A validated ultra high-pressure liquid chromatography method for separation of candesartan cilexetil impurities and its degradents in drug product-Reference-Cited by-同舟云学术

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A validated ultra high-pressure liquid chromatography method for separation of candesartan cilexetil impurities and its degradents in drug product

Published:2012-01 Issue:1 Volume:3 Page:31-39
ISSN:2229-4708
Container-title:Pharmaceutical Methods
language:en
Short-container-title:Pharmaceutical Methods

Author:

Sudhakar Babu K.,Atchuta Kumar Namala Durga,Gosada Ullas,Sharma Nitish

Publisher

EManuscript Technologies

Subject

General Medicine

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Separation and Identification of Related Substances in Candesartan Cilexetil Tablets by UHPLC-Q-TOF–MS;Chromatographia;2023-02-17

2. Chemometric Methods for Simultaneous Determination of Candesartan Cilexetil and Hydrochlorothiazide in Binary Combinations;Journal of Analytical Methods in Chemistry;2023-01-17

3. Stability-indicating RP-UPLC method for determination of antihypertensive drugs and their degradation products in tablets: application to content uniformity and dissolution studies;Journal of the Iranian Chemical Society;2023-01-04

4. Separation and identification of related substances in Candesartan cilexetil tablets by UHPLC-Q- TOF-MS;2022-08-04

5. An Overview of Advances in the Chromatography of Drugs Impurity Profiling;Critical Reviews in Analytical Chemistry;2022-02-18

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