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Wind of change challenges toxicological regulators

机译:变化之风挑战毒理学监管机构

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Background: In biomedical research, the past two decades have seen the advent of in vitro model systems based on stem cells, humanized cell lines, and engineered organotypic tissues, as well as numerous cellular assays based on primarily established tumor-derived cell lines and their genetically modified derivatives. Objective: There are high hopes that these systems might replace the need for animal testing in regulatory toxicology. However, despite increasing pressure in recent years to reduce animal testing, regulators are still reluctant to adopt in vitro approaches on a large scale. It thus seems appropriate to consider how we could realistically perform regulatory toxicity testing using in vitro assays only. D iscussion and Conclusion: Here, we suggest an in vitro-only approach for regulatory testing that will benefit consumers, industry, and regulators alike.
机译:背景:在生物医学研究中,过去二十年来,已经出现了基于干细胞,人源化细胞系和工程有机型组织的体外模型系统,以及基于主要建立的肿瘤来源的细胞系及其细胞的众多细胞测定法转基因衍生物。目的:人们寄希望于这些系统可以取代监管毒理学中对动物测试的需求。然而,尽管近年来减少动物测试的压力越来越大,但监管机构仍不愿大规模采用体外方法。因此,似乎有必要考虑我们如何仅使用体外测定法就能切实地进行调节毒性试验。讨论和结论:在这里,我们建议一种仅用于体外的法规测试方法,这将使消费者,行业和监管者都受益。

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