Bae Minju, Park Junsoo, Seong Hyeonah, Lee Hansol, Choi Wonsuk, Noh Jiyun, Kim Woojoo, Shin Sehyun
School of Mechanical Engineering, Korea University, Seoul 02841, Korea.
Department of Micro-Nano Systems, Korea University, Seoul 02841, Korea.
Diagnostics (Basel). 2022 Aug 17;12(8):1995. doi: 10.3390/diagnostics12081995.
The complex and lengthy protocol of current viral nucleic acid extraction processes limits their use outside laboratory settings. Here, we describe a rapid and reliable method for extracting nucleic acids from viral samples using a rotating blade and magnetic beads. The viral membrane can be instantly lysed using a high-speed rotating blade, and nucleic acids can be immediately isolated using a silica magnetic surface. The process was completed within 60 s by this method. Routine washing and eluting processes were subsequently conducted within 5 min. The results achieved by this method were comparable to those of a commercially available method. When the blade-based lysis and magnetic bead adsorption processes were performed separately, the RNA recovery rate was very low, and the Ct value was delayed compared to simultaneous lysis and RNA adsorption. Overall, this method not only dramatically shortens the conventional extraction time but also allows for its convenient use outside the laboratory, such as at remote field sites and for point-of-care testing.
当前病毒核酸提取过程复杂且冗长,限制了其在实验室环境之外的使用。在此,我们描述了一种使用旋转刀片和磁珠从病毒样本中提取核酸的快速可靠方法。高速旋转刀片可立即裂解病毒膜,硅胶磁性表面可立即分离核酸。此方法在60秒内完成该过程。随后在5分钟内进行常规洗涤和洗脱过程。该方法获得的结果与市售方法相当。当基于刀片的裂解和磁珠吸附过程分开进行时,RNA回收率非常低,与同时进行裂解和RNA吸附相比,Ct值延迟。总体而言,该方法不仅显著缩短了传统提取时间,还便于在实验室之外使用,如在偏远现场和即时检测中。