ArticleJournal of pharmacokinetics and pharmacodynamics2016
Steady-state volume of distribution of two-compartment models with simultaneous linear and saturated elimination.
Article in Journal of pharmacokinetics and pharmacodynamics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Mathematical analysis and drug exposure evaluation of pharmacokinetic models with endogenous production and simultaneous first-order and Michaelis-Menten elimination: the case of single dose.Journal of pharmacokinetics and pharmacodynamics · 2018Article
- Pharmacokinetics of 2,000 Milligram Ertapenem in Tuberculosis Patients.Antimicrobial agents and chemotherapy · 2018Article
Corrections and comments
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Authors and funding
3 authors.
Funding
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Abstract
The model-independent estimation of physiological steady-state volume of distribution ([Formula: see text]), often referred to non-compartmental analysis (NCA), is historically based on the linear compartment model structure with central elimination. However the NCA-based steady-state volume of distribution ([Formula: see text]) cannot be generalized to more complex models. In the current paper, two-compartment models with simultaneous first-order and Michaelis-Menten elimination are considered. In particular, two indistinguishable models [Formula: see text] and [Formula: see text], both having central Michaelis-Menten elimination, while first-order elimination exclusively either from central or peripheral compartment, are studied. The model-based expressions of the steady-state volumes of distribution [Formula: see text] and their relationships to NCA-based [Formula: see text] are derived. The impact of non-linearity and peripheral elimination is explicitly delineated in the formulas. Being concerned with model identifiability and indistinguishability issues, an interval estimate of [Formula: see text] is suggested.
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