对苯二胺二盐酸盐可能致癌性的生物测定。

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引用次数: 0

摘要

采用Fischer 344大鼠和B6C3F1小鼠对盐酸对苯二胺进行致癌性生物测定。在饲料中以两种浓度中的任何一种给药,每组50只雄性和50只雌性动物。大鼠和小鼠的对苯二胺盐酸高、低浓度分别为1250和625 ppm。复方给药103周后,大鼠和小鼠的观察期分别为2周和1周。各性别、各物种各20只作为对照进行试验。在给药的对苯二胺浓度与大鼠或小鼠的死亡率之间没有显著的正相关关系。所有组中都有足够数量的动物存活了足够长的时间,从而有患晚期肿瘤的风险。在雌性大鼠中观察到轻微的剂量相关的平均体重下降,高剂量雄性大鼠和给药雌性小鼠的平均体重相对于它们各自的对照有轻微的下降,这表明在本生物测定中给药给这些动物的对苯二胺的浓度可能接近最大耐受浓度。由于与对照组相比,雄性小鼠没有明显的平均体重下降,没有明显的死亡率加速,也没有其他毒性迹象与给药对盐酸对苯二胺有关,因此这些动物可能能够耐受较高的饮食浓度。对大鼠或小鼠的任何部位进行的统计测试,包括对雌性小鼠进行白血病或恶性淋巴瘤分析的时间,都没有显示复方给药与肿瘤发病率之间存在显著的正相关。在本生物试验条件下,没有令人信服的证据表明膳食给药对盐酸对苯二胺对Fischer 344大鼠或B6C3F1小鼠具有致癌作用。
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Bioassay of p-phenylenediamine dihydrochloride for possible carcinogenicity.

A bioassay of p-phenylenediamine dihydrochloride for possible carcinogenicity was conducted using Fischer 344 rats and B6C3F1 mice. p-Phenylenediamine dihydrochloride was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species. The high and low concentrations of p-phenylenediamine dihydrochloride were, respectively, 1,250 and 625 ppm for both rats and mice. After a 103-week period of compound administration, there were additional observation periods of 2 weeks for rats and 1 week for mice. Twenty animals of each sex and species were placed on test as controls. There were no significant positive associations between the concentrations of p-phenylenediamine dihydrochloride administered and mortality in rats or mice of either sex. Adequate numbers of animals in all groups survived sufficiently long to be at risk from late developing tumors. Slight dose-related mean body weight depression was observed in female rats and the mean body weights among high dose male rats and dosed female mice were slightly depressed in relation to their respective controls, indicating that the concentrations of p-phenylenediamine dihydrochloride administered to these animals in this bioassay may have approximated the maximum tolerated concentrations. Since no distinct mean body weight depression relative to controls, no significant accelerated mortality, and no other signs of toxicity were associated with administration of p-phenylenediamine dihydrochloride to male mice, it is possible that these animals may have been able to tolerate a higher dietary concentration. None of the statistical tests for any site in rats or mice of either sex, including time to leukemia or malignant lymphoma analysis in female mice, indicated a significant positive association between compound administration and tumor incidence. Under the conditions of this bioassay, there was no convincing evidence that dietary administration of p-phenylenediamine dihydrochloride was carcinogenic in Fischer 344 rats or B6C3F1 mice.

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