Literature DB >> 1420256

A new diffusion chamber system for the determination of drug permeability coefficients across the human intestinal epithelium that are independent of the unstirred water layer.

J Karlsson1, P Artursson.   

Abstract

A new method for determining permeability coefficients, that are independent of the unstirred water layer (UWL), has been developed. The method was used to determine the cellular permeability coefficient of the rapidly absorbed drug testosterone in monolayers of the human intestinal epithelial cell line, Caco-2. Using a new diffusion cell with an effective stirring system based on a gas lift, the cellular permeability coefficient for testosterone was (1.98 +/- 0.13).10(-4) cm/s which is 3.5-times higher than the permeability coefficient obtained in the unstirred system. The thickness of the UWL obtained with the well stirred diffusion cell was 52 +/- 4 microns. This value is much lower than those previously reported in various well stirred in vitro models. The calculated cellular permeability of testosterone was 13-23-times lower than that for an UWL of the same thickness as the epithelial cell (17-30 microns). We conclude that the permeability of the epithelial monolayer must be included in calculations of the thickness of the UWL.

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Year:  1992        PMID: 1420256     DOI: 10.1016/0005-2736(92)90312-a

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  13 in total

1.  An improved cell culture model based on 2/4/A1 cell monolayers for studies of intestinal drug transport: characterization of transport routes.

Authors:  Staffan Tavelin; Jan Taipalensuu; Finn Hallböök; Kati-Sisko Vellonen; Vanessa Moore; Per Artursson
Journal:  Pharm Res       Date:  2003-03       Impact factor: 4.200

Review 2.  Modeling kinetics of subcellular disposition of chemicals.

Authors:  Stefan Balaz
Journal:  Chem Rev       Date:  2009-05       Impact factor: 60.622

3.  The asymmetry of the unstirred water layer in permeability experiments.

Authors:  Timo Korjamo; Aki T Heikkinen; Pekka Waltari; Jukka Mönkkönen
Journal:  Pharm Res       Date:  2008-04-16       Impact factor: 4.200

4.  Quantification and imaging of mannitol transport through Caco-2 cell monolayers using a positron-emitting tracer.

Authors:  L Lazorova; J Gråsjö; P Artursson; M Bergström; F Wu; E Petterman-Bergström; M Ogren; B Långström
Journal:  Pharm Res       Date:  1998-07       Impact factor: 4.200

5.  Evidence for diminished functional expression of intestinal transporters in Caco-2 cell monolayers at high passages.

Authors:  H Yu; T J Cook; P J Sinko
Journal:  Pharm Res       Date:  1997-06       Impact factor: 4.200

Review 6.  The human intestinal epithelial cell line Caco-2; pharmacological and pharmacokinetic applications.

Authors:  V Meunier; M Bourrié; Y Berger; G Fabre
Journal:  Cell Biol Toxicol       Date:  1995-08       Impact factor: 6.691

7.  Pluronic P85 increases permeability of a broad spectrum of drugs in polarized BBMEC and Caco-2 cell monolayers.

Authors:  E V Batrakova; S Li; D W Miller; A V Kabanov
Journal:  Pharm Res       Date:  1999-09       Impact factor: 4.200

8.  Prediction of the oral absorption of low-permeability drugs using small intestine-like 2/4/A1 cell monolayers.

Authors:  Staffan Tavelin; Jan Taipalensuu; Lauri Söderberg; Rick Morrison; Saeho Chong; Per Artursson
Journal:  Pharm Res       Date:  2003-03       Impact factor: 4.200

9.  Transport of lipophilic drug molecules in a new mucus-secreting cell culture model based on HT29-MTX cells.

Authors:  I Behrens; P Stenberg; P Artursson; T Kissel
Journal:  Pharm Res       Date:  2001-08       Impact factor: 4.200

10.  The role of permeability in drug ADME/PK, interactions and toxicity--presentation of a permeability-based classification system (PCS) for prediction of ADME/PK in humans.

Authors:  Urban Fagerholm
Journal:  Pharm Res       Date:  2007-08-21       Impact factor: 4.200

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