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计算毒理学:在环境化学物质中的应用

Computational toxicology: application in environmental chemicals.

作者信息

Tan Yu-Mei, Conolly Rory, Chang Daniel T, Tornero-Velez Rogelio, Goldsmith Michael R, Peterson Shane D, Dary Curtis C

机构信息

National Exposure Research Laboratory, US Environmental Protection Agency, Research Triangle Park, NC, USA.

出版信息

Methods Mol Biol. 2012;929:9-19. doi: 10.1007/978-1-62703-050-2_2.

Abstract

This chapter provides an overview of computational models that describe various aspects of the source-to-health effect continuum. Fate and transport models describe the release, transportation, and transformation of chemicals from sources of emission throughout the general environment. Exposure models integrate the microenvironmental concentrations with the amount of time an individual spends in these microenvironments to estimate the intensity, frequency, and duration of contact with environmental chemicals. Physiologically based pharmacokinetic (PBPK) models incorporate mechanistic biological information to predict chemical-specific absorption, distribution, metabolism, and excretion. Values of parameters in PBPK models can be measured in vitro, in vivo, or estimated using computational molecular modeling. Computational modeling is also used to predict the respiratory tract dosimetry of inhaled gases and particulates [computational fluid dynamics (CFD) models], to describe the normal and xenobiotic-perturbed behaviors of signaling pathways, and to analyze the growth kinetics of preneoplastic lesions and predict tumor incidence (clonal growth models).

摘要

本章概述了描述源到健康效应连续统一体各个方面的计算模型。归宿和迁移模型描述了化学物质从排放源在整个环境中的释放、运输和转化。暴露模型将微环境浓度与个体在这些微环境中花费的时间量相结合,以估计与环境化学物质接触的强度、频率和持续时间。基于生理的药代动力学(PBPK)模型纳入了机械生物学信息,以预测化学物质特异性的吸收、分布、代谢和排泄。PBPK模型中的参数值可以在体外、体内测量,或使用计算分子建模进行估计。计算建模还用于预测吸入气体和颗粒物的呼吸道剂量学[计算流体动力学(CFD)模型],描述信号通路的正常和外源性干扰行为,以及分析癌前病变的生长动力学并预测肿瘤发生率(克隆生长模型)。

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