Moghimi S M, Patel H M
Department of Biochemistry, Charing Cross Hospital Medical School, London, UK.
J Microencapsul. 1993 Apr-Jun;10(2):155-62. doi: 10.3109/02652049309104381.
Liposomes were introduced first in 1980 for topical drug delivery and since then have attracted considerable interest and generated many speculative claims concerning their potential utility both as a drug carrier and reservoir for controlled release of drugs within various layers of the skin. A number of clinical studies have now demonstrated the superiority of liposomal drug formulations over conventional delivery systems. In this respect, liposomal formulations have been successful in treatment of a number of dermatological diseases and disorders such as psoriasis, mycoses, idiopathic hirsutism and cutaneous infections. This review emphasizes the evaluation of topically applied liposomal formulation both at experimental and clinical levels. Mechanism(s) by which liposomes facilitate deposition of drugs in various layers of the skin is also discussed.
脂质体于1980年首次被引入用于局部给药,自那时起就引起了广泛关注,并引发了许多关于其作为药物载体以及在皮肤各层中控制药物释放的储库的潜在效用的推测性说法。现在,一些临床研究已经证明脂质体药物制剂优于传统给药系统。在这方面,脂质体制剂已成功用于治疗多种皮肤病和病症,如牛皮癣、霉菌病、特发性多毛症和皮肤感染。本综述强调在实验和临床水平上对局部应用的脂质体制剂进行评估。还讨论了脂质体促进药物在皮肤各层沉积的机制。