SERS imaging-based aptasensor for ultrasensitive and reproducible detection of influenza virus A
Тип публикации: Journal Article
Дата публикации: 2020-11-01
SCImago Q1
Tоп 10% SCImago
WOS Q1
БС1
SJR: 1.833
CiteScore: 20.9
Impact factor: 10.5
ISSN: 09565663, 18734235
PubMed ID:
32818752
General Medicine
Biophysics
Electrochemistry
Biotechnology
Biomedical Engineering
Краткое описание
Surface-enhanced Raman scattering (SERS)-based aptasensors display high sensitivity for influenza A/H1N1 virus detection but improved signal reproducibility is required. Therefore, in this study, we fabricated a three-dimensional (3D) nano-popcorn plasmonic substrate using the surface energy difference between a perfluorodecanethiol (PFDT) spacer and the Au layer. This energy difference led to Au nanoparticle self-assembly; neighboring nanoparticles then created multiple hotspots on the substrate. The localized surface plasmon effects at the hot spots dramatically enhanced the incident field. Quantitative evaluation of A/H1N1 virus was achieved using the decrease of Raman peak intensity resulting from the release of Cy3-labeled aptamer DNAs from nano-popcorn substrate surfaces via the interaction between the aptamer DNA and A/H1N1 virus. The use of a Raman imaging technique involving the fast mapping of all pixel points enabled the reproducible quantification of A/H1N1 virus on nano-popcorn substrates. Average ensemble effects obtained by averaging all randomly distributed hot spots mapped on the substrate made it possible to reliably quantify target viruses. The SERS-based imaging aptasensor platform proposed in this work overcomes the issues inherent in conventional approaches (the time-consuming and labor-intensiveness of RT-PCR and low sensitivity and quantitative analysis limits of lateral flow assay kits). Our SERS-based assay for detecting A/H1N1 virus had an estimated limit of detection of 97 PFU mL −1 (approximately three orders of magnitude more sensitive than that determined by the enzyme-linked immunosorbent assay) and the approximate assay time was estimated to be 20 min. Thus, this approach provides an ultrasensitive, reliable platform for detecting viral pathogens. • SERS-based aptasensor was more sensitive in detecting influenza A/H1N1 virus than ELISA. • A 3D nano-popcorn plasmonic substrate was fabricated to improve reproducibility. • SERS-based aptasensor enabled highly efficient influenza A/H1N1 virus detection.
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Chen H. et al. SERS imaging-based aptasensor for ultrasensitive and reproducible detection of influenza virus A // Biosensors and Bioelectronics. 2020. Vol. 167. p. 112496.
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Chen H., Park S., Choi N., Moon J. I., Dang H., Das A., Lee S., Kim D., Chen L., Choo J. SERS imaging-based aptasensor for ultrasensitive and reproducible detection of influenza virus A // Biosensors and Bioelectronics. 2020. Vol. 167. p. 112496.
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TY - JOUR
DO - 10.1016/j.bios.2020.112496
UR - https://linkinghub.elsevier.com/retrieve/pii/S0956566320304887
TI - SERS imaging-based aptasensor for ultrasensitive and reproducible detection of influenza virus A
T2 - Biosensors and Bioelectronics
AU - Chen, Hao
AU - Park, Sung-Gyu
AU - Choi, Namhyun
AU - Moon, Joung Il
AU - Dang, Hajun
AU - Das, Anupam
AU - Lee, Seunghun
AU - Kim, Do-Geun
AU - Chen, Li-Song
AU - Choo, Jaebum
PY - 2020
DA - 2020/11/01
PB - Elsevier
SP - 112496
VL - 167
PMID - 32818752
SN - 0956-5663
SN - 1873-4235
ER -
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@article{2020_Chen,
author = {Hao Chen and Sung-Gyu Park and Namhyun Choi and Joung Il Moon and Hajun Dang and Anupam Das and Seunghun Lee and Do-Geun Kim and Li-Song Chen and Jaebum Choo},
title = {SERS imaging-based aptasensor for ultrasensitive and reproducible detection of influenza virus A},
journal = {Biosensors and Bioelectronics},
year = {2020},
volume = {167},
publisher = {Elsevier},
month = {nov},
url = {https://linkinghub.elsevier.com/retrieve/pii/S0956566320304887},
pages = {112496},
doi = {10.1016/j.bios.2020.112496}
}
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