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<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>Pharmaceutical Sciences</JournalTitle>
      <Issn>1735-403X</Issn>
      <Volume>22</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2016</Year>
        <Month>12</Month>
        <DAY>30</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Preparation and Physicochemical Characterization of Biodegradable mPEG-PCL Core-Shell Micelles for Delivery of Artemisinin</ArticleTitle>
    <FirstPage>234</FirstPage>
    <LastPage>243</LastPage>
    <ELocationID EIdType="doi">10.15171/PS.2016.37</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Hamid Reza</FirstName>
        <LastName>Kheiri Manjili</LastName>
      </Author>
      <Author>
        <FirstName>Hojjat</FirstName>
        <LastName>Malvandi</LastName>
      </Author>
      <Author>
        <FirstName>Mir-Sajjad</FirstName>
        <LastName>Mosavi</LastName>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Danafar</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/PS.2016.37</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>06</Month>
        <Day>09</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>10</Month>
        <Day>20</Day>
      </PubDate>
    </History>
    <Abstract>Background: Artemisinin is a sesquiterpene lactone chemical extract from Artemisia annua, is poorly resolvable in water and a fast-acting blood active in treating the acute attack of malaria.  Methods: Artemisinin was encapsulated within mPEG-PCL micelles with a single-step nano-precipitation method, leading to formation of ART/ mPEG-PCL micelles. mPEG-PCL copolymers was characterized in vitro by HNMR, FTIR and DSC techniques. Copolymers with artemisinin were self-assembled into micelles in aqueous solution. The consequential micelles were further characterized by various techniques such as DLS and AFM. Results: The results exhibited the successful formation of spherical artemisinin-loaded micelles. The artemisinin-loaded micelles showed high loading efficiency. The encapsulation efficiency of artemisinin was 63±2.31%. In vitro release of artemisinin from artemisinin-entrapped micelles followed remarkably sustained release profile. Conclusion: The results indicated that the successful formulation of artemisinin loaded mPEG-PCL micelles can improve the drug delivery of artemisinin. The results showed that nanomicelles can be promising drug delivery systems for sustaining release of artemisinin.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Artemisinin</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Drug delivery</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Micelles</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">mPEG-PCL</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>