Portable microfluidic impedance biosensor for SARS-CoV-2 detection

被引:11
|
作者
Laleh, Soroush [1 ,2 ]
Ibarlucea, Bergoi [3 ,4 ]
Stadtmueller, Marlena [5 ]
Cuniberti, Gianaurelio [3 ,4 ,6 ]
Medina-Sanchez, Mariana [1 ,2 ]
机构
[1] Leibniz IFW Dresden, Inst Emerging Elect Technol, Micro & Nanobiomed Engn Grp MNBE, Leibniz Inst Solid State & Mat Res, D-01069 Dresden, Germany
[2] Tech Univ Dresden, Chair Micro & NanoSyst, Ctr Mol Bioengn B CUBE, D-01062 Dresden, Germany
[3] Tech Univ Dresden, Inst Mat Sci, Dresden, Germany
[4] Tech Univ Dresden, Max Bergmann Ctr Biomat, Dresden, Germany
[5] Univ Klinikum Carl Gustav Carus Dresden, Dresden, Germany
[6] Tech Univ Dresden, Dresden Ctr Computat Mat Sci DCMS, Dresden, Germany
来源
基金
欧洲研究理事会;
关键词
COVID-19; diagnostics; SARS-CoV-2; biosensor; Point-of-care; Electrochemical detection; Electrochemical impedance spectroscopy; RAPID DETECTION; POINT; CORONAVIRUS; TESTS;
D O I
10.1016/j.bios.2023.115362
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Pandemics as the one we are currently facing, where fast-spreading viruses present a threat to humanity, call for simple and reliable methods to perform early diagnosis, enabling detection of very low pathogen loads even before symptoms start showing in the host. So far, standard polymerase chain reaction (PCR) is the most reliable method for doing so, but it is rather slow and needs specialized reagents and trained personnel to operate it. Additionally, it is expensive and not easily accessible. Therefore, developing miniaturized and portable sensors which perform early detection of pathogens with high reliability is necessary to not only prevent the spreading of the disease but also to monitor the effectiveness of the developed vaccines and the appearance of new pathogenic variants. Thus, in this work we develop a sensitive microfluidic impedance biosensor for the direct detection of SARS-CoV-2, towards a mobile point-of-care (POC) platform. The operational parameters are optimized with the aid of design-of-experiment (DoE), for an accurate detection of the viral antigens using electrochemical impedance spectroscopy (EIS). We perform the biodetection of buffer samples spiked with fM concentration levels and validate the biosensor in a clinical context of relevance by analyzing 15 real patient samples up to a Ct value (cycle threshold) of 27. Finally, we demonstrate the versatility of the developed platform using different settings, including a small portable potentiostat, using multiple channels for self-validation, as well as with single biosensors for a smartphone-based readout. This work contributes to the rapid and reliable diagnostics of COVID19 and can be extended to other infectious diseases, allowing the monitoring of viral load in vaccinated and unvaccinated people to anticipate a potential relapse of the disease.
引用
收藏
页数:11
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