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  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>American Journal of PharmTech Research</journal-title>
        <abbrev-journal-title abbrev-type="publisher">AJPTR</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2249-3387</issn>
      <publisher>
        <publisher-name>undefined</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">AJPTR66027</article-id>
      <title-group>
        <article-title>Development and Validation of RP-HPLC Method for Simultaneous Determination of Ranolazine In Bulk and Pharmaceutical Dosage Form</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Sharmin</surname>
            <given-names>Farhana</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Akter</surname>
            <given-names>Mariyam</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Nipa</surname>
            <given-names>Jasmin Ara</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date pub-type="epub" iso-8601-date="2016-12-01">
        <month>12</month>
        <day>01</day>
        <year>2016</year>
      </pub-date>
      <volume>6</volume>
      <issue>6</issue>
      <abstract>
        <p>This present study was undertaken with an objective to develop &amp; validate a simple, precise, cost effective, sensitive &amp; fast RP- HPLC method for the analysis of Ranolazine. A Shimazu HPLC system with Luna 5µm C18 is employed for the analysis using Methanol: Acetonitrile(50:50, v/v) as mobile phase. Signal from Ranolazine is detected at 227nm by UV Spectrophotometer. The total retention time was 5 min with a flow rate of 1.0 ml/min. % 0f RSD values for precision is found to be 0.798%.The limits of detection (LOD) and quantification (LOQ) were 0.616 and 1.86, respectively. As per ICH guidelines the proposed method is fully validated and found to be linear over a workable drug concentration, accurate, precise and robust. This fast, simple and inexpensive method is suitable for research laboratories &amp; also for quality control analysis in pharmaceutical industries.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Ranolazine</kwd>
        <kwd>RP-HPLC</kwd>
        <kwd>Acetonitrile</kwd>
        <kwd>Linearity</kwd>
        <kwd>Validation.</kwd>
      </kwd-group>
    </article-meta>
  </front>
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