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Recommendations to address uncertainties in environmental risk assessment using toxicokinetic-toxicodynamic models

机译:建议使用毒物动力学模型解决环境风险评估中不确定性的建议

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Providing reliable environmental quality standards (EQSs) is a challenging issue in environmental risk assessment (ERA). These EQSs are derived from toxicity endpoints estimated from dose-response models to identify and characterize the environmental hazard of chemical compounds released by human activities. These toxicity endpoints include the classical x% effect/lethal concentrations at a specific time t (EC/LC(x, t)) and the new multiplication factors applied to environmental exposure profiles leading to x% effect reduction at a specific time t (MF(x, t), or denoted LP(x, t) by the EFSA). However, classical dose-response models used to estimate toxicity endpoints have some weaknesses, such as their dependency on observation time points, which are likely to differ between species (e.g., experiment duration). Furthermore, real-world exposure profiles are rarely constant over time, which makes the use of classical dose-response models difficult and may prevent the derivation of MF(x, t). When dealing with survival or immobility toxicity test data, these issues can be overcome with the use of the general unified threshold model of survival (GUTS), a toxicokinetic-toxicodynamic (TKTD) model that provides an explicit framework to analyse both time- and concentration-dependent data sets as well as obtain a mechanistic derivation of EC/LC(x, t) and MF(x, t) regardless of x and at any time t of interest. In ERA, the assessment of a risk is inherently built upon probability distributions, such that the next critical step is to characterize the uncertainties of toxicity endpoints and, consequently, those of EQSs. With this perspective, we investigated the use of a Bayesian framework to obtain the uncertainties from the calibration process and to propagate them to model predictions, including LC(x, t) and MF(x, t) derivations. We also explored the mathematical properties of LC(x, t) and MF(x, t) as well as the impact of different experimental designs to provide some recommendations for a robust derivation of toxicity endpoints leading to reliable EQSs: avoid computing LC(x, t) and MF(x, t) for extreme x values (0 or 100%), where uncertainty is maximal; compute MF(x, t) after a long period of time to take depuration time into account and test survival under pulses with different periods of time between them.
机译:提供可靠的环境质量标准(EQSS)是环境风险评估(时代)的具有挑战性的问题。这些EQSS来自来自剂量 - 响应模型估计的毒性终点,以识别和表征人类活动释放的化学化合物的环境危害。这些毒性终点包括特定时间T(EC / LC(X,T)的典型X%效应/致死浓度,并且应用于环境曝光谱的新乘法因子导致特定时间T(MF的X%效应降低)(MF (x,t),或由EFSA表示的LP(x,t))。然而,用于估计毒性终点的经典剂量 - 响应模型具有一些弱点,例如它们对观察时间点的依赖性,这可能在物种(例如,实验持续时间)之间不同。此外,随着时间的推移,现实世界的曝光轮廓很少是恒定的,这使得使用经典剂量 - 响应模型困难,并且可以防止MF(X,T)的推导。在处理生存或不动毒性测试数据时,可以克服使用常规统一的存活阈值模型(肠道),一种毒族毒动力学(TKTD)模型来克服这些问题,该模型提供明确框架来分析时间和浓度 - 依赖数据集以及获得EC / LC(X,T)和MF(X,T)的机械推导,而不管x和在任何时间t的情况下。在时代,对风险的评估本质上是在概率分布时构建的,使得下一个关键步骤是表征毒性终点的不确定性,因此,方程式的不确定性。通过这种观点,我们调查了贝叶斯框架的使用来获得来自校准过程的不确定性,并将它们传播到模型预测,包括LC(x,t)和MF(x,t)衍生。我们还探索了LC(X,T)和MF(X,T)的数学特性以及不同实验设计的影响,为导致可靠的EQSS的毒性端点的强大推导提供一些建议:避免计算LC(x ,t)和mf(x,t)用于极端x值(0或100%),其中不确定性是最大的;在很长一段时间后计算MF(X,T),以考虑剩余时间并在脉冲下测试生存,在它们之间具有不同的时间段。

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