A physiologically based pharmacokinetic model of p,p'-dichlorodiphenylsulfone.
A physiologically based pharmacokinetic model of p,p'-dichlorodiphenylsulfone.
复制标题
对，对-二氯二苯砜的基于生理学的药代动力学模型。
DOI：
10.1006/taap.2002.9410
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发表时间：
2002
影响因子：
3.8
通讯作者：
Portier,CJ
中科院分区：
文献类型：
--
作者：
Parham,FredM;Matthews,HB;Portier,CJ
A physiologically based pharmacokinetic model of the absorption, distribution, metabolism, and elimination of p,p′-dichlorodiphenylsulfone (DDS) in male and female rats and mice is presented. Data used in constructing the model come from single-dose intravenous administration of DDS to male Fischer 344 rats (10 mg/kg, with data taken up to 504 h after administration), from single-dose gavage administration to male rats (10, 100, or 1000 mg/kg, with data up to 72 h after administration), and from chronic feed studies in male and female rats and male and female B6C3F1mice (studies of duration from 2 weeks up to 18 months, with feed concentrations of DDS up to 300 ppm). The model uses diffusion-limited kinetic for the distribution of the parent compound. Because fewer data are available for the metabolites of DDS (at least five of which are known to exist in the data), the model groups the metabolites into one metabolic pathway and uses simpler flow-limited kinetics for the metabolites. The data show that the kinetics of DDS are nonlinear. Possible sources of nonlinearity considered in the model were nonlinear (Michaelis-Menten) metabolism, nonlinear absorption of DDS from the gut, and induction by DDS of its own metabolism. A model using Michaelis-Menten metabolism was not found to give a significantly better fit than one using first-order linear metabolism, but omitting either of the other nonlinear effects was found to give a significantly poorer fit to the data. Because the data from mice are limited compared to those from rats, there is more confidence in the model's description of DDS kinetics in rats than in its description of kinetics in mice.
