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首页> 外文期刊>Alternatives to laboratory animals: ATLA >The bovine corneal opacity and permeability test in routine ocular irritation testing and its improvement within the limits of OECD test guideline 437.
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The bovine corneal opacity and permeability test in routine ocular irritation testing and its improvement within the limits of OECD test guideline 437.

机译:常规眼刺激性测试中的牛角膜混浊和通透性测试及其在OECD测试准则437范围内的改进。

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摘要

Data on eye irritation are generally needed for the hazard identification of chemicals. As the Bovine Corneal Opacity and Permeability (BCOP) test has been accepted by many regulatory agencies for the identification of corrosive and severe ocular irritants since September 2009 (OECD Test Guideline 437, TG 437), we evaluated this alternative method for routine testing at BASF. We demonstrated our technical proficiency by testing the reference standards recommended in TG 437, and 21 additional materials with published BCOP and in vivo data. Our results matched the published in vitro data very well, but with some intentionally selected false negatives (FNs) and false positives (FPs), the concordance was 77% (24/31), with FN and FP rates of 20% (2/10) and 24% (5/21), respectively. In addition, we tested 21 in-house materials, demonstrating the utility of the BCOP assay for our own test material panel. Histopathological assessment of the corneas by light microscopy was also conducted, as this was suggested as a means of improving the identification of FNs. The histopathology corrected the classification of some FNs, but also increased the number of FPs. Parallel to the test method evaluation, we compared three new opacitometer models with the current standard device. We recommend the use of an opacitometer developed in our BASF laboratory, which has certified components and electronic data storage, resulting in what we consider to be excellent sensitivity, stability and reproducibility.
机译:通常需要关于眼睛刺激性的数据来​​识别化学品。自2009年9月以来,牛角膜不透明性和渗透性(BCOP)测试已被许多监管机构接受,用于识别腐蚀性和严重的眼刺激物(经合组织测试准则437,TG 437),我们评估了巴斯夫这种常规测试的替代方法。我们通过测试TG 437中推荐的参考标准以及21种其他材料以及已发布的BCOP和体内数据证明了我们的技术水平。我们的结果与已公布的体外数据非常吻合,但在故意选择假阴性(FNs)和假阳性(FPs)的情况下,一致性为77%(24/31),FN和FP率为20%(2 / 10)和24%(5/21)。此外,我们测试了21种内部材料,证明了BCOP测定法在我们自己的测试材料面板中的实用性。还通过光学显微镜对角膜进行了组织病理学评估,因为这被认为是改善FN识别的一种手段。组织病理学校正了一些FN的分类,但也增加了FP的数量。在测试方法评估的同时,我们将三种新的不透明度计模型与当前的标准设备进行了比较。我们建议使用由巴斯夫实验室开发的不透明计,该不透明计具有经过认证的组件和电子数据存储,因此具有出色的灵敏度,稳定性和可重复性。

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