4.7 Article

Rapid Detection of SARS-CoV-2 Nucleocapsid Protein by a Label-Free Biosensor Based on Optical Fiber Cylindrical Micro-Resonator

Journal

IEEE SENSORS JOURNAL
Volume 23, Issue 12, Pages 12511-12518

Publisher

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/JSEN.2023.3274110

Keywords

Biosensors; optical fiber sensor; SARS-CoV-2 nucleocapsid protein (N-Protein); whispering gallery mode (WGM)

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The current global outbreak of coronavirus (COVID-19) is a severe threat to human health, and rapid, low-cost, and accurate antigen detection methods are crucial for disease diagnosis. This study validates a highly sensitive whispering gallery mode (WGM) optical cylindrical microresonator (CMR) for bioimmunoassay detection, specifically targeting the nucleocapsid protein (N-Protein) of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). The method offers advantages such as rapid assay, lower expense, easy preparation, and miniaturization, making it potentially valuable in the field of biochemistry and biomedical detection.
The current global outbreak of coronavirus (COVID-19) continues to be a severe threat to human health. Rapid, low-cost, and accurate antigen detection methods are very important for disease diagnosis. The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) nucleocapsid protein (N-Protein) is often used as the diagnostic and screening for coronavirus detection. To this end, we propose and experimentally validate a highly sensitive whispering gallery mode (WGM) optical cylindrical microresonator (CMR) for bioimmunoassay detection. To study the biokinetic process of immunoassay, the surface of the WGM micro-resonator is functionalized with N-Protein monoclonal antibody (N-Protein-mAb), which led to the specific detection of N-Proteins. The spectral characteristics of the WGM resonance dip were investigated, and it is found that the transmission spectrum of WGM shows a monotonically increasing red-shift as a function of recording time. The WGM red-shift is due to the antibody-antigen reaction and can be used for the analysis of the immunoassay process. The wavelength shift is shown to be proportional to the concentration of N-Protein, which ranges between 0.1 and 100 mu g/mL. Finally, different types of samples (concentration of 10 mu g/mL of N-Protein) were prepared and tested to simulate the specificity of the sensor in the practical application environment. This method has the merits of a rapid assay, lower expense, easy preparation, and miniaturization, which makes the sensor have the potential for broad applications in the field of biochemistry and biomedical detection.

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