Department of Chemistry and Biochemistry, Jackson State University , Jackson, Mississippi 39217, United States.
Acc Chem Res. 2016 Dec 20;49(12):2725-2735. doi: 10.1021/acs.accounts.6b00384. Epub 2016 Dec 8.
Surface-enhanced Raman spectroscopy (SERS) fingerprinting is highly promising for identifying disease markers from complex mixtures of clinical sample, which has the capability to take medical diagnoses to the next level. Although vibrational frequency in Raman spectra is unique for each biomolecule, which can be used as fingerprint identification, it has not been considered to be used routinely for biosensing due to the fact that the Raman signal is very weak. Contemporary SERS has been demonstrated to be an excellent analytical tool for practical label-free sensing applications due its ability to enhance Raman signals by factors of up to 10-10 orders of magnitude. Although SERS was discovered more than 40 years ago, its applications are still rare outside the spectroscopy community and it is mainly due to the fact that how to control, manipulate and amplify light on the "hot spots" near the metal surface is in the infancy stage. In this Account, we describe our contribution to develop nanoachitecture based highly reproducible and ultrasensitive detection capability SERS platform via low-cost synthetic routes. Using one-dimensional (1D) carbon nanotube (CNT), two-dimensional (2D) graphene oxide (GO), and zero-dimensional (0D) plasmonic nanoparticle, 0D to 3D SERS substrates have been designed, which represent highly powerful platform for biological diagnosis. We discuss the major design criteria we have used to develop robust SERS substrate to possess high density "hot spots" with very good reproducibility. SERS enhancement factor for 3D SERS substrate is about 5 orders of magnitude higher than only plasmonic nanoparticle and more than 9 orders of magnitude higher than 2D GO. Theoretical finite-difference time-domain (FDTD) stimulation data show that the electric field enhancement |E| can be more than 2 orders of magnitude in "hot spots", which suggests that SERS enhancement factors can be greater than 10 due to the formation of high density "hot spots" in 3D substrate. Next, we discuss the utilization of nanoachitecture based SERS substrate for ultrasensitive and selective diagnosis of infectious disease organisms such as drug resistance bacteria and mosquito-borne flavi-viruses that cause significant health problems worldwide. SERS based "whole-organism fingerprints" has been used to identify infectious disease organisms even when they are so closely related that they are difficult to distinguish. The detection capability can be as low as 10 CFU/mL for methicillin-resistant Staphylococcus aureus (MRSA) and 10 PFU/mL for Dengue virus (DENV) and West Nile virus (WNV). After that, we introduce exciting research findings by our group on the applications of nanoachitecture based SERS substrate for the capture and fingerprint detection of rotavirus from water and Alzheimer's disease biomarkers from whole blood sample. The SERS detection limit for β-amyloid (Aβ proteins) and tau protein using 3D SERS platform is several orders of magnitude higher than the currently used technology in clinics. Finally, we highlight the promises, major challenges and prospect of nanoachitecture based SERS in biomedical diagnosis field.
表面增强拉曼光谱(SERS)指纹图谱技术在识别临床样本中复杂混合物中的疾病标志物方面具有广阔的应用前景,它有能力将医学诊断提升到一个新的水平。尽管拉曼光谱中的振动频率对于每种生物分子都是独特的,可作为指纹识别,但由于拉曼信号非常微弱,因此尚未被常规用于生物传感。由于其能够将拉曼信号增强高达 10-10 数量级,因此当代 SERS 已被证明是一种出色的分析工具,适用于实用的无标记传感应用。尽管 SERS 早在 40 多年前就被发现,但它在光谱学领域之外的应用仍然很少,这主要是因为如何控制、操纵和放大金属表面附近“热点”上的光仍处于起步阶段。在本报告中,我们描述了我们通过低成本合成途径开发基于纳米结构的高重现性和超灵敏检测能力 SERS 平台的贡献。使用一维(1D)碳纳米管(CNT)、二维(2D)氧化石墨烯(GO)和零维(0D)等离子体纳米粒子,设计了 0D 到 3D 的 SERS 基底,它们为生物诊断提供了非常强大的平台。我们讨论了我们用于开发具有高密度“热点”且重现性非常好的稳健 SERS 基底的主要设计标准。3D SERS 基底的 SERS 增强因子比仅等离子体纳米粒子高约 5 个数量级,比 2D GO 高 9 个数量级以上。理论有限差分时域(FDTD)模拟数据表明,“热点”处的电场增强|E|可以超过 2 个数量级,这表明由于在 3D 基底中形成高密度“热点”,SERS 增强因子可以大于 10。接下来,我们讨论了基于纳米结构的 SERS 基底在超灵敏和选择性诊断传染病病原体(如耐甲氧西林金黄色葡萄球菌(MRSA)和引起全球重大健康问题的蚊媒黄病毒)方面的应用。SERS 基于“全生物体指纹”已被用于鉴定即使非常相似以至于难以区分的传染病病原体。检测能力对于耐甲氧西林金黄色葡萄球菌(MRSA)可以低至 10 CFU/mL,对于登革热病毒(DENV)和西尼罗河病毒(WNV)可以低至 10 PFU/mL。之后,我们介绍了我们小组在基于纳米结构的 SERS 基底在从水中捕获和指纹检测轮状病毒以及从全血样本中检测阿尔茨海默病生物标志物方面的令人兴奋的研究结果。使用 3D SERS 平台检测β-淀粉样蛋白(Aβ 蛋白)和tau 蛋白的 SERS 检测限比目前临床使用的技术高几个数量级。最后,我们强调了基于纳米结构的 SERS 在生物医学诊断领域的前景、主要挑战和展望。