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Preparation and characterization of gelatin surface modified PLGA microspheres

机译:明胶表面修饰的PLGA微球的制备与表征

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摘要

This study optimized conditions for preparing and characterizing gelatin surface modified poly (lactic-co-glycolic acid) (PLGA) copolymer microspheres and determined this systems interaction with fibronectin. Some gelatin microspheres have an affinity for fibronectin-bearing surfaces; these miscrospheres exploit the interaction between gelatin and fibronectin. PLGA copolymer microspheres were selected because they have reproducible and slowrelease characteristics in vivo. The PLGA microspheres were surface modified with gelatin to impart fibronectin recognition. Dexamethasone was incorporated into these microspheres because dexamethasone is beneficial in chronic human diseases associated with extra fibronectin expression (eg, cardiovascular disease, inflammatory disorders, rheumatoid arthritis). The gelatin surface modified PLGA microspheres (prepared by adsorption, conjugation, and spray coating) were investigated and characterized by encapsulation efficiency, particle size, in vitro release, and affinity for fibronectin. The gelatincoated PLGA microspheres had higher interaction with fibronectin compared with the other gelatin surface modified PLGA microspheres (adsorption and conjugation). Dexamethasone was released slowly (over 21 days) from gelatin surface modified PLGA microspheres.
机译:这项研究优化了制备和表征明胶表面改性的聚乳酸-乙醇酸共聚物(PLGA)共聚物微球的条件,并确定了该系统与纤连蛋白的相互作用。一些明胶微球对带有纤连蛋白的表面具有亲和力。这些小球利用了明胶和纤连蛋白之间的相互作用。选择PLGA共聚物微球是因为它们在体内具有可重现和缓慢释放的特性。用明胶对PLGA微球进行表面修饰,以识别纤连蛋白。地塞米松被并入这些微球中是因为地塞米松对与多余的纤连蛋白表达有关的慢性人类疾病(例如心血管疾病,炎性疾病,类风湿性关节炎)有益。研究了明胶表面改性的PLGA微球(通过吸附,结合和喷涂制备),并通过包封效率,粒径,体外释放和对纤连蛋白的亲和力进行了表征。与其他明胶表面改性的PLGA微球相比,涂明胶的PLGA微球与纤连蛋白的相互作用更高(吸附和结合)。地塞米松从明胶表面修饰的PLGA微球中缓慢释放(超过21天)。

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