Influence of 6-ketocholestanol on skin permeation of 5-aminolevulinic acid and evaluation of chemical stability

被引:11
作者
Auner, BG [1 ]
Petzenhauser, E [1 ]
Valenta, C [1 ]
机构
[1] Univ Vienna, Ctr Pharm, Inst Pharmaceut Technol & Biopharmaceut, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
6-ketocholestanol; 5-aminolevulinic acid; porcine skin; liposomes; stability; diffusion experiments;
D O I
10.1002/jps.20130
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The ability of 6-ketocholestanol to increase the skin permeation of the prodrug aminolevulinic acid (5-ALA) was investigated. 6-Ketocholestanol was incorporated together with 5-ALA in four different formulations. Preparations used were a liquid solution/suspension of 5-ALA in buffer, 5-ALA in phospholipid liposomal formulations with and without gelating agent, and finally, a complex cream formulation also including phospholipids. Standard diffusion experiments of 5-ALA using Franz-type diffusion cells and porcine skin were performed. Drug stability was monitored by analyzing the 5-ALA content in the different formulations over time and viewing the preparation for microbial contamination. The analysis of 5-ALA as a nonfluorescent probe was performed after chemical reaction, leading to a fluorescent derivative. The 5-ALA permeation through porcine skin was increased threefold by 6-ketocholestanol in the cream formulation. The chemical stability of 5-ALA in the tested formulations was in the range of about 33 to 72% after an observation period of 28 days. After that time point microbial stability was no longer evident for formulations 2 and 3. Formulation 1 could be observed until day 34, and only formulation 4 showed a microbial stability over the whole observation period of 42 days. (C) 2004 Wiley-Liss, Inc. and the American Pharmacists Association.
引用
收藏
页码:2780 / 2787
页数:8
相关论文
共 35 条
[1]   PERCUTANEOUS-ABSORPTION - A NEW PHYSICOCHEMICAL PREDICTIVE MODEL FOR MAXIMUM HUMAN INVIVO PENETRATION RATES [J].
ANDO, HY ;
SCHULTZ, TW ;
SCHNAARE, RL ;
SUGITA, ET .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1984, 73 (04) :461-467
[2]  
[Anonymous], 1987, TRANSDERMAL DELIV DR
[3]   Influence of phloretin and 6-ketocholestanol on the skin permeation of sodium-fluorescein [J].
Auner, BG ;
Valenta, C ;
Hadgraft, J .
JOURNAL OF CONTROLLED RELEASE, 2003, 89 (02) :321-328
[4]   Influence of lipophilic counter-ions in combination with phloretin and 6-ketocholestanol on the skin permeation of 5-aminolevulinic acid [J].
Auner, BG ;
Valenta, C ;
Hadgraft, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 255 (1-2) :109-116
[5]   Novel mechanisms and devices to enable successful transdermal drug delivery [J].
Barry, BW .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 14 (02) :101-114
[6]   DIPOLE POTENTIAL OF LIPID-MEMBRANES [J].
BROCKMAN, H .
CHEMISTRY AND PHYSICS OF LIPIDS, 1994, 73 (1-2) :57-79
[7]  
CALZAVARAPINTON PG, 1995, J PHOTOCH PHOTOBIO B, V29, P53
[8]   The influence of the vehicle on the synthesis of porphyrins after topical application of 5-aminolaevulinic acid. Implications in cutaneous photodynamic sensitization [J].
Casas, A ;
Fukuda, H ;
Di Venosa, G ;
Batlle, AMD .
BRITISH JOURNAL OF DERMATOLOGY, 2000, 143 (03) :564-572
[9]   ALA and ALA hexyl ester-induced porphyrin synthesis in chemically induced skin tumours: the role of different vehicles on improving photosensitization [J].
Casas, A ;
Perotti, C ;
Fukuda, H ;
Rogers, L ;
Butler, AR ;
Batlle, A .
BRITISH JOURNAL OF CANCER, 2001, 85 (11) :1794-1800
[10]   Intramembrane molecular dipoles affect the membrane insertion and folding of a model amphiphilic peptide [J].
Cladera, J ;
O'Shea, P .
BIOPHYSICAL JOURNAL, 1998, 74 (05) :2434-2442