HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF RIFAMPIN AND RELATED IMPURITIES IN PHARMACEUTICAL FORMULATIONS

被引:11
作者
GRAHAM, KC
LEBELLE, MJ
WILSON, WL
机构
[1] Drug Research Laboratories, Health Protection Branch, Health and Welfare Canada, Ottawa
来源
JOURNAL OF LIQUID CHROMATOGRAPHY | 1979年 / 2卷 / 03期
关键词
D O I
10.1080/01483917908060069
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High pressure liquid chromatography was employed for the assay of rifampin in capsules. A reverse phase RP-2 column and a mobile phase of 48% methanol, 5% tetrahydrofuran and 47% 0.05 M ammonium formate (pH 7.3) were used with detection at 254 nm. Rifampin was separated from all its major degradation products and quantitated. © 1979, Taylor & Francis Group, LLC. All rights reserved.
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页码:365 / 371
页数:7
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