亚慢性吸入毒性:90天研究(OECD TG 413)

Subchronic
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引用次数: 8

摘要

902. 该试验确定了化学品的亚慢性吸入毒性,为定量吸入危害识别/表征提供了可靠的数据。它主要用于获得监管浓度,以评估职业环境中的工人风险。它也被用于评估人类居住、交通和环境风险。给药时间为90天,首选品种为大鼠。动物在吸入室中暴露于试验物质,每周5天,每天6小时。首选的暴露方式是只暴露鼻子,但也可以使用全身暴露。OECD TG 413于1981年5月首次通过,并于2009年9月修订。虽然它尚未被证实用于检测内分泌活性物质(EASs),但该分析包含几个适合测定内分泌影响的终点。由于所有的终点都是顶点,因此仅凭这一试验很难辨别作用机制。关于作用机制的信息可能需要从体外雌激素/雄激素/甲状腺/甾体生成(E,A,T,S)试验或体内较低级别的试验中获得,如子宫营养生物测定(UT - OECD TG 440)和Hershberger生物测定(H - OECD TG 441)。激素测量不包括在这个分析中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subchronic Inhalation Toxicity: 90-Day Study (OECD TG 413)
902. This assay determines the subchronic inhalation toxicity of chemicals to provide robust data for quantitative inhalational hazard identification/characterisation. It is primarily used to derive regulatory concentrations for assessing worker risk in occupation settings. It is also used to assess human residential, transportation and environmental risk. Dosing duration is 90 days and the preferred species is the rat. Animals are exposed to test substance in inhalation chambers for six hours per day on a five day per week basis. The preferred mode of exposure is nose only, but whole body exposure may also be used. OECD TG 413 was first adopted in May 1981 and revised in September 2009. Although it has not been validated for the detection of endocrine active substances (EASs), this assay contains several endpoints that are suitable for the determination of endocrine effects. As all the endpoints are apical, it is difficult to discern mechanism of action from this test alone. Information on mechanism of action may need to be obtained from in vitro estrogen/androgen/thyroid/steroidogenesis (E,A,T,S) assays or in vivo lower tier tests such as the Uterotrophic Bioassay (UT – OECD TG 440) and the Hershberger Bioassay (H – OECD TG 441). Hormone measurements are not included in this assay.
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