Bioassay of sulfisoxazole for possible carcinogenicity.

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Abstract

A bioassay of sulfisoxazole for possible carcinogenicity was conducted by administering the chemical by gavage to Fischer 344 rats and B6C3F1 mice. Groups of 50 rats of each sex and 50 mice of each sex were administered sulfisoxazole suspended in aqueous 0.5% carboxymethyl cellulose 7 days per week at one of two doses, either 100 or 400 mg/kg body weight for the rats and either 500 or 2,000 mg/kg for the mice. Vehicle controls consisted of groups of 50 rats of each sex and 50 mice of each sex that were administered only the aqueous 0.5% carboxymethyl cellulose. Untreated controls consisted of groups of 50 rats of each sex and 50 mice of each sex. The dosed groups of the rats and mice were administered the chemical by gavage for 103 weeks, then observed for 1 to 3 additional weeks; the vehicle-control groups were similarly administered 0.5% carboxymethyl cellulose alone. All surviving rats and mice were killed at weeks 104 to 106. Mean body weights of high-dose male rats and female mice were slightly lower than those of corresponding vehicle controls during the last 40 to 50 weeks of the bioassay; mean body weights of dosed female rats and male mice were unaffected. Survival rates were unaffected by the test chemical, and adequate numbers of animals were at risk for the development of late-appearing tumors. No tumors occurred in the dosed groups of rats or mice of either sex at incidences that were significantly higher than those of the vehicle-control groups. It is concluded that under the conditions of this bioassay, sulfisoxazole was not carcinogenic for either Fischer 344 rats or B6C3F1 mice

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磺胺恶唑可能致癌性的生物测定。
通过对Fischer 344大鼠和B6C3F1小鼠灌胃磺胺恶唑进行了可能致癌性的生物测定。每组50只大鼠和50只小鼠,每周7天,按两种剂量中的一种给药,大鼠为100或400 mg/kg体重,小鼠为500或2000 mg/kg体重。载体对照包括每性别50只大鼠和每性别50只只给予0.5%羧甲基纤维素水溶液的小鼠。未经处理的对照组由各性别50只大鼠和各性别50只小鼠组成。给药组大鼠、小鼠灌胃给药103周,再观察1 ~ 3周;车辆对照组同样单独给予0.5%羧甲基纤维素。所有存活的大鼠和小鼠在第104至106周被杀死。在生物测定的最后40 ~ 50周,高剂量雄性大鼠和雌性小鼠的平均体重略低于相应的对照;雌性大鼠和雄性小鼠的平均体重未受影响。存活率没有受到试验化学物质的影响,而且有足够数量的动物有发展为晚期肿瘤的风险。在给药组的大鼠或小鼠中,无论性别,均未发生肿瘤,其发生率明显高于对照组。结果表明,在本实验条件下,磺胺恶唑对Fischer 344大鼠和B6C3F1小鼠均无致癌性
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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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