1 Ocak 2016 Dergi makalesi Açık Erişim

Ates, Muge; Kaynak, Mustafa Sinan; Sahin, Selma

Dublin Core

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<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Ates, Muge</dc:creator>
  <dc:creator>Kaynak, Mustafa Sinan</dc:creator>
  <dc:creator>Sahin, Selma</dc:creator>
  <dc:date>2016-01-01</dc:date>
  <dc:description>Objectives According to Biopharmaceutics Classification System (BCS), acyclovir is a class III (high solubility, low permeability) compound, and it is transported through paracellular route by passive diffusion. The aim of this study was to investigate the effect of various pharmaceutical excipients on the intestinal permeability of acyclovir.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/58923</dc:identifier>
  <dc:identifier>oai:zenodo.org:58923</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>JOURNAL OF PHARMACY AND PHARMACOLOGY 68(6) 781-790</dc:source>
  <dc:title>Effect of permeability enhancers on paracellular permeability of acyclovir</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
</oai_dc:dc>