TY - JOUR
T1 - Detection of SARS-CoV-2 Virus Amplification Using a Crumpled Graphene Field-Effect Transistor Biosensor
AU - Park, Insu
AU - Lim, Jongwon
AU - You, Seungyong
AU - Hwang, Michael Taeyoung
AU - Kwon, Jaehong
AU - Koprowski, Katherine
AU - Kim, Sungdae
AU - Heredia, John
AU - Stewart De Ramirez, Sarah A.
AU - Valera, Enrique
AU - Bashir, Rashid
N1 - Funding Information:
The authors would like to thank the National Science Foundation for a Rapid Response Research (RAPID) grant (Award 2028431) and Jump Applied Research through Community Health through Engineering and Simulation (ARCHES) endowment through the Health Care Engineering Systems Center at UIUC to R.B. and E.V. The authors also thank the ACES Undergraduate Research Scholarship Program for providing support to this research endeavor to K.K. The authors thank Sara Riggenbach, Gabriel Koch, and Bill Bond of OSF Healthcare (Peoria, IL) for their support of the IRB # 1602513 and patient sample acquisition for this study. The following reagent was obtained through BEI Resources, NIAID, NIH: SARS-Related Coronavirus 2, Isolate USA-WA1/2020, γ-Irradiated, NR-52287, contributed by the Centers for Disease Control and Prevention.
Publisher Copyright:
©
PY - 2021/12/24
Y1 - 2021/12/24
N2 - 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 π–π 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 104 copies/μL 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.
AB - 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 π–π 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 104 copies/μL 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.
KW - crumpled graphene FET biosensor
KW - VTM clinical samples
KW - COVID-19
KW - RT-LAMP
KW - SARS-CoV-2
KW - flat graphene FET biosensor
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U2 - 10.1021/acssensors.1c01937
DO - 10.1021/acssensors.1c01937
M3 - Article
C2 - 34878775
SN - 2379-3694
VL - 6
SP - 4461
EP - 4470
JO - ACS Sensors
JF - ACS Sensors
IS - 12
ER -