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Systematic evaluation of non-animal test methods for skin sensitisation safety assessment.

机译:用于皮肤致敏安全性评估的非动物试验方法的系统评价。

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摘要

The need for non-animal data to assess skin sensitisation properties of substances, especially cosmetics ingredients, has spawned the development of many in vitro methods. As it is widely believed that no single method can provide a solution, the Cosmetics Europe Skin Tolerance Task Force has defined a three-phase framework for the development of a non-animal testing strategy for skin sensitisation potency prediction. The results of the first phase - systematic evaluation of 16 test methods - are presented here. This evaluation involved generation of data on a common set of ten substances in all methods and systematic collation of information including the level of standardisation, existing test data, potential for throughput, transferability and accessibility in cooperation with the test method developers. A workshop was held with the test method developers to review the outcome of this evaluation and to discuss the results. The evaluation informed the prioritisation of test methods for the next phase of the non-animal testing strategy development framework. Ultimately, the testing strategy - combined with bioavailability and skin metabolism data and exposure consideration - is envisaged to allow establishment of a data integration approach for skin sensitisation safety assessment of cosmetic ingredients.
机译:需要非动物数据来评估物质(尤其是化妆品成分)的皮肤致敏特性,催生了许多体外方法的发展。人们普遍认为,没有任何一种方法可以提供解决方案,欧洲化妆品欧洲皮肤耐受性工作组已经定义了一个三阶段框架,用于开发用于皮肤敏化效力预测的非动物测试策略。第一阶段的结果-16种测试方法的系统评估-此处介绍。这项评估涉及在所有方法中生成关于一组十种物质的通用数据,并与测试方法开发人员合作,系统地整理信息,包括标准化程度,现有测试数据,通量潜力,可转让性和可及性。与测试方法开发人员举行了研讨会,以审查此评估的结果并讨论结果。评估为非动物测试策略开发框架的下一阶段确定了测试方法的优先级。最终,设想将测试策略与生物利用度和皮肤代谢数据以及暴露考虑因素相结合,以建立用于化妆品成分皮肤致敏安全性评估的数据集成方法。

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