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The dermal acute toxic class method: test procedures and biometric evaluations.

机译:皮肤急性毒性分类方法:测试程序和生物测定评估。

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摘要

A dermal acute toxic class (ATC) method is presented with the use of significantly fewer animals in comparison with the classical dermal 50% lethal dose (LD50) test. The principle of the dermal ATC method is based on the oral and the inhalation ATC method. The method was developed for three fixed starting doses. Depending on the dermal LD50, the slope, the classification system and the starting dose on average 40 to 90% fewer animals will be used in comparison to at least 30 animals with the dermal LD50 test. The method was biometrically evaluated by using the Probit model for dose-response relationships. At present, there are eight different international classification systems based on dermal LD50 values. The test procedures and the calculations of the classification probabilities demonstrate that the dermal ATC method is a reliable alternative to the dermal LD50 test with the use of significantly fewer animals. Classification probabilities are presented for all classification systems currently in use, and expected numbers of experimental and of moribund/dead animals are demonstrated for the system of chemicals in the European Union for all three starting doses. The conclusion is justified that, similarly to the inhalation ATC method, there is no need to validate the dermal ATC method with the use of experimental animals.
机译:与经典的50%皮肤致死剂量(LD50)试验相比,皮肤急性毒性等级(ATC)方法的使用明显减少。皮肤ATC方法的原理是基于口服和吸入ATC方法。该方法开发了三个固定的起始剂量。与使用皮肤LD50测试的至少30只动物相比,根据皮肤LD50的不同,斜率,分类系统和起始剂量平均减少40%至90%。通过使用Probit模型进行剂量-响应关系生物评估该方法。目前,基于皮肤的LD50值有八种不同的国际分类系统。测试程序和分类概率的计算表明,真皮ATC方法是真皮LD50测试的可靠替代方法,使用的动物少得多。列出了当前使用的所有分类系统的分类概率,并针对欧盟所有三种起始剂量的化学品系统,证明了实验动物和濒死/死动物的预期数量。结论是合理的,与吸入式ATC方法类似,无需使用实验动物来验证皮肤ATC方法。

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