Department of Chemistry and Biochemistry, University of Notre Dame , Notre Dame, Indiana, 46556 United States.
Anal Chem. 2013 Nov 5;85(21):10159-66. doi: 10.1021/ac401537k. Epub 2013 Oct 15.
Label-free, chemical specific detection in flow is important for high throughput characterization of analytes in applications such as flow injection analysis, electrophoresis, and chromatography. We have developed a surface-enhanced Raman scattering (SERS) flow detector capable of ultrasensitive optical detection on the millisecond time scale. The device employs hydrodynamic focusing to improve SERS detection in a flow channel where a sheath flow confines analyte molecules eluted from a fused silica capillary over a planar SERS-active substrate. Increased analyte interactions with the SERS substrate significantly improve detection sensitivity. The performance of this flow detector was investigated using a combination of finite element simulations, fluorescence imaging, and Raman experiments. Computational fluid dynamics based on finite element analysis was used to optimize the flow conditions. The modeling indicates that a number of factors, such as the capillary dimensions and the ratio of the sheath flow to analyte flow rates, are critical for obtaining optimal results. Sample confinement resulting from the flow dynamics was confirmed using wide-field fluorescence imaging of rhodamine 6G (R6G). Raman experiments at different sheath flow rates showed increased sensitivity compared with the modeling predictions, suggesting increased adsorption. Using a 50 ms acquisition, a sheath flow rate of 180 μL/min, and a sample flow rate of 5 μL/min, a linear dynamic range from nanomolar to micromolar concentrations of R6G with a limit of detection (LOD) of 1 nM is observed. At low analyte concentrations, rapid analyte desorption is observed, enabling repeated and high-throughput SERS detection. The flow detector offers substantial advantages over conventional SERS-based assays such as minimal sample volumes and high detection efficiency.
无标记、化学特异性的流动检测对于高通量分析物的特征描述非常重要,例如在流动注射分析、电泳和色谱等应用中。我们开发了一种表面增强拉曼散射(SERS)流动检测器,能够在毫秒时间尺度上进行超灵敏的光学检测。该设备采用流体力学聚焦,在流道中提高 SERS 检测能力,其中鞘流将从熔融石英毛细管中洗脱的分析物分子限制在平面 SERS 活性衬底上。分析物与 SERS 衬底的相互作用增加,显著提高了检测灵敏度。该流动检测器的性能通过有限元模拟、荧光成像和拉曼实验的组合进行了研究。基于有限元分析的计算流体动力学用于优化流动条件。建模表明,许多因素,如毛细管尺寸和鞘流与分析物流速的比例,对于获得最佳结果至关重要。通过对罗丹明 6G(R6G)的宽场荧光成像,证实了由于流动动力学而产生的样品限制。与建模预测相比,不同鞘流率下的拉曼实验显示出更高的灵敏度,表明吸附增加。使用 50 ms 的采集时间、180 μL/min 的鞘流率和 5 μL/min 的样品流率,观察到 R6G 的纳摩尔到微摩尔浓度范围内的线性动态范围,检测限(LOD)为 1 nM。在低分析物浓度下,观察到快速的分析物解吸,从而实现了重复和高通量的 SERS 检测。与传统的基于 SERS 的分析相比,流动检测器具有显著的优势,例如样品体积小和检测效率高。