Ethosomes - novel vesicular carriers for enhanced delivery: characterization and skin penetration properties

被引:979
作者
Touitou, E
Dayan, N
Bergelson, L
Godin, B
Eliaz, M
机构
[1] Hebrew Univ Jerusalem, Fac Med, Sch Pharm, Dept Pharmaceut, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Fac Med, Sch Pharm, Unit Lipid Res, IL-91120 Jerusalem, Israel
[3] Hebrew Univ Jerusalem, David R Bloom Ctr Pharm, IL-91120 Jerusalem, Israel
关键词
ethosome; liposome; ethanol; transdermal; phospholipid; minoxidil; testosterone;
D O I
10.1016/S0168-3659(99)00222-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work describes a novel carrier for enhanced skin delivery, the ethosomal system, which is composed of phospholipid, ethanol and water. Ethosomal systems were much more efficient at delivering a fluorescent probe to the skin in terms of quantity and depth, than either liposomes or hydroalcoholic solution. The ethosomal system dramatically enhanced the skin permeation of minoxidil in vitro compared with either ethanolic or hydroethanolic solution or phospholipid ethanolic micellar solution of minoxidil. In addition, the transdermal delivery of testosterone from an ethosomal patch was greater both in vitro and in vivo than from commercially available patches. Skin permeation of ethosomal components, ethanol and phospholipid, was demonstrated in diffusion-cell experiments. Ethosomal systems composed of soy phosphatidylcholine 2%, ethanol 30% and water were shown by electron microscopy to contain multilamellar vesicles. P-31-NMR studies confirmed the bilayer configuration of the lipids. Calorimetry and fluorescence measurements suggested that the vesicular bilayers are flexible, having a relatively low T-m and fluorescence anisotropy compared with liposomes obtained in the absence of ethanol. Dynamic light scattering measurements indicated that ethanol imparted a negative charge to the vesicles. The average vesicle size, as measured by dynamic light scattering, was modulated by altering the ethosome composition. Experiments using fluorescent probes and ultracentrifugation showed that the ethosomes had a high entrapment capacity for molecules of various lyophilicities. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:403 / 418
页数:16
相关论文
共 28 条
[1]   SINGLE BILAYER LIPOSOMES PREPARED WITHOUT SONICATION [J].
BATZRI, S ;
KORN, ED .
BIOCHIMICA ET BIOPHYSICA ACTA, 1973, 298 (04) :1015-1019
[2]  
Bergelson L., 1978, METHODS MEMBR BIOL, V9, P275
[3]   LIPID-SPECIFIC FLUORESCENT-PROBES IN STUDIES OF BIOLOGICAL-MEMBRANES [J].
BERGELSON, LD ;
MOLOTKOVSKY, JG ;
MANEVICH, YM .
CHEMISTRY AND PHYSICS OF LIPIDS, 1985, 37 (02) :165-195
[4]  
Berner B., 1995, PERCUTANEOUS PENETRA, P45
[5]   INTERACTION OF PHOSPHOLIPID LIPOSOMES WITH LIPID MODEL MIXTURES FOR STRATUM-CORNEUM LIPIDS [J].
BLUME, A ;
JANSEN, M ;
GHYCZY, M ;
GAREISS, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 99 (2-3) :219-228
[6]  
BRAUNFALCO O, 1992, GRIESB C LIP DERM
[7]   Ultraflexible vesicles, transfersomes, have an extremely low pore penetration resistance and transport therapeutic amounts of insulin across the intact mammalian skin [J].
Cevc, G ;
Gebauer, D ;
Stieber, J ;
Schätzlein, A ;
Blume, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1368 (02) :201-215
[8]  
CHIN JH, 1997, MOL PHARMACOL, V13, P435
[9]   BIOAVAILABILITY OF PROPRANOLOL FOLLOWING ORAL AND TRANSDERMAL ADMINISTRATION IN RABBITS [J].
CORBO, M ;
LIU, JC ;
CHIEN, YW .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (07) :584-587
[10]  
Dayan Nava, 1997, Pharmaceutical Research (New York), V14, pS318