Comparing computational times for simulations when using PBPK model template and stand-alone implementations of PBPK models

Journal Article · 18 February 2025 · Frontiers in Toxicology

DOI: https://doi.org/10.3389/ftox.2025.1518769 · OSTI ID:2520222

Bernstein, Amanda S.; Schlosser, Paul M.; Kapraun, Dustin F.

Introduction We previously developed a PBPK model template that consists of a single model “superstructure” with equations and logic found in many physiologically based pharmacokinetic (PBPK) models. Using the template, one can implement PBPK models with different combinations of structures and features. Methods To identify factors that influence computational time required for PBPK model simulations, we conducted timing experiments using various implementations of PBPK models for dichloromethane and chloroform, including template and stand-alone implementations, and simulating four different exposure scenarios. For each experiment, we measured the required computational time and evaluated the impacts of including various model features (e.g., number of output variables calculated) and incorporating various design choices (e.g., different methods for estimating blood concentrations). Results We observed that model implementations that treat body weight and dependent quantities as constant (fixed) parameters can result in a 30% time savings compared with options that treat body weight and dependent quantities as time-varying. We also observed that decreasing the number of state variables by 36% in our PBPK model template led to a decrease of 20–35% in computational time. Other factors, such as the number of output variables, the method for implementing conditional statements, and the method for estimating blood concentrations, did not have large impacts on simulation time. In general, simulations with PBPK model template implementations of models required more time than simulations with stand-alone implementations, but the flexibility and (human) time savings in preparing and reviewing a model implemented using the PBPK model template may justify the increases in computational time requirements. Conclusion Our findings concerning how PBPK model design and implementation decisions impact computational speed can benefit anyone seeking to develop, improve, or apply a PBPK model, with or without the PBPK model template.

• Sponsoring Organization: USDOE
• OSTI ID: 2520222
• Journal Information: Frontiers in Toxicology, Journal Name: Frontiers in Toxicology Vol. 7; ISSN 2673-3080
• Publisher: Frontiers Media SACopyright Statement
• Country of Publication: Switzerland
• Language: English