Afterglow Nanoprobe-Enabled Quantitative Lateral Flow Immunoassay by a Palm-Size Device for Household Healthcare

被引:17
作者
Guo, Jiuchuan [1 ]
Zhou, Yudong [2 ,3 ]
Cheng, Jie [1 ]
Chen, Fuli [4 ]
Xu, Jiahui [2 ,3 ]
Yang, Lirong [2 ,3 ]
Shi, Huifang [2 ,3 ]
An, Zhongfu [2 ,3 ]
Guo, Jinhong [5 ]
Ma, Xing [4 ]
机构
[1] Univ Elect Sci & Technol China, Chengdu 611731, Peoples R China
[2] Nanjing Tech Univ NanjingTech, Key Lab Flexible Elect KLOFE, Nanjing 211816, Peoples R China
[3] Nanjing Tech Univ NanjingTech, Inst Adv Mat IAM, Nanjing 211816, Peoples R China
[4] Harbin Inst Technol Shenzhen, Sch Mat Sci & Engn, Sauvage Lab Smart Mat, Shenzhen 518055, Peoples R China
[5] Shanghai Jiao Tong Univ, Sch Sensing Sci & Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
ORGANIC PHOSPHORESCENCE; NANOPARTICLES; ASSAYS;
D O I
10.1021/acs.analchem.3c05448
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Lateral flow immunoassay (LFIA), a classical point-of-care testing (POCT) technique, plays an important role in disease screening and healthcare monitoring. However, traditional LFIA is either designed for qualitative analysis or requires expensive equipment for quantification, limiting its use in household diagnosis. In this study, we proposed a new generation of LFIA for household health monitoring by using ultralong organic phosphorescence (UOP) nanomaterials as afterglow nanoprobes with a self-developed palm-size sensing device. The UOP nanoprobes exhibit a phosphorescence signal with a second-level lifetime, which completely avoids the interference from excitation light and biological background fluorescence. Therefore, an ultraminiaturized and low-cost UOP nanosensor was successfully designed by eliminating the complex optical path and filtering systems. We chose an inflammatory factor, C-reactive protein (CRP), for household POCT validation. The whole analysis was completed within 9 min. A limit of detection (LOD) of 0.54 ng/mL of CRP antigen was achieved with high stability and good specificity, which is comparable to laboratory instruments and fully satisfying the clinical diagnosis requirement.
引用
收藏
页码:4891 / 4900
页数:10
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