<?xml version="1.0"?>
<Articles JournalTitle="Acta Medica Iranica">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Acta Medica Iranica</JournalTitle>
      <Issn>0044-6025</Issn>
      <Volume>45</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2007</Year>
        <Month>04</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">SIMPLE AND RAPID GAS-CHROMATOGRAPHIC METHOD FOR QUANTITATION OF TOTAL AND FREE VALPROIC ACID IN HUMAN SERUM</title>
    <FirstPage>85</FirstPage>
    <LastPage>90</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>H. R. Falahat-Pisheh</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>T. R. Neyestani  M. Bigdeli</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>09</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Valproic acid (VPA) is one of the mostly used antiepileptic drugs that may have some side effects so, it is highly recommended to evaluate its serum concentrations. The aim of this study was to develop a simple, fast and economic method using gas-chromatography equipped with flame ionization detector (GC/FID) and VPA analysis. To do this, 200 &#xB5;l of serum was mixed with an aliquot of caproic acid (200 &#xB5;L, methanolic solution) as internal standard and extracted by stepwise addition of hydrochloric acid and chloroform with slight agitation between each step. After centrifugation, 1.0 &#xB5;l of the bottom layer was injected into a wide-bore nonpolar capillary column. Injectable samples for analysis of unbonded VPA were prepared by ultra filtration followed by solid phase extraction (SPE). Caproic acid and VPA were eluted after 1.5 min and 3.0 min, respectively (total GC run time about 3.2 minutes). This GC/FID method was linear over a range of 2.5-6400 &#xB5;g/ml with the mean recovery of 92%. The intra- and inter-assay precision in the range of 25-100 &#xB5;g/ml was 1.50-, 2.95, and 2.35- 3.22%, respectively. The simplicity of sample preparation with no derivatization, short run-time and high sensitivity sufficient to detect low concentrations of the drug makes this method suitable for research as well as routine use.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/3248</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/3248/3226</pdf_url>
  </Article>
</Articles>
