VITO NV (Flemish Institute for Technological Research), Mol, Belgium.
L'Oréal Research & Innovation, Aulnay-sous-Bois, France.
Toxicol In Vitro. 2018 Jun;49:11-20. doi: 10.1016/j.tiv.2017.06.012. Epub 2017 Jun 15.
Assessment of ocular irritancy is an international regulatory requirement and a necessary step in the safety evaluation of industrial and consumer products. Although a number of in vitro ocular irritation assays exist, none are capable of fully categorizing chemicals as a stand-alone assay. Therefore, the CEFIC-LRI-AIMT6-VITO CON4EI (CONsortium for in vitro Eye Irritation testing strategy) project was developed with the goal of assessing the reliability of eight in vitro/alternative test methods as well as establishing an optimal tiered-testing strategy. One of the in vitro assays selected was the validated SkinEthic™ Human Corneal Epithelium Eye Irritation Test method (SkinEthic™ HCE EIT). The SkinEthic™ HCE EIT has already demonstrated its capacity to correctly identify chemicals (both substances and mixtures) not requiring classification and labelling for eye irritation or serious eye damage (No Category). The goal of this study was to evaluate the performance of the SkinEthic™ HCE EIT test method in terms of the important in vivo drivers of classification. For the performance with respect to the drivers all in vivo Cat 1 and No Cat chemicals were 100% correctly identified. For Cat 2 chemicals the liquids and the solids had a sensitivity of 100% and 85.7%, respectively. For the SkinEthic™ HCE EIT test method, 100% concordance in predictions (No Cat versus No prediction can be made) between the two participating laboratories was obtained. The accuracy of the SkinEthic™ HCE EIT was 97.5% with 100% sensitivity and 96.9% specificity. The SkinEthic™ HCE EIT confirms its excellent results of the validation studies.
眼刺激性评估是国际监管要求,也是工业和消费品安全评估的必要步骤。尽管存在许多体外眼刺激性检测方法,但没有一种方法能够单独对化学品进行充分分类。因此,CEFIC-LRI-AIMT6-VITO CON4EI(体外眼刺激性测试策略联合会)项目旨在评估八种体外/替代测试方法的可靠性,并建立最佳的分层测试策略。选定的体外检测方法之一是经过验证的 SkinEthic™ 人角膜上皮眼刺激性检测方法(SkinEthic™ HCE EIT)。SkinEthic™ HCE EIT 已经证明其能够正确识别不需要分类和标签的化学品(包括物质和混合物),这些化学品不会引起眼刺激或严重眼损伤(无类别)。本研究的目的是评估 SkinEthic™ HCE EIT 检测方法在分类的重要体内驱动因素方面的性能。对于与驱动因素相关的性能,所有体内 Cat 1 和无 Cat 化学品均被 100%正确识别。对于 Cat 2 化学品,液体和固体的灵敏度分别为 100%和 85.7%。对于 SkinEthic™ HCE EIT 检测方法,两个参与实验室之间的预测(无 Cat 与无预测)之间获得了 100%的一致性。SkinEthic™ HCE EIT 的准确性为 97.5%,具有 100%的敏感性和 96.9%的特异性。SkinEthic™ HCE EIT 证实了其验证研究的优异结果。