TY - JOUR
T1 - Rapid point-of-care detection of SARS-CoV-2 RNA with smartphone-based upconversion luminescence diagnostics
AU - Song, Menglin
AU - Wong, Man Chung
AU - Li, Lihua
AU - Guo, Feng
AU - Liu, Yuan
AU - Ma, Yingjing
AU - Lao, Xinyue
AU - Wang, Pui
AU - Chen, Honglin
AU - Yang, Mo
AU - Hao, Jianhua
N1 - Funding Information:
The research was supported by the grant from the Research Grants Council of the Hong Kong Special Administrative Region, China (Project No. CRF No. PolyU C5110-20G ) and PolyU Internal Research Fund ( 1-CD4S , 1-W21G ).
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2023/2/15
Y1 - 2023/2/15
N2 - Accurate COVID-19 screening via molecular technologies is still hampered by bulky instrumentation, complicated procedure, high cost, lengthy testing time, and the need for specialized personnel. Herein, we develop point-of-care upconversion luminescence diagnostics (PULD), and a streamlined smartphone-based portable platform facilitated by a ready-to-use assay for rapid SARS-CoV-2 nucleocapsid (N) gene testing. With the complementary oligo-modified upconversion nanoprobes and gold nanoprobes specifically hybridized with the target N gene, the luminescence resonance energy transfer effect leads to a quenching of fluorescence intensity that can be detected by the easy-to-use diagnostic system. A remarkable detection limit of 11.46 fM is achieved in this diagnostic platform without the need of target amplification, demonstrating high sensitivity and signal-to-noise ratio of the assay. The capability of the developed PULD is further assessed by probing 9 RT-qPCR-validated SARS-CoV-2 variant clinical samples (B.1.1.529/Omicron) within 20 min, producing reliable diagnostic results consistent with those obtained from a standard fluorescence spectrometer. Importantly, PULD is capable of identifying the positive COVID-19 samples with superior sensitivity and specificity, making it a promising front-line tool for rapid, high-throughput screening and infection control of COVID-19 or other infectious diseases.
AB - Accurate COVID-19 screening via molecular technologies is still hampered by bulky instrumentation, complicated procedure, high cost, lengthy testing time, and the need for specialized personnel. Herein, we develop point-of-care upconversion luminescence diagnostics (PULD), and a streamlined smartphone-based portable platform facilitated by a ready-to-use assay for rapid SARS-CoV-2 nucleocapsid (N) gene testing. With the complementary oligo-modified upconversion nanoprobes and gold nanoprobes specifically hybridized with the target N gene, the luminescence resonance energy transfer effect leads to a quenching of fluorescence intensity that can be detected by the easy-to-use diagnostic system. A remarkable detection limit of 11.46 fM is achieved in this diagnostic platform without the need of target amplification, demonstrating high sensitivity and signal-to-noise ratio of the assay. The capability of the developed PULD is further assessed by probing 9 RT-qPCR-validated SARS-CoV-2 variant clinical samples (B.1.1.529/Omicron) within 20 min, producing reliable diagnostic results consistent with those obtained from a standard fluorescence spectrometer. Importantly, PULD is capable of identifying the positive COVID-19 samples with superior sensitivity and specificity, making it a promising front-line tool for rapid, high-throughput screening and infection control of COVID-19 or other infectious diseases.
KW - COVID-19
KW - Luminescence resonance energy transfer (LRET)
KW - Point-of-care diagnostics
KW - SARS-CoV-2
KW - Upconversion nanoparticles
KW - Viral RNA detection
UR - http://www.scopus.com/inward/record.url?scp=85143867450&partnerID=8YFLogxK
U2 - 10.1016/j.bios.2022.114987
DO - 10.1016/j.bios.2022.114987
M3 - Journal article
C2 - 36495722
AN - SCOPUS:85143867450
SN - 0956-5663
VL - 222
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
M1 - 114987
ER -