PEI-Mediated Assembly of Fe3O4 onto SiO2-Encapsulated CsPbBr3 for Highly Sensitive Fluorescent Lateral Flow Immunoassay

被引:4
|
作者
Shang, Yanxue [1 ]
Wang, Jinling [1 ]
Xia, Hongkun [1 ]
Jiao, Chunpeng [1 ]
Wu, Yanfang [2 ]
Jiang, Yongzhong [3 ]
Wu, Xian [4 ]
Wen, Congying [1 ]
Zeng, Jingbin [1 ]
机构
[1] China Univ Petr East China, Coll Chem & Chem Engn, State Key Lab Chem Safety, Qingdao 266580, Peoples R China
[2] Univ New South Wales, Sch Chem, Sydney, NSW 2052, Australia
[3] Hubei Prov Ctr Dis Control & Prevent, Wuhan 430065, Peoples R China
[4] Peking Univ First Hosp, Dept Clin Lab, Beijing 100034, Peoples R China
基金
中国国家自然科学基金;
关键词
SALMONELLA DETECTION; QUANTUM DOTS; NANOCRYSTALS; CSPBX3;
D O I
10.1021/acs.analchem.4c00648
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The conventional lateral flow immunoassay (LFIA) method using colloidal gold nanoparticles (Au NPs) as labeling agents faces two inherent limitations, including restricted sensitivity and poor quantitative capability, which impede early viral infection detection. Herein, we designed and synthesized CsPbBr3 perovskite quantum dot-based composite nanoparticles, CsPbBr3@SiO2@Fe3O4 (CSF), which integrated fluorescence detection and magnetic enrichment properties into LFIA technology and achieved rapid, sensitive, and convenient quantitative detection of the SARS-CoV-2 virus N protein. In this study, CsPbBr3 served as a high-quantum-yield fluorescent signaling probe, while SiO2 significantly enhanced the stability and biomodifiability of CsPbBr3. Importantly, the SiO2 shell shows relatively low absorption or scattering toward fluorescence, maintaining a quantum yield of up to 74.4% in CsPbBr3@SiO2. Assembly of Fe3O4 nanoparticles mediated by PEI further enhanced the method's sensitivity and reduced matrix interference through magnetic enrichment. Consequently, the method achieved a fluorescent detection range of 1 x 10(2) to 5 x 10(6) pg<middle dot>mL(-1) after magnetic enrichment, with a limit of detection (LOD) of 58.8 pg<middle dot>mL(-1), representing a 13.3-fold improvement compared to nonenriched samples (7.58 x 10(2) pg<middle dot>mL(-1)) and a 2-orders-of-magnitude improvement over commercial colloidal gold kits. Furthermore, the method exhibited 80% positive and 100% negative detection rates in clinical samples. This approach holds promise for on-site diagnosis, home-based quantitative tests, and disease procession evaluation.
引用
收藏
页码:6065 / 6071
页数:7
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