Preparation of microspheres by the solvent evaporation technique

被引:622
作者
ODonnell, PB [1 ]
McGinity, JW [1 ]
机构
[1] UNIV TEXAS,COLL PHARM,DRUG DYNAM INST,AUSTIN,TX 78712
关键词
microspheres; solvent evaporation; water soluble compounds; peptides; proteins; multiple emulsion;
D O I
10.1016/S0169-409X(97)00049-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The microencapsulation process in which the removal of the hydrophobic polymer solvent is achieved by evaporation has been widely reported in recent years for the preparation of microspheres and microcapsules based on biodegradable polymers and copolymers of hydroxy acids. The properties of biodegradable microspheres of poly(lactic acid) (PLA) and poly(lactic-co-glycolic acid) (PLGA) have been extensively investigated. The encapsulation of highly water soluble compounds including proteins and peptides presents formidable challenges to the researcher. The successful encapsulation of such entities requires high drug loading in the microspheres, prevention of protein degradation by the encapsulation method, and predictable release of the drug compound from the microspheres. To achieve these goals, multiple emulsion techniques and other innovative modifications have been made to the conventional solvent evaporation process. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:25 / 42
页数:18
相关论文
共 76 条
[1]  
Aftabrouchad C., 1992, STP PHARMA SCI, V2, P365
[2]  
ALPAR HO, 1994, EUR J PHARM BIOPHARM, V40, P198
[3]   CLINICAL-EVALUATION OF INJECTABLE BIODEGRADABLE CONTRACEPTIVE SYSTEM [J].
BECK, LR ;
RAMOS, RA ;
FLOWERS, CE ;
LOPEZ, GZ ;
LEWIS, DH ;
COWSAR, DR .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1981, 140 (07) :799-806
[4]  
BENOIT JP, 1996, P INT S CONTR REL BI, P379
[5]  
BITZ C, 1995, WORLD M PHARM BIOPH, P409
[6]   SOLVENT SELECTION IN THE PREPARATION OF POLY(DL-LACTIDE) MICROSPHERES PREPARED BY THE SOLVENT EVAPORATION METHOD [J].
BODMEIER, R ;
MCGINITY, JW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1988, 43 (1-2) :179-186
[7]   THE EFFECT OF THE ADDITION OF LOW-MOLECULAR WEIGHT POLY(DL-LACTIDE) ON DRUG RELEASE FROM BIODEGRADABLE POLY(DL-LACTIDE) DRUG DELIVERY SYSTEMS [J].
BODMEIER, R ;
OH, KH ;
CHEN, H .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 51 (01) :1-8
[10]   THE PREPARATION AND EVALUATION OF DRUG-CONTAINING POLY(DL-LACTIDE) MICROSPHERES FORMED BY THE SOLVENT EVAPORATION METHOD [J].
BODMEIER, R ;
MCGINITY, JW .
PHARMACEUTICAL RESEARCH, 1987, 4 (06) :465-471