Wen Ruoxi, Yang Xiaoxi, Hu Ligang, Sun Cheng, Zhou Qunfang, Jiang Guibin
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, China.
School of Earth and Space Science, University of Science and Technology of China, Anhui, 230026, China.
J Appl Toxicol. 2016 Mar;36(3):445-53. doi: 10.1002/jat.3260. Epub 2015 Nov 20.
The wide applications of silver nanoparticles (AgNPs) have been concerned regarding their unintentional toxicities. Different exposure modes may cause distinct accumulation, retention and elimination profiles, which are closely related with their toxicities. Unlike silver accumulation profiles through other regular administration modes, the biodistribution, accumulation and elimination of AgNPs by intranasal instillation are not fully understood. This study conducted intranasal instillation of polyvinylpyrrolidone-coated AgNPs in neonatal Sprague-Dawley rats at doses of 1 and 0.1 mg kg(-1) day(-1) for 4 and 12 weeks, respectively. The 4-week recovery was also designed after the 12-week exposure. Silver concentrations in the main tissues or organs were periodically monitored. Parallel exposures using silver ion were performed for the comparative studies. No physiological alterations were observed in AgNP exposures. In comparison, 1 mg kg(-1) day(-1) silver ions decreased body weight gain and caused mortality of 18.2%, showing ionic silver had a relatively higher toxicity than AgNPs. A relatively higher silver accumulation was observed in silver ion groups than AgNP groups. The silver ion release could not fully explain silver accumulation in AgNP exposures, showing silver distribution caused by particulate silver occurred in vivo. The highest silver concentration was in the liver at week 4, while it shifted to the brain after a 12-week exposure. Dose-related silver accumulation occurred for both AgNP and silver ion groups. The time course revealed a uniquely high concentration and retention of brain silver, implying chronic intranasal instillation caused brain-targeted silver accumulation. These findings provided substantial evidence on the potential neuronal threat from the intranasal administration of AgNPs or silver colloid-based products.
银纳米颗粒(AgNPs)的广泛应用引发了人们对其意外毒性的关注。不同的暴露模式可能导致不同的积累、滞留和消除情况,这与它们的毒性密切相关。与通过其他常规给药方式的银积累情况不同,经鼻滴注AgNPs后的生物分布、积累和消除情况尚未完全明确。本研究分别以1和0.1 mg kg⁻¹天⁻¹的剂量对新生Sprague-Dawley大鼠经鼻滴注聚乙烯吡咯烷酮包覆的AgNPs,持续4周和12周。在12周暴露后还设计了4周的恢复期。定期监测主要组织或器官中的银浓度。使用银离子进行平行暴露以进行对比研究。在AgNP暴露中未观察到生理改变。相比之下,1 mg kg⁻¹天⁻¹的银离子降低了体重增加,并导致18.2%的死亡率,表明离子银的毒性相对高于AgNPs。在银离子组中观察到的银积累相对高于AgNP组。银离子释放不能完全解释AgNP暴露中的银积累,表明体内存在由颗粒银引起的银分布。第4周时肝脏中的银浓度最高,而在12周暴露后转移到了大脑。AgNP组和银离子组均出现了与剂量相关的银积累。时间进程显示大脑中的银具有独特的高浓度和滞留现象,这意味着慢性经鼻滴注会导致大脑靶向性银积累。这些发现为经鼻给药AgNPs或基于银胶体的产品对神经元的潜在威胁提供了大量证据。