Method Validation for Simultaneous Quantification of Olmesartan and Hydrochlorothiazide in Human Plasma Using LC-MS/MS and Its Application Through Bioequivalence Study in Healthy Volunteers

Author:

Kumar Arvind,Dwivedi Surya Prakash,Prasad Tulika

Publisher

Frontiers Media SA

Subject

Pharmacology (medical),Pharmacology

Reference31 articles.

1. LC-MS/MS method for simultaneous estimation of candesartan and hydrochlorothiazide in human plasma and its use in clinical pharmacokinetics;Bharathi;Bioanalysis,2012

2. Safety, tolerability, and efficacy of a fixed dose combination of olmesartan 40 mg and hydrochlorothiazide 12.5/25 mg in daily practice;Bramlage;Vasc. Health Risk Manag.,2013

3. Evaluation of antihypertensive therapy with the combination of olmesartan medoxomil and hydrochlorothiazide;Chrysant;Am. J. Hypertens.,2004

4. Validated reversed phase High Performance Liquid Chromatography method for simultaneous estimation of olmesartan medoxomil, hydrochlorothiazide and amlodipine besylate in newly designed pharmaceutical dosage forms;Doshi;Int. Res. J. Pharm.,2012

5. Simultaneous determination of amlodipine, valsartan and hydrochlorothiazide by LC–ESI-MS/MS and its application to pharmacokinetics in rats;Gadepalli;J. Pharm. Anal.,2014

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