表面增强拉曼光谱检测血液中病毒性传染病的研究进展

Y. Yeh
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摘要

拉曼光谱是一种光学光谱技术,通常用于识别物质的振动模式。然而,激发拉曼散射的效率非常低,大约每106个声子中有1个通过拉曼散射被吸收和发射。这种微弱的效率极大地限制了拉曼光谱的信号强度。研究表明,金属纳米粒子可以通过基于纳米粒子的局部等离子体共振(LSPR)显著增强拉曼散射。这种拉曼信号的增强使得检测可以降低到单分子水平(~皮摩尔)[1,2]。表面增强拉曼光谱(SERS)是一种利用激光激发在金属或介质材料附近诱导局部表面等离子体以增强拉曼信号的技术。这种基于表面的检测技术可以通过分子吸附在粗糙的金属表面上将拉曼信号增强到1010,并且如果目标分子靠近金属表面,则可以检测单个生物分子[3,4]。在检测病毒时,有两种常规方法使目标病毒接近粗金属,一种是通过抗体结合的纳米颗粒,另一种是通过表面工程金属纳米结构。下面,我们将重点综述基于SERS的不同传染病检测方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of the Viral Infectious Diseases in Blood by Surface-Enhanced Raman Spectroscopy: Mini Review
Raman spectroscopy is an optical spectroscopic technique that is commonly used to identify the vibrational modes of a substance. However, the efficiency of exciting Raman scattering is very weak—approximately 1 out of 106 phonons are absorbed and emitted through Raman scattering. This weak efficiency dramatically limits the signal intensity of Raman spectroscopy. Studies have shown that metal nanoparticles can dramatically enhance Raman scattering via a nanoparticles-based localized plasmon resonance (LSPR). This enhancement of the Raman signal enables detection down to the single molecule level (~picomolar) [1,2]. Surface-enhanced Raman spectroscopy (SERS) is a technique which induces local surface plasmons at the vicinity of a metal or dielectric material by laser excitation to enhance the Raman signal. This surface-based detection technique can enhance the Raman signal up to 1010 by molecular adsorption on a rough metal surface and makes single biomolecular detection possible if the target molecule is near the metal surface [3,4]. When detecting viruses there are two conventional approaches to bringing the target virus close to the rough metal, one is through antibody-conjugated nanoparticles, and the other is through surface engineered metal nanostructures. In the following, we will focus on reviewing SERS based detection for different infectious diseases.
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