SENSORS AND ACTUATORS B-CHEMICAL | 卷:349 |
A nanoenzyme linked immunochromatographic sensor for rapid and quantitative detection of SARS-CoV-2 nucleocapsid protein in human blood | |
Article | |
Liang, Chaolan1  Liu, Bochao1,2,3  Li, Jinfeng4  Lu, Jinhui1  Zhang, Enhui1  Deng, Qitao1  Zhang, Ling1  Chen, Ruiai5,6  Li, Chengyao1  Li, Tingting1  | |
[1] Southern Med Univ, Dept Transfus Med, Sch Lab Med & Biotechnol, Guangzhou 510515, Peoples R China | |
[2] Guangzhou Bai Rui Kang BRK Biol Sci & Technol Ltd, Guangzhou, Peoples R China | |
[3] Guangzhou Blood Ctr, Guangzhou, Peoples R China | |
[4] Shenzhen Ctr Dis Control & Prevent, Shenzhen Key Lab Mol Epidemiol, Shenzhen, Peoples R China | |
[5] Guangdong Lab Lingnan Modern Agr Sci & Technol, Zhaoqing Branch Ctr, Zhaoqing, Peoples R China | |
[6] South China Agr Univ, Coll Vet Med, Guangzhou, Peoples R China | |
关键词: SARS-CoV-2; Rapid detection; Immunochromatography; Photometer; Smartphone; | |
DOI : 10.1016/j.snb.2021.130718 | |
来源: Elsevier | |
【 摘 要 】
The establishment of a simple, low-cost, high-sensitive and rapid immunoassay for detecting SARS-CoV-2 antigen in human blood is an effective mean of discovering early SARS-CoV-2 infection and controlling the pandemic of COVID-19. Herein, a smartphone based nanozyme linked immunochromatographic sensor (NLICS) for the detection of SARS-CoV-2 nucleocapsid protein (NP) has been developed on demand. The system is integrated by disposable immunochromatography assay (ICA) and optical sensor devices. Immunoreaction and enzyme-catalyzed substrate color reaction were carried out on the chromatographic strip in a device, of which the light signal was read by a photometer through a biosensor channel, and the data was synchronously transmitted via the Bluetooth to the app in-stored smartphone for reporting the result. With a limit of detection (LOD) of 0.026 ng/mL NP, NLICS had the linear detection range (LDR) between 0.05 and 1.6 ng/mL NP, which was more sensitive than conventional ICA. NLICS took 25 min for reporting results. For detection of NP antigen in clinical serum samples from 21 COVID-19 patients and 80 healthy blood donor controls, NLICS and commercial enzyme linked immunosorbent assay (ELISA) had 76.2% or 47.6% positivity, and 100% specificity, respectively (P = 0.057), while a good correlation coefficient (r = 0.99) for quantification of NP between two assays was obtained. In conclusion, the NLICS was a rapid, simple, cheap, sensitive and specific immunochromatographic sensing assay for early diagnosis of SARS-CoV-2 infection.
【 授权许可】
Free
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
10_1016_j_snb_2021_130718.pdf | 1168KB | download |