涕灭威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,对涕灭威可能的致癌性进行了生物测定。每组各50只大鼠和50只小鼠,按两种剂量(2 ppm或6 ppm)中的一种给药103周,然后再观察0至2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。所有幸存的动物在第103周至第105周被杀死。给药的雄性和雌性大鼠的平均体重与相应的对照组基本相同。给药的雄性和雌性小鼠的平均体重也与相应的对照组基本相同。在给药组的小鼠中发现了多动症。大鼠和小鼠的存活率在给药组中都没有受到显著影响,在第90周时,所有给药组和对照组的存活率都达到72%或更高。有足够数量的动物有发展为晚期肿瘤的风险。在大鼠和小鼠身上都没有发生肿瘤,其发生率显然与试验化学物质的施用有关。然而,在大鼠和小鼠中,无论是通过体重抑制还是早期死亡率,都没有迹象表明使用了最大耐受剂量水平。因此,这些研究可能没有使用最大灵敏度来评估涕灭威可能的致癌性。在本实验条件下,技术级灭蚊威对F344大鼠和B6C3F1小鼠均无致癌作用。
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Bioassay of aldicarb for possible carcinogenicity.

A bioassay of aldicarb for possible carcinogenicity was conducted by administering the test chemical in feed to F344 rats and B6C3F1 mice. Groups of 50 rats and 50 mice of each sex were administered aldicarb at one of two doses, either 2 or 6 ppm, for 103 weeks and then observed for an additional 0 to 2 weeks. Matched controls consisted of 25 untreated rats and 25 untreated mice of each sex. All surviving animals were killed at weeks 103 to 105. Mean body weights of the dosed male and female rats were essentially the same as those of the corresponding controls. Mean body weights of the dosed male and female mice also were essentially the same as those of corresponding controls. Hyperactivity was noted in the dosed groups of mice. Survival was not affected significantly in dosed groups of either the rats or the mice and was 72% or greater in all dosed or control groups at week 90. Sufficient numbers of animals were at risk for the development of late-appearing tumors. No tumors occurred in either the rats or mice at incidences that could clearly be related to administration of the test chemical. In both rats and mice, however, there was no indication either through weight depression or early mortality that maximum tolerated dose levels were used. Therefore, the studies may not have been conducted using maximum sensitivity for the assessment of the possible carcinogenicity of aldicarb. It is concluded that under the conditions of this bioassay, technical-grade aldicarb was not carcinogenic for F344 rats or B6C3F1 mice of either sex.

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Bioassay of sulfisoxazole for possible carcinogenicity. Bioassay of diazinon for possible carcinogenicity. Bioassay of aldicarb for possible carcinogenicity. Bioassay of malaoxon for possible carcinogenicity. Bioassay of C.I. vat yellow 4 for possible carcinogenicity.
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