冠状病毒
2019-20冠状病毒爆发
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒学
电阻抗
纳米技术
生物传感器
Sars病毒
电化学
材料科学
2019年冠状病毒病(COVID-19)
化学
医学
传染病(医学专业)
电极
工程类
疾病
病理
电气工程
物理化学
爆发
作者
Hana Cho,Suhyun Shim,Won Woo Cho,Sungbo Cho,Hanseung Baek,Sang-Myung Lee,Dong‐Sik Shin
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2022-06-02
卷期号:7 (6): 1676-1684
被引量:29
标识
DOI:10.1021/acssensors.2c00317
摘要
Diagnosis of coronavirus disease (COVID-19) is important because of the emergence and global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Real-time polymerase chain reaction (PCR) is widely used to diagnose COVID-19, but it is time-consuming and requires sending samples to test centers. Thus, the need to detect antigens for rapid on-site diagnosis rather than PCR is increasing. We quantified the nucleocapsid (N) protein in SARS-CoV-2 using an electro-immunosorbent assay (El-ISA) and a multichannel impedance analyzer with a 96-interdigitated microelectrode sensor (ToAD). The El-ISA measures impedance signals from residual detection antibodies after sandwich assays and thus offers highly specific, label-free detection of the N protein with low cross-reactivity. The ToAD sensor enables the real-time electrochemical detection of multiple samples in conventional 96-well plates. The limit of detection for the N protein was 0.1 ng/mL with a detection range up to 10 ng/mL. This system did not detect signals for the S protein. While this study focused on detecting the N protein in SARS-CoV-2, our system can also be widely applicable to detecting various biomolecules involved in antigen-antibody interactions.
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