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DARU Journal of Pharmaceutical Sciences
2010;18(2) : 97-102
 
Original Article
Development and validation of a rapid HPLC- fluorescence method for simultaneous determination of venlafaxine and its major metabolites in human plasma

1Ardakani Y. H., 2Foroumadi A., *1Rouini M.R.

1Biopharmaceutics and Pharmacokinetics Division, Department of Pharmaceutics, Faculty of Pharmacy, 2Drug Design & Development Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Corresponding Author:
 

Rouini M.R

Received:September 9,2009
Accepted: February 15,2010
Available online:June 19,2010
Abstract:

 Background and the purpose of the study:To develop a simple, rapid and accurate HPLC method for the measurement of the venlafaxine and its main metabolites, O-desmethylvenlafaxine and O,N-didesmethylvenlafaxine in pharmacokinetic studies and therapeutic drug monitoring.Method: Chromatographic separation was achieved with a ChromolithTM Performance RP-18e 100 mm×4.6 mm column equipped with a Fluorescence detectore (λex 200 nm/λem 300 nm) The mobile phase of methanol:water (35:65, v/v) adjusted to pH 2.5 by phosphoric acid was passed through the column in an isocratic mode at flow rate of 2 ml/min. The sample preparation involved a simple, one-step, extraction with ethyl acetate.

Results:The calibration curves were linear in the concentration range of 1-300 ng/ml for all analytes (r2 > 0.998). The lower limit of quantification was 1 ng/ml for all analytes. Within and between day precisions in the measurement of quality control (QC) of samples were in the range of 1.8-14.1% for all analytes.

Conclusion:The developed procedure was used to assess the pharmacokinetics of venlafaxine and its main metabolites following oral administration of 75 mg venlafaxine to a healthy subject.

Keywords:
Venlafaxine ،  Metabolite ،  Pharmacokinetics ،  HPLC
Permanent Link: http://journals.tums.ac.ir/abs/15739
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