检出限
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019年冠状病毒病(COVID-19)
病毒学
材料科学
逆转录酶
逆转录聚合酶链式反应
冠状病毒
聚合酶链反应
纳米技术
生物
传染病(医学专业)
医学
信使核糖核酸
色谱法
化学
基因
生物化学
疾病
病理
作者
Hyun‐June Jang,Wen Zhuang,Xiaoyu Sui,Byunghoon Ryu,Xiaodan Huang,Min Chen,Xiaolei Cai,Hongting Pu,Kathleen G. Beavis,Jun Huang,Junhong Chen
标识
DOI:10.1021/acsami.3c00331
摘要
Rapid diagnosis of coronavirus disease 2019 (COVID-19) is key for the long-term control of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) amid renewed threats of mutated SARS-CoV-2 around the world. Here, we report on an electrical label-free detection of SARS-CoV-2 in nasopharyngeal swab samples directly collected from outpatients or in saliva-relevant conditions by using a remote floating-gate field-effect transistor (RFGFET) with a 2-dimensional reduced graphene oxide (rGO) sensing membrane. RFGFET sensors demonstrate rapid detection (<5 min), a 90.6% accuracy from 8 nasal swab samples measured by 4 different devices for each sample, and a coefficient of variation (CV) < 6%. Also, RFGFET sensors display a limit of detection (LOD) of pseudo-SARS-CoV-2 that is 10 000-fold lower than enzyme-linked immunosorbent assays, with a comparable LOD to that of reverse transcription-polymerase chain reaction (RT-PCR) for patient samples. To achieve this, comprehensive systematic studies were performed regarding interactions between SARS-CoV-2 and spike proteins, neutralizing antibodies, and angiotensin-converting enzyme 2, as either a biomarker (detection target) or a sensing probe (receptor) functionalized on the rGO sensing membrane. Taken together, this work may have an immense effect on positioning FET bioelectronics for rapid SARS-CoV-2 diagnostics.
科研通智能强力驱动
Strongly Powered by AbleSci AI