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Pharmacokinetic Evaluation of Metolazone Tablets using healthy Human Volunteers

Basvan Babu*, Selvadurai Muralidharan, Subramaniya Nainar Meyyanathan and
Bhojraj Suresh
Department of Pharmaceutical Analysis, J.S.S.College of Pharmacy, (Off Campus of JSS University, Mysore) Ootacamund, Rocklands, Ooty
*Corresponding author: Dr. Basvan Babu,
Department of Pharmaceutical Analysis,
J.S.S.College of pharmacy, Tamilnadu, India,
Tel: +91-423- 2443393,
Fax: +91-423-2442937,
E-mail: thammababu@yahoo.co.in
Received November 25, 2009; Accepted December 22, 2009; Published December 22, 2009
Citation: Babu B, Muralidharan S, Meyyanathan SN, Suresh B (2009) Pharmacokinetic Evaluation of Metolazone Tablets using healthy Human Volunteers. J Bioanal Biomed 1: 039-040. doi:10.4172/1948-593X.1000008
Copyright: © 2009 Babu B, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
A sensitive and reproducible high performance liquid chromatography (HPLC) method has been developed and validated for the quantification of metolazone in human plasma, after solid phase extraction (SPE). A Good resolution was achieved on a reverse-phase LichroCART Purospher® C18 column using the mobile phase acetonitrile– 0.5% triethylamine (35:65) in isocratic elution with a total run time of 15 min. The analyte, metolazone, was detected by using high performance liquid chromatography with the support of photo diode array detector. Limit of detection and Lower limit of quantification was found to be 1 and 2.5 ng/mL. The present method was successfully applied in the pharmacokinetic study of metolazone in human plasma.
 
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