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Trace analysis of mercury(II) ions using aptamer-modified Au/Ag core-shell nanoparticles and SERS spectroscopy in a microdroplet channel

机译:适体修饰的Au / Ag核壳纳米粒子和SERS光谱在微滴通道中痕量分析汞(II)离子

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摘要

We report the rapid and highly sensitive trace analysis of mercury(n) ions in water using a surface-enhanced Raman scattering (SERS)-based microdroplet sensor. Aptamer-modified Au/Ag core-shell nanoparticles have been fabricated and utilized as highly functional sensing probes. All detection processes for the reaction between mercury(II) ions and aptamer-modified nanoparticles were performed in a specially designed microdroplet channel. Small water droplets that included sample reagents were separated from each other by an oil phase that continuously flowed along the channel. This two-phase liquid-liquid segmented flow system prevented the adsorption of aggregated colloids to the channel walls due to localized reagents within encapsulated droplets. The result was reduced residence time distributions. The limit of detection (LOD) of mercury(II) ions in water was determined by the SERS-based microdroplet sensor to be below 10 pM, which is three orders below the EPA-defined maximum contaminant level. This combination of a SERS-based microfluidic sensor with aptamer-based functional nanoprobes can be used for in-the-field sensing platforms, due to its size and simplicity.
机译:我们报告使用基于表面增强的拉曼散射(SERS)的微滴传感器对水中的汞离子进行快速,高度灵敏的痕量分析。适体修饰的Au / Ag核-壳纳米粒子已被制造出来,并用作高功能的传感探针。汞(II)离子与适体修饰的纳米颗粒之间反应的所有检测过程均在专门设计的微滴通道中进行。包含样品试剂的小水滴通过沿通道连续流动的油相彼此分离。这种两阶段的液-液分段流动系统可防止由于包囊液滴内的局部试剂而使聚集的胶体吸附到通道壁上。结果是减少了停留时间分布。通过基于SERS的微滴传感器确定的水中汞(II)离子的检测极限(LOD)低于10 pM,这比EPA定义的最大污染物水平低了三个数量级。基于SERS的微流体传感器与基于适体的功能性纳米探针的结合,由于其尺寸和简单性,可用于现场传感平台。

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