﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>Pharmaceutical Sciences</JournalTitle>
      <Issn>1735-403X</Issn>
      <Volume>23</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2017</Year>
        <Month>12</Month>
        <DAY>30</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Modelling the Preferential Solvation of Ferulic Acid in {2-Propanol (1) + Water (2)} Mixtures at 298.15 K</ArticleTitle>
    <FirstPage>330</FirstPage>
    <LastPage>334</LastPage>
    <ELocationID EIdType="doi">10.15171/PS.2017.48</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Abolghasem</FirstName>
        <LastName>Jouyban</LastName>
      </Author>
      <Author>
        <FirstName>Fleming</FirstName>
        <LastName>Martínez</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/PS.2017.48</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>09</Month>
        <Day>22</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>11</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <Abstract>Background: Recently Haq et al. reported the equilibrium solubility in {2-propanol (1) + water (2)} mixtures at several temperatures with some numerical correlation analysis. Nevertheless, no attempt was made to evaluate the preferential solvation of this compound by the solvents. Methods: Preferential solvation of ferulic acid in the saturated mixtures at 298.15 K was analyzed based on the inverse Kirkwood-Buff integrals as described in the literature. Results: Ferulic acid is preferentially solvated by water in water-rich mixtures (0.00 &lt; x1 &lt; 0.19) but preferentially solvated by 2-propanol in mixtures with composition 0.19 &lt; x1 &lt; 1.00. Conclusion: These results could be interpreted as a consequence of hydrophobic hydration around the non-polar groups of the solute in the former case (0.00 &lt; x1 &lt; 0.19). Moreover, in the last case (0.19 &lt; x1 &lt; 1.00), the observed trend could be a consequence of the acid behavior of ferulic acid in front to 2-propanol molecules because this cosolvent is more basic than water as described by the respective solvatochromic parameters.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Ferulic acid</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Antibacterial-{2-Propanol (1) + water (2)} mixture</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Preferential solvation</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">IKBI</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>