4.8 Article

Plasmon color-preserved gold nanoparticle clusters for high sensitivity detection of SARS-CoV-2 based on lateral flow immunoassay

期刊

BIOSENSORS & BIOELECTRONICS
卷 205, 期 -, 页码 -

出版社

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2022.114094

关键词

Gold nanoparticle cluster; Plasmonic; Lateral flow immunoassay; SARS-CoV-2; Colorimetric sensor; COVID-19

资金

  1. National Research Foundation - Ministry of Science, ICT, and Future Planning [NRF2021R1A2B5B3001417]
  2. BioNano Health Guard Research Center - Ministry of Science, ICT, and Future Planning of Korea [H-GUARD_NRF-2019M3A6B2060097]
  3. Gwangju Institute of Science and Technology (GIST)
  4. Korea Innovation Foundation - Ministry of Science and ICT [2020-GJ-RD-0170]
  5. UKRI, Engineering and Physical Sci-ences Research Council [EP/V001019/1]
  6. National Research Foundation of Korea [2020-GJ-RD-0170] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study developed AuNP clusters to improve the detection sensitivity of lateral flow immunoassays (LFI) for diseases, including SARS-CoV-2. The AuNP clusters maintained the red color of isolated individual AuNPs while increasing the colorimetric readout. The PLASCOP AuNP clusters showed high sensitivity and good specificity for SARS-CoV-2 nucleocapsid proteins, making them a promising sensing tool for LFI applications.
Lateral flow immunoassays (LFI) have shown great promise for point-of-care (POC) sensing applications, however, its clinical translation is often hindered by insufficient sensitivity for early detection of diseases, including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This is mainly due to weak absorption signals of single gold nanoparticles (AuNPs). Here, we developed AuNP clusters that maintain the red color of isolated individual AuNPs, but increase the colorimetric readout to improve the detection sensitivity. The plasmon colorpreserved (PLASCOP) AuNP clusters is simply made by mixing streptavidin-coated AuNP core with satellite AuNPs coated with biotinylated antibodies. The biotinylated antibody-streptavidin linker forms a gap size over 15 nm to avoid plasmon coupling between AuNPs, thus maintaining the plasmonic color while increasing the overall light absorption. LFI sensing using PLASCOP AuNP clusters composed of 40 nm AuNPs showed a high detection sensitivity for SARS-CoV-2 nucleocapsid proteins with a limit of detection (LOD) of 0.038 ng mL-1, which was 23.8- and 5.9-times lower value than that of single 15 nm and 40 nm AuNP conjugates, respectively. The PLASCOP AuNP clusters-based LFI sensing also shows good specificity for SARS-CoV-2 nucleocapsid proteins from other influenza and coronaviruses. In a clinical feasibility test, we demonstrated that SARS-CoV-2 particles spiked in human saliva could be detected with an LOD of 54 TCID50 mL-1. The developed PLASCOP AuNP clusters are promising colorimetric sensing reporters that present improved sensitivity in LFI sensing for broad POC sensing applications beyond SARS-CoV-2 detection.

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