PAMPA - a drug absorption in vitro model 11. Matching the in vivo unstirred water layer thickness by individual-well stirring in microtitre plates

被引:134
作者
Avdeef, A [1 ]
Nielsen, PE [1 ]
Tsinman, O [1 ]
机构
[1] pION INC, Woburn, MA 01801 USA
关键词
PAMPA; unstirred water layer; Flux-pK(a); oral absorption; permeability; in vivo-in vitro correlations; progesterone; itraconazole; amiodarone; terfenadine;
D O I
10.1016/j.ejps.2004.04.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Many plate-based in vitro assays of membrane permeability (e.g., Caco-2, MDCK, PAMPA) of sparingly soluble candidate molecules report permeability of water, and not of the intended membrane barrier. This is so because the unstirred water layer on both sides of the membrane barrier is rate limiting for these highly permeable molecules. The thickness of this water layer can be 1500-4000 mum in unstirred assays. Under in vivo conditions, however, the unstirred water layer is believed to be 30-100 mum thick. Lightly stirred in vitro assays, using plate shakers, cannot lower the thickness of the water layer to match that found in vivo. In this study, 55 lipophilic drugs were employed to characterize the effect of stirring in parallel artificial membrane permeability assay (PAMPA). Highly efficient individual-well magnetic stirring at speeds greater than 110 rpm has been demonstrated to lower the unstirred water layer thickness to the in vivo range. Stirring at 622 rpm has lowered the layer thickness to 13 mum in some cases, which had not been previously achieved for plate-based permeability assays. With diminished water layer contribution at 622 rpm, for example, the effective permeability of progesterone, is 2754 x 10(-6) cm/s. The new stirring apparatus used in this study is not only suitable for PAMPA, but can also be used in Caco-2 assays. Because of the diminished resistance of the thinner water layer, the stirred PAMPA permeation time has decreased from the usual 15 It to about 15 min for lipophilic compounds. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:365 / 374
页数:10
相关论文
共 27 条
  • [1] PASSIVE DIFFUSION OF WEAK ORGANIC ELECTROLYTES ACROSS CACO-2 CELL MONOLAYERS - UNCOUPLING THE CONTRIBUTIONS OF HYDRODYNAMIC, TRANSCELLULAR, AND PARACELLULAR BARRIERS
    ADSON, A
    BURTON, PS
    RAUB, TJ
    BARSUHN, CL
    AUDUS, KL
    HO, NFH
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (10) : 1197 - 1204
  • [2] [Anonymous], 1970, Handbook of Biochemistry: Selected Data for Molecular Biology
  • [3] Drug absorption in vitro model:: filter-immobilized artificial membranes 2.: Studies of the permeability properties of lactones in Piper methysticum Forst
    Avdeef, A
    Strafford, M
    Block, E
    Balogh, MP
    Chambliss, W
    Khan, I
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 14 (04) : 271 - 280
  • [4] Avdeef A., 2003, ABSORPTION DRUG DEV, P116
  • [5] AVDEEF A, 2003, DRUG BIOAVAILABILITY, P46
  • [6] Avdeef Alex, 2001, Current Topics in Medicinal Chemistry, V1, P277, DOI 10.2174/1568026013395100
  • [7] CUSSLER EL, 1999, DIFFUSION MASS TRANS, P70
  • [8] Profiling drug-like properties in discovery research
    Di, L
    Kerns, EH
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 2003, 7 (03) : 402 - 408
  • [9] MASS-TRANSPORT PHENOMENA AND MODELS - THEORETICAL CONCEPTS
    FLYNN, GL
    YALKOWSKY, SH
    ROSEMAN, TJ
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1974, 63 (04) : 479 - 510
  • [10] DIFFUSION OF WEAK ACIDS ACROSS LIPID BILAYER MEMBRANES - EFFECTS OF CHEMICAL REACTIONS IN UNSTIRRED LAYERS
    GUTKNECHT, J
    TOSTESON, DC
    [J]. SCIENCE, 1973, 182 (4118) : 1258 - 1261