Institute of Chemical Technologies and Analytics, Vienna University of Technology, Getreidemarkt 9/151, A-1060 Vienna, Austria; Departement of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Assiut University, 71526 Assiut, Egypt.
Talanta. 2013 Nov 15;116:972-7. doi: 10.1016/j.talanta.2013.07.059. Epub 2013 Jul 31.
This paper reports an improved way for performing highly reproducible surface enhanced Raman scattering of different analytes using an automated flow system. The method uses a confocal Raman microscope to prepare SERS active silver spots on the window of a flow cell by photo-reduction of silver nitrate in the presence of citrate. Placement of the flow cell on an automated x and y stages of the Raman microscope allows to prepare a fresh spot for every new measurement. This procedure thus efficiently avoids any carry over effects which might result from adsorption of the analyte on the SERS active material and enables highly reproducible SERS measurements. For reproducible liquid handling the used sequential injection analysis system as well as the Raman microscope was operated by the flexible LabVIEW based software ATLAS developed in our group. Quantitative aspects were investigated using Cu(PAR)2 as a model analyte. Concentration down to 5×10(-6) M provided clear SERS spectra, a linear concentration dependence of the SERS intensities at 1333 cm(-1) was obtained from 5×10(-5) to 1×10(-3) with a correlation coefficient r=0.999. The coefficient of variation of the method Vxo was found to be 5.6% and the calculated limit of detection 1.7×10(-5) M. The results demonstrate the potential of SERS spectroscopy to be used as a molecular specific detector in aqueous flow systems.
本文报道了一种使用自动化流动系统进行高重现性表面增强拉曼散射(SERS)分析不同分析物的改进方法。该方法使用共焦拉曼显微镜通过在柠檬酸存在下用光还原硝酸银在流动池窗口上制备 SERS 活性银点。将流动池放置在拉曼显微镜的自动化 x 和 y 台上,可在每次新测量时制备一个新的活性点。因此,该方法有效地避免了由于分析物在 SERS 活性材料上的吸附而可能导致的任何残留效应,并实现了高重现性的 SERS 测量。为了实现可重现的液体处理,所使用的顺序注射分析系统以及拉曼显微镜都由我们小组开发的基于灵活的 LabVIEW 的软件 ATLAS 操作。使用 Cu(PAR)2 作为模型分析物研究了定量方面。在 5×10(-6) M 浓度下可获得清晰的 SERS 光谱,从 5×10(-5) 到 1×10(-3) 获得了 1333 cm(-1)处 SERS 强度的线性浓度依赖性,相关系数 r=0.999。该方法的变异系数 Vxo 为 5.6%,计算出的检测限为 1.7×10(-5) M。结果表明,SERS 光谱法具有作为水相流动系统中分子特异性检测器的潜力。