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Table 1 Model description of the seven compartmental models used and estimated parameters

From: Pharmacokinetic and pharmacodynamic characterization of a novel formulation containing co-formulated interferons alpha-2b and gamma in healthy male volunteers

Model

Description

Parameters

I

Mono-compartmental with zero order absorption and bioavailability

Tk0, F, V, k

II

Mono-compartmental with first order absorption and bioavailability

ka, F, V, k

III

Bi-compartmental with first order absorption and bioavailability

ka, F, V, k, k12, k21

IV

Mono-compartmental with simultaneous zero order and first order absorption

Tk0, ka, F, V, k

V

Mono-compartmental with consecutive zero order and first order absorption. One bioavailability value

Tk0, ka, F, V, k

VI

Mono-compartmental with two simultaneous first order absorptions

ka1, F, ka2, V, k

VII

Mono-compartmental with consecutive zero order and first order absorption. One bioavailability value for each absorption component

Tk0, ka, F1, F2, V, k

  1. Tk0 duration of zero order absorption, F bioavailability associated to absorption processes, V volume of distribution of central compartment, ka rate constant of first order absorption, k first order elimination rate constant, k12 and k21: first order inter-compartmental rate constants