Balogh A, Merkel U, Looks A, Vollandt R, Wollina U
Institute of Clinical Pharmacology, Friedrich Schiller University, Jena, Germany.
Exp Toxicol Pathol. 1998 Sep;50(4-6):397-401. doi: 10.1016/S0940-2993(98)80025-0.
Recently, a new therapy involving an extracorporal activation of orally administered 8-methoxypsoralen (8-MOP), photosensitizing furocoumarin, is established for the treatment of different skin diseases, extracorporeal photopheresis (ECP). The pharmacokinetic profile of 8-MOP has been pursued as part of a clinical study which should assess the efficacy of ECP in patients with progressive systemic sclerosis and cutaneous T-cell lymphoma. The enormous intra-individual variations proofed for plasma as well as buffy coat concentration are unfavourable for oral 8-MOP therapy. Therefore, the introduction of liquid 8-MOP formulation that allows the direct administration of the drug in to the treatment bag of the ECP device is challenging.
最近,一种新的治疗方法被确立用于治疗不同的皮肤病,即体外光化学疗法(ECP),该方法涉及对口服的8-甲氧基补骨脂素(8-MOP)进行体外激活,8-MOP是一种光敏性呋喃香豆素。作为一项临床研究的一部分,人们一直在研究8-MOP的药代动力学特征,该临床研究旨在评估ECP对进行性系统性硬化症和皮肤T细胞淋巴瘤患者的疗效。血浆和血沉棕黄层浓度存在巨大的个体内差异,这对口服8-MOP治疗不利。因此,引入可直接将药物注入ECP设备治疗袋的液体8-MOP制剂具有挑战性。