Effect of chemical enhancers and iontophoresis on thiocolchicoside permeation across rabbit and human skin in vitro

被引:42
作者
Artusi, M
Nicoli, S
Colombo, P
Bettini, R
Sacchi, A
Santi, P
机构
[1] Univ Parma, Dipartimento Farmaceut, I-43100 Parma, Italy
[2] Univ Naples Federico II, Dipartimento Chim Farmaceut & Tossicol, I-80181 Naples, Italy
关键词
transdermal; permeation enhancers; iontophoresis; permeability; skin;
D O I
10.1002/jps.20152
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
The aim of this work was to study the permeation of thiocolchicoside across the skin in vitro. The effect of the chemical enhancer lauric acid and the physical technique of iontophoresis was investigated. Permeation experiments were performed in vitro using rabbit ear skin as barrier. The effect of lauric acid at different concentrations (2% and 4%) and of the vehicle (water, ethanol, or ethanol/water) was investigated. The primary effect of lauric acid was on the partitioning parameter, whereas the diffusive parameter did not change significantly. When human epidermis was used, the permeation parameters were generally lower, although not significantly different from rabbit ear skin. The data obtained with full-thickness human skin indicate that, despite the hydrophilic nature of thiocolchicoside, the resistance to drug transport is not limited to the stratum corneum, but that the underlying dermal tissue can also contribute. Iontophoresis enhanced the flux of thiocolchicoside compared with the passive control. The mechanism by which iontophoresis enhanced thiocolchicoside transport across the skin was electroosmosis. The permeation of thiocolchicoside across the skin can be enhanced using chemical or physical penetration enhancers. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:2431 / 2438
页数:8
相关论文
共 31 条
[1]
Buccal delivery of thiocolchicoside: in vitro and in vivo permeation studies [J].
Artusi, M ;
Santi, P ;
Colombo, P ;
Junginger, HE .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 250 (01) :203-213
[2]
Drug delivery routes in skin: a novel approach [J].
Barry, BW .
ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 :S31-S40
[3]
Mechanism of transport enhancement of LHRH through porcine epidermis by terpenes and iontophoresis: Permeability and lipid extraction studies [J].
Bhatia, KS ;
Singh, J .
PHARMACEUTICAL RESEARCH, 1998, 15 (12) :1857-1862
[4]
Synergistic effect of iontophoresis and a series of fatty acids on LHRH permeability through porcine skin [J].
Bhatia, KS ;
Singh, J .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (04) :462-469
[5]
Transdermal application of bupivacaine-loaded poly (acrylamide(A)-co-monomethyl itaconate) hydrogels [J].
Blanco, MD ;
Bernardo, MV ;
Teijón, C ;
Sastre, RL ;
Teijón, JM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 255 (1-2) :99-107
[6]
In vitro permeation screening of a new formulation of thiocolchicoside containing various enhancers [J].
Ceschel, GC ;
Maffei, P ;
Porzio, S ;
Melillo, G ;
Caselli, GF ;
Dragani, MC ;
Gentile, MM ;
Clavenna, G .
DRUG DELIVERY, 2002, 9 (04) :259-263
[7]
Design and evaluation of a lorazepam transdermal delivery system [J].
Costa, P ;
Ferreira, DC ;
Morgado, R ;
Lobo, JMS .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1997, 23 (10) :939-944
[8]
CHARACTERIZATION OF CONVECTIVE SOLVENT FLOW DURING IONTOPHORESIS [J].
DELGADOCHARRO, MB ;
GUY, RH .
PHARMACEUTICAL RESEARCH, 1994, 11 (07) :929-935
[9]
Development and evaluation on transdermal delivery of enoxacin via chemical enhancers and physical iontophoresis [J].
Fang, JY ;
Lin, HH ;
Chen, HI ;
Tsai, YH .
JOURNAL OF CONTROLLED RELEASE, 1998, 54 (03) :293-304
[10]
Influence of Transcutol® CG on the skin accumulation and transdermal permeation of ultraviolet absorbers [J].
Godwin, DA ;
Kim, NH ;
Felton, LA .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2002, 53 (01) :23-27