Egbaria K, Ramachandran C, Weiner N
College of Pharmacy, University of Michigan, Ann Arbor.
Skin Pharmacol. 1990;3(1):21-8. doi: 10.1159/000210837.
The kinetics and extent of uptake of ciclosporin in various strata of hairless mouse skin upon topical application of several ciclosporin formulations were determined by in vitro diffusion cell experiments. The ciclosporin formulations tested included a hydroalcoholic solution, an oil-in-water emulsion and two liposomal systems. The accumulation of drug in stratum corneum is in the order: 'skin lipid' liposomes greater than 'phospholipid' liposomes greater than emulsion greater than hydroalcoholic solution. The total combined amount of drug in the deeper skin strata and the receiver compartment followed the order: hydroalcoholic solution much greater than 'phospholipid' liposomes greater than 'skin lipid' liposomes greater than emulsion. The results suggest that topically applied liposomes, particularly those prepared from lipid mixtures having compositions similar to the stratum corneum, may provide sustained, enhanced levels of ciclosporin in the stratum corneum (the reservoir) while minimizing high levels in strata associated with blood and lymph supplies.
通过体外扩散池实验,测定了在局部应用几种环孢素制剂后,环孢素在无毛小鼠皮肤各层中的摄取动力学和摄取程度。所测试的环孢素制剂包括水醇溶液、水包油乳液和两种脂质体系统。药物在角质层中的蓄积顺序为:“皮肤脂质”脂质体大于“磷脂”脂质体大于乳液大于水醇溶液。在较深皮肤层和接受室中药物的总蓄积量顺序为:水醇溶液远大于“磷脂”脂质体大于“皮肤脂质”脂质体大于乳液。结果表明,局部应用脂质体,尤其是由与角质层组成相似的脂质混合物制备的脂质体,可能会在角质层(储存库)中提供持续增强的环孢素水平,同时使与血液和淋巴供应相关层中的高水平降至最低。