Immunoassay of SARS-CoV-2 nucleocapsid proteins using novel red emission-enhanced carbon dot-based silica spheres

• Published in: Analyst (London) Vol. 146; no. 16; pp. 555 - 56
• Main Authors: Xu, Lai-Di, Zhu, Jin, Ding, Shou-Nian
• Format: Journal Article
• Language: English
• Published: London Royal Society of Chemistry 09.08.2021
• Subjects: Aqueous solutions; Carbon dots; Coronaviruses; COVID-19; Emission spectra; Excitation; Fluorescence; Immunoassay; Proteins; Sensitivity; Severe acute respiratory syndrome coronavirus 2; Silicon dioxide; Ultraviolet radiation
• ISSN: 0003-2654; 1364-5528
• DOI: 10.1039/d1an01010g

It is imminent to develop a new type of rapid COVID-19 detection method with high sensitivity. Here, we used novel red emission-enhanced carbon dot (CD)-based silica (RCS) spheres as the signals of lateral flow immunochromatography (LFI) to ultrasensitively detect novel severe acute respiratory syndrome coronavirus 2 nucleocapsid proteins (SARS-CoV-2 NPs). The red emission of CDs can be enhanced and enriched in silica spheres by a simple way. The amino ends of the N -β-(aminoethyl)-γ-aminopropyltrimethoxy anchor carboxyl-rich CDs and enhance the red emission, while the other end is embedded in the silica carrier. Then, the composite silica spheres werecoated with 3-(triethylsilyl) propylamine to protect the CDs, promote bioconjugation and obtain RCS spheres. The optimal emission peaks of the aqueous solution and the solid state of RCS spheres were at 634 nm and 638 nm, respectively, with quantum yields (QYs) of 48.5% and 35.7%, respectively. Their red emission has a wide excitation range (from the ultraviolet region to the red region), and the best excitation wavelength is about 580 nm. Two fluorescence detection modes of the RCS-LFI technology for the SARS-CoV-2 NP assay are available: the simple mode of observation under ultraviolet light has a sensitivity of 100 pg mL −1 ; the advanced mode of detection under a fluorescence microscope has a sensitivity of 10 pg mL −1 . This assay also exhibits the advantages of fast detection speed, high specificity, and simple operation. In addition, the feasibility of this method in actual sample detection was verified in human serum by the standard-addition method, and the results show that the method has excellent practicability. We believe that this method will be a valuable supplement for the diagnosis of COVID-19. The fluorescence enhancement of red emissive CDs and the casting of its aggregates were realized, and then, applied to the immunoassay of SARS-CoV-2 nucleocapsid proteins.