二氧化钛可能致癌性的生物测定。

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引用次数: 0

摘要

通过给Fischer 344大鼠和B6C3F1小鼠喂食饲料中的试验化学品,对二氧化钛可能的致癌性进行了生物测定。每组各50只雌雄大鼠和50只雌雄小鼠,以两种剂量(2.5万ppm或5万ppm)中的一种喂食二氧化钛103周,然后再观察1周。配对的对照组由各性别50只未治疗的大鼠和各性别50只未治疗的小鼠组成。所有存活的大鼠和小鼠在104周时被杀死。施用二氧化钛对大鼠或小鼠的平均体重没有明显的影响。除了白色粪便外,没有其他临床症状被认为与使用二氧化钛有关。大鼠和雄性小鼠在生物测定结束时的存活率不受试验化学品的影响;雌性小鼠的死亡率与剂量有关。有足够数量的剂量大鼠和对照小鼠,不论性别,都有发生晚期肿瘤的风险。雌性大鼠c细胞腺瘤或甲状腺癌的发生率与剂量相关(P=0.013),但未达到Bonferroni标准(对照1/48,低剂量0/47,高剂量6/44)要求的P=0.025水平(高剂量组与对照组直接比较P=0.043)。因此,这些甲状腺肿瘤不被认为与试验化学品的施用有关。在雄性和雌性小鼠中,剂量组未发生肿瘤,发生率显著高于相应的对照组。由此可见,在本实验条件下,口服方式的二氧化钛对Fischer 344大鼠和B6C3F1小鼠均无致癌性。
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Bioassay of titanium dioxide for possible carcinogenicity.

A bioassay of titanium dioxide for possible carcinogenicity was conducted by administering the test chemical in feed to Fischer 344 rats and B6C3F1 mice. Groups of 50 rats of each sex and 50 mice of each sex were administered titanium dioxide in the diet at one of two doses, either 25,000 or 50,000 ppm, for 103 weeks and then observed for 1 additional week. Matched controls consisted of 50 untreated rats of each sex and 50 untreated mice of each sex. All surviving rats and mice were killed at 104 weeks. Administration of the titanium dioxide had no appreciable effect on the mean body weights of rats or mice of either sex. With the exception of white feces, there was no other clinical sign that was judged to be related to the administration of titanium dioxide. Survival of the rats and the male mice at the end of the bioassay was not affected by the test chemical; mortality in female mice was dose related. Sufficient numbers of dosed and control rats and mice of each sex were at risk for development of late-appearing tumors. In the female rats, C-cell adenomas or carcinomas of the thyroids occurred at incidences that were dose related (P=0.013), but were not high enough (P=0.043 for direct comparison of the high-dose group with the control group) to meet the level of P=0.025 required by the Bonferroni criterion (controls 1/48, low-dose 0/47, high-dose 6/44). Thus, these tumors of the thyroid were not considered to be related to the administration of the test chemical. In male and female mice, no tumors occurred in dosed groups at incidences that were significantly higher than those for corresponding control groups. It is concluded that under the conditions of this bioassay, titanium dioxide was not carcinogenic by the oral route for Fischer 344 rats or B6C3F1 mice.

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