Schmid J, Brickl R, Koss F W
Abteilung Biochemie der Dr. Karl Thomae GmbH, Biberach an der Riss.
Derm Beruf Umwelt. 1988 Nov-Dec;36(6):177-85.
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.
基于大约60篇出版物,并鉴于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银屑病光化学疗法(PUVA)中的后果进行了全面综述。目前认为8-MOP与DNA的相互作用是最可能的作用方式。8-MOP具有强烈的首过效应,血浆水平存在相当大的个体差异。药物剂量和光照剂量的精确 timing 对于成功治疗至关重要,同时将PUVA治疗的潜在短期和长期风险降至最低。