Department of Applied Chemistry, National Chiayi University, 300 Syuefu Road, Chiayi City, 60004, Taiwan.
Mikrochim Acta. 2018 Jan 17;185(2):120. doi: 10.1007/s00604-017-2662-9.
Making good use of interactions between analyte molecules and the metal nanoparticles is key to impact the detection limit in a surface-enhanced Raman scattering (SERS) based detections. SERS was applied to the analysis of catechin and it was found that the relative abundance of catechin in the sample to citrate-capped AgNPs and the aggregation agent NaCl plays a critical role in the quality of detection. At a component volume ratio of 6:2:1 (catechin:AgNPs:NaCl), catechin can be detected at µM levels. When the ratio is 12:2:1, Raman signals are discernible even at the attomolar concentration level (10 M). Under these conditions, the SERS mechanisms and the force of laser tweezers function best. The extent of signal enhancement enabled an ultrasensitive and reproducible Raman spectroscopic determination of catechin. Graphical abstract At a component volume ratio of 6:2:1 (catechin:AgNPs:NaCl), catechin was detected at 10 M to 10 M. When the ratio was 12:2:1, the discernible concentration of catechin was found to reach the attomolar level (10 M).
充分利用分析物分子与金属纳米粒子之间的相互作用是影响基于表面增强拉曼散射(SERS)检测的检测限的关键。SERS 被应用于儿茶素的分析,结果发现样品中儿茶素与柠檬酸封端的 AgNPs 和聚集剂 NaCl 的相对丰度对检测质量起着关键作用。在 6:2:1(儿茶素:AgNPs:NaCl)的组分体积比下,儿茶素可以在 µM 水平检测到。当比例为 12:2:1 时,即使在飞摩尔浓度水平(10−18 M)下也可以分辨出拉曼信号。在这些条件下,SERS 机制和激光镊子的力的作用最佳。信号增强的程度实现了儿茶素的超灵敏和可重现的拉曼光谱测定。