Combined chemical and electrical enhancement modulates stratum corneum structure

被引:11
作者
de Graaff, AM
Li, GL
van Aelst, AC
Bouwstra, JA
机构
[1] Leiden Univ, Leiden Amsterdam Ctr Drug Res, Dept Pharmaceut Technol, Gorlaeus Labs, NL-2300 RA Leiden, Netherlands
[2] Lab Plant Cytol & Morphol, Wageningen, Netherlands
关键词
iontophoresis; surfactant pretreatment; freeze fracture electron microscopy; cryo-scanning electron microscopy;
D O I
10.1016/S0168-3659(03)00134-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In a previous in vitro study it has been shown that pretreatment with a water-based surfactant formulation results in a two-fold increase in transdermal iontophoretic transport of R-apomorphine compared to iontophoresis only. The aim of the study presented in this paper was to unravel the mechanisms involved in the increased iontophoretic delivery. Freeze fracture electron microscopy and cryo-scanning electron microscopy were used to visualise the ultrastucture of human stratum corneum after (i) application of the surfactant formulation, (ii) iontophoresis and (iii) application of the surfactant formulation followed by iontophoresis. Non-occlusive application of the surfactant formulation did not exert any detectable changes in the ultrastructure of the stratum corneum, except for swelling of the outermost corneocyte layers. Application of a current density of 0.5 mA/cm(2) for 9 h induced a swelling of the corneocytes and the formation of water pools that were occasionally present in the intercellular regions. Application of the surfactant formulation followed by iontophoresis resulted in a further swelling of the corneocytes and a frequent presence of water pools in the intercellular regions throughout the whole stratum corneum. The observed changes in the ultrastructure of the stratum corneum can explain the increased R-apomorphine transport during iontophoresis. (C) 2003 Published by Elsevier Science B.V.
引用
收藏
页码:49 / 58
页数:10
相关论文
共 22 条
[1]  
BHATIA KS, 1996, P INT S CONTR REL BI, V23, P287
[2]   Transdermal water mobility in the presence of electrical fields using MR microscopy [J].
Caban, JB ;
Moerland, TS ;
Gibbs, SJ ;
McFadden, L ;
Locke, BR .
MAGNETIC RESONANCE IMAGING, 1999, 17 (08) :1183-1191
[3]   High-resolution cryo-scanning electron microscopy study of the macromolecular structure of fibronectin fibrils [J].
Chen, Y ;
Zardi, L ;
Peters, DMP .
SCANNING, 1997, 19 (05) :349-355
[4]   The pretreatment effect of chemical skin penetration enhancers in transdermal drug delivery using iontophoresis [J].
Choi, EH ;
Lee, SH ;
Ahn, SK ;
Hwang, SM .
SKIN PHARMACOLOGY AND APPLIED SKIN PHYSIOLOGY, 1999, 12 (06) :326-335
[5]  
CraaneVanHinsberg IWHM, 1997, MICROSC RES TECHNIQ, V37, P200, DOI 10.1002/(SICI)1097-0029(19970501)37:3<200::AID-JEMT5>3.0.CO
[6]  
2-R
[7]   Transdermal macromolecular delivery: Real-time visualization of iontophoretic and chemically enhanced transport using two-photon excitation microscopy [J].
Grewal, BS ;
Naik, A ;
Irwin, WJ ;
Gooris, G ;
de Grauw, GJ ;
Gerritsen, HG ;
Bouwstra, JA .
PHARMACEUTICAL RESEARCH, 2000, 17 (07) :788-795
[8]  
Honeywell-Nguyen PL, 2000, P INT S CONTR REL BI, V27, P237
[9]  
JADOUL P, 1998, J INVEST DERMATOL, V3, P159
[10]  
LI GL, 2002, IN PRESS PHARM RES