Kim Hwang-Soo, Abbas Naseem, Shin Sehyun
Department of Mechanical Engineering, Korea University, Seoul, 02841, Republic of Korea.
Nano-Biofluignostic Research Center, Korea University, Seoul, 02841, Republic of Korea.
Biosens Bioelectron. 2021 Apr 1;177:113005. doi: 10.1016/j.bios.2021.113005. Epub 2021 Jan 18.
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.
2019年冠状病毒病(COVID-19)大流行是2020年一项重大的公共卫生挑战。COVID-19的早期诊断是控制疾病传播和预防进一步死亡的最有效方法。因此,迫切需要一种高精度、快速且经济的检测方法。在此,我们提出一种创新方法,利用在含有多个微流控孔的网格上进行核酸等温扩增来检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)。病原体DNA与固定化探针杂交通过滚环扩增形成DNA水凝胶,结果如观察到的那样,会堵塞孔以阻止流体流动。在对包括孔径、网格位置和精密微流控等几个因素进行优化后,确定在15分钟孵育时SARS-CoV-2的检测限(LOD)为0.7 aM。这些结果表明,通过远程即时检测,无需任何复杂设备,就能以适度的检测限快速、简便且有效地检测目标病原体。