Closed pburkat closed 3 years ago
Maybe the following tutorial is helpful: doi:10.1002/psp4.12134 Besides describing a typical overall strategy to build a PBPK model, also typically adjusted parameters are mentioned.
How does one simulate drug concentration in compartments aside from peripheral venous blood and create a plot?
For individual simulations: s. Running a simulation in an individual and Analyzing results for a simulation in an individual For population simulations: s. Running a population simulation and Analyzing a population simulation
How does one increase simulation resolution in PKSim?
You can change the resolution here:
Where can I find information on how PKSIM handles compound transport into brain and all of its compartments?
Are the differential equations in PK Sim permeability limited? Of which form?
Please disregard my last 2 questions.
@pburkat , please open a new issue for each new question, otherwise your questions might be missed.
For the "permeability limited" question, please see https://github.com/Open-Systems-Pharmacology/Forum/issues/700
Good morning, I am new to PBPK modeling, but have extensive experience with pharmacodynamic kinetic modeling. Are there any resources available that help in decision making for parameter modification to improve model fits to data?