Ding Xiong, Li Ziyue, Avery Lori, Ballesteros Enrique, Makol Rohit, Liu Changchun
Department of Biomedical Engineering University of Connecticut Health Center 263 Farmington Ave Farmington CT 06030 USA.
Department of Pathology and Laboratory Medicine University of Connecticut Health Center Farmington CT 06030 USA.
Adv Nanobiomed Res. 2022 Feb;2(2):2100101. doi: 10.1002/anbr.202100101. Epub 2021 Dec 7.
The ongoing pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused millions of deaths worldwide. However, most SARS-CoV-2 detection methods depend on time-consuming sample preparation and large detection instruments. Herein, a method employing nonbleeding pH paper to achieve both RNA extraction and visual isothermal amplification is proposed, enabling rapid, instrument-free SARS-CoV-2 detection. By taking advantage of capillary forces, pH-paper-based RNA extraction can be accomplished within 1 min without need for any equipment. Further, the pH paper can mediate dye-free visual isothermal amplification detection. In less than a 46-min sample-to-answer time, pH-paper-based extraction and visual detection (termed pH-EVD) can consistently detect 1200 genome equivalents per microliter of SARS-CoV-2 in saliva, which is comparable to TaqMan probe-based quantitative reverse transcription PCR (RT-qPCR). Through coupling with a chemically heated incubator called a smart cup, the instrument-free, pH-EVD-based SARS-CoV-2 detection method on 30 nasopharyngeal swab samples and 33 contrived saliva samples is clinically validated. Thus, the pH-EVD method provides simple, rapid, reliable, low-cost, and instrument-free SARS-CoV-2 detection and has the potential to streamline onsite COVID-19 diagnostics.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病(COVID-19)大流行已在全球造成数百万人死亡。然而,大多数SARS-CoV-2检测方法依赖于耗时的样本制备和大型检测仪器。在此,提出了一种使用非出血pH试纸实现RNA提取和可视化等温扩增的方法,能够快速、无需仪器地检测SARS-CoV-2。利用毛细作用力,基于pH试纸的RNA提取可在1分钟内完成,无需任何设备。此外,pH试纸可介导无染料可视化等温扩增检测。在不到46分钟的样本到结果时间内,基于pH试纸的提取和可视化检测(称为pH-EVD)能够一致地检测唾液中每微升1200个基因组当量的SARS-CoV-2,这与基于TaqMan探针的定量逆转录PCR(RT-qPCR)相当。通过与一种名为智能杯的化学加热培养箱相结合,对30份鼻咽拭子样本和33份人工合成唾液样本进行了基于pH-EVD的无仪器SARS-CoV-2检测方法的临床验证。因此,pH-EVD方法提供了简单、快速、可靠、低成本且无需仪器的SARS-CoV-2检测,并且有可能简化现场COVID-19诊断。