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    <depositor>
      <depositor_name>Editor</depositor_name>
      <email_address>editor.jddt@gmail.com</email_address>
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    <registrant>UJPR</registrant>
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    <journal>
      <journal_metadata>
        <full_title>Universal Journal of Pharmaceutical Research</full_title>
        <abbrev_title>Univ J Pharm Res</abbrev_title>
        <issn media_type="electronic">2456-8058</issn>
      </journal_metadata>
      <journal_issue>
        <publication_date media_type="online">
          <month>04</month>
          <day>11</day>
          <year>2018</year>
        </publication_date>
      </journal_issue>
      <journal_article xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1" publication_type="full_text" metadata_distribution_opts="any">
        <titles>
          <title>TOLNAFTATE LOADED LIPOSOMES- DESIGN, AND IN-VITRO EVALUATION</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first">
            <given_name>Dingwoke Francis</given_name>
            <surname>John</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Unus A</given_name>
            <surname>A</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Udokwu Japheth</given_name>
            <surname>Chigbo</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Ugwoke Sunday</given_name>
            <surname>Paul</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Ezeaku</given_name>
            <surname>Ikenna</surname>
          </person_name>
        </contributors>
        <jats:abstract xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1">
          <jats:p>Liposomes are colloidal particles formed as concentric bimolecular layers that are capable of encapsulating drugs. Liposomes have the potential for extending the duration of action for days or months. Tolnaftate  is is used as the topical antifungal agent.  The purpose of this study was to provide the delivery of the topical drug at a sustained rate across intact skin to improve bioavailability.  In present study, four different liposomes  formulations of Tolnaftate were prepared by ethanol (solvent) injection method by varying the concentrations of phospholipids. The prepared liposomes were characterized for  size, shape, entrapment efficiency, zeta potential, in-vitro drug release. An in vitro drug release of about 82.114 % in 10 h was observed from optimum formulation of batch LS4.&#13;
Google Scholar</jats:p>
        </jats:abstract>
        <publication_date media_type="online">
          <month>11</month>
          <day>01</day>
          <year>2016</year>
        </publication_date>
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          <doi>10.22270/ujpr.v1i2.R6</doi>
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