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采用复乳溶剂挥发法制备含油包水型乳液的聚(D,L-乳酸)和聚(D,L-乳酸-共-乙醇酸)多相微球。

Preparation of multi-phase microspheres of poly(D,L-lactic acid) and poly(D,L-lactic-co-glycolic acid) containing a W/O emulsion by a multiple emulsion solvent evaporation technique.

作者信息

Iwata M, McGinity J W

机构信息

Department of Pharmaceutical Technology, Dainippon Pharmaceutical Co. Ltd, Osaka, Japan.

出版信息

J Microencapsul. 1992 Apr-Jun;9(2):201-14. doi: 10.3109/02652049109021237.

Abstract

Multi-phase microspheres of poly(D,L-lactic acid) (PLA) or poly(D,L-lactic-co-glycolic acid) (PLGA) containing a water-in-oil (W/O) emulsion were prepared by a multiple emulsion solvent evaporation technique. Acetonitrile was used as the solvent for the polymers and light mineral oil as the dispersion medium for the encapsulation procedure. Process and formulation parameters to optimize the microencapsulation of a W/O emulsion containing water-soluble drugs were investigated. Drug loading efficiencies of 80-100 per cent were obtained under specific preparative conditions. The drug loading efficiency in the microspheres was dependent upon the ratio of the W/O emulsion to polymer and the concentration of surfactant in the mineral oil. Compared to conventional microspheres, in which fine drug particles are homogeneously dispersed in the polymer beads, the multi-phase microspheres permit the higher encapsulation efficiency of water-soluble drugs and eliminate partitioning into the polymer-acetonitrile phase which results in low encapsulation efficiency with conventional solvent evaporation techniques.

摘要

通过复乳溶剂蒸发技术制备了含有油包水(W/O)乳液的聚(D,L-乳酸)(PLA)或聚(D,L-乳酸-共-乙醇酸)(PLGA)多相微球。乙腈用作聚合物的溶剂,轻质矿物油用作包封过程的分散介质。研究了优化含水溶性药物的W/O乳液微囊化的工艺和配方参数。在特定的制备条件下,药物负载效率达到80%-100%。微球中的药物负载效率取决于W/O乳液与聚合物的比例以及矿物油中表面活性剂的浓度。与传统微球(其中细药物颗粒均匀分散在聚合物珠粒中)相比,多相微球允许更高的水溶性药物包封效率,并消除了药物分配到聚合物-乙腈相中,而这会导致传统溶剂蒸发技术的包封效率较低。

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