2019年冠状病毒病(COVID-19)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
微流控
免疫分析
纺纱
抗体
冠状病毒
病毒学
医学
纳米技术
材料科学
免疫学
2019-20冠状病毒爆发
传染病(医学专业)
内科学
疾病
复合材料
爆发
作者
Fanwu Gong,Hua-Xing Wei,Ji Qi,Huan Ma,Lianxin Liu,Jianping Weng,Xucai Zheng,Qiangsheng Li,Dan Zhao,Haopeng Fang,Liu Liu,Hongliang He,Cuichen Ma,Jinglong Han,Anyuan Sun,Baolong Wang,Tengchuan Jin,Bowei Li,Bofeng Li
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2021-07-15
卷期号:6 (7): 2709-2719
被引量:53
标识
DOI:10.1021/acssensors.1c00773
摘要
The spread of Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2), resulting in a global pandemic with around four million deaths. Although there are a variety of nucleic acid-based tests for detecting SARS-CoV-2, these methods have a relatively high cost and require expensive supporting equipment. To overcome these limitations and improve the efficiency of SARS-CoV-2 diagnosis, we developed a microfluidic platform that collected serum by a pulling-force spinning top and paper-based microfluidic enzyme-linked immunosorbent assay (ELISA) for quantitative IgA/IgM/IgG measurements in an instrument-free way. We further validated the paper-based microfluidic ELISA analysis of SARS-CoV-2 receptor-binding domain (RBD)-specific IgA/IgM/IgG antibodies from human blood samples as a good measurement with higher sensitivity compared with traditional IgM/IgG detection (99.7% vs 95.6%) for early illness onset patients. In conclusion, we provide an alternative solution for the diagnosis of SARS-CoV-2 in a portable manner by this smart integration of pulling-force spinning top and paper-based microfluidic immunoassay.
科研通智能强力驱动
Strongly Powered by AbleSci AI