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. 2013 Jul 24;53(1):73–87. doi: 10.1007/s40262-013-0097-y

Table 3.

Interacting concentrations used depending on the selected physiologically based pharmacokinetic models for perpetrators

Liver transporter function Permeability limited Perfusion limited
Efflux IuIW I Liv fu/(K p Liv)
Uptake IuEW I Liv fu/(K p Liv)

EW extracellular water, I perpetrator concentration affecting other victim moieties, fu fraction unbound in plasma of the perpetrator, IW intracellular water, K p tissue-to-plasma partition coefficient, Liv liver, u unbound