Role of edge activators and surface charge in developing ultradeformable vesicles with enhanced skin delivery

小泡 渗透 化学 透皮 药物输送 毒品携带者 色谱法 生物物理学 药理学 生物化学 医学 有机化学 生物
作者
Ghada M. El-Zaafarany,Gehanne A.S. Awad,Samar Mansour Holayel,Nahed D. Mortada
出处
期刊:International Journal of Pharmaceutics [Elsevier]
卷期号:397 (1-2): 164-172 被引量:381
标识
DOI:10.1016/j.ijpharm.2010.06.034
摘要

Transfersomes are highly efficient edge activator (EA)-based ultraflexible vesicles capable of, non-invasively, trespassing skin by virtue of their high, self-optimizing deformability. This investigation presents different approaches for the optimization of Transfersomes for enhanced transepidermal delivery of Diclofenac sodium (DS). Different methods of preparation, drug and lipid concentrations and vesicle compositions were employed, resulting in ultraflexible vesicles with diverse membrane characteristics. Evaluation of Transfersomes was implemented in terms of their shapes, sizes, entrapment efficiencies (EE%), relative deformabilities and in vitro skin permeation. Transfersomes prepared with 95:5% (w/w) (PC:EA) ratio showed highest EE% (Span 85>Span 80>Na cholate>Na deoxycholate>Tween 80). Whereas, those prepared using 85:15% (w/w) ratio showed highest deformability (Tween 80 was superior to bile salts and spans). Transfersomes were proved significantly superior in terms of, the amount of drug deposited in the skin and the amount permeated, with an enhancement ratio of 2.45, when compared to a marketed product. The study proved that the type and concentration of EA, as well as, the method of preparation had great influences on the properties of Transfersomes. Hence, optimized Transfersomes can significantly increase transepidermal flux and prolong the release of DS, when applied non-occlusively.
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