/侵蚀机制降解微球后,微球CPC可用于在体内环境中生成多孔支架。

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