Ethosomes: New prospects in transdermal delivery

被引:169
作者
Godin, B
Touitou, E [1 ]
机构
[1] Hebrew Univ Jerusalem, Dept Pharmaceut, Sch Pharm, Fac Med, IL-91120 Jerusalem, Israel
[2] Univ Bradford, Bradford BD7 1DP, W Yorkshire, England
来源
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS | 2003年 / 20卷 / 01期
关键词
liposomes; dermal delivery; permeation enhancement;
D O I
10.1615/CritRevTherDrugCarrierSyst.v20.i1.20
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ethosomes are noninvasive delivery carriers that enable drugs to reach the deep skin layers and/or the systemic circulation. Although ethosomal systems are conceptually sophisticated, they are characterized by simplicity in their preparation, safety, and efficacy a combination that can highly expand their application. Ethosomes are soft, malleable vesicles tailored for enhanced delivery of active agents. This article reviews work carried out in vitro, in vivo, in animal models, and in humans with various ethosomal systems incorporating a wide range of drugs. Because of their unique structure, ethosomes are able to encapsulate and deliver through the skin highly lipophilic molecules such as cannabinoids, testosterone, and minoxidil, as well as cationic drugs such as propranolol and trihexyphenidil. Results obtained in a double-blind two-armed randomized clinical study showed that treatment with the ethosomal acyclovir formulation significantly improved all the evaluated parameters. Preliminary studies with plasmids and insulin revealed that the ethosomal carrier may be used for enhanced delivery of these agents. In further work, the ethosomal technology was broadened to introduce agents into cultured cells and microorganisms. Enhanced delivery of bioactive molecules through the skin and cellular membranes by means of an ethosomal carrier opens numerous challenges and opportunities for the research and future development of novel improved therapies.
引用
收藏
页码:63 / 102
页数:40
相关论文
共 139 条
[1]   A novel tetraester construct that reduces cationic lipid-associated cytotoxicity. Implications for the onset of cytotoxicity [J].
Aberle, AM ;
Tablin, F ;
Zhu, J ;
Walker, NJ ;
Gruenert, DC ;
Nantz, MH .
BIOCHEMISTRY, 1998, 37 (18) :6533-6540
[2]  
AGURELL S, 1986, PHARMACOL REV, V38, P21
[4]   EFFICACY OF GENTAMICIN OR CEFTAZIDIME ENTRAPPED IN LIPOSOMES WITH PROLONGED BLOOD-CIRCULATION AND ENHANCED LOCALIZATION IN KLEBSIELLA PNEUMONIAE-INFECTED LUNG-TISSUE [J].
BAKKERWOUDENBERG, IAJM ;
TENKATE, MT ;
STEARNECULLEN, LET ;
WOODLE, MC .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (04) :938-947
[5]   HYDROGEL-BASED IONTOTHERAPEUTIC DELIVERY DEVICES FOR TRANSDERMAL DELIVERY OF PEPTIDE PROTEIN DRUGS [J].
BANGA, AK ;
CHIEN, YW .
PHARMACEUTICAL RESEARCH, 1993, 10 (05) :697-702
[6]   Iontophoresis and electroporation: comparisons and contrasts [J].
Banga, AK ;
Bose, S ;
Ghosh, TK .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 179 (01) :1-19
[7]   TRANSDERMAL IONTOPHORETIC DELIVERY AND DEGRADATION OF VASOPRESSIN ACROSS HUMAN CADAVER SKIN [J].
BANGA, AK ;
KATAKAM, M ;
MITRA, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 116 (02) :211-216
[8]   Assessing the potential of skin electroporation for the delivery of protein- and gene-based drugs [J].
Banga, AK ;
Prausnitz, MR .
TRENDS IN BIOTECHNOLOGY, 1998, 16 (10) :408-412
[9]   Antibiotic resistance: a current perspective [J].
Barker, KF .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1999, 48 (02) :109-124
[10]  
Barry WB, 1983, DERMATOLOGICAL FORMU