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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">AJPTR36056</article-id>
      <title-group>
        <article-title>Formulation and Evaluation of Proniosomal Gel of Flurbiprofen</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Chandra</surname>
            <given-names>Dinesh</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Kumar</surname>
            <given-names>Ashish</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>singh</surname>
            <given-names>Rakesh</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Raj</surname>
            <given-names>Tirth</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Verma</surname>
            <given-names>Jayant Kumar Maurya1  Shrikant</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date pub-type="epub" iso-8601-date="2013-12-01">
        <month>12</month>
        <day>01</day>
        <year>2013</year>
      </pub-date>
      <volume>3</volume>
      <issue>6</issue>
      <abstract>
        <p>The aim of present study,  To formulate and characterized  proniosome contain flurbiprofen in a gel formulation for the treatment of rheumatoid arthritis and enhanced skin targeted effect, sustained &amp; prolonged drug release, enhanced skin bioavailability by using different type of non ionic surfactant &amp; cholesterol. The batches were designed using Box Behnken Design and prepared by coacervation phase separation method. Optimized formulation (PNGopt) showed drug entrapment efficiency of 74.46% and particle size 215nm. In-vitro drug release from PNGopt was found to be 84.15 in 24 hrs. The In-vitro drug release was best explained by zero order kinetics as the plot showed highest linearity and release was governed by Quasi Fickian diffusion.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Proniosomes</kwd>
        <kwd>Flurbiprofen</kwd>
        <kwd>Brij93</kwd>
        <kwd>in-vitro release</kwd>
        <kwd>Stability  studies</kwd>
      </kwd-group>
    </article-meta>
  </front>
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