4.8 Article

Nanozyme chemiluminescence paper test for rapid and sensitive detection of SARS-CoV-2 antigen

Journal

BIOSENSORS & BIOELECTRONICS
Volume 173, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2020.112817

Keywords

SARS-CoV-2; Antigen detection; Paper test; Nanozyme; Chemiluminescence

Funding

  1. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB29040101]
  2. National Science and Technology Major Project [2018ZX10101004002004]
  3. CAS Engineering Laboratory Project [KFJ-PTXM-013]
  4. Frontier Science Major Project of the Chinese Academy of Sciences [QYZDB-SSWSMC013]

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The nanozyme-based chemiluminescence paper assay offers a new method for rapid and sensitive detection of SARS-CoV-2 antigen. The test is specific to the SARS-CoV-2 antigen and can be completed within 16 minutes.
COVID-19 has evolved into a global pandemic. Early and rapid detection is crucial to control of the SARS-CoV-2 transmission. While representing the gold standard for early diagnosis, nucleic acid tests for SARS-CoV-2 are often complicated and time-consuming. Serological rapid antibody tests are characterized by high rates of false-negative diagnoses, especially during early infection. Here, we developed a novel nanozyme-based chemiluminescence paper assay for rapid and sensitive detection of SARS-CoV-2 spike antigen, which integrates nanozyme and enzymatic chemiluminescence immunoassay with the lateral flow strip. The core of our paper test is a robust Co-Fe@hemin-peroxidase nanozyme that catalyzes chemiluminescence comparable with natural peroxidase HRP and thus amplifies immune reaction signal. The detection limit for recombinant spike antigen of SARS-CoV-2 was 0.1 ng/mL, with a linear range of 0.2-100 ng/mL. Moreover, the sensitivity of test for pseudovirus could reach 360 TCID50/mL, which was comparable with ELISA method. The strip recognized SARS-CoV2 antigen specifically, and there was no cross reaction with other coronaviruses or influenza A subtypes. This testing can be completed within 16 min, much shorter compared to the usual 1-2 h required for currently used nucleic acid tests. Furthermore, signal detection is feasible using the camera of a standard smartphone. Ingredients for nanozyme synthesis are simple and readily available, considerably lowering the overall cost. In conclusion, our paper test provides a high-sensitive point-of-care testing (POCT) approach for SARS-CoV-2 antigen detection, which should greatly facilitate early screening of SARS-CoV-2 infections, and considerably lower the financial burden on national healthcare resources.

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