State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, China.
Nanoscale. 2018 Jun 21;10(24):11564-11577. doi: 10.1039/c8nr01248b.
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.
QD 在动物体内的毒性已得到广泛研究;然而,其对哺乳期啮齿动物的生殖毒性目前尚不清楚。因此,本研究旨在评估产后 QD 暴露于两个剂量(每只大鼠 5 和 1 nmol)对母体和后代的潜在毒性,并阐明 QD 是否可以通过母乳喂养转移到幼仔体内。通过检查体重、血液学、生物化学、组织病理学变化和性激素水平,观察了 QD 对母体的剂量依赖性全身毒性。结果发现,QD 在注射后 1 天(dpi)主要在母体的肝脏和脾脏中积累,但在 18 dpi 时在肾脏中发现了最高浓度。在幼仔的母乳、胃和肠中检测到少量 QD;这表明 QD 通过血液循环传递到母乳中,然后通过母乳喂养传递给幼仔。高剂量 QD 诱导严重的生长抑制和 71.08%的幼仔死亡率,而低剂量组的幼仔在 90 dpi 内表现出生长受限。此外,血液学、生物化学和组织学结果表明,长期来看,对后代的慢性毒性有限。本研究为哺乳期动物中纳米材料暴露评估和 QD 在生物医学领域的应用提供了理论基础。