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Evaluation of 2-week repeated oral dose toxicity of 100 nm zinc oxide nanoparticles in rats

机译:评估100 nm氧化锌纳米颗粒在大鼠中2周重复口服剂量的毒性

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摘要

The aim of this study was to verify subacute oral dose toxicity of positively charged 100 nm zinc oxide (ZnOAE100[+]) nanoparticles (NPs) in Sprague-Dawley rats. ZnOAE100[+] NPs were administered to rats of each sex by gavage at 0, 500, 1,000, and 2,000 mg/kg/day for 14 days. During the study period, clinical signs, mortality, body weight, food consumption, hematology, serum biochemistry, gross pathology, organ weight, and histopathology were examined. Increased mortality and clinical signs, decreased body weight, feed consumption, hemoglobin (HB), hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), platelet (PT), and lymphocyte (LYM) and increased white blood cells (WBCs), neutrophils (NEUs), alkaline phosphatase (ALP), and histopathological alterations in the spleen, stomach, and pancreas were observed at 2,000 mg/kg/day. Increased clinical signs, decreased body weight, feed consumption, HB, HCT, MCV, MCH, MCHC, and LYM and increased WBCs, NEUs, ALP, and histopathological alterations in the spleen, stomach, and pancreas were seen at 1,000 mg/kg/day. Increased clinical signs, decreased MCV and MCH and increased histopathological alterations in the stomach and pancreas were found at 500 mg/kg/day. These results suggest that the target organs were the spleen, stomach, and pancreas in rats. The no-observed-adverse-effect level was <500 mg/kg for both sexes.
机译:这项研究的目的是验证正电荷的100 nm氧化锌(ZnO AE100 [+] )纳米粒子(NPs)在Sprague-Dawley大鼠中的亚急性口服剂量毒性。 ZnO AE100 [+] NPs分别以0、500、1,000和2,000 mg / kg / day的剂量灌胃给各性别大鼠,持续14天。在研究期间,检查了临床体征,死亡率,体重,食物消耗,血液学,血清生化,大体病理学,器官重量和组织病理学。死亡率和临床症状增加,体重,饲料消耗减少,血红蛋白(HB),血细胞比容(HCT),平均红细胞体积(MCV),平均红细胞血红蛋白(MCH),平均红细胞血红蛋白浓度(MCHC),血小板(PT),每天2,000 mg / kg / day观察到淋巴细胞(LYM)和白细胞(WBCs),中性粒细胞(NEUs),碱性磷酸酶(ALP)的增加以及脾,胃和胰腺的组织病理学改变。在1000 mg / kg / kg时,临床体征增加,体重减轻,饲料消耗减少,HB,HCT,MCV,MCH,MCHC和LYM升高,并且WBC,NEU,ALP以及脾,胃和胰腺的组织病理学改变增加天。以500 mg / kg / day的剂量,发现临床症状增加,MCV和MCH降低以及胃和胰腺的组织病理学改变增加。这些结果表明,目标器官是大鼠的脾脏,胃和胰腺。男女的未观察到的不良反应水平是<500 mg / kg。

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