Development of a dialysis in vitro release method for biodegradable microspheres

被引：6

作者：

D'Souza S.S. ^{[1
]}

DeLuca P.P. ^{[1
,2
]}

机构：

[1] University of Kentucky, College of Pharmacy, Lexington

[2] Faculty of Pharmaceutical Sciences, University of Kentucky, College of Pharmacy, Lexington

来源：

AAPS PharmSciTech | / 6卷 / 2期

关键词：

Biodegradable microspheres; Dialysis; In vitro release methods;

D O I：

10.1208/pt060242

中图分类号：

学科分类号：

摘要：

The purpose of this research was to develop a simple and convenient in vitro release method for biodegradable microspheres using a commercially available dialyzer. A 25 KD MWCO Float-a-Lyzer was used to evaluate peptide diffusion at 37°C and 55°C in different buffers and assess the effect of peptide concentration. In vitro release of Leuprolide from PLGA microspheres, having a 1-month duration of action, was assessed using the dialyzer and compared with the commonly used sample and separate method with and without agitation. Peptide diffusion through the dialysis membrane was rapid at 37°C and 55°C in all buffers and was independent of peptide concentration. There was no detectable binding to the membrane under the conditions of the study. In vitro release of Leuprolide from PLGA microspheres was tri-phasic and was complete in 28 days with the dialysis technique. With the sample and separate technique, linear release profiles were obtained with complete release occurring under conditions of agitation. Diffusion through the dialysis membrane was sufficiently rapid to qualify the Float-a-Lyzer for an in vitro release system for microparticulate dosage forms. Membrane characteristics render it useful to study drug release under real-time and accelerated conditions. Copyright ©2003. All Rights Reserved.

引用

页数：9

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