Adjustment factors for toluene, styrene and methyl chloride by population modeling of toxicokinetic variability

•We present data-driven AFs for human kinetic variability for 3 organic solvents.•The AFs are derived by population PBPK modeling.•We explore effects of age, gender and various workplace conditions.•For most groups and conditions our AFs are below 2.2.•For certain occupational exposure scenarios the...

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Veröffentlicht in:Regulatory toxicology and pharmacology 2014-06, Vol.69 (1), p.78-90
Hauptverfasser: Mörk, Anna-Karin, Jonsson, Fredrik, Johanson, Gunnar
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Sprache:eng
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Zusammenfassung:•We present data-driven AFs for human kinetic variability for 3 organic solvents.•The AFs are derived by population PBPK modeling.•We explore effects of age, gender and various workplace conditions.•For most groups and conditions our AFs are below 2.2.•For certain occupational exposure scenarios the AFs are up to 5.0. The availability of experimental data suitable as a basis to quantify human variability in response to chemical exposure has increased in recent years. It has enabled scientifically based, data driven adjustment factors (AF) to be deployed in the risk assessment process. As part of this development, we derive AF for human toxicokinetic variability (HK) for three lipophilic organic solvents; toluene, styrene and methyl chloride using physiologically based pharmacokinetic (PBPK) models in a population framework. The Monte Carlo simulations cover the influence of age and gender on toxicokinetic variability in the general population, as well as workplace ventilation rates and fluctuations in exposure level and workload in adult male and female workers. The derived AFHK are below 2.2 (95th percentile) for all subpopulations, exposure scenarios and chemicals, except for markers of acute effects in workers, where the factors are up to 5.0.
ISSN:0273-2300
1096-0295
1096-0295
DOI:10.1016/j.yrtph.2014.02.015