Paolino Donatella, Cosco Donato, Muzzalupo Rita, Trapasso Elena, Picci Nevio, Fresta Massimo
Department of Experimental and Clinical Medicine, Faculty of Medicine, University Magna Graecia of Catanzaro, Campus Universitario, Building of BioSciences, Viale Europa, Germaneto (CZ), Italy.
Int J Pharm. 2008 Apr 2;353(1-2):233-42. doi: 10.1016/j.ijpharm.2007.11.037. Epub 2007 Nov 28.
An innovative niosomal system made up of alpha,omega-hexadecyl-bis-(1-aza-18-crown-6) (Bola), Span 80 and cholesterol (2:5:2 molar ratio) was proposed as a topical delivery system for 5-fluorouracil (5-FU), largely used in the treatment of different forms of skin cancers. Bola-niosomes showed a mean size of approximately 400 nm, which were reduced to approximately 200 nm by a sonication procedure with a polydispersion index value of 0.1. Bola-niosomes showed a loading capacity of approximately 40% with respect to the amount of 5-FU added during the preparation. 5-FU-loaded bola-niosomes were tested on SKMEL-28 (human melanoma) and HaCaT (non-melanoma skin cancer with a specific mutations in the p53 tumor suppressor gene) to assess the cytotoxic activity with respect to the free drug. 5-FU-loaded bola-niosomes showed an improvement of the cytotoxic effect with respect to the free drug. Confocal laser scanning microscopy studies were carried out to evaluate both the extent and the time-dependent bola-niosome-cell interaction. The percutaneous permeation of 5-FU-loaded niosomes was evaluated by using human stratum corneum and epidermis membranes. Bola-niosomes provided an increase of the drug penetration of 8- and 4-folds with respect to a drug aqueous solution and to a mixture of empty bola-niosomes with a drug aqueous solution.
一种由α,ω-十六烷基-双-(1-氮杂-18-冠-6)(bola)、司盘80和胆固醇(摩尔比为2:5:2)组成的创新型非离子型脂质体系统被提出作为5-氟尿嘧啶(5-FU)的局部给药系统,5-FU在不同形式皮肤癌的治疗中广泛应用。bola-脂质体的平均尺寸约为400nm,通过超声处理后尺寸减小至约200nm,多分散指数值为0.1。bola-脂质体相对于制备过程中添加的5-FU量显示出约40%的载药量。将负载5-FU的bola-脂质体在SKMEL-28(人黑色素瘤)和HaCaT(在p53肿瘤抑制基因中有特定突变的非黑色素瘤皮肤癌)上进行测试,以评估相对于游离药物的细胞毒性活性。负载5-FU的bola-脂质体相对于游离药物显示出细胞毒性作用的改善。进行共聚焦激光扫描显微镜研究以评估bola-脂质体与细胞相互作用的程度和时间依赖性。使用人角质层和表皮膜评估负载5-FU的脂质体的经皮渗透。相对于药物水溶液以及空bola-脂质体与药物水溶液的混合物,bola-脂质体使药物渗透率提高了8倍和4倍。