Evaluation of in silico model predictions for mammalian acute oral toxicity and regulatory application in pesticide hazard and risk assessment

IF 3 4区 医学 Q1 MEDICINE, LEGAL
Patricia L. Bishop , Kamel Mansouri , William P. Eckel , Michael B. Lowit , David Allen , Amy Blankinship , Anna B. Lowit , D. Ethan Harwood , Tamara Johnson , Nicole C. Kleinstreuer
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引用次数: 0

Abstract

The United States Environmental Protection Agency (USEPA) uses the lethal dose 50% (LD50) value from in vivo rat acute oral toxicity studies for pesticide product label precautionary statements and environmental risk assessment (RA). The Collaborative Acute Toxicity Modeling Suite (CATMoS) is a quantitative structure-activity relationship (QSAR)-based in silico approach to predict rat acute oral toxicity that has the potential to reduce animal use when registering a new pesticide technical grade active ingredient (TGAI). This analysis compared LD50 values predicted by CATMoS to empirical values from in vivo studies for the TGAIs of 177 conventional pesticides. The accuracy and reliability of the model predictions were assessed relative to the empirical data in terms of USEPA acute oral toxicity categories and discrete LD50 values for each chemical. CATMoS was most reliable at placing pesticide TGAIs in acute toxicity categories III (>500–5000 mg/kg) and IV (>5000 mg/kg), with 88% categorical concordance for 165 chemicals with empirical in vivo LD50 values ≥ 500 mg/kg. When considering an LD50 for RA, CATMoS predictions of 2000 mg/kg and higher were found to agree with empirical values from limit tests (i.e., single, high-dose tests) or definitive results over 2000 mg/kg with few exceptions.

评估哺乳动物急性口服毒性的硅学模型预测以及在农药危害和风险评估中的监管应用
美国环境保护局 (USEPA) 在农药产品标签防范说明和环境风险评估 (RA) 中使用体内大鼠急性经口毒性研究得出的致死剂量 50% (LD50) 值。急性毒性合作建模套件 (CATMoS) 是一种基于定量结构-活性关系 (QSAR) 的硅学方法,用于预测大鼠急性经口毒性,有可能在登记新农药技术级活性成分 (TGAI) 时减少动物用量。这项分析比较了 CATMoS 预测的 LD50 值和 177 种常规农药技术级活性成分的体内研究经验值。根据 USEPA 急性经口毒性类别和每种化学品的离散 LD50 值,评估了模型预测与经验数据相比的准确性和可靠性。CATMoS 在将农药 TGAI 列入急性毒性类别 III(500-5000 毫克/千克)和 IV(5000 毫克/千克)方面最为可靠,对于体内 LD50 经验值≥ 500 毫克/千克的 165 种化学品,分类一致性达到 88%。在考虑 RA 的半数致死剂量时,CATMoS 预测的 2000 mg/kg 或更高值与极限试验(即单次高剂量试验)的经验值或超过 2000 mg/kg 的确定结果一致,只有少数例外。
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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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