4.6 Article

Detection of SARS-CoV-2 Virus Amplification Using a Crumpled Graphene Field-Effect Transistor Biosensor

期刊

ACS SENSORS
卷 6, 期 12, 页码 4461-4470

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.1c01937

关键词

crumpled graphene FET biosensor; flat graphene FET biosensor; SARS-CoV-2; RT-LAMP; COVID-19; VTM clinical samples

资金

  1. National Science Foundation [2028431]
  2. ACES Undergraduate Research Scholarship Program
  3. Sara Riggenbach
  4. Gabriel Koch
  5. Bill Bond of OSF Healthcare (Peoria, IL) [1602513]
  6. Div Of Electrical, Commun & Cyber Sys
  7. Directorate For Engineering [2028431] Funding Source: National Science Foundation

向作者/读者索取更多资源

The rapid and unexpected spread of SARS-CoV-2 has caused disruptions in daily life and highlighted the need for rapid and accurate diagnoses. By combining RT-LAMP techniques with cgFETs, a portable detection device capable of detecting the presence of the virus in clinical samples was developed.
The rapid and unexpected spread of SARS-CoV-2 worldwide has caused unprecedented disruption to daily life and has brought forward critical challenges for public health. The disease was the largest cause of death in the United States in early 2021. Likewise, the COVID-19 pandemic has highlighted the need for rapid and accurate diagnoses at scales larger than ever before. To improve the availability of current gold standard diagnostic testing methods, the development of point-of-care devices that can maintain gold standard sensitivity while reducing the cost and providing portability is much needed. In this work, we combine the amplification capabilities of reverse transcriptase loop-mediated isothermal amplification (RT-LAMP) techniques with high-sensitivity end-point detection of crumpled graphene field-effect transistors (cgFETs) to develop a portable detection cell. This electrical detection method takes advantage of the ability of graphene to adsorb single-stranded DNA due to noncovalent pi-pi bonds but not double-stranded DNA. These devices have demonstrated the ability to detect the presence of the SARS-CoV-2 virus in a range from 10 to 10(4) copies/mu L in 20 viral transport medium (VTM) clinical samples. As a result, we achieved 100% PPV, NPV, sensitivity, and specificity with 10 positive and 10 negative VTM clinical samples. Further, the cgFET devices can differentiate between positive and negative VTM clinical samples in 35 min based on the Dirac point shift. Likewise, the improved sensing capabilities of the crumpled gFET were compared with those of the traditional flat gFET devices.

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