Janus-structured colorimetric and fluorescent nanocomposites with highly luminescent retention to enhance point-of-care diagnosis

被引:2
|
作者
Shen, Xuan-ang [1 ,2 ]
Chen, Xirui [1 ,2 ]
Zhou, Haoxiang [1 ,2 ]
Chen, Song [3 ]
Wu, Jinyu [1 ,2 ]
Li, Xiangmin [2 ,4 ]
Huang, Xiaolin [1 ,2 ]
Xiong, Yonghua [1 ,2 ,4 ]
机构
[1] Nanchang Univ, State Key Lab Food Sci & Resources, Nanchang 330047, Peoples R China
[2] Nanchang Univ, Sch Food Sci & Technol, Nanchang 330047, Peoples R China
[3] Guangzhou Dev Dist, AIE Inst, Guangzhou Dev Dist, Guangzhou 510530, Peoples R China
[4] Nanchang Univ, Jiangxi OAI Joint Res Inst, Nanchang 330047, Jiangxi, Peoples R China
关键词
Colorimetric-fluorescent bifunctional; nanocomposite; Janus structure; Aggregation-induced emission luminogen; Lateral flow immunoassay; C -reaction protein; aflatoxin M 1; AGGREGATION-INDUCED EMISSION; AFLATOXIN M1; MILK; IMMUNOASSAY; ASSAY;
D O I
10.1016/j.cej.2024.154825
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Lateral flow immunoassay (LFIA) with dual-readout signals offers significant advantages in point-of-care testing due to its adaptability to various analysis scenarios. However, colorimetric and fluorescent nanocomposites (cfNCs) composed of plasmonic and luminescent components often suffer from low luminescent efficiency because of severe optical interference between the two functional components. Herein, we propose a simple self-assembly strategy for fabricating novel cf-NCs with a Janus structure (J-cf-NCs) using oleylamine ligand-coated gold nanoparticles (OA-AuNPs) and aggregation-induced emission luminogens (AIEgens) as building blocks. For comparison, two other cf-NCs with core-shell (CS-cf-NCs) and co-embedding (CE-cf-NCs) structures were synthesized to explore the effects of spatial intersection of OA-AuNPs and AIEgens on their optical properties. Our results demonstrate that J-cf-NCs exhibit the highest fluorescence retention (75 %), as the face-to-face spatial distribution of OA-AuNPs and AIEgens effectively prevents fluorescence resonance energy transfer and minimizes inner-filter effect-induced fluorescence quenching. When integrated with the LFIA platform, the developed J-cfNC-LFIA demonstrated excellent detection performance for both qualitative and quantitative determination of various target analytes in sandwich and competitive formats. Specifically, the visual limit of detection (vLOD) for C-reactive protein using J-cf-NC-LFIA showed approximately an eight-fold improvement compared to the classical colloidal gold test strip, while the quantitative sensitivity was two orders of magnitude greater than that of colorimetric readout. Furthermore, the vLOD for aflatoxin M1 in milk samples was 0.5 ng center dot mL-1, with a quantitative sensitivity 38-fold higher than that of the colorimetric pattern. Overall, the proposed J-cf-NCs exhibit significant potential for enhancing the detection performance of LFIA platforms.
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页数:10
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