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评估水动力色谱法与电感耦合等离子体质谱法联用对溶解态和纳米颗粒态金和银的形态分析。

Evaluation of hydrodynamic chromatography coupled to inductively coupled plasma mass spectrometry for speciation of dissolved and nanoparticulate gold and silver.

机构信息

Group of Analytical Spectroscopy and Sensors (GEAS), Institute of Environmental Sciences (IUCA), University of Zaragoza, Pedro Cerbuna 12, 50009, Zaragoza, Spain.

出版信息

Anal Bioanal Chem. 2021 Mar;413(6):1689-1699. doi: 10.1007/s00216-020-03132-3. Epub 2021 Feb 2.

DOI:10.1007/s00216-020-03132-3
PMID:33528600
Abstract

In this study, hydrodynamic chromatography coupled to inductively coupled plasma mass spectrometry has been evaluated for the simultaneous determination of dissolved and nanoparticulate species of gold and silver. Optimization of mobile phase was carried out with special attention to the column recovery of the different species and the resolution between them. Addition of 0.05 mM penicillamine to the mobile phase allowed the quantitative recovery of ionic gold and gold nanoparticles up to 50 nm, whereas 1 mM penicillamine was necessary for quantitative recovery of ionic silver and silver nanoparticles up to 40 nm. The resolution achieved between ionic gold and 10-nm gold nanoparticles was 0.7, whereas it ranged between 0.31 and 0.93 for ionic silver and 10-nm silver nanoparticles, depending on the composition of mobile phase. Best-case mass concentration detection limits for gold and silver species were 0.05 and 0.75 μg L, respectively. The developed methods allowed the simultaneous detection of nanoparticulate and dissolved species of gold and silver in less than 10 min. Size determination and quantification of gold and silver species were carried out in different dietary supplements, showing good agreement with the results obtained by electron microscopy and total and ultrafiltrable contents, respectively. Due to the attainable resolution, the quality of the quantitative results is affected by the relative abundance of nanoparticulate and dissolved species of the element and the size of the nanoparticles if present.

摘要

在这项研究中,采用水动力学色谱与电感耦合等离子体质谱联用的方法,同时测定了溶解态和纳米颗粒态的金和银。通过特别关注不同物种在柱上的回收率和它们之间的分辨率,对流动相进行了优化。在流动相中添加 0.05 mM 青霉胺可定量回收离子态金和粒径达 50 nm 的金纳米颗粒,而定量回收离子态银和粒径达 40 nm 的银纳米颗粒则需要 1 mM 青霉胺。离子态金和 10nm 金纳米颗粒之间的分辨率为 0.7,而离子态银和 10nm 银纳米颗粒之间的分辨率范围为 0.31 至 0.93,这取决于流动相的组成。金和银的最佳质量浓度检测限分别为 0.05 和 0.75 μg/L。所开发的方法可在不到 10 分钟的时间内同时检测到金和银的纳米颗粒态和溶解态。在不同的膳食补充剂中进行了金和银物种的粒径测定和定量分析,与电子显微镜以及总含量和超滤含量的结果分别具有良好的一致性。由于可实现的分辨率,如果存在纳米颗粒,则定量结果的质量会受到元素的纳米颗粒态和溶解态的相对丰度以及纳米颗粒的粒径的影响。

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