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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>18</Volume><Issue>2</Issue></Journal><ArticleTitle>Development and validation of a rapid HPLC- fluorescence method for simultaneous determination of venlafaxine and its major metabolites in human plasma.</ArticleTitle><FirstPage>97</FirstPage><LastPage>102</LastPage><AuthorList><Author><FirstName>Y H</FirstName><LastName>Ardakani</LastName></Author><Author><FirstName>A</FirstName><LastName>Foroumadi</LastName></Author><Author><FirstName>M R</FirstName><LastName>Rouini</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>11</Month><Day>09</Day></PubDate></History><Abstract>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.Chromatographic separation was achieved with a ChromolithTM Performance RP-18e 100 mm×4.6 mm column equipped with a Fluorescence detectore (λ(ex) 200 nm/λ(em) 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.The calibration curves were linear in the concentration range of 1-300 ng/ml for all analytes (r2&gt;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.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.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/483</web_url></Article></Articles>
