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Ionic-liquid-based microextraction method for the determination of silver nanoparticles in consumer products

机译:基于离子液体的微萃取方法,用于测定消费品中的银纳米粒子

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A simple method to determine hazardous silver nanoparticles (AgNPs) based on ionic liquid (IL) dispersive liquid-liquid microextraction and back-extraction is described. This approach involves AgNP stabilization using a cationic surfactant followed by extraction from the sample matrix by means of an IL as an extraction phase. Certain ILs have high affinity for metals, and preliminary experiments showed that those ILs consisting of imidazolium cation efficiently extracted AgNPs in the presence of a cationic surfactant and a chelating agent. Afterward, histamine was used as a dispersing agent to promote phase transfer of differently coated AgNPs from the IL in aqueous solution to be subsequently analyzed by UV-visible spectrometry. The analytical procedure allows AgNPs to be recovered from the sample matrix in an aqueous medium, the enrichment factor being up to 4, preserving both AgNP size and AgNP shape as demonstrated by transmission electron microscopy images and the localized surface plasmon resonance band characteristic of each AgNP. The present method exhibited a linear response for AgNPs in the range from 3 to 20 mu g/mL, the limit of detection being 0.15 mu g/mL. Method efficiency was assessed in spiked orange juice and face cream, yielding recoveries ranging from 75.7% to 96.6%. The method was evaluated in the presence of other nanointerferents (namely, gold nanoparticles). On the basis of diverse electrophoretic mobilities and surface plasmon resonance bands for metal nanoparticles, capillary electrophoresis was used to prove the lack of interaction of the target AgNPs with gold nanoparticles during the whole protocol; thus, interferents do not affect AgNP determination. As a consequence, the analytical approach described has great potential for the analysis of engineered nanosilver in consumer products.
机译:描述了一种基于离子液体(IL)色散液 - 液微萃取和背萃取的危险银纳米颗粒(AgNP)的简单方法。这种方法涉及使用阳离子表面活性剂的AgNP稳定化,然后通过作为萃取相的IL从样品基质中提取。某些ILS对金属具有很高的亲和力,并且初步实验表明,那些由咪唑阳溶阳离子组成的ILS在阳离子表面活性剂和螯合剂存在下有效地提取AgNP。之后,使用组胺作为分散剂,以促进从IL中的不同涂覆的AgNP的相转移随后通过UV可见光光谱法分析。分析程序允许从水性介质中的样品基质中回收AgNP,富集因子高达4,保持AGNP尺寸和AgNP形状,通过透射电子显微镜图像和每个AGNP的局部表面等离子体谐振带特性证明。本方法表现出直线响应的agnps在3至20μg/ ml的范围内,检测极限为0.15μg/ ml。在尖刺的橙汁和面霜中评估了方法效率,产生的回收率为75.7%至96.6%。该方法在其他纳诺子系(即金纳米颗粒)的存在下进行评估。基于多样化的电泳迁移率和用于金属纳米颗粒的表面等离子体共振带,使用毛细管电泳来证明整个方案期间靶酰胺与金纳米颗粒的缺乏相互作用;因此,干扰不会影响AGNP测定。因此,描述的分析方法具有巨大的消费产品分析工程纳米液的潜力。

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