Department of Chemistry, Tokyo Institute of Technology, Meguro-ku, Tokyo, 152-8551, Japan.
Mikrochim Acta. 2021 Nov 3;188(11):406. doi: 10.1007/s00604-021-05055-x.
Raman spectroscopy is a powerful method to characterize molecules in various media. Although surface-enhanced Raman scattering (SERS) is often employed to compensate for the intrinsically poor sensitivity of Raman spectroscopy, there remain serious tasks, such as simple preparations of SERS substrates, sensitivity control, and reproducible measurements. Here, we propose freezing as an efficient way to overcome these problems in SERS measurements using DNA bases as model targets. Solutes are expelled from ice crystals and concentrated in the liquid phase upon freezing. Silver nanoparticles (AgNPs) are also concentrated in the liquid phase to aggregate with Raman target analytes. The SERS signal intensity is maximized when the AgNP concentration exceeds the critical aggregation value. Freezing allows up to 5000 times enhancements of the SERS signal. Thus, an efficient SERS platform is prepared by simple freezing. The simultaneous detection of four DNA bases effectively eliminates variations of signal intensities and allows the reliable determination of concentration ratios.
拉曼光谱是一种在各种介质中对分子进行特征分析的强大方法。尽管表面增强拉曼散射(SERS)常用于补偿拉曼光谱固有的灵敏度低的问题,但仍然存在严重的任务,如 SERS 基底的简单制备、灵敏度控制和可重现的测量。在这里,我们提出冷冻作为一种有效的方法,使用 DNA 碱基作为模型靶标来克服 SERS 测量中的这些问题。溶质从冰晶中排出并在冷冻时浓缩在液相中。银纳米粒子(AgNPs)也集中在液相中与拉曼目标分析物聚集。当 AgNP 浓度超过临界聚集值时,SERS 信号强度最大化。冷冻可将 SERS 信号增强高达 5000 倍。因此,通过简单的冷冻制备了高效的 SERS 平台。同时检测四种 DNA 碱基可有效地消除信号强度的变化,并允许可靠地确定浓度比。