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一种用于快速检测新型冠状病毒肺炎的微流控集成侧向流动重组酶聚合酶扩增(MI-IF-RPA)检测方法。

A microfluidic-integrated lateral flow recombinase polymerase amplification (MI-IF-RPA) assay for rapid COVID-19 detection.

作者信息

Liu Dan, Shen Haicong, Zhang Yuqian, Shen Danyu, Zhu Mingyang, Song Yanling, Zhu Zhi, Yang Chaoyong

机构信息

School of Biomedical Sciences, Huaqiao University, Xiamen 362000, China.

The MOE Key Laboratory of Spectrochemical Analysis & Instrumentation, The Key Laboratory of Chemical Biology of Fujian Province, State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, Department of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.

出版信息

Lab Chip. 2021 May 18;21(10):2019-2026. doi: 10.1039/d0lc01222j.

Abstract

The COVID-19 pandemic, caused by SARS-CoV-2, currently poses an urgent global medical crisis for which there remains a lack of affordable point-of-care testing (POCT). In particular, resource-limited areas need simple and easily disseminated testing solutions to manage the outbreak. In this work, a microfluidic-integrated lateral flow recombinase polymerase amplification (MI-IF-RPA) assay was developed for rapid and sensitive detection of SARS-CoV-2, which integrates the reverse transcription recombinase polymerase amplification (RT-RPA) and a universal lateral flow (LF) dipstick detection system into a single microfluidic chip. The single-chamber RT-RPA reaction components are mixed with running buffer, and then delivered to the LF detection strips for biotin- and FAM-labelled amplified analyte sequences, which can provide easily interpreted positive or negative results. Testing requires only a simple nucleic acid extraction and loading, then incubation to obtain results, approximately 30 minutes in total. SARS-CoV-2 armored RNA particles were used to validate the MI-IF-RPA system, which showed a limit of detection of 1 copy per μL, or 30 copies per sample. Chip performance was further evaluated using clinically diagnosed cases of COVID-19 and revealed a sensitivity of 97% and specificity of 100%, highly comparable to current reverse transcription-polymerase chain reaction (RT-PCR)-based diagnostic assays. This MI-IF-RPA assay is portable and comprises affordable materials, enabling mass production and decreased risk of contamination. Without the need for specialized instrumentation and training, MI-IF-RPA assay can be used as a complement to RT-PCR for low-cost COVID-19 screening in resource-limited areas.

摘要

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,目前给全球带来了紧迫的医疗危机,而目前仍缺乏经济实惠的即时检测(POCT)方法。特别是在资源有限的地区,需要简单且易于推广的检测解决方案来应对疫情。在这项工作中,开发了一种微流控集成侧流重组酶聚合酶扩增(MI-IF-RPA)检测方法,用于快速、灵敏地检测SARS-CoV-2,该方法将逆转录重组酶聚合酶扩增(RT-RPA)和通用侧流(LF)试纸条检测系统集成到单个微流控芯片中。单腔RT-RPA反应组分与运行缓冲液混合,然后输送到LF检测条上,用于检测生物素和荧光素标记的扩增分析物序列,可提供易于解读的阳性或阴性结果。检测仅需简单的核酸提取和加样,然后孵育即可获得结果,总共约30分钟。使用SARS-CoV-2装甲RNA颗粒对MI-IF-RPA系统进行验证,结果显示检测限为每微升1拷贝,或每个样本30拷贝。使用COVID-19临床诊断病例进一步评估芯片性能,结果显示灵敏度为97%,特异性为100%,与当前基于逆转录聚合酶链反应(RT-PCR)的诊断检测方法高度可比。这种MI-IF-RPA检测方法便于携带,材料成本低,能够进行大规模生产并降低污染风险。无需专门的仪器和培训,MI-IF-RPA检测方法可作为RT-PCR的补充,用于资源有限地区低成本的COVID-19筛查。

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