| Literature DB >> 32837510 |
Fei Tian1,2, Chao Liu1,2, Jinqi Deng1,2, Ziwei Han1,2, Lu Zhang3, Qinghua Chen1, Jiashu Sun1,2.
Abstract
The outbreak of virus-induced infectious diseases poses a global public-health challenge. Nucleic acid amplification testing (NAAT) enables early detection of pandemic viruses and plays a vital role in preventing onward transmission. However, the requirement of skilled operators, expensive instrumentation, and biosafety laboratories has hindered the use of NAAT for screening and diagnosis of suspected patients. Here we report development of a fully automated centrifugal microfluidic system with sample-in-answer-out capability for sensitive, specific, and rapid viral nucleic acid testing. The release of nucleic acids and the subsequent reverse transcription loop-mediated isothermal amplification (RT-LAMP) were integrated into the reaction units of a microfluidic disc. The whole processing steps such as injection of reagents, fluid actuation by rotation, heating and temperature control, and detection of fluorescence signals were carried out automatically by a customized instrument. We validate the centrifugal microfluidic system using oropharyngeal swab samples spiked with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) armored RNA particles. The estimated limit of detection for armored RNA particles is 2 copies per reaction, the throughput is 21 reactions per disc, and the assay sample-to-answer time is approximately 70 min. This enclosed and automated microfluidic system efficiently avoids viral contamination of aerosol, and can be readily adapted for virus detection outside the diagnostic laboratory. ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s11426-020-9800-6 and is accessible for authorized users. © Science China Press and Springer-Verlag GmbH Germany, part of Springer Nature 2020.Entities:
Keywords: automation; microfluidics; nucleic acid testing; sample-to-answer; virus
Year: 2020 PMID: 32837510 PMCID: PMC7387882 DOI: 10.1007/s11426-020-9800-6
Source DB: PubMed Journal: Sci China Chem ISSN: 1869-1870 Impact factor: 9.445