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Detection of the SARS-CoV-2 humanized antibody with paper-based ELISA
Surasak Kasetsirikul1, Muhammad Umer2, Narshone Soda3
1School of Engineering and Build Environment (EBE), Griffith University, Nathan Campus, QLD 4222, Australia and Queensland Micro-and Nanotechnology Centre (QMNC), Griffith University, Nathan Campus, QLD 4111, Australia. nam-trung.nguyen@griffith.edu.au m.shiddiky@griffith.edu.au.
Abstract:
This work reports the development of a rapid, simple and inexpensive colorimetric paper-based assay for the detection of the severe acute respiratory symptom coronavirus 2 (SARS-CoV-2) humanized antibody. The paper device was prepared with lamination for easy sample handling and coated with the recombinant SARS-CoV-2 nucleocapsid antigen. This assay employed a colorimetric reaction, which is followed by horseradish peroxidase (HRP) conjugated detecting antibody in the presence of the 3,3',5,5'-tetramethylbenzidine (TMB) substrate. The colorimetric readout was evaluated and quantified for specificity and sensitivity. The characterization of this assay includes determining the linear regression curve, the limit of detection (LOD), the repeatability, and testing complex biological samples. We found that the LOD of the assay was 9.00 ng μL-1 (0.112 IU mL-1). The relative standard deviation was approximately 10% for a sample number of n = 3. We believe that our proof-of-concept assay has the potential to be developed for clinical screening of the SARS-CoV-2 humanized antibody as a tool to confirm infected active cases or to confirm SARS-CoV-2 immune cases during the process of vaccine development.
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