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High-performance portable graphene field-effect transistor device for detecting Gram-positive and -negative bacteria

Authors
Kim, Kyung HoPark, Seon JooPark, Chul SoonSeo, Sung EunLee, JiyeonKim, JinyeongLee, Seung HwanLee, SoohyunKim, Jun-SeobRyu, Choong-MinYong, DongeunYoon, HyeonseokSong, Hyun SeokLee, Sang HunKwon, Oh Seok
Issue Date
Nov-2020
Publisher
Pergamon Press Ltd.
Keywords
Portable biosensor; Graphene field-effect transistor; Interfacing chemistry; Microfluidics; Real-time monitoring; Bioprobes
Citation
Biosensors and Bioelectronics, v.167, pp 1 - 12
Pages
12
Indexed
SCIE
SCOPUS
Journal Title
Biosensors and Bioelectronics
Volume
167
Start Page
1
End Page
12
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/765
DOI
10.1016/j.bios.2020.112514
ISSN
0956-5663
1873-4235
Abstract
Current techniques for Gram-typing and for diagnosing a pathogen at the early infection stage rely on Gram stains, cultures, Enzyme linked immunosorbent assay (ELISA), polymerase chain reaction (PCR), and gene microarrays, which are labor-intensive and time-consuming approaches. In addition, a delayed or imprecise diagnosis of clinical pathogenic bacteria leads to a life-threatening emergency or overuse of antibiotics and a high-rate occurrence of antimicrobial-resistance microbes. Herein, we report high-performance antibiotics (as bioprobes) conjugated graphene micropattern field-effect transistors (ABX-GMFETs) to facilitate on-site Gram-typing and help in the detection of the presence or absence of Gram-negative and -positive bacteria in the samples. The ABX-GMFET platform, which consists of recognition probes and GM transistors conjugated with novel interfacing chemical compounds, was integrated into the microfluidics to minimize the required human intervention and facilitate automation. The mechanism of binding of ABX-GMFET was based on a charge or chemical moiety interaction between the bioprobes and target bacteria. Subsequently, ABX-GMFETs exhibited unprecedented high sensitivity with a limit of detection (LOD) of 10(0) CFU/mL (1-9 CFU/mL), real-time target specificity.
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LEE, SEUNG HWAN
ERICA 공학대학 (DEPARTMENT OF BIONANO ENGINEERING)
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