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        <datestamp>2024-06-20T06:49:23Z</datestamp>
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          <dc:title>生体膜輸送の分子機構に関する生物薬剤学的研究</dc:title>
          <dc:title xml:lang="en">Biopharmaceutical studies on molecular mechanisms of membrane transport</dc:title>
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            <jpcoar:nameIdentifier nameIdentifierURI="https://kaken.nii.ac.jp/ja/search/?qm=10019664" nameIdentifierScheme="e-Rad">10019664</jpcoar:nameIdentifier>
            <jpcoar:creatorName>Tsuji, Akira</jpcoar:creatorName>
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          <datacite:description descriptionType="Abstract">By incorporating the transporter-mediated or receptor-mediated transport process in physiologically based pharmacokinetic models, we succeeded in the quantitative prediction of plasma and tissue concentrations of β-lactam antibiotics, insulin, pentazocine, quinolone antibacterial agents, and inaperizone and digoxin. The author's research on transporter-mediated pharmacokinetics focuses on the molecular and functional characteristics of drug transporters such as oligopeptide transporter, monocarboxylic acid transporter, anion antiporter, organic anion transporters, organic cation/carnitine transporters (OCTNs), and the ATP-binding cassette transporters P-glycoprotein and MRP2. We have successfully demonstrated that these transporters play important roles in the influxes and/or effluxes of drugs in intestinal and renal epithelial cells, hepatocytes, and brain capillary endothelial cells that form the blood-brain barrier. In the systemic carnitine defficiency (SCD) phenotype mouse model, juvenile visceral steatosis (jvs) mouse, a mutation in the OCTN2 gene was found. Furthermore, several types of mutation in human SCD patients were found, demonstrating that OCTN2 is a physiologically important carnitine transporter. Interestingly, OCTNs transport carnitine in a sodium-dependent manner and various cationic drugs transport it in a sodium-independent manner. OCTNs are thought to be multifunctional transporters for the uptake of carnitine into tissue cells and for the elimination of intracellular organic cationic drugs. © 2002 The Pharmaceutical Society of Japan.</datacite:description>
          <datacite:description descriptionType="Other">金沢大学薬学部</datacite:description>
          <datacite:description descriptionType="Other">金沢大学医薬保健研究域薬学系</datacite:description>
          <dc:publisher>日本薬学会</dc:publisher>
          <datacite:date dateType="Issued">2002-12-01</datacite:date>
          <datacite:date>2017-10-04</datacite:date>
          <dc:language>jpn</dc:language>
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          <jpcoar:identifier identifierType="HDL">http://hdl.handle.net/2297/14413</jpcoar:identifier>
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            <jpcoar:relatedIdentifier identifierType="DOI">10.1248/yakushi.122.1037</jpcoar:relatedIdentifier>
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          <jpcoar:sourceIdentifier identifierType="NCID">AN00241525</jpcoar:sourceIdentifier>
          <jpcoar:sourceIdentifier identifierType="ISSN">0031-6903</jpcoar:sourceIdentifier>
          <jpcoar:sourceTitle>藥學雜誌 = Yakugaku Zasshi</jpcoar:sourceTitle>
          <jpcoar:volume>122</jpcoar:volume>
          <jpcoar:issue>12</jpcoar:issue>
          <jpcoar:pageStart>1307</jpcoar:pageStart>
          <jpcoar:pageEnd>1058</jpcoar:pageEnd>
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            <datacite:date dateType="Available">2017-10-04</datacite:date>
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