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跨部门审查急性系统毒性测试的驱动因素和可用 3R 方法。

Cross-sector review of drivers and available 3Rs approaches for acute systemic toxicity testing.

机构信息

Research & Toxicology Department, Humane Society International, B-1030 Brussels, Belgium.

出版信息

Toxicol Sci. 2010 Aug;116(2):382-96. doi: 10.1093/toxsci/kfq143. Epub 2010 May 19.

Abstract

Acute systemic toxicity studies are carried out in many sectors in which synthetic chemicals are manufactured or used and are among the most criticized of all toxicology tests on both scientific and ethical grounds. A review of the drivers for acute toxicity testing within the pharmaceutical industry led to a paradigm shift whereby in vivo acute toxicity data are no longer routinely required in advance of human clinical trials. Based on this experience, the following review was undertaken to identify (1) regulatory and scientific drivers for acute toxicity testing in other industrial sectors, (2) activities aimed at replacing, reducing, or refining the use of animals, and (3) recommendations for future work in this area.

摘要

急性全身毒性研究在许多制造或使用合成化学品的领域进行,这些研究在科学和伦理方面都受到了最严厉的批评。对制药行业中急性毒性测试的驱动因素进行了审查,导致了一种范式转变,即在进行人体临床试验之前,不再常规要求体内急性毒性数据。基于这一经验,进行了以下审查,以确定:(1) 其他工业领域急性毒性测试的监管和科学驱动因素;(2) 旨在替代、减少或改进动物使用的活动;(3) 对该领域未来工作的建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a19/2905404/b1d54823110f/toxscikfq143f01_ht.jpg

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