Comparison of the lipid composition of porcine buccal and esophageal permeability barriers

被引:66
作者
Diaz-del-Consuelo, I
Jacques, Y
Pizzolato, GP
Guy, RH
Falson, F
机构
[1] Ctr Interuniv Rech & Enseignement Pharmapeptides, F-74160 Archamps, France
[2] Univ Geneva, Sch Pharmaceut Sci, CH-1211 Geneva, Switzerland
[3] Univ Lyon 1, ISPB, Lab Rech & Dev Pharm Galen Ind, F-69373 Lyon, France
[4] Hop Cantonal Geneva, Unite Neuropathol, Dept Clin Pathol, CH-1211 Geneva, Switzerland
[5] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
关键词
esophageal epithelium; buccal epithelium; membrane lipids; permeability; AMD-HPTLC;
D O I
10.1016/j.archoralbio.2005.04.008
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
Pig esophageal mucosa has been shown to be a useful and practical substitute for buccal mucosa in in vitro permeability studies in that it offers a Larger surface area and it is much easier to prepare. Further, the tissues demonstrate similar histological. characteristics. The objectives of this work were to characterize the lipid composition of the esophageal. mucosa, to compare it to that of the buccal. tissue, and to correlate lipid composition with the membranes' permeabitity to fentanyl. The major lipid classes of buccal. and esophageal. epithelia were separated and analysed by automated multiple development high-performance thin-layer chromatography (AMD-HPTLC). The two epithelia presented a very similar lipid pattern. In general, there were more polar lipids than non-polar; glycosylceramides were relatively abundant whereas the amount of ceramides present was very small. The flux of fentanyl. applied as the citrate in aqueous solution was comparable across the buccal. and esophageal. barriers. Lipid extraction provoked a significant increase in permeability. In conclusion, this research confirms the suitability of the esophageal. mucosa as a model for buccal. permeability studies. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:981 / 987
页数:7
相关论文
共 24 条
[1]
Chen S.-Y., 1984, STRUCTURE FUNCTION O, P7
[2]
CHARACTERIZATION OF THE BARRIER PROPERTIES OF MUCOSAL MEMBRANES [J].
CORBO, DC ;
LIU, JC ;
CHIEN, YW .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (03) :202-206
[3]
DELCONSUELO ID, 2003, CONTR REL SOC 30 ANN, P514
[4]
DEVRIES ME, 1991, CRIT REV THER DRUG, V8, P271
[5]
Lipid extracting effect of ethanol on keratinized oral mucosa [J].
Ganem-Quintanar, A ;
Jacques, Y ;
Falson-Rieg, F ;
Buri, P .
PHARMACEUTICAL RESEARCH, 1998, 15 (03) :495-498
[6]
A HISTOLOGICAL METHOD FOR THE VISUALIZATION OF THE INTER-CELLULAR PERMEABILITY BARRIER IN MAMMALIAN STRATIFIED SQUAMOUS EPITHELIA [J].
HILL, MW ;
SQUIER, CA ;
LINDER, JE .
HISTOCHEMICAL JOURNAL, 1982, 14 (04) :641-648
[7]
Effects of the penetration enhancer glycodeoxycholate on the lipid integrity in porcine buccal epithelium in vitro [J].
Hoogstraate, AJ ;
Wertz, PW ;
Squier, CA ;
Bos-van Geest, A ;
Abraham, W ;
Garrison, MD ;
Verhoef, JC ;
Junginger, HE ;
Bodde, HE .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 5 (04) :189-198
[8]
ESOPHAGEAL DEFENSE-MECHANISMS [J].
HOPWOOD, D .
DIGESTION, 1995, 56 :5-8
[9]
HOPWOOD D, 1978, VIRCHOWS ARCH B, V26, P345
[10]
UPTAKE OF HORSERADISH-PEROXIDASE BY HUMAN ESOPHAGEAL EXPLANTS OVER 24-H [J].
HOPWOOD, D ;
MILNE, G ;
JANKOWSKI, J ;
HOWAT, K ;
WORMSLEY, KG .
HISTOCHEMICAL JOURNAL, 1991, 23 (09) :409-414