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Intestinal absorption-partition relationships: a tentative functional nonlinear model

J M Plá-Delfina, J Moreno

    Journal of Pharmacokinetics and Biopharmaceutics
    |April 1, 1981
    PubMed
    Summary
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    This study reviews models of passive intestinal absorption, proposing a new model that incorporates pore transport for smaller molecules. This unified model explains previously contradictory absorption-partition data.

    Area of Science:

    • Pharmacokinetics
    • Physical Chemistry
    • Biophysical Chemistry

    Background:

    • Passive intestinal absorption is crucial for drug bioavailability.
    • Existing models often predict sigmoidal, hyperbolic, parabolic, or bilinear relationships between absorption rate constant (ka) and partition coefficients (P).
    • These models struggle to reconcile diverse experimental data, particularly for compounds of varying molecular weights.

    Purpose of the Study:

    • To review existing models of passive intestinal absorption.
    • To propose a novel, unified model that reconciles contradictory absorption-partition data.
    • To investigate the role of pore transport in intestinal absorption.

    Main Methods:

    • Analysis of the relationship between absorption rate constant (ka) and partition coefficients (P).

    Related Experiment Videos

  • Review of classical nonlinear physical models (nonstirred layer, equilibrium extraction).
  • Development of an alternative model incorporating the Wagner-Sedman equilibrium extraction model and pore transport.
  • Main Results:

    • Classical models predict distinct relationships (sigmoidal, hyperbolic, parabolic, bilinear) between ka and P.
    • The proposed model integrates equilibrium extraction with pore transport for compounds < 250 Da.
    • The new model demonstrates high consistency with previously contradictory absorption-partition literature data.

    Conclusions:

    • The proposed model offers a more comprehensive explanation for passive intestinal absorption mechanisms.
    • Pore transport is a significant factor for the absorption of low molecular weight compounds.
    • This unified approach enhances the understanding of drug absorption and disposition.