Highly sensitive detection of high-risk bacterial pathogens using SERS-based lateral flow assay strips

被引:125
|
作者
Wang, Rui [1 ]
Kim, Kihyun [1 ]
Choi, Namhyun [1 ]
Wang, Xiaokun [1 ]
Lee, Jiyoung [1 ]
Jeon, Jun Ho [2 ]
Rhie, Gi-eun [2 ]
Choo, Jaebum [1 ]
机构
[1] Hanyang Univ, Dept Bionano Technol, Ansan 15588, South Korea
[2] Korea Cts Dis Control & Prevent, Lab Control Infect Dis, Div High Risk Pathogens, Chungju 28159, South Korea
基金
新加坡国家研究基金会;
关键词
Yersinia pestis; Francisella tularensis; Bacillus anthraces; Surface enhanced Raman scattering; Lateral flow assay; YERSINIA-PESTIS; FRANCISELLA-TULARENSIS; GENOME SEQUENCE; RAPID DETECTION; IMMUNOASSAY; PLAGUE; NANOPARTICLES; TRANSMISSION; TULAREMIA; AGENT;
D O I
10.1016/j.snb.2018.04.162
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Bacterial pathogens such as Yersinia pestis, Francisella tularensis, and Bacillus anthraces are classified into the highest rank of potential bioterrorism agents. Colorimetric lateral flow assay (LFA) strips are commercially available but these conventional strips have drawbacks in terms of low sensitivity and limit of quantitative analysis. Therefore, there is an urgent need for a new sensing platform to detect these pathogens in the early contamination stage. In this study, a novel surface-enhanced Raman scattering (SERS)-based LFA strip was developed for sensitive detection of bacterial pathogens. Target-specific SERS nanotags (Raman reporter-labeled gold nanoparticles) were used as an alternative to the gold nanoparticles in conventional LFA strips. Using these SERS nanotags the presence of bacteria could be identified through a simple color change in the test line. Additionally, highly sensitive and accurate quantitative analysis could be performed by monitoring the characteristic Raman peak intensity of SERS nanotags that were captured in the test line. This highly sensitive method required a short assay time (15 min) and a tiny volume of pathogen sample (40 mu L). We believe that the proposed SERS-based LFA technique has great potential as a valuable tool in the early detection of specific bacterial pathogens in the field due to its excellent analytical sensitivity. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 79
页数:8
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