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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">AJPTR36038</article-id>
      <title-group>
        <article-title>Enantioselectivity Transport of Timolol Maleate Through Hairless Mice Skin is A Single-Valued Function of the Concentrations of Chiral Terpene Enhancer(D-Limonene)</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Afouna</surname>
            <given-names>Mohsen I.</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 purposes of the present study were: 1).To study the relationship between different concentrations of the chiral enhancer D-Limonene (D-LM) on the solubility of individual enantiomer and racemate Timolol maleate (TM). 2). To study the preferential enhancement of D-LM upon S-TM, R-TM, and racemate across the hairless mice skin. For solubility studies, excess of R-, S-, or racemate with wide-range of different concentrations of D-LM were prepared.  Samples were agitated, centrifuged and filtered and analyzed by HPLC using chiral column at 294nm.  For skin transport studies, formulations containing 0.5% solutions of S-TM, R-TM, or racemate in buffer solution with predetermined concentrations of D-LM were studied. Samples of 1-ml were withdrawn and quantitatively analyzed for their TM contents.  The steady-state fluxes (Jss), permeability coefficients and the enhancement factor were calculated. In solubility studies, D-LM significantly enhances solubility of all forms of TM in a concentration dependent manner.  In permeation studies, presence of D-LM significantly enhances the flux values of both enantiomers and racemate.  However, D-LM immensely increased all permeability characteristics of the S-isomer compared to those of R-isomer. Solubilities of all forms of TM were found to be a single-valued function of D-LM concentration. Moreover, addition of D-LM has enhanced the transport of S-, R-TM enantiomers and that of racemate across hairless mice skin.  For all tested formulations, the overall permeability characteristics of the therapeutically active TM (i.e., S-TM) were superior results obtained with the R-TM either as enantiomer or racemate.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Timolol</kwd>
        <kwd>Terpene</kwd>
        <kwd>Chiral</kwd>
        <kwd>Enhancer</kwd>
        <kwd>D-Limonene</kwd>
        <kwd>Enantioselective</kwd>
      </kwd-group>
    </article-meta>
  </front>
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