首页> 外文期刊>Toxicology Letters: An International Journal Providing a Forum for Original and Pertinent Contributions in Toxicology Research >The integration of data on physico-chemical properties, in vitro-derived toxicity data and physiologically based kinetic and dynamic as modelling a tool in hazard and risk assessment. A commentary.
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The integration of data on physico-chemical properties, in vitro-derived toxicity data and physiologically based kinetic and dynamic as modelling a tool in hazard and risk assessment. A commentary.

机译:物理化学特性数据,体外毒性数据以及基于生理学的动力学和动力学方面的数据集成,是危害和风险评估的建模工具。评论。

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摘要

Toxicity of a compound for an organism is dependent on the route of exposure, the amount (or concentration), the way in which the compound is taken up, distributes and is eliminated from the organism (ADME, kinetics) and the intrinsic properties (reactivity; mode of action, dynamics) of the compound towards the organism. These three elements: exposure, kinetics and dynamics form the basis of hazard and risk evaluations. Developments in our knowledge of the way in which physico-chemical properties of chemicals (on the one side) and physiological processes in the organism (on the other side) determine a compound's toxicity have greatly increased our understanding of toxicological processes and our ability to interpret experimental results. This has now resulted in the development of model systems in which the above-mentioned processes can be described mathematically. Biokinetic modelling is currently of great interest, but the further development of toxicodynamic modelling is equally important. The combination of both allows the estimation of a compound's critical amount/concentration on the critical site of action, which ideally would be the basis for hazard and risk assessments. In vitro systems have been extremely useful in studying the molecular basis of a chemical's biological activity, including its mechanism(s) of toxic action. Other achievements include the prediction of biological reactivity on the basis of a compound's physico-chemical properties and the construction of quantitative structure-activity relationships (QSARs). However, for the incorporation of in vitro-derived data as well as the results of QSARs, kinetic modelling is indispensable. Thus, biokinetic and toxicodynamic modelling are important (if not crucial) tools in toxicological research and there are increasing opportunities to incorporate the results of this work in hazard and risk assessments. Their implementation will allow a much more scientifically-based and a better structured risk assessment, which will be to a much lesser extent relying on animal experimentation.
机译:化合物对生物体的毒性取决于暴露途径,量(或浓度),化合物的吸收,分布和从生物体中消除的方式(ADME,动力学)以及内在特性(反应性)。化合物对生物体的作用方式,动力学)。这三个要素:暴露,动力学和动力学构成危害和风险评估的基础。我们对化学物质(一方面)和生物体的生理过程(另一方面)决定化合物毒性的方式的了解的发展极大地增进了我们对毒理学过程的理解和解释能力实验结果。现在,这导致了模型系统的开发,其中可以数学地描述上述过程。目前对生物动力学建模非常感兴趣,但是毒物动力学建模的进一步发展同样重要。两者的结合可以估算化合物在关键作用部位上的关键量/浓度,理想情况下,这将是进行危害和风险评估的基础。体外系统在研究化学物质生物学活性的分子基础(包括其毒性作用机理)方面非常有用。其他成就包括根据化合物的理化性质预测生物反应性和建立定量构效关系(QSAR)。但是,对于合并体外来源的数据以及QSAR的结果,动力学建模是必不可少的。因此,生物动力学和毒物动力学模型是毒理学研究中的重要工具(如果不是很关键的话),并且越来越多的机会将这项工作的结果纳入危害和风险评估。它们的实施将允许进行更加科学的评估和更好的结构化风险评估,而在较小程度上依赖于动物实验。

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