Fukana Nutnaree, Park Joowon, Silva Junior Gilberto J, Malsick Lauren E, Gallichotte Emily N, Ebel Gregory D, Geiss Brian J, Dandy David S, Bertotti Mauro, Nacapricha Duangjai, Baldo Thaisa A, Henry Charles S
Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok, 10400, Thailand; Flow Innovation-Research for Science and Technology Laboratories (Firstlabs), Thailand; Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
Biosens Bioelectron. 2025 Mar 1;271:117048. doi: 10.1016/j.bios.2024.117048. Epub 2024 Dec 7.
The COVID-19 pandemic highlighted the need for rapid and sensitive diagnostic tools. In this work, the Magnetophoretic Slider Assay (MeSA) was integrated with electrochemical detection (eMeSA) using screen-printed carbon electrodes for the first time for the detection of SARS-CoV-2 nucleocapsid protein (NP). A sandwich enzyme-linked immunosorbent assay (ELISA) was performed on streptavidin-labeled magnetic beads (MBs). The streptavidin MB/biotinylated antibody/NP complexes were added into the sample inlet, where the beads were trapped using an external magnet while the solution rehydrated the HRP-labeled antibody (HRP-Ab) and 3,3',5,5'-tetramethylbenzidine (TMB) pads. By sliding the external magnet along the channel, the bead complexes were moved to the reservoir under the HRP-Ab pad, forming sandwich complexes. These complexes were subsequently moved back across the device to reach the electrochemical detection zone, where they reacted with released TMB, which underwent oxidation upon reacting with HRP attached to the detection antibody, followed by reduction due to the voltage applied to the working electrode (0.0 V vs. Ag reference electrode). The assay showed promising results in detecting SARS-CoV-2 in 10 min, with a limit of detection of 8.89 ng/mL NP and 78.02 PFU/mL inactivated virus. The results from 15 human samples demonstrated 100% clinical specificity and 100% clinical sensitivity for samples with RT-PCR cycle threshold (C) values from 19 to 30, meeting WHO criteria for COVID-19 diagnostics. The eMeSA offers an alternative to traditional ELISA for a wide range of point-of-care and point-of-need diagnostic applications.
新冠疫情凸显了对快速且灵敏的诊断工具的需求。在本研究中,首次将磁泳滑块分析法(MeSA)与电化学检测(eMeSA)相结合,采用丝网印刷碳电极检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)核衣壳蛋白(NP)。在链霉亲和素标记的磁珠(MBs)上进行夹心酶联免疫吸附测定(ELISA)。将链霉亲和素MB/生物素化抗体/NP复合物加入样品入口,在此处使用外部磁铁捕获磁珠,同时溶液使辣根过氧化物酶标记的抗体(HRP-Ab)和3,3',5,5'-四甲基联苯胺(TMB)垫重新水化。通过沿通道滑动外部磁铁,磁珠复合物被移动到HRP-Ab垫下方的储液器中,形成夹心复合物。随后这些复合物反向移动穿过该装置到达电化学检测区,在那里它们与释放的TMB反应,TMB与附着在检测抗体上的HRP反应后发生氧化,随后由于施加到工作电极的电压(相对于银参比电极0.0 V)而发生还原。该检测方法在10分钟内检测SARS-CoV-2方面显示出有前景的结果,检测限为8.89 ng/mL NP和78.02 PFU/mL灭活病毒。15份人类样本的结果表明,对于逆转录聚合酶链反应(RT-PCR)循环阈值(C)值为19至30的样本,临床特异性和临床敏感性均为100%,符合世界卫生组织(WHO)的新冠诊断标准。eMeSA为广泛的即时检测和即时需求诊断应用提供了一种替代传统ELISA的方法。