Development and validation of a LC-ESI-MS/MS method for simultaneous quantification of olmesartan and hydrochlothiazide in human K3 EDTA plasma and its application to pharmacokinetic biostudy-Reference-Cited by-同舟云学术

Development and validation of a LC-ESI-MS/MS method for simultaneous quantification of olmesartan and hydrochlothiazide in human K3 EDTA plasma and its application to pharmacokinetic biostudy

Published:2013-10-29 Issue:1 Volume:31 Page:6-23
ISSN:1060-1333
Container-title:Clinical Research and Regulatory Affairs
language:en
Short-container-title:Clinical Research and Regulatory Affairs

Author:

Kumar Ajay,Prasad Verma Priya Ranjan,Monif Tausif,Khuroo Arshad H.,Iyer Sunil S.

Publisher

Informa UK Limited

Subject

Pharmacology (medical),Pharmaceutical Science,Pharmacology

Link

http://www.tandfonline.com/doi/pdf/10.3109/10601333.2013.849267

Reference17 articles.

1. Pharmacokinetic Estimation of Losartan, Losartan Carboxylic Acid and Hydrochlorothiazide in Human Plasma by LC/MS/MS Validated Method

2. 2003 European Society of Hypertension???European Society of Cardiology guidelines for the management of arterial hypertension*

3. Evaluation of antihypertensive therapy with the combination of olmesartan medoxomil and hydrochlorothiazide

4. Olmesartan medoxomil combined with hydrochlorothiazide for the treatment of hypertension

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