Investigation on physicochemical and biological differences of cefpodoxime proxetil enantiomers

被引:10
|
作者
Kakumanu, Vasu Kumar
Arora, Vinod
Bansal, Arvind K.
机构
[1] NIPER, Dept Pharmaceut Technol Formulat, Punjab 160062, India
[2] Ranbaxy Res Labs, Gurgaon, Haryana, India
关键词
cefpodoxime proxetil; enantiomers; differences; enzymes; segments; regional metabolism; GIT; physicochemical; biological;
D O I
10.1016/j.ejpb.2006.05.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cefpodoxime proxetil (CP) is a prodrug of cefpodoxime acid (CA), and is supplied as racemic mixture of R- and S-enantiomers. CP has only 50% absolute bioavailability, and the reasons responsible for low bioavailability remain poorly understood. The present work ascertains physicochemical and biological properties of individual isomers of CP and explores their capacity to optimize delivery of CP. Both isomers showed similar pH stability behavior, but R-isomer was more susceptible to enzymatic metabolism compared to S-isomer, when incubated with enzymes collected from various segments of GIT. Based on the in vitro and in vivo results, use of S-isomer for development of a dosage form such as gastro-retentive dosage form can improve oral bioavailability of CP. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:255 / 259
页数:5
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