Corvaro M, Gehen S, Andrews K, Chatfield R, Macleod F, Mehta J
Dow AgroSciences Ltd - European Development Centre, Milton Park, Abingdon, OX14 4RN, UK.
Dow AgroSciences LLC - Headquarters, 9330 Zionsville Road, Indianapolis, IN 46268, USA.
Regul Toxicol Pharmacol. 2017 Oct;89:131-147. doi: 10.1016/j.yrtph.2017.06.014. Epub 2017 Jun 28.
Analysis of the prevalence of health effects in large scale databases is key in defining testing strategies within the context of Integrated Approaches on Testing and Assessment (IATA), and is relevant to drive policy changes in existing regulatory toxicology frameworks towards non-animal approaches. A retrospective analysis of existing results from in vivo skin irritation, eye irritation, and skin sensitisation studies on a database of 223 agrochemical formulations is herein published. For skin or eye effects, high prevalence of mild to non-irritant formulations (i.e. per GHS, CLP or EPA classification) would generally suggest a bottom-up approach. Severity of erythema or corneal opacity, for skinor eye effects respectively, were the key drivers for classification, consistent with existing literature. The reciprocal predictivity of skin versus eye irritation and the good negative predictivity of the GHS additivity calculation approach (>85%) provided valuable non-testing evidence for irritation endpoints. For dermal sensitisation, concordance on data from three different methods confirmed the high false negative rate for the Buehler method in this product class. These results have been reviewed together with existing literature on the use of in vitro alternatives for agrochemical formulations, to propose improvements to current regulatory strategies and to identify further research needs.
在大规模数据库中分析健康影响的患病率是在测试与评估综合方法(IATA)背景下定义测试策略的关键,并且对于推动现有监管毒理学框架朝着非动物方法的政策变化具有重要意义。本文发表了对223种农用化学品制剂数据库中现有体内皮肤刺激性、眼睛刺激性和皮肤致敏性研究结果的回顾性分析。对于皮肤或眼睛影响,轻度至无刺激性制剂的高患病率(即根据全球统一制度、化学品分类和标签协调制度或美国环境保护局分类)通常表明应采用自下而上的方法。皮肤红斑或眼睛角膜混浊的严重程度分别是皮肤或眼睛影响分类的关键驱动因素,这与现有文献一致。皮肤与眼睛刺激性的相互预测性以及全球统一制度相加性计算方法的良好阴性预测性(>85%)为刺激性终点提供了有价值的非测试证据。对于皮肤致敏性,三种不同方法的数据一致性证实了该产品类别中Buehler方法的高假阴性率。这些结果与关于农用化学品制剂体外替代方法使用的现有文献一起进行了审查,以提出对当前监管策略的改进建议并确定进一步的研究需求。