PBPK modelling of inter-individual variability in the pharmacokinetics of environmental chemicals
Open accessAbstract
Generic PBPK models, applicable to a large number of substances, coupled to parameter databases and QSAR modules, are now available for predictive modelling of inter-individual variability in the absorption, distribution, metabolism and excretion of environmental chemicals. When needed, Markov chain Monte Carlo methods and multilevel population models can be jointly used for a Bayesian calibration of a PBPK model, to improve our understanding of the determinants of population heterogeneity and differential susceptibility. This article reviews those developments and illustrates them with recent applications to environmentally relevant questions.
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Another significant source of uncertainty in half-life estimation could be due to the possible ongoing and/or unaccounted background exposures, and to the possible role of individual determinants (such as sex, age, genetics and general health), which may contribute to interindividual variation.
“Another significant source of uncertainty in half-life estimation could be due to the possible ongoing and/or unaccounted background exposures (Dourson and Gadagbui, 2021), and to the possible role of individual determinants (such as sex, age, genetics and general health), which may contribute to interindividual variation (Bois et al., 2010; Chiu et al., 2022).”
From Estimation of per- and polyfluoroalkyl substances (PFAS) half-lives in human studies: a systematic review and meta-analysis (2024) · cites this paper as Bois et al., 2010
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References 173 · Cited by 194
- Authors
- Bois, F. Y., Jamei, M., & Clewell, H. J.
- Affiliations
- Université de Technologie de Compiègne (FR)
- Simcyp (United Kingdom) (GB)
- Corresponding author
- Bois, Frédéric Y.
- Venue
- Toxicology
- Publisher
- Elsevier BV
- Published
- 2010-12
- Volume
- 278
- Issue
- 3
- Pages
- 256-267
- ISSN
- 0300-483X (ISSN-L)
- OpenAlex
- W2055526313
- Cited by
- 194
- References
- 173
- Citations by year
- 2026: 7 · 2025: 12 · 2024: 6 · 2023: 7 · 2022: 7 · 2021: 8 · 2020: 25 · 2019: 13 · 2018: 16 · 2017: 17 · 2016: 15 · 2015: 9 · 2014: 13 · 2013: 14 · 2012: 17
- FWCI
- 1.26
- Type
- journal article
- Language
- en
- Open access
- green
- ineris.hal.science
- Licence
- Locations
- Toxicology (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- Topics
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Toxic Organic Pollutants Impact
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Physical Sciences › Computer Science › Computational Theory and Mathematics › Computational Drug Discovery Methods
- Keywords
- physiologically based pharmacokinetic modelling, interindividual variability, environmental chemicals, population heterogeneity, differential susceptibility, Bayesian calibration, Markov chain Monte Carlo, QSAR, parameter database, ADME
- MeSH terms
- Animals, Drug Interactions, Environmental Pollutants, Humans, Models, Biological, Monte Carlo Method, Risk Assessment
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