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Quantum dots cause acute systemic toxicity in lactating rats and growth restriction of offspring

机译:量子点导致急性全身毒性哺乳期大鼠和增长的限制后代

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The in vivo toxicity of QDs in animals has been broadly studied; however, their reproductive toxicity towards lactating rodents is currently unknown. This study therefore aims to assess the potential toxicity against dams and offspring after postnatal QD exposure at two doses (5 and 1 nmol per rat) and unravel whether QDs can translocate to pups via breastfeeding. The dose-dependent systemic toxicity of QDs in dams was observed by examining the body weight, hematology, biochemistry, histopathological changes, and sex hormone levels. It was found that the QDs primarily accumulated in the liver and spleen of dams at 1 day post injection (dpi), but the highest concentrations were found in the kidneys at 18 dpi. A few QDs were detected in breast milk and stomach and intestine of pups; this suggested that the QDs were transmitted to breast milk via blood circulation and then transferred to pups via breastfeeding. High-dose QDs induced severe growth inhibition and a 71.08% offspring mortality, while pups showed growth restriction within 90 dpi in the low-dose group. Moreover, the hematology, biochemistry, and histology results showed limited chronic toxicity against offspring in the long term. This study provides a theoretical foundation for the exposure assessment of nanomaterials in lactating animals and for the advancement of QDs in the biomedical field.
机译:量子点的体内毒性的动物广泛的研究;对哺乳期啮齿动物目前毒性未知的。潜在的毒性对大坝和后代产后QD曝光后两剂(5和1nmol /老鼠)和揭开量子点是否可以把通过母乳喂养幼崽。存在剂量依赖的相关性系统性毒性量子点的大坝观察通过检查体重,血液学、生物化学、组织病理学变化,性激素水平。量子点,主要积累在肝脏和脾脏的水坝在一天后注入(dpi),但最高的浓度被发现肾脏在18 dpi。母乳和幼崽的胃和小肠;这表明量子点的传播通过血液循环,然后母乳转移到通过母乳喂养幼崽。成为诱发严重的生长抑制和71.08%后代的死亡率,而小狗出现了增长低剂量组的限制在90 dpi。此外,血液学、生化和组织学结果显示有限的慢性毒性对后代的长期。提供了一个理论基础纳米材料在哺乳期暴露评估动物和量子点的进步的生物医学领域。

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