4.7 Article

Ultrasensitive supersandwich-type electrochemical sensor for SARS-CoV-2 from the infected COVID-19 patients using a smartphone

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 327, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2020.128899

关键词

SARS-CoV-2; Electrochemical biosensor; Supersandwich-type biosensor; Smartphone; Calixarene

资金

  1. National Natural Science Foundation of China [31760311, 21764005]
  2. Key Projects of Yunnan Natural Science Foundation [2018FA005]
  3. Key Research and Development Projects of Yunnan [2018BC005]
  4. Major Science and Technology Special Project of Yunnan Province (Biomedicine)
  5. Program for Excellent Young Talents of Yunnan University
  6. Program for Donglu Scholars of Yunnan University

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The study developed an ultrasensitive electrochemical detection technology using calixarene functionalized graphene oxide for targeting SARS-CoV-2 RNA without the need for nucleic acid amplification and reverse transcription. The biosensor demonstrated high specificity and selectivity, offering a rapid and convenient method for SARS-CoV-2 detection at the point of care.
The recent pandemic outbreak of COVID-19 caused by a novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), poses a threat to public health globally. Thus, developing a rapid, accurate, and easy-to-implement diagnostic system for SARS-CoV-2 is crucial for controlling infection sources and monitoring illness progression. Here, we reported an ultrasensitive electrochemical detection technology using calixarene functionalized graphene oxide for targeting RNA of SARS-CoV-2. Based on a supersandwich-type recognition strategy, the technology was confirmed to practicably detect the RNA of SARS-CoV-2 without nucleic acid amplification and reverse-transcription by using a portable electrochemical smartphone. The biosensor showed high specificity and selectivity during in silico analysis and actual testing. A total of 88 RNA extracts from 25 SARS-CoV-2-confirmed patients and eight recovery patients were detected using the biosensor. The detectable ratios (85.5 % and 46.2 %) were higher than those obtained using RT-qPCR (56.5 % and 7.7 %). The limit of detection (LOD) of the clinical specimen was 200 copies/mL, which is the lowest LOD among the published RNA measurement of SARS-CoV-2 to date. Additionally, only two copies (10 mu L) of SARS-CoV-2 were required for per assay. Therefore, we developed an ultrasensitive, accurate, and convenient assay for SARS-CoV-2 detection, providing a potential method for point-of-care testing.

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