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如何在不进行动物试验的情况下评估化妆品的致突变潜力?

How to assess the mutagenic potential of cosmetic products without animal tests?

机构信息

Universität Ulm, Institut für Humangenetik, Oberer Eselsberg M25, D-89069 Ulm, Germany.

出版信息

Mutat Res. 2009 Aug;678(2):108-12. doi: 10.1016/j.mrgentox.2009.04.006. Epub 2009 Apr 18.

Abstract

Animal experiments (in vivo tests) currently play a key role in genotoxicity testing. Results from in vivo tests are, in many cases, decisive for the assessment of a mutagenic potential of a test compound. The Seventh Amendment to the European Cosmetics Directive will, however, ban the European marketing of cosmetic/personal care products that contain ingredients that have been tested in animal experiments. If genotoxicity testing is solely based on the currently established in vitro tests, the attrition rate for chemicals used in cosmetic products will greatly increase due to irrelevant positive in vitro test results. There is urgent need for new and/or improved in vitro genotoxicity tests and for modified test strategies. Test strategies should consider all available information on chemistry of the test substance/the chemical class (e.g. SAR, metabolic activation and dermal adsorption). Test protocols for in vitro genotoxicity tests should be sensitive and robust enough to ensure that negative results can be accepted with confidence. It should be excluded that positive in vitro test results are due to high cytotoxicity or secondary genotoxic effects which may be thresholded and/or only occur under in vitro test conditions. Consequently, further research is needed to establish the nature of thresholds in in vitro assays and to determine the potential for incorporation of mode of action data into future risk assessments. New/improved tests have to be established and validated, considering the use of (metabolically competent) primary (skin) cells, 3D skin models and cells with defined capacity for metabolic activation (e.g. genetically engineered cell lines). The sensitivity and specificity of new and improved genotoxicity tests has to be determined by testing a battery of genotoxic and non-genotoxic chemicals. New or adapted international guidelines will be needed for these tests. The establishment of such a new genotoxicity testing strategy will take time and the new in vitro genotoxicity testing will become much more complex and will require greater mechanistic understanding to build a weight of evidence decision, which will be demanding and time-consuming. At present, no validated alternative methods for the follow-up of positive results from the standard genotoxicity battery are available and an appropriate evaluation of the mutagenic potential of cosmetic ingredients without animal experiments is therefore not possible in many cases.

摘要

动物实验(体内测试)目前在遗传毒性测试中起着关键作用。在许多情况下,体内测试的结果对于评估测试化合物的致突变潜力具有决定性作用。然而,《欧洲化妆品指令》第七修正案将禁止在欧洲市场销售含有已在动物实验中测试过的成分的化妆品/个人护理产品。如果遗传毒性测试仅基于当前建立的体外测试,由于无关的体外阳性测试结果,用于化妆品产品的化学品的淘汰率将会大大增加。迫切需要新的和/或改进的体外遗传毒性测试以及修改后的测试策略。测试策略应考虑测试物质/化学物质类别(例如 SAR、代谢激活和皮肤吸收)的所有可用化学信息。体外遗传毒性测试的测试方案应足够灵敏和稳健,以确保可以有信心地接受阴性结果。应排除阳性体外测试结果是由于高细胞毒性或可能是阈值化的二次遗传毒性效应引起的,这些效应可能仅在体外测试条件下发生。因此,需要进一步研究以确定体外测定中阈值的性质,并确定将作用模式数据纳入未来风险评估的潜力。需要建立和验证新的/改进的测试,同时考虑使用(代谢能力强)原代(皮肤)细胞、3D 皮肤模型和具有定义代谢激活能力的细胞(例如基因工程细胞系)。需要通过测试一系列遗传毒性和非遗传毒性化学品来确定新的和改进的遗传毒性测试的敏感性和特异性。这些测试将需要新的或改编的国际准则。建立这样一个新的遗传毒性测试策略需要时间,新的体外遗传毒性测试将变得更加复杂,并且需要更多的机制理解来建立证据权重决策,这将是具有挑战性和耗时的。目前,没有经过验证的替代方法可用于跟踪标准遗传毒性电池的阳性结果,因此在许多情况下,无法在没有动物实验的情况下对化妆品成分的致突变潜力进行适当评估。

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