Literature DB >> 21120752

Physiologically based pharmacokinetic (PBPK) tool kit for environmental pollutants--metals.

P Ruiz1, B A Fowler, J D Osterloh, J Fisher, M Mumtaz.   

Abstract

The Agency for Toxic Substances and Disease Registry (ATSDR) is mandated by the US Congress to identify significant human exposure levels, develop methods to determine such exposures, and design strategies to mitigate them. Physiologically based pharmacokinetic (PBPK) models are increasingly being used to evaluate toxicity of environmental pollutants through multiple exposure pathways. As part of its translational research project, ATSDR is developing a human 'PBPK model tool kit' that consists of a series of published models re-coded in a common simulation language. The tool kit currently consists of models, at various stages of development, for priority environmental contaminants including solvents and persistent organic pollutants. Presented here are results of translational activities of re-coding models for cadmium, mercury, and arsenic. As part of this work, following re-coding each new model was evaluated for fidelity followed by sensitivity analysis. Good agreement was generally obtained for all three models when predictions of original and re-coded model simulations were compared. Also presented is an application of the cadmium toxicokinetic model to interpret biomonitoring data from the National Health and Nutrition Examination Survey (NHANES). The PBPK tool kit will enable ATSDR scientists to perform simulations of exposures from contaminated environmental media at sites of concern and to better interpret site-specific biomonitoring data.

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Year:  2010        PMID: 21120752     DOI: 10.1080/1062936X.2010.528942

Source DB:  PubMed          Journal:  SAR QSAR Environ Res        ISSN: 1026-776X            Impact factor:   3.000


  9 in total

1.  Application of pharmacokinetic modelling for 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure assessment.

Authors:  P Ruiz; L L Aylward; M Mumtaz
Journal:  SAR QSAR Environ Res       Date:  2014-11-14       Impact factor: 3.000

2.  Exploring Mechanistic Toxicity of Mixtures Using PBPK Modeling and Computational Systems Biology.

Authors:  Patricia Ruiz; Claude Emond; Evad D McLanahan; Shivanjali Joshi-Barr; Moiz Mumtaz
Journal:  Toxicol Sci       Date:  2020-03-01       Impact factor: 4.849

Review 3.  Exposure to Mixtures of Metals and Neurodevelopmental Outcomes: A Multidisciplinary Review Using an Adverse Outcome Pathway Framework.

Authors:  Katherine von Stackelberg; Elizabeth Guzy; Tian Chu; Birgit Claus Henn
Journal:  Risk Anal       Date:  2015-06-10       Impact factor: 4.000

4.  Physiologically based pharmacokinetic toolkit to evaluate environmental exposures: Applications of the dioxin model to study real life exposures.

Authors:  Claude Emond; Patricia Ruiz; Moiz Mumtaz
Journal:  Toxicol Appl Pharmacol       Date:  2016-12-10       Impact factor: 4.219

5.  Modeling cadmium exposures in low- and high-exposure areas in Thailand.

Authors:  Soisungwan Satarug; Witaya Swaddiwudhipong; Werawan Ruangyuttikarn; Muneko Nishijo; Patricia Ruiz
Journal:  Environ Health Perspect       Date:  2013-02-22       Impact factor: 9.031

6.  Translational research to develop a human PBPK models tool kit-volatile organic compounds (VOCs).

Authors:  M Moiz Mumtaz; Meredith Ray; Susan R Crowell; Deborah Keys; Jeffrey Fisher; Patricia Ruiz
Journal:  J Toxicol Environ Health A       Date:  2012

Review 7.  Development of a human Physiologically Based Pharmacokinetic (PBPK) Toolkit for environmental pollutants.

Authors:  Patricia Ruiz; Meredith Ray; Jeffrey Fisher; Moiz Mumtaz
Journal:  Int J Mol Sci       Date:  2011-10-31       Impact factor: 5.923

8.  Application of physiologically based pharmacokinetic models in chemical risk assessment.

Authors:  Moiz Mumtaz; Jeffrey Fisher; Benjamin Blount; Patricia Ruiz
Journal:  J Toxicol       Date:  2012-03-19

Review 9.  Dietary Cadmium Intake and Its Effects on Kidneys.

Authors:  Soisungwan Satarug
Journal:  Toxics       Date:  2018-03-10
  9 in total

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