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人眼角膜模型用于眼部刺激性测试:生产质量控制、可靠性和预测能力。

A human hemi-cornea model for eye irritation testing: quality control of production, reliability and predictive capacity.

机构信息

University of Bremen, FB2, Leobener Straße 2, 28359 Bremen, Germany.

出版信息

Toxicol In Vitro. 2013 Feb;27(1):458-68. doi: 10.1016/j.tiv.2012.07.011. Epub 2012 Aug 8.

Abstract

We have developed a 3-dimensional human hemi-cornea which comprises an immortalized epithelial cell line and keratocytes embedded in a collagen stroma. In the present study, we have used MTT reduction of the whole tissue to clarify whether the production of this complex 3-D-model is transferable into other laboratories and whether these tissues can be constructed reproducibly. Our results demonstrate the reproducible production of the hemi-cornea model according to standard operation procedures using 15 independent batches of reconstructed hemi-cornea models in two independent laboratories each. Furthermore, the hemi-cornea tissues have been treated with 20 chemicals of different eye-irritating potential under blind conditions to assess the performance and limitations of our test system comparing three different prediction models. The most suitable prediction model revealed an overall in vitro-in vivo concordance of 80% and 70% in the participating laboratories, respectively, and an inter-laboratory concordance of 80%. Sensitivity of the test was 77% and specificity was between 57% and 86% to discriminate classified from non-classified chemicals. We conclude that additional physiologically relevant endpoints in both epithelium and stroma have to be developed for the reliable prediction of all GHS classes of eye irritation in one stand alone test system.

摘要

我们已经开发出一种 3 维人类角膜模型,它由一个永生化的上皮细胞系和嵌入在胶原基质中的角膜细胞组成。在本研究中,我们使用整个组织的 MTT 还原来阐明这种复杂的 3-D 模型的产生是否可以转移到其他实验室,以及这些组织是否可以可重复地构建。我们的结果表明,根据标准操作程序,使用来自两个独立实验室的 15 个独立批次的重建角膜模型,可重复地生产角膜模型。此外,还对 20 种不同眼部刺激性潜力的化学物质对角膜组织进行了盲法处理,以评估我们的测试系统的性能和局限性,并比较了三种不同的预测模型。在参与的两个实验室中,最适合的预测模型的整体体外-体内一致性分别为 80%和 70%,实验室间的一致性为 80%。测试的敏感性为 77%,特异性为 57%-86%,可区分分类和非分类的化学物质。我们得出结论,需要在上皮组织和基质中开发更多与生理相关的终点,以便在一个独立的测试系统中可靠地预测所有 GHS 类别的眼部刺激性。

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