OECD 402/OCSPP 870.1200: Acute dermal toxicity
Acute
当在最大24小时内以一个或多个剂量施用时,通过活性成分产生急性毒性。该测试使用两种哺乳动物,包括一个不探测。
The objective is to identify doses causing no adverse effect and doses causing major, life-threatening toxicity.
Information obtained from single-dose studies is useful in choosing doses for repeat-dose studies, providing preliminary identification of target organs of toxicity.
急性毒性研究也可以帮助选择I阶段人类研究的起始剂量,并提供与人类急性过量的信息。