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细菌病原体表面等离子体共振生物传感器的研究进展,涉及远程表面等离子体和磁性纳米粒子检测方法。

Bacterial pathogen surface plasmon resonance biosensor advanced by long range surface plasmons and magnetic nanoparticle assays.

机构信息

Austrian Institute of Technology, Muthgasse 11/2, 1190 Vienna, Austria.

出版信息

Anal Chem. 2012 Oct 2;84(19):8345-50. doi: 10.1021/ac301904x. Epub 2012 Sep 12.

Abstract

A new approach to surface plasmon resonance (SPR) biosensors for rapid and highly sensitive detection of bacterial pathogens is reported. It is based on the spectroscopy of grating-coupled long-range surface plasmons (LRSPs) combined with magnetic nanoparticle (MNP) assay. The interrogation of LRSPs allows increasing the biosensor figure of merit (FOM), and the employment of MNPs further enhances the sensor response by a fast delivery of the analyte to the sensor surface and through the amplified refractive index changes associated with the capture of target analyte. This amplification strategy is particularly attractive for detection of large analytes that diffuse slowly from the analyzed sample to the sensor surface. The potential of the presented approach is demonstrated in a model experiment in which Escherichia coli O157:H7 was detected at concentrations as low as 50 cfu mL(-1), 4 orders of magnitude better than the limit of detection achieved by regular grating-coupled SPR with direct detection format.

摘要

一种用于快速高灵敏度检测细菌病原体的新型表面等离子体共振(SPR)生物传感器方法被报道。它基于光栅耦合长程表面等离子体(LRSP)的光谱学与磁性纳米粒子(MNP)检测相结合。LRSP 的询问允许提高生物传感器的品质因数(FOM),并且通过快速将分析物输送到传感器表面并通过与捕获目标分析物相关的放大折射率变化来增强传感器响应,MNP 的使用进一步增强了传感器的响应。这种放大策略对于检测从分析样品缓慢扩散到传感器表面的大分析物特别有吸引力。在大肠杆菌 O157:H7 检测的模型实验中证明了所提出方法的潜力,其浓度低至 50 cfu mL(-1),比直接检测格式的常规光栅耦合 SPR 达到的检测限高出 4 个数量级。

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