Development and Validation of a Stability-Indicating Liquid Chromatographic Method for Estimating Olmesartan Medoxomil Using Quality by Design-Reference-Cited by-同舟云学术

Development and Validation of a Stability-Indicating Liquid Chromatographic Method for Estimating Olmesartan Medoxomil Using Quality by Design

Published:2015-01-12 Issue:7 Volume:53 Page:1048-1059
ISSN:0021-9665
Container-title:Journal of Chromatographic Science
language:en
Short-container-title:J Chromatogr Sci

Author:

Beg Sarwar,Sharma Gajanand,Katare O.P.,Lohan Shikha,Singh Bhupinder

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Analytical Chemistry

Link

http://academic.oup.com/chromsci/article-pdf/53/7/1048/1031657/bmu165.pdf

Reference42 articles.

1. Brunner H.R. ; The new oral angiotensin II antagonist olmesartan medoxomil: a concise overview; Journal of Human Hypertension, (2002); 16: S13–S16.

2. The pharmacokinetic and metabolic profile of olmesartan medoxomil limits the risk of clinically relevant drug interaction

3. Olmesartan medoxomil: current status of its use in monotherapy

4. The relative bioavailability and fasting pharmacokinetics of three formulations of olmesartan medoxomil 20-mg capsules and tablets in healthy Chinese male volunteers: An open-label, randomized-sequence, single-dose, three-way crossover study

5. Raghunathan K. Reddy J.M. Manasa R. ; Stability indicating RP-HPLC method development and validation of Olmesartan medoxomil; Asian Journal of Pharmaceutical and Biological Research, (2011); 1: 79–86.

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