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用于新冠病毒现场快速诊断的模块化微型聚合酶链反应系统

Modular micro-PCR system for the onsite rapid diagnosis of COVID-19.

作者信息

Nguyen Phuong Quoc Mai, Wang Ming, Ann Maria Nelisha, Li Adelicia Yongling, Tan Hsih Yin, Xiong Gordon Minru, Tan Meng-Kwang Marcus, Bhagat Ali Asgar S, Ong Catherine W M, Lim Chwee Teck

机构信息

Institute for Health Innovation and Technology (iHealthtech), National University of Singapore, MD6, 14 Medical Drive #14-01, Singapore, 117599 Singapore.

Department of Biomedical Engineering, National University of Singapore, 4 Engineering Drive 3, Block 4, #04-08, Singapore, 117583 Singapore.

出版信息

Microsyst Nanoeng. 2022 Jul 19;8:82. doi: 10.1038/s41378-022-00400-3. eCollection 2022.

DOI:10.1038/s41378-022-00400-3
PMID:35860034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9294789/
Abstract

Effective containment of the COVID-19 pandemic requires rapid and accurate detection of the pathogen. Polymerase chain reaction (PCR) remains the gold standard for COVID-19 confirmation. In this article, we report the performance of a cost-effective modular microfluidic reverse transcription (RT)-PCR and RT-loop mediated isothermal amplification (RT-LAMP) platform, Epidax®, for the point-of-care testing and confirmation of SARS-CoV-2. This platform is versatile and can be reconfigured either for screening using endpoint RT-PCR or RT-LAMP tests or for confirmatory tests using real-time RT-PCR. Epidax® is highly sensitive and detects as little as 1 RNA copy per µL for real-time and endpoint RT-PCR, while using only half of the reagents. We achieved comparable results with those of a commercial platform when detecting SARS-CoV-2 viruses from 81 clinical RNA extracts. Epidax® can also detect SARS-CoV-2 from 44 nasopharyngeal samples without RNA extraction by using a direct RT-PCR assay, which shortens the sample-to-answer time to an hour with minimal user steps. Furthermore, we validated the technology using an RT-LAMP assay on 54 clinical RNA extracts. Overall, our platform provides a sensitive, cost-effective, and accurate diagnostic solution for low-resource settings.

摘要

有效遏制新冠疫情需要快速、准确地检测病原体。聚合酶链反应(PCR)仍然是新冠病毒确诊的金标准。在本文中,我们报告了一种具有成本效益的模块化微流控逆转录(RT)-PCR和RT环介导等温扩增(RT-LAMP)平台Epidax®在即时检测和确诊严重急性呼吸综合征冠状病毒2(SARS-CoV-2)方面的性能。该平台用途广泛,既可以重新配置用于使用终点RT-PCR或RT-LAMP检测进行筛查,也可以用于使用实时RT-PCR进行确诊检测。Epidax®高度灵敏,实时和终点RT-PCR检测低至每微升1个RNA拷贝,同时试剂用量仅为一半。从81份临床RNA提取物中检测SARS-CoV-2病毒时,我们获得了与商业平台相当的结果。通过直接RT-PCR检测,Epidax®还可以从44份鼻咽样本中检测SARS-CoV-2,无需进行RNA提取,这将样本到结果的时间缩短至1小时,且用户操作步骤最少。此外,我们使用RT-LAMP检测对54份临床RNA提取物验证了该技术。总体而言,我们的平台为资源匮乏地区提供了一种灵敏、经济高效且准确的诊断解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eef8/9296627/7270fb212c53/41378_2022_400_Fig5_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eef8/9296627/b711bbfce95a/41378_2022_400_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eef8/9296627/181bbcc70e79/41378_2022_400_Fig3_HTML.jpg
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