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Updated: Dec 6, 2025

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Published on: July 11, 2025
A workflow to build PBTK models for novel species
Sebastian Schneckener1, Thomas G Preuss2, Lars Kuepfer3
1Applied Mathematics, Engineering and Technology, Bayer AG, Leverkusen, Germany.
Developing physiology-based pharmacokinetic/toxicokinetic (PBPK/TK) models for new species is streamlined by a best practice workflow. This approach identifies key parameters, significantly aiding ecotoxicology and drug development research.
Area of Science:
- Ecotoxicology
- Pharmacokinetics
- Toxicokinetics
Background:
- Physiology-based pharmacokinetic/toxicokinetic (PBPK/TK) models simulate xenobiotic concentrations in organisms.
- These models are vital in life sciences but limited for novel species in ecotoxicology.
- A standardized workflow is needed to build PBPK/TK models for new animal models.
Purpose of the Study:
- To present a best practice workflow for constructing PBPK/TK models for novel species.
- To assess parameter sensitivity across multiple species-specific PBPK/TK models.
- To develop guidelines for efficient PBPK/TK model development in new animal species.
Main Methods:
- Extrapolated eight rabbit PBPK/TK models to six additional mammalian species (human, beagle, rat, monkey, mouse, minipig).
- Utilized existing PBPK/TK models for species-specific physiological data.
- Systematically assessed parameter sensitivity in 56 resulting PBPK/TK models.
Main Results:
- Over 80% of 609 model parameters showed negligible sensitivity across all models.
- Approximately 5% of parameters exhibited high sensitivity in at least one model.
- Parameter relevance was ranked, informing model development priorities.
Conclusions:
- The study provides a best practice workflow for developing PBPK/TK models for novel species.
- This workflow enhances the efficiency and applicability of PBPK/TK modeling in ecotoxicology and related fields.
- The findings support the development of PBPK/TK models for new animal species, advancing research.
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