Fischell Department of Bioengineering, University of Maryland, College Park, Maryland 20742, USA.
Biomicrofluidics. 2012 Mar;6(1):14105-141059. doi: 10.1063/1.3677369. Epub 2012 Jan 13.
We report the demonstration of an optofluidic surface enhanced Raman spectroscopy (SERS) device that leverages a nanoporous microfluidic matrix to improve the SERS detection performance by more than two orders of magnitude as compared to a typical open microfluidic channel. Although it is a growing trend to integrate optical biosensors into microfluidic channels, this basic combination has been detrimental to the sensing performance when applied to SERS. Recently, however, synergistic combinations between microfluidic functions and photonics (i.e., optofluidics) have been implemented that improve the detection performance of SERS. Conceptually, the simplest optofluidic SERS techniques reported to date utilize a single nanofluidic channel to trap nanoparticle-analyte conjugates as a method of preconcentration before detection. In this work, we leverage this paradigm while improving upon the simplicity by forming a 3D nanofluidic network with packed nanoporous silica microspheres in a microfluidic channel; this creates a concentration matrix that traps silver nanoclusters and adsorbed analytes into the SERS detection volume. With this approach, we are able to achieve a detection limit of 400 attomoles of Rhodamine 6G after only 2 min of sample loading with high chip-to-chip repeatability. Due to the high number of fluidic paths in the nanoporous channel, this approach is less prone to clogging than single nanofluidic inlets, and the loading time is decreased compared to previous reports. In addition, fabrication of this microsystem is quite simple, as nanoscale fabrication is not necessary. Finally, integrated multimode fiber optic cables eliminate the need for optical alignment, and thus the device is relevant for portable and automated applications in the field, including point-of-sample and point-of-care detection. To illustrate a relevant field-based application, we demonstrate the detection of 12 ppb of the organophosphate malathion in water using the nanofluidic SERS microsystem.
我们报告了一种光流控表面增强拉曼光谱(SERS)器件的演示,该器件利用纳米多孔微流控基质通过与典型的开放式微流道相比,将 SERS 检测性能提高了两个数量级以上。虽然将光学生物传感器集成到微流道中是一种日益增长的趋势,但当应用于 SERS 时,这种基本组合对传感性能不利。然而,最近已经实现了微流控功能和光子学(即光流控)之间的协同组合,提高了 SERS 的检测性能。从概念上讲,迄今为止报道的最简单的光流控 SERS 技术利用单个纳米流道来捕获纳米粒子-分析物缀合物,作为检测前的预浓缩方法。在这项工作中,我们利用了这一范例,同时通过在微流道中形成具有纳米多孔二氧化硅微球的 3D 纳米流控网络来改进其简单性;这创建了一个浓度矩阵,将银纳米簇和吸附的分析物捕获到 SERS 检测体积中。通过这种方法,我们能够在仅 2 分钟的样品加载后实现 400 飞摩尔的 Rhodamine 6G 的检测限,并且具有较高的芯片间重复性。由于纳米多孔通道中存在大量的流体路径,与单个纳米流道入口相比,这种方法不易堵塞,与以前的报告相比,加载时间也缩短了。此外,这种微系统的制造非常简单,因为不需要纳米级制造。最后,集成的多模光纤电缆消除了对光学对准的需求,因此该设备适用于现场的便携式和自动化应用,包括样品点和护理点检测。为了说明相关的现场应用,我们使用纳米流控 SERS 微系统演示了在水中检测 12ppb 的有机磷马拉硫磷。