Electrochemiluminescence Lateral Flow Immunoassay Using Ruthenium(II) Complex-Loaded Dendritic Mesoporous Silica Nanospheres for Highly Sensitive and Quantitative Detection of SARS-CoV-2 Nucleocapsid Protein

被引:5
|
作者
Fu, Wenxuan [1 ]
Wang, Xuexue [2 ]
Ying, Xudong [1 ]
Sun, Tao [3 ]
Wang, Yafeng [4 ]
Wang, Jing [2 ]
Su, Bin [1 ]
机构
[1] Zhejiang Univ, Inst Analyt Chem, Dept Chem, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310014, Peoples R China
[3] Zhejiang Univ, Afiliated Hosp 2, Sch Med, Dept Lab Med, Hangzhou 310019, Peoples R China
[4] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Dept Clin Lab, Hangzhou 310016, Peoples R China
基金
中国国家自然科学基金;
关键词
dendritic mesoporous silica nanospheres; electrochemiluminescence; lateral flow immunoassay; paper electrode; SARS-CoV-2; ELECTROGENERATED CHEMILUMINESCENCE; NANOPARTICLES; SERS;
D O I
10.1002/adfm.202409632
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lateral flow immunoassays (LFIA) are widely used for the cost-effective and rapid detection of diverse analytes. However, traditional LFIA suffers from difficulties in providing quantitative results and has low sensitivity. Herein, LFIA is combined with electrochemiluminescence (ECL), a leading transduction technique with high sensitivity and wide dynamic range, to achieve highly sensitive and quantitative detection of severe acute respiratory syndrome coronavirus nucleocapsid protein (SARS-CoV-2 N protein). Ruthenium(II)-based complexes are synthesized and loaded into dendritic mesoporous silica nanospheres (PEI-Ru/dSiO2), which possessed central-radial pore channels and served as tags for ECL-LFIA. The electrodes are fabricated on a nitrocellulose (NC) membrane, which simplifies the structure of the ECL-LFIA. PEI-Ru/dSiO2 is captured on the electrode surface via a sandwich immunoreaction, which enhances the ECL signal by decreasing the distance between PEI-Ru/dSiO2 and the electrode surface. Using 2,2-bis(hydroxymethyl)-2,2 ',2 ''-nitrilotriethanol (BIS-TRIS) as coreactant, the ECL-LFIA is used for detecting SARS-CoV-2 N protein, with a linear range of 1-104 ng mL-1 and a limit of detection (LOD) of 0.52 ng mL-1. ECL-LFIA can also be used to detect analytes in complex matrices. These results demonstrate that the prepared ECL-LFIA has great potential as a point-of-care testing platform for the rapid and quantitative detection of disease biomarkers. Electrochemiluminescence lateral flow immunoassay (ECL-LFIA) strips are prepared by fabricating three electrodes on a nitrocellulose membrane, which simplifies electrode fixation and reduces the distance between the ECL luminophore and electrode surface, promoting ECL reactions. Using ruthenium(II) complex-loaded dendritic mesoporous silica nanospheres as tags (PEI-Ru/dSiO2), the ECL-LFIA strip enables the rapid and quantitative detection of disease biomarkers. image
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页数:10
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