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J Pharm Biomed Anal ; 26(1): 7-14, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11451637

ABSTRACT

A sensitive high-performance liquid chromatographic assay for the quantitative determination of gemfibrozil is described in this work. Ibuprofen was used as internal standard. The assay involved a single cyclohexane extraction and LC analysis with fluorescence detection. Chromatography was performed at 40 degrees C on a Hypersil ODS column. The mobile phase was a mixture of a solution of phosphoric acid 0.4% and acetonitrile (45:55). The method was validated. The detection limit of this method was 0.025 microg ml(-1); only 0.5 ml of the plasma sample was required for the determination. The calibration graph was linear from 0.05 to 0.5 microg ml(-1) and required a cubic equation from 0.5 to 30 microg ml(-1). Intra and inter-day precision (C.V.) did no exceed 15%. Mean recoveries were of 90.15+/-6.9% (C.V.'s<8%) for gemfibrozil and 93.10% for ibuprofen Applicability of the method was demonstrated by a pharmacokinetic study in normal volunteers who received gemfibrozil by oral route.


Subject(s)
Chromatography, High Pressure Liquid/methods , Gemfibrozil/blood , Hypolipidemic Agents/blood , Area Under Curve , Drug Stability , Gemfibrozil/pharmacokinetics , Humans , Hypolipidemic Agents/pharmacokinetics
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