An open source physiologically based kinetic model for the chicken (Gallus gallus domesticus): Calibration and validation for the prediction residues in tissues and eggs

•Open source PBK model for the chicken using WHO criteria for model evaluation.•Physiological parameters, model calibration and validation are described.•Applications to predict in vivo kinetics, tissue and egg residues for 7 chemicals.•Refinement of PBK models in chicken and other avian species is...

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Veröffentlicht in:Environment international 2020-03, Vol.136, p.105488, Article 105488
Hauptverfasser: Lautz, L.S., Nebbia, C., Hoeks, S., Oldenkamp, R., Hendriks, A.J., Ragas, A.M.J., Dorne, J.L.C.M.
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Sprache:eng
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Zusammenfassung:•Open source PBK model for the chicken using WHO criteria for model evaluation.•Physiological parameters, model calibration and validation are described.•Applications to predict in vivo kinetics, tissue and egg residues for 7 chemicals.•Refinement of PBK models in chicken and other avian species is discussed. Xenobiotics from anthropogenic and natural origin enter animal feed and human food as regulated compounds, environmental contaminants or as part of components of the diet. After dietary exposure, a chemical is absorbed and distributed systematically to a range of organs and tissues, metabolised, and excreted. Physiologically based kinetic (PBK) models have been developed to estimate internal concentrations from external doses. In this study, a generic multi-compartment PBK model was developed for chicken. The PBK model was implemented for seven compounds (with log Kow range −1.37–6.2) to quantitatively link external dose and internal dose for risk assessment of chemicals. Global sensitivity analysis was performed for a hydrophilic and a lipophilic compound to identify the most sensitive parameters in the PBK model. Model predictions were compared to measured data according to dataset-specific exposure scenarios. Globally, 71% of the model predictions were within a 3-fold change of the measured data for chicken and only 7% of the PBK predictions were outside a 10-fold change. While most model input parameters still rely on in vivo experiments, in vitro data were also used as model input to predict internal concentration of the coccidiostat monensin. Future developments of generic PBK models in chicken and other species of relevance to animal health risk assessment are discussed.
ISSN:0160-4120
1873-6750
DOI:10.1016/j.envint.2020.105488