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Fluorescence polarization system for rapid COVID-19 diagnosis.
Lee, Chang Yeol; Degani, Ismail; Cheong, Jiyong; Lee, Jae-Hyun; Choi, Hyun-Jung; Cheon, Jinwoo; Lee, Hakho.
  • Lee CY; Institute for Basic Science (IBS), Center for Nanomedicine, Seoul, South Korea; Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA.
  • Degani I; Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA; Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Cheong J; Institute for Basic Science (IBS), Center for Nanomedicine, Seoul, South Korea; Graduate Program of Nano Biomedical Engineering (NanoBME), Advanced Science Institute, Yonsei University, Seoul, South Korea.
  • Lee JH; Institute for Basic Science (IBS), Center for Nanomedicine, Seoul, South Korea; Graduate Program of Nano Biomedical Engineering (NanoBME), Advanced Science Institute, Yonsei University, Seoul, South Korea.
  • Choi HJ; Department of Laboratory Medicine, Chonnam National University Medical School and Chonnam National University Hospital, Gwangju, South Korea. Electronic address: hyunjung.choi@chonnam.ac.kr.
  • Cheon J; Institute for Basic Science (IBS), Center for Nanomedicine, Seoul, South Korea; Graduate Program of Nano Biomedical Engineering (NanoBME), Advanced Science Institute, Yonsei University, Seoul, South Korea; Department of Chemistry, Yonsei University, Seoul, South Korea. Electronic address: jcheon@yon
  • Lee H; Institute for Basic Science (IBS), Center for Nanomedicine, Seoul, South Korea; Center for Systems Biology, Massachusetts General Hospital Research Institute, Boston, MA, USA; Graduate Program of Nano Biomedical Engineering (NanoBME), Advanced Science Institute, Yonsei University, Seoul, South Korea
Biosens Bioelectron ; 178: 113049, 2021 Apr 15.
Article in English | MEDLINE | ID: covidwho-1056383
ABSTRACT
Prompt diagnosis, patient isolation, and contact tracing are key measures to contain the coronavirus disease 2019 (COVID-19). Molecular tests are the current gold standard for COVID-19 detection, but are carried out at central laboratories, delaying treatment and control decisions. Here we describe a portable assay system for rapid, onsite COVID-19 diagnosis. Termed CODA (CRISPR Optical Detection of Anisotropy), the method combined isothermal nucleic acid amplification, activation of CRISPR/Cas12a, and signal generation in a single assay, eliminating extra manual steps. Importantly, signal detection was based on the ratiometric measurement of fluorescent anisotropy, which allowed CODA to achieve a high signal-to-noise ratio. For point-of-care operation, we built a compact, standalone CODA device integrating optoelectronics, an embedded heater, and a microcontroller for data processing. The developed system completed SARS-CoV-2 RNA detection within 20 min of sample loading; the limit of detection reached 3 copy/µL. When applied to clinical samples (10 confirmed COVID-19 patients; 10 controls), the rapid CODA test accurately classified COVID-19 status, in concordance with gold-standard clinical diagnostics.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Biosensing Techniques / Fluorescence Polarization / COVID-19 Nucleic Acid Testing / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Biosens Bioelectron Journal subject: Biotechnology Year: 2021 Document Type: Article Affiliation country: J.bios.2021.113049

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Biosensing Techniques / Fluorescence Polarization / COVID-19 Nucleic Acid Testing / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: Biosens Bioelectron Journal subject: Biotechnology Year: 2021 Document Type: Article Affiliation country: J.bios.2021.113049