Development and validation of predictive permeability and partitioning models for organic contaminants within physiologically-based toxicokinetic models

基于生理的毒代动力学模型中有机污染物的预测渗透性和分配模型的开发和验证

基本信息

  • 批准号:
    371792-2009
  • 负责人:
  • 金额:
    $ 1.97万
  • 依托单位:
  • 依托单位国家:
    加拿大
  • 项目类别:
    Discovery Grants Program - Individual
  • 财政年份:
    2012
  • 资助国家:
    加拿大
  • 起止时间:
    2012-01-01 至 2013-12-31
  • 项目状态:
    已结题

项目摘要

Environmental contaminant exposure is an escalating concern and assessing the human risks associated with such exposure continues to be an inexact science. Risks are largely based upon the extrapolation of exposure and effect in animals to those in human. The use of modeling and simulation has been used as an aid for understanding the relationship between chemical exposure, from food or air, and response. By building virtual organisms in computers to represent both laboratory animals and humans, the movement of the contaminant in the human body can be modeled based on experimental tests in animals. Because we cannot ethically expose humans to contaminants, this represents the best means at predicting human exposure. These virtual organisms must accurately represent the true form and this proposal aims to ensure that the movement of chemical from external exposure to internal or organ exposure is well represented. Since response is based on organ concentrations of the chemical, understanding this process is imperative. This will allow predictions of how the external exposure relates to organ exposure across different species.
环境污染物暴露是一个日益严重的问题,评估与这种暴露有关的人类风险仍然是一门不精确的科学。风险很大程度上是基于对动物暴露和对人类影响的推断。建模和模拟的使用已被用来帮助理解从食物或空气中接触化学物质与反应之间的关系。通过在计算机中构建虚拟生物体来代表实验动物和人类,污染物在人体中的运动可以基于动物的实验测试来建模。因为从道德上讲,我们不能让人类暴露在污染物中,所以这是预测人类暴露的最佳方法。这些虚拟生物必须准确地代表真实形式,本提案旨在确保化学物质从外部暴露到内部或器官暴露的运动得到很好的代表。由于反应是基于器官的化学物质浓度,了解这一过程是必要的。这将有助于预测外部暴露与不同物种的器官暴露之间的关系。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Edginton, Andrea其他文献

Routine clinical care data for population pharmacokinetic modeling: the case for Fanhdi/Alphanate in hemophilia A patients
A Blended Learning Approach to Teaching Basic Pharmacokinetics and the Significance of Face-to-Face Interaction
Parameterization of small intestinal water volume using PBPK modeling
  • DOI:
    10.1016/j.ejps.2014.10.016
  • 发表时间:
    2015-01-25
  • 期刊:
  • 影响因子:
    4.6
  • 作者:
    Maharaj, Anil;Fotaki, Nikoletta;Edginton, Andrea
  • 通讯作者:
    Edginton, Andrea
A Mechanistic Bayesian Inferential Workflow for Estimation of In Vivo Skin Permeation from In Vitro Measurements
  • DOI:
    10.1016/j.xphs.2021.11.028
  • 发表时间:
    2022-03-04
  • 期刊:
  • 影响因子:
    3.8
  • 作者:
    Hamadeh, Abdullah;Troutman, John;Edginton, Andrea
  • 通讯作者:
    Edginton, Andrea
Effects of acepromazine or dexmedetomidine on fentanyl disposition in dogs during recovery from isoflurane anesthesia
  • DOI:
    10.1111/vaa.12271
  • 发表时间:
    2016-01-01
  • 期刊:
  • 影响因子:
    1.7
  • 作者:
    Keating, Stephanie;Kerr, Carolyn;Edginton, Andrea
  • 通讯作者:
    Edginton, Andrea

Edginton, Andrea的其他文献

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{{ truncateString('Edginton, Andrea', 18)}}的其他基金

PBTK modeling and simulation framework to identify critical data requirements for efficient and effective pediatric risk assessment
PBTK 建模和模拟框架,用于确定高效且有效的儿科风险评估的关键数据要求
  • 批准号:
    RGPIN-2017-05056
  • 财政年份:
    2021
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Discovery Grants Program - Individual
PBTK modeling and simulation framework to identify critical data requirements for efficient and effective pediatric risk assessment
PBTK 建模和模拟框架,用于确定高效且有效的儿科风险评估的关键数据要求
  • 批准号:
    RGPIN-2017-05056
  • 财政年份:
    2020
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Discovery Grants Program - Individual
PBTK modeling and simulation framework to identify critical data requirements for efficient and effective pediatric risk assessment
PBTK 建模和模拟框架,用于确定高效且有效的儿科风险评估的关键数据要求
  • 批准号:
    RGPIN-2017-05056
  • 财政年份:
    2019
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Discovery Grants Program - Individual
PBTK modeling and simulation framework to identify critical data requirements for efficient and effective pediatric risk assessment
PBTK 建模和模拟框架,用于确定高效且有效的儿科风险评估的关键数据要求
  • 批准号:
    RGPIN-2017-05056
  • 财政年份:
    2018
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Discovery Grants Program - Individual
PBTK modeling and simulation framework to identify critical data requirements for efficient and effective pediatric risk assessment
PBTK 建模和模拟框架,用于确定高效且有效的儿科风险评估的关键数据要求
  • 批准号:
    RGPIN-2017-05056
  • 财政年份:
    2017
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Discovery Grants Program - Individual
Development and validation of predictive permeability and partitioning models for organic contaminants within physiologically-based toxicokinetic models
基于生理的毒代动力学模型中有机污染物的预测渗透性和分配模型的开发和验证
  • 批准号:
    371792-2009
  • 财政年份:
    2015
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Discovery Grants Program - Individual
Development and validation of predictive permeability and partitioning models for organic contaminants within physiologically-based toxicokinetic models
基于生理的毒代动力学模型中有机污染物的预测渗透性和分配模型的开发和验证
  • 批准号:
    371792-2009
  • 财政年份:
    2011
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Discovery Grants Program - Individual
Development and validation of predictive permeability and partitioning models for organic contaminants within physiologically-based toxicokinetic models
基于生理的毒代动力学模型中有机污染物的预测渗透性和分配模型的开发和验证
  • 批准号:
    371792-2009
  • 财政年份:
    2010
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Discovery Grants Program - Individual
Development and validation of predictive permeability and partitioning models for organic contaminants within physiologically-based toxicokinetic models
基于生理的毒代动力学模型中有机污染物的预测渗透性和分配模型的开发和验证
  • 批准号:
    371792-2009
  • 财政年份:
    2009
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Discovery Grants Program - Individual
Correlating gene expression with biochemical responses in Xenopus tropicalis to chemicals that modulate thyroid hormone function
将基因表达与热带爪蟾对调节甲状腺激素功能的化学物质的生化反应相关联
  • 批准号:
    305050-2004
  • 财政年份:
    2005
  • 资助金额:
    $ 1.97万
  • 项目类别:
    Postdoctoral Fellowships

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  • 批准号:
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开发快速剂量测定系统,用于快速评估大规模放射事件受害者的急性辐射暴露、个体放射敏感性和损伤
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