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<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>Pharmaceutical Sciences</JournalTitle>
      <Issn>1735-403X</Issn>
      <Volume>21</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2015</Year>
        <Month>11</Month>
        <DAY>30</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Solubility of Sodium Phenytoin in Propylene Glycol + Water Mixtures in the Presence of B-Cyclodextrin</ArticleTitle>
    <FirstPage>152</FirstPage>
    <LastPage>156</LastPage>
    <ELocationID EIdType="doi">10.15171/PS.2015.30</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Arezoo</FirstName>
        <LastName>Mabhoot</LastName>
      </Author>
      <Author>
        <FirstName>Abolghasem</FirstName>
        <LastName>Jouyban</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/PS.2015.30</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>08</Month>
        <Day>31</Day>
      </PubDate>
    </History>
    <Abstract>Poor aqueous solubility of drugs is still a challenging aspect in drug discovery and development. Solubilization techniques such as cosolvency and complexation are used to solubilize poorly soluble drugs. A number of mathematical models presented for predicting the solubility of drugs in water+cosolvent mixtures and the Jouyban-Acree model promises more accuracy when compared with other algorithms. Methods: Solubility of sodium phenytoin in binary mixtures of propylene glycol + water in the presence of beta-cyclodextrin (b-CD) along with the solubility of sodium phenytoin in this solvent mixture in the absence of b-CD using saturating shake flask method were studied. The generated solubility data was fitted to the Jouyban-Acree model and the solubility profile of drug in the presence of b-CD was compared with solubility data in the absence of b-CD. Results: The solubility was increased by addition of propylene glycol and was decreased by addition of beta-cyclodextrin. The measured solubility data were used to evaluate the correlation ability of the Jouyban-Acree model employing the solubility data in monosolvent. These findings are supported by acceptable mean relative deviations values obtained when comparing the estimated and experimental solubilities. Conclusion: The addition of b-CD was decreased the solubilization power of propylene glycol.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">sodium phenytoin</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">propylene glycol</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">cyclodextrin</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>