TY - JOUR
T1 - A rapid diagnosis of SARS-CoV-2 using DNA hydrogel formation on microfluidic pores
AU - Kim, Hwang soo
AU - Abbas, Naseem
AU - Shin, Sehyun
N1 - Funding Information:
This research was supported by the National Research Foundation of Korea (NRF) funded by the Korean Government Ministry of Science and ICT (MSIT, Korea) [grant number 2016R1A5A1010148 ] as well as by the Korea Evaluation Institute of Industrial Technology (KEIT) funded by the Korean Government Ministry of Trade, Industry & Energy (MOTIE, Korea) [grant number 20012427 ].
Publisher Copyright:
© 2021 The Authors
PY - 2021/4/1
Y1 - 2021/4/1
N2 - The coronavirus disease 2019 (COVID-19) pandemic has been a major public health challenge in 2020. Early diagnosis of COVID-19 is the most effective method to control disease spread and prevent further mortality. As such, a high-precision and rapid yet economic assay method is urgently required. Herein, we propose an innovative method to detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) using isothermal amplification of nucleic acids on a mesh containing multiple microfluidic pores. Hybridization of pathogen DNA and immobilized probes forms a DNA hydrogel by rolling circle amplification and, consequently, blocks the pores to prevent fluid movement, as observed. Following optimization of several factors, including pore size, mesh location, and precision microfluidics, the limit of detection (LOD) for SARS-CoV-2 was determined to be 0.7 aM at 15-min incubation. These results indicate rapid, easy, and effective detection with a moderate-sized LOD of the target pathogen by remote point-of-care testing and without the requirement of any sophisticated device.
AB - The coronavirus disease 2019 (COVID-19) pandemic has been a major public health challenge in 2020. Early diagnosis of COVID-19 is the most effective method to control disease spread and prevent further mortality. As such, a high-precision and rapid yet economic assay method is urgently required. Herein, we propose an innovative method to detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) using isothermal amplification of nucleic acids on a mesh containing multiple microfluidic pores. Hybridization of pathogen DNA and immobilized probes forms a DNA hydrogel by rolling circle amplification and, consequently, blocks the pores to prevent fluid movement, as observed. Following optimization of several factors, including pore size, mesh location, and precision microfluidics, the limit of detection (LOD) for SARS-CoV-2 was determined to be 0.7 aM at 15-min incubation. These results indicate rapid, easy, and effective detection with a moderate-sized LOD of the target pathogen by remote point-of-care testing and without the requirement of any sophisticated device.
KW - COVID-19
KW - Hydrogel
KW - Microfluidics
KW - Micropores
KW - Nucleic acid
KW - Rolling circle amplification
UR - http://www.scopus.com/inward/record.url?scp=85100202027&partnerID=8YFLogxK
U2 - 10.1016/j.bios.2021.113005
DO - 10.1016/j.bios.2021.113005
M3 - Article
C2 - 33486135
AN - SCOPUS:85100202027
SN - 0956-5663
VL - 177
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
M1 - 113005
ER -