苯胺的可能致癌性生物测定(CAS No. 101-05-3)。

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摘要

通过给Fischer 344大鼠和B6C3F1小鼠喂食饲料,对苯胺嗪进行了可能致癌性的生物测定。每组各50只大鼠和50只小鼠,按两种剂量(500或1,000 ppm)中的一种给药103周,然后再观察1-6周。配对的对照组由25只未治疗的大鼠和25只未治疗的小鼠组成。103 ~ 104周处死存活大鼠;在107-109周时杀死所有存活小鼠。给药苯胺嗪对大鼠和雌鼠的体重没有明显影响;然而,给药的雄性小鼠的平均体重增加有所减少。生存率也基本未受影响。在90周研究结束时,除雄性对照组小鼠外,所有给药组和对照组大鼠和小鼠的存活率至少为80%;因此,在大多数组中,有足够数量的动物处于发展为晚期肿瘤的风险中。在给药的大鼠或雌雄小鼠中均未发生肿瘤,其发生率明显高于相应的对照组。雄性、雌性大鼠和雌性小鼠可能能够承受更高的剂量。结果表明,在本实验条件下,苯胺嗪对Fischer 344大鼠和B6C3F1小鼠均无致癌性。
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Bioassay of anilazine for possible carcinogenicity (CAS No. 101-05-3).

A bioassay of anilazine for possible carcinogenicity was conducted by administering the test chemical in feed to Fischer 344 rats and B6C3F1 mice. Groups of 50 rats and 50 mice of each sex were administered anilazine at one of two doses, either 500 or 1,000 ppm, for 103 weeks and then observed for 1-6 additional weeks. Matched controls consisted of 25 untreated rats and 25 untreated mice of each sex. All surviving rats were killed at 103-104 weeks; all surviving mice were killed at 107-109 weeks. Administration of the anilazine had no appreciable effect on body weight in the rats and female mice; however, there was a decreased gain in mean body weight in the dosed male mice. Survival also was essentially unaffected. Survival in all groups of dosed and control rats and mice was at least 80% at the end of 90 weeks on study, except for the male control mice; thus, sufficient numbers of animals were at risk in most groups for development of late-appearing tumors. No tumors occurred in dosed rats or mice of either sex at incidences that were significantly higher than those in corresponding controls. Male and female rats and female mice may have been able to tolerate higher doses. It is concluded that under the conditions of this bioassay, anilazine was not carcinogenic for either Fischer 344 rats or B6C3F1 mice.

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