8-甲氧基补骨脂素的药代动力学和毒理学分析。安全有效的PUVA治疗的基础]。

J Schmid, R Brickl, F W Koss
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引用次数: 0

摘要

在大约60篇出版物的基础上,根据我们自己的研究结果,我们对8-甲氧基补骨脂素(8-MOP)的作用方式、药代动力学、代谢和毒理学及其在PUVA治疗银屑病中的作用进行了全面的综述。目前认为8-MOP与DNA的相互作用是最可能的作用方式。8-MOP受强烈的首过效应影响,血浆水平有相当大的个体差异。药物剂量和光剂量的精确时间是成功治疗的关键,同时最大限度地减少PUVA治疗的潜在短期和长期风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The pharmacokinetic and toxicologic profile of 8-methoxypsoralen. The basis for safe and effective PUVA therapy].

On the basis of approximately 60 publications and in view of our own results we present a comprehensive review as to the mode of action, the pharmacokinetics, the metabolism and the toxicology of 8-methoxypsoralen (8-MOP) and its consequences in the PUVA therapy of psoriasis. The interaction of 8-MOP with DNA is presently considered to be the most likely mode of action. 8-MOP is subject to strong first-pass effects with considerable individual variations in plasma levels. An exact timing of drug dose and light dose is essential for a successful therapy, simultaneously minimizing the potential short-term and long-term risks of PUVA therapy.

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