The paper considers the structural identifiability of a parent-metabolite p
harmacokinetic model for ivabradine and one of its metabolites. The model,
which is linear, is consider ed initially for intravenous administration of
ivabradine, and then for a combined intravenous and oral administration. I
n both cases, the model is shown to be unidentifiable. Simplification of th
e model (for both forms of administration! to that proposed by Duffull et a
l. (1) results in a globally structurally identifiable model. The analysis
could be applied In the modeling of any drug undergoing first-pass metaboli
sm, with plasma concentrations available from drug and metabolite.