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癌患者中N-天冬氨酰氯in e6的药代动力学

Pharmacokinetics of N-aspartyl chlorin e6 in cancer patients.

作者信息

Kessel D

机构信息

Department of Pharmacology, Wayne State University School of Medicine, Detroit, MI 48201, USA.

出版信息

J Photochem Photobiol B. 1997 May;39(1):81-3. doi: 10.1016/s1011-1344(96)00009-7.

Abstract

We examined the pharmacokinetics of the photosensitizer N-aspartyl chlorin e6 in a group of cancer patients. While the drug persisted in plasma for as long as six weeks, there was no evidence of fluorescent NPe6 metabolites during this interval. Kinetics of drug elimination from plasma were consistent with a 2-compartment model with half-lives of approximately 9 hr (57%) and 134 hr (43%). The drug was bound to plasma albumin+other heavy proteins (65%) > HDL (35%) > > LDL (1-2%). These relative values did not change for as long as 21 days after drug administration. The long persistence of NPe6 in plasma was not associated with extended skin photosensitization.

摘要

我们研究了一组癌症患者中光敏剂N-天冬氨酰氯高铁血红素e6的药代动力学。虽然该药物在血浆中持续存在长达六周,但在此期间没有荧光NPe6代谢物的证据。药物从血浆中消除的动力学符合二室模型,半衰期约为9小时(57%)和134小时(43%)。该药物与血浆白蛋白+其他重蛋白结合(65%)>高密度脂蛋白(35%)>>低密度脂蛋白(1-2%)。给药后长达21天,这些相对值没有变化。NPe6在血浆中的长期持续存在与皮肤光敏性延长无关。

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