期刊
JOURNAL OF CHROMATOGRAPHIC SCIENCE
卷 -, 期 -, 页码 -出版社
OXFORD UNIV PRESS INC
DOI: 10.1093/chromsci/bmad001
关键词
-
A sensitive, selective, precise and stability-indicating HPTLC method was developed for simultaneous estimation of remogliflozin etabonate and vildagliptin and their degradation products. The method showed good separation on a silica gel G60F(254) pre-coated TLC plate using methanol:ethyl acetate:toluene:ammonia (1.5:4:4.5:0.1, v/v/v/v) as mobile phase and detection at 212 nm. Degradation studies in various stress conditions were conducted and the method also met the validation requirements by ICH. The method was successfully applied to tablets without interference from excipients and was considered highly selective.
A sensitive, selective, precise and stability-indicating high-performance thin-layer chromatographic (HPTLC) method is developed for the simultaneous estimation of remogliflozin etabonate and vildagliptin in the presence of their degradation products. The separation was performed in thin layer chromatography plate precoated with silica gel G60F(254). The mobile phase consists of methanol:ethyl acetate:toluene:ammonia (1.5:4:4.5:0.1, v/v/v/v). Detection and quantification are performed with densitometer at 212 nm. The R-f values of remogliflozin etabonate and vildagliptin are 0.53 and 0.42, respectively. Degradation studies for the two drugs were carried out in acidic, alkaline, neutral, oxidative, photolytic and thermal stress conditions and analyzed. The suitability of this method for the quantitative determination of the compounds is proved by validation in accordance with the requirements laid down by International Conference on Harmonization (ICH). Linearity was found over the concentration range of 200-1000 ng/band with correlation coefficient of 0.9936 for remogliflozin etabonate and 100-500 ng/band with correlation coefficient of 0.9912 for vildagliptin. The method was successively applied to tablets containing two drugs and found to have no chromatographic interferences from the tablet excipients. The degradant formed was not interfering with estimation of two drugs makes the method more selective for the purpose intended.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据