Literature DB >> 9044169

New perspectives on the theory of permeability and resistance in the study of drug transport and absorption.

W L Chiou1.   

Abstract

Permeability coefficient (P) expressed as distance per unit time has been commonly interpreted to represent the velocity of drug movement across a heterogeneous medium such as skin and intestinal epithelium. The basis of such an interpretation is questioned on several grounds. For example, the basic assumption for calculating P (as defined conventionally) according to the Fick's law of diffusion requires the entire medium to be homogeneous and rate-limiting in transport. The theoretical basis of the widely used total resistance or resistance additivity concept is reviewed. Such a concept is shown to be applicable to the study of total transit time across the medium but may not be applicable to the study of steady-state flux or absorption across the medium under normal conditions. Based on the diffusional, compartmental, absorptive clearance or carrier-mediated-transport analysis it is shown that only the first transport resistance from the bulk medium across the surface (such as cellular membranes) of the permeation medium (such as a cell or a tissue) is usually the deciding factor in drug transport or absorption. Resistances on the other side of the surface barrier usually only affect the drug accumulation vs. time profile in the medium, but not the steady-state flux or absorption. The role of unstirred water layer adjacent to the internal capillary wall is postulated to play an important role in causing the blood-flow dependency in absorption, a phenomenon that cannot be rationalized by the conventional effective permeability concept. The conventional concept of sink conditions on the serosal side is questioned. The present analysis further supports the use of the absorptive or transport clearance concept in absorption or transport study. Effective permeability is regarded as a mathematical operator for transport across a barrier or a tissue, and may be unrelated to the Fick's law of diffusion under most conditions. The velocity unit for P is regarded simply as a "collapsed" unit based on the absorptive or transport clearance per unit gross surface area. It is hoped that this commentary will stimulate further research and discussions in this general area of drug transport and absorption. It appears that there is a need to experimentally confirm the total resistance theory in biological systems.

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Year:  1996        PMID: 9044169     DOI: 10.1007/bf02353521

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  16 in total

Review 1.  We may not measure the correct intestinal wall permeability coefficient of drugs: alternative absorptive clearance concept.

Authors:  W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1995-06

2.  Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells.

Authors:  P Artursson; J Karlsson
Journal:  Biochem Biophys Res Commun       Date:  1991-03-29       Impact factor: 3.575

3.  The validation of the intestinal permeability approach to predict oral fraction of dose absorbed in humans and rats.

Authors:  W L Chiou
Journal:  Biopharm Drug Dispos       Date:  1995-01       Impact factor: 1.627

4.  Effect of 'unstirred' water layer in the intestine on the rate and extent of absorption after oral administration.

Authors:  W L Chiou
Journal:  Biopharm Drug Dispos       Date:  1994-11       Impact factor: 1.627

5.  Regional rectal perfusion: a new in vivo approach to study rectal drug absorption in man.

Authors:  H Lennernäs; U Fagerholm; Y Raab; B Gerdin; R Hällgren
Journal:  Pharm Res       Date:  1995-03       Impact factor: 4.200

6.  A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability.

Authors:  G L Amidon; H Lennernäs; V P Shah; J R Crison
Journal:  Pharm Res       Date:  1995-03       Impact factor: 4.200

7.  Estimating human oral fraction dose absorbed: a correlation using rat intestinal membrane permeability for passive and carrier-mediated compounds.

Authors:  G L Amidon; P J Sinko; D Fleisher
Journal:  Pharm Res       Date:  1988-10       Impact factor: 4.200

8.  Closed rat jejunal segment in situ: role of pre-epithelial diffusion resistance (unstirred layer) in the absorption process and model analysis.

Authors:  D Winne; H Görig; U Müller
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1987-02       Impact factor: 3.000

9.  First-pass accumulation of salicylic acid in gut tissue after absorption in anesthetized rat.

Authors:  Y M Choi; S M Chung; W L Chiou
Journal:  Pharm Res       Date:  1995-09       Impact factor: 4.200

10.  Influence of anesthetic regimens on the intestinal absorption of 5-fluorouracil in rats.

Authors:  H Yuasa; K Matsuda; J Watanabe
Journal:  Biol Pharm Bull       Date:  1995-05       Impact factor: 2.233

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  8 in total

1.  Profound effect of plasma protein binding on the polarized transport of furosemide and verapamil in the Caco-2 model.

Authors:  S M Chung; E J Park; S M Swanson; T C Wu; W L Chiou
Journal:  Pharm Res       Date:  2001-04       Impact factor: 4.200

2.  Linear correlation of the fraction of oral dose absorbed of 64 drugs between humans and rats.

Authors:  W L Chiou; A Barve
Journal:  Pharm Res       Date:  1998-11       Impact factor: 4.200

3.  The size of the unstirred layer as a function of the solute diffusion coefficient.

Authors:  P Pohl; S M Saparov; Y N Antonenko
Journal:  Biophys J       Date:  1998-09       Impact factor: 4.033

4.  Evaluation of using dog as an animal model to study the fraction of oral dose absorbed of 43 drugs in humans.

Authors:  W L Chiou; H Y Jeong; S M Chung; T C Wu
Journal:  Pharm Res       Date:  2000-02       Impact factor: 4.200

5.  Apparent lack of effect of P-glycoprotein on the gastrointestinal absorption of a substrate, tacrolimus, in normal mice.

Authors:  W L Chiou; S M Chung; T C Wu
Journal:  Pharm Res       Date:  2000-02       Impact factor: 4.200

6.  Comparison of oral absorption and bioavailablity of drugs between monkey and human.

Authors:  Win L Chiou; Paul W Buehler
Journal:  Pharm Res       Date:  2002-06       Impact factor: 4.200

7.  Metronidazole or Cotrimoxazole therapy is associated with a decrease in intestinal bioavailability of common antiretroviral drugs.

Authors:  Flore Dossou-Yovo; Godefroy Mamadou; Imar Djibrine Soudy; Nicolas Limas-Nzouzi; Joe Miantezila; Jehan-François Desjeux; Bruno Eto
Journal:  PLoS One       Date:  2014-02-26       Impact factor: 3.240

Review 8.  Developments in Methods for Measuring the Intestinal Absorption of Nanoparticle-Bound Drugs.

Authors:  Wei Liu; Hao Pan; Caiyun Zhang; Liling Zhao; Ruixia Zhao; Yongtao Zhu; Weisan Pan
Journal:  Int J Mol Sci       Date:  2016-07-21       Impact factor: 5.923

  8 in total

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