MatTek In Vitro Life Science Laboratories, Bratislava, Slovakia.
MatTek In Vitro Life Science Laboratories, Bratislava, Slovakia.
Toxicol In Vitro. 2018 Jun;49:21-33. doi: 10.1016/j.tiv.2017.07.002. Epub 2017 Jul 8.
Assessment of the acute eye irritation potential is part of the international regulatory requirements for testing of chemicals. The objective of the CON4EI project was to develop tiered testing strategies for eye irritation assessment. A set of 80 reference chemicals (38 liquids and 42 solids) was tested with eight different methods. Here, the results obtained with the EpiOcular™ Eye Irritation Test (EIT), adopted as OECD TG 492, are shown. The primary aim of this study was to evaluate of the performance of the test method to discriminate between chemicals not requiring classification for serious eye damage/eye irritancy (No Category) and chemicals requiring classification and labelling. In addition, the predictive capacity in terms of in vivo drivers of classification (i.e. corneal opacity, conjunctival redness and persistence at day 21) was investigated. EpiOcular™ EIT achieved a sensitivity of 97%, a specificity of 87% and accuracy of 95% and also confirmed its excellent reproducibility (100%) from the original validation. The assay was applicable to all chemical categories tested in this project and its performance was not limited to the particular driver of the classification. In addition to the existing prediction model for dichotomous categorization, a new prediction model for Cat 1 is suggested.
急性眼刺激潜能评估是化学品测试国际监管要求的一部分。CON4EI 项目的目的是开发分级测试策略以评估眼刺激。用八种不同方法测试了一组 80 种参考化学品(38 种液体和 42 种固体)。这里显示了采用 OECD TG 492 的 EpiOcular™ 眼刺激测试(EIT)获得的结果。本研究的主要目的是评估该测试方法区分不需要严重眼损伤/眼刺激性分类(无类别)和需要分类和标签的化学品的性能。此外,还研究了分类的体内驱动因素(即角膜混浊、结膜充血和第 21 天的持续时间)的预测能力。EpiOcular™ EIT 的灵敏度为 97%,特异性为 87%,准确性为 95%,并且还证实了其出色的重现性(100%),这是从最初的验证中得出的。该测定法适用于本项目中测试的所有化学类别,并且其性能不受分类的特定驱动因素限制。除了现有的二项分类预测模型外,还建议了一种用于 Cat 1 的新预测模型。