Metabolite mean transit times in the liver as predicted by various models of hepatic elimination


Autoria(s): Mellick, GD; Anissimov, YG; Bracken, AJ; Roberts, MS
Data(s)

01/01/1997

Resumo

Predicted area under curve (AUC), mean transit time (MTT) and normalized variance (CV2) data have been compared for parent compound and generated metabolite following an impulse input into the liver, Models studied were the well-stirred (tank) model, tube model, a distributed tube model, dispersion model (Danckwerts and mixed boundary conditions) and tanks-in-series model. It is well known that discrimination between models for a parent solute is greatest when the parent solute is highly extracted by the liver. With the metabolite, greatest model differences for MTT and CV2 occur when parent solute is poorly extracted. In all cases the predictions of the distributed tube, dispersion, and tasks-in-series models are between the predictions of the rank and tube models. The dispersion model with mixed boundary conditions yields identical predictions to those for the distributed tube model (assuming an inverse gaussian distribution of tube transit times). The dispersion model with Danckwerts boundary conditions and the tanks-in series models give similar predictions to the dispersion (mixed boundary conditions) and the distributed tube. The normalized variance for parent compound is dependent upon hepatocyte permeability only within a distinct range of permeability values. This range is similar for each model but the order of magnitude predicted for normalized variance is model dependent. Only for a one-compartment system is the MIT for generated metabolite equal to the sum of MTTs for the parent compound and preformed metabolite administered as parent.

Identificador

http://espace.library.uq.edu.au/view/UQ:34758

Idioma(s)

eng

Palavras-Chave #Pharmacology & Pharmacy #Hepatic Elimination Models #Metabolite Kinetics #Dispersion Model #Distributed Tube Model #Area Under Curve #Mean Transit Time #Normalized Variance #Hepatocyte Permeability #Impulse-response #Perfused-rat-liver #2-compartment Dispersion Model #Multiple-indicator Dilution #Formation In-vivo #Protein-binding #Distribution Kinetics #Drug Elimination #Salicylic-acid #Clearance #Discrimination
Tipo

Journal Article