Rapid detection of SARS-CoV-2 antibodies using electrochemical impedance-based detector

被引:143
|
作者
Rashed, Mohamed Z. [1 ]
Kopechek, Jonathan A. [2 ]
Priddy, Mariah C. [2 ]
Hamorsky, Krystal T. [3 ]
Palmer, Kenneth E. [3 ]
Mittal, Nikhil [4 ]
Valdez, Joseph [4 ]
Flynn, Joseph [5 ]
Williams, Stuart J. [1 ]
机构
[1] Univ Louisville, Dept Mech Engn, 200 Sackett Hall, Louisville, KY 40208 USA
[2] Univ Louisville, Dept Bioengn, Louisville, KY 40208 USA
[3] Univ Louisville, Ctr Predict Med Biodefense & Emerging Infect Dis, Louisville, KY 40208 USA
[4] Agilent Technolo Inc, ACEA Biosci, San Diego, CA 92121 USA
[5] Norton Healthcare Inc, Louisville, KY 40202 USA
来源
关键词
Impedance spectroscopy; SARS-CoV-2; Capacitive immunosensors; Antibodies; Label-free; DIELECTRIC-SPECTROSCOPY;
D O I
10.1016/j.bios.2020.112709
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Coronavirus disease (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was classified as a pandemic by the World Health Organization and has caused over 550,000 deaths worldwide as of July 2020. Accurate and scalable point-of-care devices would increase screening, diagnosis, and monitoring of COVID-19 patients. Here, we demonstrate rapid label-free electrochemical detection of SARS-CoV-2 antibodies using a commercially available impedance sensing platform. A 16-well plate containing sensing electrodes was pre-coated with receptor binding domain (RBD) of SARS-CoV-2 spike protein, and subsequently tested with samples of anti-SARS-CoV-2 monoclonal antibody CR3022 (0.1 mu g/ml, 1.0 mu g/ml, 10 mu g/ml). Subsequent blinded testing was performed on six serum specimens taken from COVID-19 and non-COVID-19 patients (1:100 dilution factor). The platform was able to differentiate spikes in impedance measurements from a negative control (1% milk solution) for all CR3022 samples. Further, successful differentiation and detection of all positive clinical samples from negative control was achieved. Measured impedance values were consistent when compared to standard ELISA test results showing a strong correlation between them (R-2 = 0.9). Detection occurs in less than five minutes and the well-based platform provides a simplified and familiar testing interface that can be readily adaptable for use in clinical settings.
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页数:6
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