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Making PBPK models more reproducible in practice
E. Domínguez-Romero, S. Mazurenko, M. Scheringer, VAP. Martins Dos Santos, CT. Evelo, M. Anton, JM. Hancock, A. Županič, M. Suarez-Diez
Language English Country England, Great Britain
Document type Journal Article
Grant support
857560
European Union's Horizon 2020 Research and Innovation Programme
ESFRI ELIXIR LM2023055
Czech Ministry of Education, Youth and Sports
HBM4EU
European Union's Horizon 2020
NWA-ORC 1292.19.272
Netherlands Research Council
NLK
Directory of Open Access Journals
from 2024
PubMed Central
from 2008
Medline Complete (EBSCOhost)
from 2000-01-01
Oxford Journals Open Access Collection
from 2000
PubMed
39494970
DOI
10.1093/bib/bbae569
Knihovny.cz E-resources
- MeSH
- Models, Biological * MeSH
- Pharmacokinetics * MeSH
- Humans MeSH
- Computer Simulation MeSH
- Reproducibility of Results MeSH
- Software * MeSH
- Systems Biology * methods MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Systems biology aims to understand living organisms through mathematically modeling their behaviors at different organizational levels, ranging from molecules to populations. Modeling involves several steps, from determining the model purpose to developing the mathematical model, implementing it computationally, simulating the model's behavior, evaluating, and refining the model. Importantly, model simulation results must be reproducible, ensuring that other researchers can obtain the same results after writing the code de novo and/or using different software tools. Guidelines to increase model reproducibility have been published. However, reproducibility remains a major challenge in this field. In this paper, we tackle this challenge for physiologically-based pharmacokinetic (PBPK) models, which represent the pharmacokinetics of chemicals following exposure in humans or animals. We summarize recommendations for PBPK model reporting that should apply during model development and implementation, in order to ensure model reproducibility and comprehensibility. We make a proposal aiming to harmonize abbreviations used in PBPK models. To illustrate these recommendations, we present an original and reproducible PBPK model code in MATLAB, alongside an example of MATLAB code converted to Systems Biology Markup Language format using MOCCASIN. As directions for future improvement, more tools to convert computational PBPK models from different software platforms into standard formats would increase the interoperability of these models. The application of other systems biology standards to PBPK models is encouraged. This work is the result of an interdisciplinary collaboration involving the ELIXIR systems biology community. More interdisciplinary collaborations like this would facilitate further harmonization and application of good modeling practices in different systems biology fields.
ELIXIR Wellcome Genome Campus Hinxton Cambridgeshire CB10 1SD United Kingdom
RECETOX Faculty of Science Masaryk University Kotlarska 2 611 37 Brno Czech Republic
References provided by Crossref.org
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