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Effects of material hydrophobicity on physical properties of polymeric microspheres formed by double emulsion process

机译:材料疏水性对双乳液法制备聚合物微球物理性能的影响

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Human serum albumin (HSA) was encapsulated as a model protein in microspheres of biodegradable and biocompatible polymers by the water-in-oil-in-water (w/o/w) emulsion solvent extraction/evaporation (double emulsion) technique for purpose of controlled release. To improve the properties and control the rate of drug release of the delivery vehicle, materials with different hydrophobicity from that of their conventional counterparts, such as poly(lactide-co-ethylene glycol) (PELA) in place of poly(lactide-co-glycolide) (PLGA) as the polymer matrix, ethyl acetate/acetone in place of dichloride methane (DCM) as the (co)solvent and d-alpha tocopheryl polyethylene glycol 1000 succinate (vitamin E TPGS) as the additive, were used to prepare the microspheres. It has been found that PELA microspheres, compared with PLGA ones, were slightly smaller in size if prepared at identical emulsification strength. They had more porous surface and internal structure, higher encapsulation efficiency (EE) and more rapid in vitro release rate. Furthermore, the physical properties of the microspheres were also affected by the presence of solvents and additives and their properties. Our results suggest that these materials could have interesting potential applications in preparation of polymeric microspheres for controlled protein release. (C) 2002 Elsevier Science B.V. All rights reserved. [References: 28]
机译:通过将水包油包水(w / o / w)乳液溶剂萃取/蒸发(双重乳液)技术的目的,将人血清白蛋白(HSA)作为模型蛋白封装在可生物降解和生物相容性聚合物的微球中。控释。为了改善传递载体的特性并控制药物释放速率,具有不同于传统对应材料疏水性的材料,例如聚丙交酯-乙二醇共聚物(PELA)代替聚丙交酯-乙二醇乙交酯(PLGA)作为聚合物基质,用乙酸乙酯/丙酮代替二氯甲烷(DCM)作为(共)溶剂,并使用d-α生育酚聚乙二醇1000琥珀酸酯(维生素E TPGS)作为制备原料微球。已经发现,如果以相同的乳化强度制备,则PELA微球与PLGA微球相比尺寸稍小。它们具有更多的多孔表面和内部结构,更高的包封效率(EE)和更快的体外释放速率。此外,微球的物理性质还受到溶剂和添加剂的存在及其性质的影响。我们的结果表明,这些材料在制备可控蛋白质释放的聚合物微球方面可能具有有趣的潜在应用。 (C)2002 Elsevier Science B.V.保留所有权利。 [参考:28]

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