Automated enzyme-linked immunosorbent assay for point-of-care COVID-19 testing

被引:1
作者
Baldo, Thaisa A. [1 ]
Ataide, Vanessa N. [1 ,2 ]
Park, Joowon [1 ]
Panraksa, Yosita [1 ,3 ]
Martinez, Brandaise [1 ]
Anderson, Loran B. R. [3 ]
Malsick, Lauren E. [3 ]
Gallichotte, Emily N. [3 ]
Ebel, Gregory D. [3 ]
Geiss, Brian J. [3 ,5 ]
Dandy, David S. [4 ,5 ]
Paixao, Thiago R. L. C. [2 ]
Henry, Charles S. [1 ,4 ,5 ]
机构
[1] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
[2] Univ Sao Paulo, Dept Fundamental Chem, BR-05508000 Saao Paulo, SP, Brazil
[3] Colorado State Univ, Dept Microbiol Immunol & Pathol, Ft Collins, CO 80523 USA
[4] Colorado State Univ, Dept Chem & Biol Engn, Ft Collins, CO 80523 USA
[5] Colorado State Univ, Sch Biomed Engn, Ft Collins, CO 80523 USA
基金
巴西圣保罗研究基金会;
关键词
Coronavirus; Electrochemical biosensors; Immunoassay; Microfluidic device; Point-of-care devices; Nasal swab samples; SARS-COV-2; INFECTIVITY; DIAGNOSIS; TRENDS; FLOW;
D O I
10.1016/j.electacta.2024.144525
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The COVID-19 pandemic pushed the demand for readily available monitoring tools, leading to the development of electrochemical point-of-care devices. This work presents an electrochemical capillary-driven immunoassay (eCaDI) device based on polyethylene terephthalate (PET) and adhesive films featuring a screen-printed carbon electrode (SPCE) for the detection of SARS-CoV-2 nucleocapsid (N) protein in clinical samples. The SPCE was modified with protein A and capture antibodies (Ab 1 ) to ensure biomolecule immobilization and enhance sensitivity to detect N protein. The eCaDI automates an enzyme-linked immunosorbent assay (ELISA) through sequential reagent delivery, allowing for one-step sample addition. This process involves capturing the N protein by Ab 1 , followed by the automated delivery of HRP-labelled antibody and 3,3 ' ,5,5 ' -tetramethylbenzidine (TMB) followed by electrochemical detection through TMB reduction. The SPCEs are sensitive and selective for SARSCoV-2 N protein and stable for four weeks. Inactivated virus was used to determine a limit of detection (LOD) of 627 PFU/mL. The results obtained through immunoassay on eCADI were consistent with those of the RT-PCR method, showing a coefficient of determination (R 2 ) of 0.816 for 27 nasal swab samples from SARS-CoV-2 infected individuals. The developed eCADI is an alternative to conventional ELISA, given the device ' s low cost (less than $1), low consumption of samples and reagents, low waste generation, and short analysis time (5 min). Moreover, the immunoassay has shown potential for diagnosing COVID-19 in decentralized areas.
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页数:9
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