作者: Kazuhiko Arimori
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摘要: Purpose. The purpose of this work was to investigate the role hepatic and intestinal P-glycoprotein (P-gp) canalicular multispecific organic anion transporter /multidrug resistance-associated protein 2 (cMOAT/MRP2) on both biliary excretion exsorption irinotecan hydrochloride (CPT-11) its metabolite, SN-38, in lactone carboxylate forms. Cyclosporin A (CsA) used modulate P-gp cMOAT/MRP2.