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生理药物代谢动力学模型及其在二甲苯危险度评价中的应用 被引量:1

Physiologically Based Pharmacokinetic Models for Use in Risk Assessment of Xylene
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摘要 作为一种估测组织放射量的成熟工具,生理药物代谢动力学(PBPK)模型可用于模拟从化学物质的外暴露到靶位点的内暴露这一过程,以支持人体健康危险度的定量预测。笔者将从建立模型的一般步骤、评估模型的标准和模型在危险度评价中的应用三个方面进行综述,并以二甲苯为例详细介绍PBPK模型在危险度评价中的应用。 As a mature tool for estimating tissue dosimetry, physiologically based pharmacokinetic (PBPK) models are being used to simulate the process from an external chemical exposure to an internal exposure at a target site, for supporting quantitative predictions of risks to human health. This paper reviewed these models from three aspects: the general steps of model construction, the criteria of model evaluation, the use of model in risk assessment and taking xylene as an example particularly described the third aspect.
作者 熊成香
出处 《环境与健康杂志》 CAS CSCD 北大核心 2008年第5期467-469,共3页 Journal of Environment and Health
关键词 生理药物代谢动力学模型 危险度评价 二甲苯 Physiologically based pharmacokinetic model Risk assessment Xylene
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参考文献21

  • 1Andersen ME. Toxicokinetic modeling and its application in chemical risk assessment [J ]. Toxicol Lett, 2003, 138: 9-27.
  • 2Clewell HJ 3rd, Andersen ME. Applying mode-of-action and phannacokinetic considerations in contemporary cancer risk assessments: an example with trichloroethylene [J ]. Crit Rev Toxicol, 2004, 34: 385-445.
  • 3USEPA. Approaches for the application of physiologically based pharmacokinetic(PBPK) models and supporting data in risk assessment [ OL ].http://cfpub.epa.gov/ncea/cfm/recordisplay.cfm?deid = 135427. 2005-07-28.
  • 4Robert SD. PBPK models in risk assessment: a focus on chloroprene [J ]. Chem Biol Interact, 2007, 166:352-359.
  • 5郝守进,王斌.挥发性有机化合物的代谢动力学研究进展与应用[J].中华预防医学杂志,1999,33(3):182-184. 被引量:2
  • 6Rory BC. Biologically motivated quantitative models and the mixture toxicity problem[J ]. Toxicol Sci, 2001, 63:125-131.
  • 7陆亚松,Raymond S.H.Yang.以1,1,1-三氯乙烷为例介绍生理药代动力学模型的建立[J].环境与职业医学,2006,23(4):330-338. 被引量:14
  • 8Weihsueh AC, Hugh AB, Robert SD, et al. Evaluation of physiologically based pharmacokinetic models for use in risk assessment [J ]. J Appl Toxicol, 2001, 63:218-237.
  • 9Chao C, Robert DW. Improving risk assessment through the use of physiologieaUy-basedmodels [ OL ]. http://oaspub.epa.gov/eims/eimscomm. getfile?p_download_id=434178. 2007-09.
  • 10USEPA. Toxicological review of xylenes [ OL ]. http://www.epa.gov/IRIS/ toxreviews/0270-tr.pdf. 2003-01.

二级参考文献49

  • 1Jepson GW,Hoover DK,Black RK,et al.A partition coefficient determination method for nonvolatile chemicals in biological tissues[J].Fundam Appl Toxicol,1994,22:519-524.
  • 2Sato A,Nakajima T.A vial-equilibration method to evaluate the drugmetabolizing enzyme activity for volatile hydrocarbons[J].Toxicol Appl Pharmacol,1979,47:41-46.
  • 3Staats DA,Fisher JW,Connolly RB.Gastrointestinal absorption of xenobiotics in physiologically based pharmacokinetic models.A two-compartment description[J].Drug Metab Dispos,1991,19:144-148.
  • 4Bungay PM,Dedrick RL,Matthews HB.Enteric transport of chlordecone (Kepone) in the rat[J].J Pharmacokinet Biopharm,1981,9:309-341.
  • 5Cong D,Doherty M,Pang KS.A new physiologically based,segregated-flow model to explain route-dependent intestinal metabolism[J].Drug Metab Dispos,2000,28:224-235.
  • 6Semino G,Lilly P,Andersen ME.A pharmacokinetic model describing pulsatile uptake of orally-administered carbon tetrachloride[J].Toxicology,1997,117:25-33.
  • 7Ramsey JC,Andersen ME.A physiologically based description of the inhalation pharmacokinetics of styrene in rats and humans[J].Toxicol Appl Pharmacol,1984,73:159-175.
  • 8Woodruff TJ,Bois FY,Auslander D,et al.Structure and parameterization of pharmacokinetic models:their impact on model predictions[J].Risk Anal,1992,12:189-201.
  • 9Clewell HJ,3rd,Lee TS,Carpenter RL.Sensitivity of physiologically based pharmacokinetic models to variation in model parameters:methylene[J] chloride.Risk Anal,1994,14:521-531.
  • 10Dallas CE,Ramanathan R,Muralidhara S,et al.The uptake and elimination of 1,1,1-trichloroethane during and following inhalation exposures in rats[J].Toxicol Appl Pharmacol,1989,98:385-397.

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