Gasparro F P, Dall'Amico R, Goldminz D, Simmons E, Weingold D
Department of Dermatology, Yale University School of Medicine, New Haven, Connecticut 06510.
Yale J Biol Med. 1989 Nov-Dec;62(6):579-93.
8-methoxypsoralen (8-MOP), activated upon exposure to long-wavelength ultraviolet radiation, is used therapeutically to treat the diseased blood cells of cutaneous T-cell lymphoma patients. The factors responsible for the efficacy of this therapy are reviewed. Primary among these are the plasma level of 8-MOP at the time of irradiation and the effective dose of UVA. 8-MOP plasma levels determined in a series of six patients demonstrated that the drug is absorbed at a highly variable rate (122 ng/ml +/- 67). A new liquid form of 8-MOP is absorbed with a modest increase in plasma levels (170 ng/ml) but with no improvement in the variability (+/- 163). An examination of the dose-response relationship between 8-MOP concentration and UVA dose indicated that properties such as 8-MOP photoadduct formation and PHA response are proportional to the combined doses of these two factors. A new molecular target for 8-MOP photomodification, cell membrane DNA, is described.
8-甲氧基补骨脂素(8-MOP)在暴露于长波紫外线辐射后被激活,用于治疗皮肤T细胞淋巴瘤患者的病变血细胞。本文综述了该疗法疗效的相关影响因素。其中主要因素包括照射时8-MOP的血浆水平以及UVA的有效剂量。对6例患者进行的一系列检测发现,8-MOP的血浆水平显示该药物的吸收速率变化很大(122纳克/毫升±67)。一种新的8-MOP液体制剂吸收后血浆水平略有升高(170纳克/毫升),但变异性没有改善(±163)。对8-MOP浓度与UVA剂量之间剂量反应关系的研究表明,诸如8-MOP光加合物形成和PHA反应等特性与这两个因素的联合剂量成正比。本文还描述了8-MOP光修饰的一个新分子靶点——细胞膜DNA。