FIG. 3.
Example of a fit of the pharmacokinetic model to the data of an individual subject, for comodelling of intravenous and oral data of (+) dOTC (A) and (−) dOTC (B). Circles, post-oral dose plasma drug concentrations; squares, post-intravenous dose plasma drug concentrations. The solid lines associated with each are the predicted concentrations of the pharmacokinetic model.
