首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Detection and characterization of silver nanoparticles and dissolved species of silver in culture medium and cells by AsFlFFF-UV-Vis- ICPMS: application to nanotoxicity tests
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Detection and characterization of silver nanoparticles and dissolved species of silver in culture medium and cells by AsFlFFF-UV-Vis- ICPMS: application to nanotoxicity tests

机译:AsFlFFF-UV-Vis-ICPMS检测和表征培养基和细胞中的银纳米颗粒和银的溶解物种:应用于纳米毒性测试

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摘要

A methodology based on Asymmetric Flow Field-Flow Fractionation (AsFlFFF) coupled with UV-Vis absorption spectrometry and ICP mass spectrometry (ICPMS) has been developed and applied to the study of silver nanoparticles (AgNPs) and dissolved species of silver in culture media and cells used in cytotoxicity tests. The effect of a nano-silver based product (protein stabilized silver nanoparticles ca. 15 nm average diameter) on human hepatoma (HepG2) cell viability has been studied. UV-Vis absorption spectrometry provided information about the nature (organic vs. nanoparticle) of the eluted species, whereas the silver was monitored by ICPMS. A shift towards larger hydrodynamic diameters was observed in the AgNPs after a 24 hour incubation period in the culture medium, which suggests a "protein corona" effect. Silver(I) associated with proteins present in the culture medium has also been detected, as a consequence of the oxidation process experimented by the AgNPs. However, the Ag(I) released into the culture medium did not justify the toxicity levels observed. AgNPs associated with the cultured HepG2 cells were also identified by AsFlFFF, after applying a solubilisation process based on the use of tetramethylammonium hydroxide (TMAH) and Triton X-100. These results have been confirmed by transmission electronic microscopy (TEM) analysis of the fractions collected from the AsFlFFF. The effect of AgNPs on HepG2 cells has been compared to that caused by silver(I) as AgNO_3 under the same conditions. The determination of the total content of silver in the cells confirms that a much larger mass of silver as AgNPs with respect to AgNO_3 (16 to 1) is needed to observe a similar toxicity.
机译:已开发出一种基于非对称流场流分馏(AsFlFFF)结合UV-Vis吸收光谱法和ICP质谱法(ICPMS)的方法,并将其用于研究银纳米颗粒(AgNPs)和培养基中银的溶解种类,细胞毒性试验中使用的细胞。研究了纳米银基产品(蛋白质稳定的银纳米粒子,平均直径约15 nm)对人肝癌(HepG2)细胞生存能力的影响。 UV-Vis吸收光谱法可提供有关洗脱物质的性质(有机粒子与纳米粒子)的信息,而银则通过ICPMS进行监测。在培养基中孵育24小时后,在AgNP中观察到向更大的流体力学直径的转变,这表明存在“蛋白电晕”效应。由于AgNPs的氧化过程,还检测到了与培养基中存在的蛋白质相关的银(I)。然而,释放到培养基中的Ag(I)不能证明所观察到的毒性水平是合理的。在使用基于氢氧化四甲基铵(TMAH)和Triton X-100的增溶过程后,还通过AsFlFFF鉴定了与培养的HepG2细胞相关的AgNP。这些结果已经通过透射电子显微镜(TEM)分析从AsF1FFF收集的级分证实。已经比较了在相同条件下,AgNP对HepG2细胞的作用与银(I)作为AgNO_3引起的作用。确定细胞中银的总含量证实,相对于AgNO_3(16比1),需要更大质量的银作为AgNPs才能观察到类似的毒性。

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