检出限
抗体
病毒学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019年冠状病毒病(COVID-19)
微流控
免疫
免疫系统
2019-20冠状病毒爆发
化学
免疫学
生物
色谱法
纳米技术
医学
材料科学
爆发
病理
疾病
传染病(医学专业)
作者
Minghui Wu,Siying Wu,Gaobo Wang,Wengang Liu,Lok Ting Chu,Tianyi Jiang,Hoi Kwan Kwong,Hiu Lam Chow,Iris Wai Sum Li,Ting‐Hsuan Chen
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-06-03
卷期号:8 (22)
被引量:18
标识
DOI:10.1126/sciadv.abn6064
摘要
Various COVID-19 vaccines are currently deployed, but their immunization varies and decays with time. Antibody level is a potent correlate to immune protection, but its quantitation relies on intensive laboratory techniques. Here, we report a decentralized, instrument-free microfluidic device that directly visualizes SARS-CoV-2 antibody levels. Magnetic microparticles (MMPs) and polystyrene microparticles (PMPs) can bind to SARS-CoV-2 antibodies simultaneously. In a microfluidic chip, this binding reduces the incidence of free PMPs escaping from magnetic separation and shortens PMP accumulation length at a particle dam. This visual quantitative result enables use in either sensitive mode [limit of detection (LOD): 13.3 ng/ml; sample-to-answer time: 70 min] or rapid mode (LOD: 57.8 ng/ml; sample-to-answer time: 20 min) and closely agrees with the gold standard enzyme-linked immunosorbent assay. Trials on 91 vaccinees revealed higher antibody levels in mRNA vaccinees than in inactivated vaccinees and their decay in 45 days, demonstrating the need for point-of-care devices to monitor immune protection.
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