Isotianil (2nd edition) (Pesticides)

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Abstract

Abstract Food Safety Commission of Japan (FSCJ) conducted a risk assessment of isotianil (CAS No. 224049-04-1), an isothiazole agent for induced resistance to blast disease. This evaluation was requested from Ministry of Agriculture, Forestry and Fisheries (MAFF) on the reevaluation article of Agricultural Chemicals Regulation Act. Additional information including the fate in livestock (goats and chickens) and genotoxicity, and also the list of published scientific literature were newly submitted from the MAFF. The following data were used in the assessment; fate in plants (including paddy rice and potatoes), residues in crops, fate in livestock (goats and chickens), residues in livestock products, fate in animals (rats), subacute toxicity (rats, mice and dogs), chronic toxicity (rats and dogs), carcinogenicity (rats and mice), two-generation reproductive toxicity (rats), developmental toxicity (rats and rabbits), and genotoxicity. Major adverse effects of isotianil were observed in the stomach (mucosal epithelium hyperplasia of the forestomach limiting ridge in rats), the liver (including organ weight gain), and the kidney (including chronic nephropathy). No adverse effects were observed on carcinogenicity, fertility, teratogenicity, and genotoxicity. The lowest no-observed-adverse-effect level (NOAEL) obtained from the studies described above was 2.83 mg/kg bw per day in a one-year chronic toxicity study in rats. FSCJ specified an acceptable daily intake (ADI) of 0.028 mg/kg bw per day based on the NOAEL after applying a safety factor of 100. An acute reference dose (ARfD) was judged unnecessary to be specified, based on the results of a single oral administration of isotianil and other related tests.
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异噻菌胺(第 2 版)(杀虫剂)
摘要 日本食品安全委员会(FSCJ)对异噻菌胺(化学文摘社编号:224049-04-1)进行了风险评估。该评估是农林水产省(MAFF)根据《农业化学品管理法》的重新评估条款要求进行的。农林渔业部新近提交了其他信息,包括在牲畜(山羊和鸡)体内的转归和遗传毒性,以及已发表的科学文献清单。评估采用了以下数据:在植物(包括水稻和马铃薯)中的转归、在作物中的残留、在牲畜(山羊和鸡)中的转归、在畜产品中的残留、在动物(大鼠)中的转归、亚急性毒性(大鼠、小鼠和狗)、慢性毒性(大鼠和狗)、致癌性(大鼠和小鼠)、两代生殖毒性(大鼠)、发育毒性(大鼠和兔子)以及遗传毒性。在胃部(大鼠林胃边缘脊粘膜上皮增生)、肝脏(包括器官重量增加)和肾脏(包括慢性肾病)中观察到异噻菌胺的主要不良影响。在致癌性、生育能力、致畸性和遗传毒性方面未观察到不良影响。在对大鼠进行的为期一年的慢性毒性研究中,上述研究得出的最低无观测不良效应水平(NOAEL)为每天 2.83 毫克/千克体重。根据无观测不良效应水平,FSCJ 规定每日允许摄入量为 0.028 毫克/千克体重,安全系数为 100。根据一次口服异噻尼尔和其他相关试验的结果,判定没有必要规定急性参考剂量(ARfD)。
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