Skin-PAMPA: A new method for fast prediction of skin penetration

被引:140
作者
Sinko, Balint [1 ]
Garrigues, Teresa M. [2 ]
Balogh, Gyoergy T. [3 ]
Nagy, Zsombor K. [4 ]
Tsinman, Oksana [5 ]
Avdeef, Alex [5 ]
Takacs-Novak, Krisztina [1 ]
机构
[1] Semmelweis Univ, Dept Pharmaceut Chem, H-1092 Budapest, Hungary
[2] Univ Valencia, Dept Pharm & Pharmaceut, E-46100 Valencia, Spain
[3] Gedeon Richter Nyrt, H-1103 Budapest, Hungary
[4] Budapest Univ Technol & Econ, Dept Organ Chem & Technol, H-1111 Budapest, Hungary
[5] pION INC, Billerica, MA 01821 USA
基金
美国国家科学基金会;
关键词
Skin permeability; PAMPA; In vitro high-throughput model; Transdermal drug penetration; Artificial membrane permeability assay; IN-VITRO MODEL; PERCUTANEOUS-ABSORPTION; LOG-P; PERMEATION; MEMBRANE; BARRIER; ASSAY; PKA;
D O I
10.1016/j.ejps.2012.01.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The goal of this study was to develop a quick, reliable, and cost-effective permeability model for predicting transdermal penetration of compounds. The Parallel Artificial Membrane Permeability Assay (PAMPA) was chosen for this purpose, as it already has been successfully used for estimating passive gastrointestinal absorption and blood-brain barrier permeability. To match the permeability of the rate-limiting barrier in human skin, synthetic certramides, which are analogs of the ceramides present in the stratum corneum, were selected for the skin-PAMPA model. The final skin-PAMPA membrane lipid mixture (certramide, free fatty acid, and cholesterol) was selected and optimized based on data from three different human skin databases and the final model was found to correlate well to all of the databases. The reproducibility of the skin-PAMPA model was investigated and compared to that of other PAMPA models. The homogeneity of the filter-impregnated lipid mixture membrane was confirmed with Raman microscopy. It was shown that skin-PAMPA is a quick and cost-effective research tool that can serve as a useful model of skin penetration in pharmaceutical and cosmetic research. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:698 / 707
页数:10
相关论文
共 41 条
[1]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[2]   PAMPA - A drug absorption in vitro model 13. Chemical selectivity due to membrane hydrogen bonding: In combo comparisons of HDM-, DOPC-, and DS-PAMPA models [J].
Avdeef, A ;
Tsinman, O .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2006, 28 (1-2) :43-50
[3]  
Avdeef A., 2003, ABSORPTION DRUG DEV
[4]   PAMPA - Critical factors for better predictions of absorption [J].
Avdeef, Alex ;
Bendels, Stefanie ;
Di, Li ;
Faller, Bernard ;
Kansy, Manfred ;
Sugano, Kiyohiko ;
Yamauchi, Yukinori .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (11) :2893-2909
[5]  
Avdeef Alex, 2005, Expert Opin Drug Metab Toxicol, V1, P325, DOI 10.1517/17425255.1.2.325
[6]   Unexpected skin barrier influence from nonionic emulsifiers [J].
Bárány, E ;
Lindberg, M ;
Lodén, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 195 (1-2) :189-195
[7]   Structure of the skin barrier and its modulation by vesicular formulations [J].
Bouwstra, JA ;
Honeywell-Nguyen, PL ;
Gooris, GS ;
Ponec, M .
PROGRESS IN LIPID RESEARCH, 2003, 42 (01) :1-36
[8]   Inter- and intralaboratory variation of in vitro diffusion cell measurements:: An international multicenter study using quasi-standardized methods and materials [J].
Chilcott, RP ;
Barai, N ;
Beezer, AE ;
Brain, SI ;
Brown, MB ;
Bunge, AL ;
Burgess, SE ;
Cross, S ;
Dalton, CH ;
Dias, M ;
Farinha, A ;
Finnin, BC ;
Gallagher, SJ ;
Green, DM ;
Gunt, H ;
Gwyther, RL ;
Heard, CM ;
Jarvis, CA ;
Kamiyama, F ;
Kasting, GB ;
Ley, EE ;
Lim, ST ;
Mcnaughton, GS ;
Morris, A ;
Nazemi, MH ;
Pellett, MA ;
Du Plessis, J ;
Quan, YS ;
Raghavan, SL ;
Roberts, M ;
Romonchuk, W ;
Roper, CS ;
Schenk, D ;
Simonsen, L ;
Simpson, A ;
Traversa, BD ;
Trottet, L ;
Watkinson, A ;
Wilkinson, SC ;
Williams, FM ;
Yamamoto, A ;
Hadgraft, J .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 94 (03) :632-638
[9]  
Fl/p F., 2010, GYOGYSZERESZI KEMIA
[10]  
Franz T J, 1978, Curr Probl Dermatol, V7, P58