邻苯二胺可能致癌性的生物测定。

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引用次数: 0

摘要

通过给F344大鼠和B6C3F1小鼠喂食饲料,对邻苯二胺可能的致癌性进行了生物测定。每组50只雌雄老鼠被注射两种剂量中的一种,雄性注射1.5万或3万ppm,雌性注射5000或1万ppm,持续106周。每组50只雌雄老鼠分别以两种剂量中的一种(雄性为25000 ppm或50000 ppm)和三种剂量中的一种(雌性为6200 ppm、12500 ppm或25000 ppm)进行103或105周的试验。配对的对照包括各20只未经治疗的大鼠、20只未经治疗的雄鼠和两组各20只未经治疗的雌鼠。所有幸存的大鼠和小鼠在给药结束时被杀死。给药组的大鼠和小鼠的平均体重要么略低于相应的对照组,要么基本上不受给药的影响。此外,除了高剂量组和中剂量组雌性小鼠的早期死亡外,大鼠和小鼠的存活率没有受到影响。除雌鼠高剂量组(36%)外,所有给药组和各物种、性别的对照组在生物测定结束时的存活率为66%或更高。除了高剂量的雌性小鼠外,所有组中都有足够数量的动物处于晚期肿瘤发展的风险中。在大鼠或小鼠中,无论雌雄,均未发生肿瘤,但剂量组的发生率明显高于相应的对照组。然而,邻苯二胺在雄性和雌性大鼠的肝脏以及雌性大鼠和小鼠的泌尿系统中产生毒性病变。非肿瘤性病变提示MTD可能已经使用或超过。在本实验条件下,邻苯二胺对F344大鼠和B6C3F1小鼠均无致癌性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioassay of phthalamide for possible carcinogenicity.

A bioassay of phthalamide for possible carcinogenicity was conducted by administering the test chemical in feed to F344 rats and B6C3F1 mice. Groups of 50 rats of each sex were administered phthalamide at one of two doses, either 15,000 or 30,000 ppm for the males and either 5,000 or 10,000 ppm for the females, for 106 weeks. Groups of 50 mice of each sex were administered the test chemical at one of two doses, 25,000 or 50,000 ppm for the males, and at one of three doses, 6,200, 12,500, or 25,000 ppm, for the females, for 103 or 105 weeks. Matched controls consisted of 20 untreated rats of each sex, 20 untreated male mice, and two groups of 20 untreated female mice. All surviving rats and mice were killed at the end of administration of the test chemical. Mean body weights of the dosed groups of rats and mice were either slightly lower than those of corresponding control groups or essentially unaffected by administration of the test chemical. Also, survival was unaffected in the rats and mice except for early deaths in the high- and mid-dose groups of female mice. Survival was 66% or greater at the end of the bioassay in all dosed groups and control groups of each species and sex except for the high-dose group of female mice (36%). With the exception of the high-dose female mice, sufficient numbers of animals were at risk in all groups for the development of late-appearing tumors. No tumors occurred in the rats or mice of either sex at incidences that were significantly higher in the dosed groups than in the corresponding control groups. However, phthalamide produced toxic lesions in the livers of male and female rats and the urinary systems of female rats and mice. The presence of nonneoplastic lesions suggests that the MTD may have been used or exceeded. It is concluded that under the conditions of this bioassay, phthalamide was not carcinogenic for F344 rats or B6C3F1 mice of either sex.

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