首页> 外文会议>Conference on microfluidics, bioMEMS, and medical microsystems XII >Monolithically integrated microfluidic nanoporous gold disk (NPGD) surface-enhanced Raman scattering (SERS) sensor for rapid and label-free biomolecular detection
【24h】

Monolithically integrated microfluidic nanoporous gold disk (NPGD) surface-enhanced Raman scattering (SERS) sensor for rapid and label-free biomolecular detection

机译:单片集成的微流控纳米多孔金盘(NPGD)表面增强拉曼散射(SERS)传感器,用于快速,无标记的生物分子检测

获取原文

摘要

We present a novel microfluidic surface-enhanced Raman scattering (SERS) sensor for rapid and label-free biomolecular detection. Our sensor design mitigates a common limiting factor in microfluidic SERS sensors that utilize integrated nanostructures: low-efficiency transport of biomolecules to nanostructured surface which adversely impacts sensitivity. Our strategy is to increase the total usable nanostructured surface area, which provides more adsorption sites for biomolecules. Specifically, nanoporous gold disk (NPGD) array, a highly effective SERS substrate, has been monolithically integrated inside a microfluidic chip. Individual NPGD is known to feature an order of magnitude larger surface area than its projected disk area. The increased surface area arises from nanoscale pores and ligaments 3-dimensionally distributed in the NPGD, which manifest themselves as high-density SERS hot-spots. High-density NPGD arrays further guarantee large coverage of these hot-spots on the microchannel floor. The SERS-active NPGD arrays enable highly-reproducible SERS measurements with relative intensity variations from 8% to -8%. R6G solutions in the concentrations ranging from 1 μM to 1 mM have been detected and quantitatively evaluated, and the performance of the sensor in continuous-flow condition has been assessed. Moreover, the sensor's capabilities have been studied by detecting and identifying a physiological metabolite (urea), and the results show lower detection limit compared to best results from most recent work using integrated nanostructured surface inside microchannels. We expect that the sensor would be applicable for detecting, identifying and quantifying molecules for some point-of-care applications, i.e. urine screening.
机译:我们提出了一种新型的微流控表面增强拉曼散射(SERS)传感器,用于快速且无标签的生物分子检测。我们的传感器设计减轻了利用集成纳米结构的微流控SERS传感器的一个共同限制因素:生物分子向纳米结构表面的低效率转运,这会对灵敏度产生不利影响。我们的策略是增加总的可用纳米结构表面积,从而为生物分子提供更多的吸附位点。具体而言,纳米多孔金盘(NPGD)阵列(一种高效的SERS衬底)已单片集成在微流控芯片内部。已知单个NPGD的表面积要比其投影磁盘的表面积大一个数量级。表面积的增加是由NPGD中3维分布的纳米级孔和韧带引起的,它们表现为高密度SERS热点。高密度NPGD阵列进一步确保了微通道底板上这些热点的大量覆盖。 SERS活性NPGD阵列可实现高度可重复的SERS测量,相对强度范围为8%至-8%。已检测并定量评估了浓度范围为1μM至1 mM的R6G溶液,并评估了传感器在连续流动条件下的性能。此外,已经通过检测和识别生理代谢物(尿素)来研究传感器的功能,与最近的使用微通道内部集成纳米结构表面的最新成果相比,该结果显示出较低的检测限。我们期望该传感器将适用于检测,识别和定量某些医疗点应用中的分子,即尿液筛查。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号