Pharmacokinetic modeling of polychlorinated dibenzo-p-dioxins (PCDDs) and furans (PCDFs) in cows

A physiologically based pharmacokinetic (PB-PK) model for 2,3,7,8-TCDD in cows is described. Uptake in tissues appears to be blood flow limited except in adipose. Sensitive model parameters are fat tissue volume and bioavailability. The agreement between predicted and experimental data is fairly goo...

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Veröffentlicht in:Chemosphere (Oxford) 1994-02, Vol.28 (4), p.711-715
Hauptverfasser: Derks, H.J.G.M., Berende, P.L.M., Olling, M., Everts, H., Liem, A.K.D., de Jong, A.P.J.M.
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Sprache:eng
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Zusammenfassung:A physiologically based pharmacokinetic (PB-PK) model for 2,3,7,8-TCDD in cows is described. Uptake in tissues appears to be blood flow limited except in adipose. Sensitive model parameters are fat tissue volume and bioavailability. The agreement between predicted and experimental data is fairly good.
ISSN:0045-6535
1879-1298
DOI:10.1016/0045-6535(94)90222-4