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  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>American Journal of Pharmacy and Health Research</journal-title>
        <abbrev-journal-title abbrev-type="publisher">AJPHR</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2321-3647</issn>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">AJPHR17007</article-id>
      <title-group>
        <article-title>RP-HPLC Method Development and Validation of Telmisartan and Hydrochlorothiazide in Combination Dosage Form &lt;Tablets&gt;</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Bala</surname>
            <given-names>Saroj</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Mahatma</surname>
            <given-names>O.P.</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Azim</surname>
            <given-names>Md. Sabir</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date pub-type="epub" iso-8601-date="2013-10-01">
        <month>10</month>
        <day>01</day>
        <year>2013</year>
      </pub-date>
      <volume>1</volume>
      <issue>7</issue>
      <abstract>
        <p>A simple, accurate, precise and fast reverse phase, gradient RP-HPLC method was developed for the separation of telmisartan and hydrochlorothiazide in combination dosage form of Tablets. The method was carried out by using Kromasil, C18, 4.6 x 150mm, 5 μm enhanced polar selectivity column and mobile phase comprised of potassium dihydrogen phosphate buffer pH adjusted to 3.2 ± 0.5 with orthophosphoric acid and acetonitrile, and degassed under ultrasonication. The flow rate was 1.5 mL/min and the effluent was monitored at 225nm. The retention time of hydrochlorothiazide and telmisartan were 2.7 ± 0.5 and 7.3 ± 0.5 respectively. The method was validated as per ICH guideline. The proposed method is suitable for simultaneous determination of telmisartan and hydrochlorothiazide in pharmaceutical dosage form.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Telmisartan</kwd>
        <kwd>Hydrochlorothiazide</kwd>
        <kwd>RP-HPLC</kwd>
        <kwd>Kromasil</kwd>
        <kwd>ICH Guideline.</kwd>
      </kwd-group>
    </article-meta>
  </front>
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