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Computational toxicology: Physiologically based pharmacokinetic models (PBPK) for lifetime exposure and bioaccumulation of polybrominated diphenyl ethers (PBDEs) in marine mammalsPeer reviewed article
Weijs, L.; Covaci, A.; Yang, R.S.H.; Das, K.; Blust, R. (2012). Computational toxicology: Physiologically based pharmacokinetic models (PBPK) for lifetime exposure and bioaccumulation of polybrominated diphenyl ethers (PBDEs) in marine mammals Environ. Pollut. 163: 134-141. dx.doi.org/10.1016/j.envpol.2011.12.037
In: Environmental Pollution. Elsevier: London. ISSN 0269-7491, meer

Beschikbaar in Auteurs 
    VLIZ: Open Repository 233031 [ OMA ]

Trefwoorden
    Modellen; Polybrominated biphenyls; Zeezoogdieren; ANE, Noordzee [gazetteer]; MED, Zwarte Zee [gazetteer]; Marien

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Abstract
    Due to migration of harbour porpoises towards more polluted areas like the North Sea and their sensitivity towards pollution, there is a need for proper conservation measures for this species. As a consequence, knowledge about the pollutant’s kinetics is required. The present study is the first to investigate the kinetics of PBDEs in marine mammals using PBPK modeling as a non-destructive tool for describing the chemical’s kinetics in a protected animal species. The models were developed and parameterized using data from the literature and Black Sea harbour porpoises through computer optimization. The predictability of these models in time was assessed by reverse dosimetry modeling using data from North Sea porpoises (1990–2008). From these predictions, PBDE 99 levels were found to decrease the fastest, followed by PBDE 153, 47 and 100. Results show that the PBPK models can be applied for harbour porpoises from different regions and also simulate time trends.

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