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使用便携式表面增强拉曼散射-侧向流分析读取器快速准确地现场免疫诊断高传染性严重急性呼吸综合征冠状病毒 2

Rapid and Accurate On-Site Immunodiagnostics of Highly Contagious Severe Acute Respiratory Syndrome Coronavirus 2 Using Portable Surface-Enhanced Raman Scattering-Lateral Flow Assay Reader.

机构信息

Department of Chemistry, Chung-Ang University, Seoul 06974, South Korea.

Nanoscope Systems Inc., Daejeon 34016, South Korea.

出版信息

ACS Sens. 2022 Nov 25;7(11):3470-3480. doi: 10.1021/acssensors.2c01808. Epub 2022 Nov 14.

DOI:10.1021/acssensors.2c01808
PMID:36374202
Abstract

In early 2022, the number of people infected with the highly contagious mutant severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), called Omicron, was increasing worldwide. Therefore, several countries approved the lateral flow assay (LFA) strip as a diagnostic method for confirming SARS-CoV-2 instead of reverse transcription-polymerase chain reaction (RT-PCR), which takes a long time to generate the results. However, owing to the limitation of detection sensitivity, commercial LFA strips have high false-negative diagnosis rates for patients with low virus concentrations. Therefore, in this study, we developed a portable surface-enhanced Raman scattering (SERS)-LFA reader based on localized surface plasmon effects to solve the sensitivity problem of the commercial LFA strip. We tested 54 clinical samples using this portable SERS-LFA reader, which generated 49 positive and 5 negative results. Out of the 49 positive results, SERS-LFA classified only 2 as false negative, while the commercial LFA classified 21 as false negative. This confirmed that the false-negative rate had significantly improved compared to that of commercial LFA strips. We believe that the proposed SERS-LFA system can be utilized as a point-of-care diagnostic system to quickly and accurately determine a virus infection that could spread significantly within a short period.

摘要

2022 年初,传染性极强的变异严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2),即奥密克戎(Omicron),在全球范围内感染人数不断增加。因此,一些国家批准了侧向流动检测(LFA)条作为确诊 SARS-CoV-2 的诊断方法,而非需要较长时间才能出结果的逆转录-聚合酶链反应(RT-PCR)。然而,由于检测灵敏度的限制,商业 LFA 条对病毒浓度较低的患者存在较高的假阴性诊断率。因此,在本研究中,我们开发了一种基于局域表面等离激元效应的便携式表面增强拉曼散射(SERS)-LFA 读取器,以解决商业 LFA 条的灵敏度问题。我们使用这种便携式 SERS-LFA 读取器测试了 54 个临床样本,其中 49 个为阳性,5 个为阴性。在这 49 个阳性结果中,SERS-LFA 仅将 2 个归类为假阴性,而商业 LFA 将 21 个归类为假阴性。这证实与商业 LFA 条相比,假阴性率显著提高。我们相信,所提出的 SERS-LFA 系统可以用作即时护理诊断系统,快速准确地确定可能在短时间内广泛传播的病毒感染。

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