Transdermal delivery from liposomal formulations - Evolution of the technology over the last three decades

被引:113
作者
Ashtikar, Mukul [1 ]
Nagarsekar, Kalpa [2 ]
Fahr, Alfred [3 ]
机构
[1] Fraunhofer Inst Mol Biol & Appl Ecol, Project Grp Translat Med & Pharmacol, D-60596 Frankfurt, Germany
[2] Goethe Univ, Inst Pharmaceut Technol, D-60438 Frankfurt, Germany
[3] Friedrich Schiller Univ Jena, Inst Pharm, Lessingstr 8, D-07743 Jena, Germany
关键词
Skin; Penetration mechanism; Permeation; Liposome; Nanosystem; NONIONIC SURFACTANT VESICLES; TEMOPORFIN-LOADED INVASOMES; HUMAN STRATUM-CORNEUM; VITRO PERCUTANEOUS PERMEATION; TRADITIONAL DIFFUSION CELLS; ATR-FTIR SPECTROSCOPY; SKIN IN-VITRO; DRUG-DELIVERY; TOPICAL DELIVERY; HAIR-FOLLICLES;
D O I
10.1016/j.jconrel.2016.09.008
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Strong barrier properties of stratum corneum often limits the efficiency of drug delivery through skin. Several strategies were tried to improve permeation of drug through skin for local as well as systemic drug delivery. Incorporation of the drug within flexible liposomal vesicles has been one of the popular and well-studied approaches for delivering drug to deeper layers of the skin or even systemic circulation. Flexible/deformable/elastic liposomal systems such as invasomes, Transfersomes (R), ethosomes, niosomes, etc. have demonstrated encouraging results in delivering small molecules and large proteins to the skin. It is necessary to recognize the promising concepts and analyze their potential, since a clear understanding of the drawbacks and advantages of these approaches will lead towards future development. In the current review we have attempted to give an overview of different liposomal drug carriers for transdermal drug delivery and their efficiency as drug delivery system through different in vivo and in vitro studies. Also, an overview of the studies which investigated the interactions between skin and vesicles, which have lead us to our current understanding of the skin penetration mechanisms of liposomal formulations is presented. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:126 / 140
页数:15
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