Development and evaluation of an in vitro method for prediction of human drug absorption - I. Assessment of artificial membrane composition

被引:33
作者
Corti, G [1 ]
Maestrelli, F [1 ]
Cirri, M [1 ]
Furlanetto, S [1 ]
Mura, P [1 ]
机构
[1] Univ Florence, Fac Pharm, Dept Pharmaceut Sci, I-50019 Florence, Italy
关键词
artificial membrane; in vitro permeation method; naproxen; experimental design; mixture design;
D O I
10.1016/j.ejps.2005.11.004
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
A study was undertaken aimed at developing a dynamic in vitro method based on the use of artificial membranes for screening and prediction of the absorption properties of drugs. The development of a suitable artificial membrane simulating the behaviour of the natural gastrointestinal one is the critical step for the fulfilment of this research and it has been the aim of the present work. A series of filters of different chemical nature and different characteristics (pore size, percent of porosity, thickness) were evaluated and compared in order to select the most suitable one to use as support for the artificial lipid membrane preparation. Permeation experiments were performed by using naproxen as reference model drug. The target was to achieve a naproxen apparent permeability (P-app) value close to that previously obtained using a Caco-2 cell dynamic methodology (4.88 x 10(-5) cm s(-1)), which related well to the fraction of dose absorbed in vivo in human. Filters of cellulose nitrate-acetate mixture with a porosity of 70% and 0.025 mu m pore size were selected on the basis of the highest reproducibility of results and suitable drug P-app value obtained. Mixture design experiments were then carried out in order to optimize the composition of the lipid mixture to use for porous support impregnation to obtain the desired P-app value. Sixteen different lipid mixtures were prepared according to mixture experimental plan and evaluated by diffusion experiments. The contour plot obtained was used to select an optimum lipidic mixture (cholesterol 2.10%; Lipoid(R) E 80 1.70%; n-octanol 96.2%) for the cellulose nitrate-acetate membrane impregnation. The experimental response obtained from diffusion experiments performed by utilising the optimised lipidic impregnation mixture, was 4.88 x 10(-5) cm s(-1), matching exactly the prefixed target. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:346 / 353
页数:8
相关论文
共 36 条
[1]
[Anonymous], [No title captured]
[2]
Caco-2 monolayers in experimental and theoretical predictions of drug transport (Reprinted from Advanced Drug Delivery Reviews, vol 22, pg 67-84, 1996) [J].
Artursson, P ;
Palm, K ;
Luthman, K .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 46 (1-3) :27-43
[3]
EPITHELIAL TRANSPORT OF DRUGS IN CELL-CULTURE .1. A MODEL FOR STUDYING THE PASSIVE DIFFUSION OF DRUGS OVER INTESTINAL ABSORPTIVE (CACO-2) CELLS [J].
ARTURSSON, P .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (06) :476-482
[4]
AVDEEF A, 2003, DRUG BIOAVAILABILITY, P46
[5]
Absorption classification of oral drugs based on molecular surface properties [J].
Bergström, CAS ;
Strafford, M ;
Lazorova, L ;
Avdeef, A ;
Luthman, K ;
Artursson, P .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (04) :558-570
[6]
Brereton R. G., 2004, CHEMOMETRICS DATA AN
[7]
Differential scanning calorimetry differences in micronized and unmicronized nimesulide uptake processes in biomembrane models [J].
Castelli, F ;
Sarpietro, MG ;
Messina, C ;
De Lazzari, A ;
Di Rosa, D ;
Giannetto, A .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 19 (04) :237-243
[8]
Castro J. L., 1991, P INT FUZZ ENG S 91, V1, P70
[9]
Cornell JA., 1990, EXPT MIXTURES
[10]
*COUNC EUR, 2002, EUR PHARM, P194