Hi
I am trying to build a PopPk model for a drug with its metabolite (active) as a joint model. I found a published model where they modeled the portion of the metabolite formed from the parent drug in GI (pre-systemic). I tried to build a similar model using the graphical interface option in NLME.
For pre-systemic metabolism, I created a deposit compartment using the (Duration) function in the absorption compartment and then two absorption rates, one to the central compartment of the parent drug and another directly to the central compartment of the metabolite. I am unsure if this defined the pre-systemic metabolism step described in the published model.
The other issue, I am trying to model the fraction of parent drug clearance attributed to metabolite formation and the fraction to other not active metabolites (not needed to be included in the model). I do not know how to do that using NLME.
Can I get help with this issue?
I attached the model file I created and the pharmacokinetic model structure for the published paper.
AZT meta.phxproj (846 KB)