Literature DB >> 11042605

Commentary: using the convection-dispersion model and transit time density functions in the analysis of organ distribution kinetics.

M S Roberts1, Y G Anissimov, M Weiss.   

Abstract

The convection-dispersion model and its extended form have been used to describe solute disposition in organs and to predict hepatic availabilities. A range of empirical transit-time density functions has also been used for a similar purpose. The use of the dispersion model with mixed boundary conditions and transit-time density functions has been queried recently by Hisaka and Sugiyama in this journal. We suggest that, consistent with soil science and chemical engineering literature, the mixed boundary conditions are appropriate providing concentrations are defined in terms of flux to ensure continuity at the boundaries and mass balance. It is suggested that the use of the inverse Gaussian or other functions as empirical transit-time densities is independent of any boundary condition consideration. The mixed boundary condition solutions of the convection-dispersion model are the easiest to use when linear kinetics applies. In contrast, the closed conditions are easier to apply in a numerical analysis of nonlinear disposition of solutes in organs. We therefore argue that the use of hepatic elimination models should be based on pragmatic considerations, giving emphasis to using the simplest or easiest solution that will give a sufficiently accurate prediction of hepatic pharmacokinetics for a particular application. Copyright 2000 Wiley-Liss Inc.

Mesh:

Year:  2000        PMID: 11042605     DOI: 10.1002/1520-6017(200012)89:12<1579::aid-jps8>3.0.co;2-y

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  9 in total

Review 1.  Enterohepatic circulation: physiological, pharmacokinetic and clinical implications.

Authors:  Michael S Roberts; Beatrice M Magnusson; Frank J Burczynski; Michael Weiss
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

2.  A compartmental model of hepatic disposition kinetics: 1. Model development and application to linear kinetics.

Authors:  Yuri G Anissimov; Michael S Roberts
Journal:  J Pharmacokinet Pharmacodyn       Date:  2002-04       Impact factor: 2.745

Review 3.  Advanced pharmacokinetic models based on organ clearance, circulatory, and fractal concepts.

Authors:  K Sandy Pang; Michael Weiss; Panos Macheras
Journal:  AAPS J       Date:  2007-06-29       Impact factor: 4.009

4.  A note on population analysis of dissolution-absorption models using the inverse Gaussian function.

Authors:  Jian Wang; Michael Weiss; David Z D'Argenio
Journal:  J Clin Pharmacol       Date:  2008-03-21       Impact factor: 3.126

5.  Fractal structure of the liver: effect on drug elimination.

Authors:  Michael Weiss
Journal:  J Pharmacokinet Pharmacodyn       Date:  2012-12-05       Impact factor: 2.745

6.  Reassessing models of hepatic extraction.

Authors:  D Ridgway; J A Tuszynski; Y K Tam
Journal:  J Biol Phys       Date:  2003-03       Impact factor: 1.365

7.  Application of the convection-dispersion equation to modelling oral drug absorption.

Authors:  Jan I Freijer; Teun M Post; Bart A Ploeger; Joost DeJongh; Meindert Danhof
Journal:  Bull Math Biol       Date:  2006-10-06       Impact factor: 1.758

Review 8.  Drug structure-transport relationships.

Authors:  Michael S Roberts
Journal:  J Pharmacokinet Pharmacodyn       Date:  2010-11-24       Impact factor: 2.745

9.  Developing transmission line equations of oxygen transport for predicting oxygen distribution in the arterial system.

Authors:  Fei Yan; Wen-Tao Jiang; Zhi Xu; Qing-Yuan Wang; Yu-Bo Fan; Ming Zhang
Journal:  Sci Rep       Date:  2018-03-29       Impact factor: 4.379

  9 in total

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