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银纳米颗粒在雄性 Wistar 大鼠体内的时相分布和排泄。

Time-dependent biodistribution and excretion of silver nanoparticles in male Wistar rats.

机构信息

Warsaw University of Life Sciences, Warsaw, Poland.

出版信息

J Appl Toxicol. 2012 Nov;32(11):920-8. doi: 10.1002/jat.2758. Epub 2012 Jun 13.

DOI:10.1002/jat.2758
PMID:22696427
Abstract

Silver nanoparticles (AgNPs) are the most commonly used nanoparticles owing to their antimicrobial properties. The motivation of the present study was (1) to analyze the effect of silver particle size on rat tissue distribution at different time points, (2) to determine the accumulation of AgNPs in potential rat target organs, (3) to analyze the intracellular distribution of AgNPs and (4) to examine the excretion of AgNPs by urine and feces. AgNPs were characterized by dynamic light scattering (DLS), zeta potential measurements, BET surface area measurements, transmission and scanning electron microscopy. AgNPs (20 and 200 nm) were administered intravenously (i.v.) to male Wistar rats at a dose of 5 mg kg(-1) of body weight. Biological material was sampled 24 h, 7 and 28 days after injection. Using inductively coupled plasma-mass spectrometry (ICP-MS) and transmission electron microscopy (TEM) it was observed that AgNPs translocated from the blood to the main organs and the concentration of silver in tissues was significantly higher in rats treated with 20 nm AgNPs as compared with 200 nm AgNPs. The highest concentration of silver was found in the liver after 24 h. After 7 days, a high level of silver was observed in the lungs and spleen. The silver concentration in the kidneys and brain increased during the experiment and reached the highest concentration after 28 days. Moreover, the highest concentration of AgNPs was observed in the urine 1 day after the injection, maintained high for 14 days and then decreased. The fecal level of silver in rats was the highest within 2 days after AgNPs administration and then decreased.

摘要

银纳米粒子(AgNPs)由于其抗菌性能而被广泛应用。本研究的目的是:(1)分析不同时间点银颗粒尺寸对大鼠组织分布的影响;(2)确定 AgNPs 在潜在大鼠靶器官中的积累;(3)分析 AgNPs 的细胞内分布;(4)通过尿液和粪便检查 AgNPs 的排泄情况。AgNPs 通过动态光散射(DLS)、zeta 电位测量、BET 比表面积测量、透射和扫描电子显微镜进行表征。AgNPs(20nm 和 200nm)以 5mgkg(-1)的体重静脉内(i.v.)给予雄性 Wistar 大鼠。在注射后 24h、7 天和 28 天采集生物材料。使用电感耦合等离子体质谱(ICP-MS)和透射电子显微镜(TEM)观察到,AgNPs 从血液转移到主要器官,并且与 200nm AgNPs 相比,20nm AgNPs 处理的大鼠组织中银的浓度明显更高。在 24h 时,肝脏中银的浓度最高。7 天后,肺部和脾脏中观察到高浓度的银。在实验过程中,肾脏和大脑中的银浓度增加,在 28 天后达到最高浓度。此外,在注射后 1 天尿液中观察到 AgNPs 的最高浓度,维持 14 天,然后降低。在给予 AgNPs 后 2 天内,大鼠粪便中的银浓度最高,然后降低。

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