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首页> 外文期刊>Journal of Colloid and Interface Science >Preparation of uniform-sized PELA microspheres with high encapsulation efficiency of antigen by premix membrane emulsification
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Preparation of uniform-sized PELA microspheres with high encapsulation efficiency of antigen by premix membrane emulsification

机译:通过预混膜乳化制备具有高抗原包封率的均一尺寸的PELA微球

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Relatively uniform-sized poly(lactide-co-ethylene glycol) (PELA) microspheres with high encapsulation efficiency were prepared rapidly by a novel method combining emulsion-solvent extraction and premix membrane emulsification. Briefly, preparation of coarse double emulsions was followed by additional premix membrane emulsification, and antigen-loaded microspheres were obtained by further solidification. Under the optimum condition, the particle size was about 1 pm and the coefficient of variation (CV) value was 18.9%. Confocal laser scanning microscope and flow cytometer analysis showed that the inner droplets were small and evenly dispersed and the antigen was loaded uniformly in each microsphere when sonication technique was occupied to prepare primary emulsion. Distribution pattern of PEG segment played important role on the properties of microspheres. Compared with triblock copolymer PLA-PEG-PLA, the diblock copolymer PLA-mPEG yielded a more stable interfacial layer at the interface of oil and water phase, and thus was more Suitable to stabilize primary emulsion and protect coalescence of inner droplets and external water phase, resulting in high encapsulation efficiency (90.4%). On the other hand, solidification rate determined the time for coalescence during microspheres fabrication, and thus affected encapsulation efficiency. Taken together, improving the polymer properties and solidification rate are considered as two effective strategies to yield high encapsulation. (c) 2008 Elsevier Inc. All rights reserved.
机译:采用乳液-溶剂萃取与预混膜乳化相结合的新方法,快速制备了具有较高包封率的相对均匀大小的聚乳酸-丙二醇(PELA)微球。简而言之,在制备粗制双乳状液后再进行预混膜乳化,并通过进一步固化获得负载抗原的微球。在最佳条件下,粒径约为1 pm,变异系数(CV)值为18.9%。共聚焦激光扫描显微镜和流式细胞仪分析表明,当采用超声处理技术制备初级乳剂时,内部液滴很小且分散均匀,抗原均匀地负载在每个微球中。 PEG片段的分布方式对微球的性质起着重要作用。与三嵌段共聚物PLA-PEG-PLA相比,二嵌段共聚物PLA-mPEG在油和水相界面处产生更稳定的界面层,因此更适合稳定初级乳液并保护内部液滴和外部水相的聚结。 ,因此封装效率很高(90.4%)。另一方面,固化速率决定了微球制备过程中的聚结时间,因此影响了包封效率。综上所述,改善聚合物性能和固化速率被认为是实现高封装的两种有效策略。 (c)2008 Elsevier Inc.保留所有权利。

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