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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Capillary electrophoresis coupled with inductively coupled mass spectrometry as an alternative to cloud point extraction based methods for rapid quantification of silver ions and surface coated silver nanoparticles
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Capillary electrophoresis coupled with inductively coupled mass spectrometry as an alternative to cloud point extraction based methods for rapid quantification of silver ions and surface coated silver nanoparticles

机译:毛细管电泳与电感耦合质谱法相结合,可替代基于浊点提取的银离子和表面涂覆的银纳米粒子的快速定量方法

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Speciation and accurate quantification of ionic silver and metallic silver nanoparticles are critical to investigate silver toxicity and to determine the shelf-life of products that contain nano silver under various storage conditions. We developed a rapid method for quantification of silver ions and silver nanoparticles using capillary electrophoresis (CE) interfaced with inductively-coupled plasma mass spectrometry (ICPMS). The addition of 2-mercaptopropionylglycine (tiopronin) to the background electrolyte was used to facilitate the chromatographic separation of ionic silver and maintain the oxidation state of silver. The obtained limits of detection were 0.05 mu g kg(-1) of silver nanoparticles and 0.03 mu g kg(-1) of ionic silver. Nanoparticles of varied sizes (10-110 nm) with different surface coating, including citrate acid, lipoic acid, polyvinylpyrrolidone and bovine serum albumin (BSA) were successfully analyzed. Particularly good recoveries (>93%) were obtained for both ionic silver and silver nanoparticle in the presence of excess amount of BSA. The method was further tested with six commercially available dietary supplements which varied in concentration and matrix components. The summed values of silver ions and silver nanoparticles correlated well with the total silver concentration determined by ICPMS after acid digestion. This method can serve as an alternative to cloud point extraction technique when the extraction efficiency for protein coated nanoparticles is low. (C) 2015 Elsevier B.V. All rights reserved.
机译:离子银和金属银纳米粒子的形态和准确定量对于研究银的毒性以及确定在各种储存条件下含有纳米银的产品的货架期至关重要。我们开发了一种使用毛细管电泳(CE)与电感耦合等离子体质谱(ICPMS)接口的定量银离子和银纳米颗粒的快速方法。将2-巯基丙酰甘氨酸(硫普罗宁)添加到本底电解液中可用于促进离子银的色谱分离并保持银的氧化态。获得的检出限为0.05微克kg(-1)的银纳米颗粒和0.03微克kg(-1)的离子银。成功地分析了具有不同表面涂层的各种尺寸(10-110 nm)的纳米颗粒,包括柠檬酸,硫辛酸,聚乙烯吡咯烷酮和牛血清白蛋白(BSA)。在过量的BSA存在下,离子银和银纳米粒子的回收率都特别高(> 93%)。用六种市售的膳食补充剂进一步测试了该方法,这些膳食补充剂的浓度和基质成分均不同。酸消解后,银离子和银纳米颗粒的总和与ICPMS测定的总银浓度高度相关。当蛋白包被的纳米颗粒的提取效率较低时,该方法可以替代浊点提取技术。 (C)2015 Elsevier B.V.保留所有权利。

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