Label-free direct detection of melamine using functionalized gold nanoparticles-based dual-fluorescence colorimetric nanoswitch sensing platform

被引:5
作者
Xiong, Jincheng [1 ,2 ,3 ]
Sun, Boyan [1 ,2 ]
Wang, Sihan [1 ,2 ]
Zhang, Shuai [1 ,2 ]
Qin, Linqian [1 ,2 ]
Jiang, Haiyang [1 ,2 ]
机构
[1] China Agr Univ, Coll Vet Med, Natl Key Lab Vet Publ Hlth Secur, Beijing 100193, Peoples R China
[2] China Agr Univ, Beijing Key Lab Detect Technol Anim Derived Food S, Beijing 100193, Peoples R China
[3] Southern Univ Sci & Technol, Dept Biomed Engn, Guangdong Prov Key Lab Adv Biomat, Shenzhen Key Lab Smart Healthcare Engn, Shenzhen 518055, Guangdong, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Gold nanoparticles; Triton X-100; Gold nanoclusters; Inner filter effect; Melamine; RAW-MILK; VISUAL DETECTION;
D O I
10.1016/j.talanta.2024.126335
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Developing a simple, economical, sensitive, and selective method for label-free direct detection analytes is attractive, especially the strategies that could achieve signal amplification without complicated operations. Herein, a dual-fluorescence colorimetric nanoswitch sensing platform for label-free direct melamine (MEL) detection was established. We first explored the relationship between MEL-induced aggregation of gold nanoparticles (AuNPs) and size and determined the optimal size to be 37 nm. Using surfactant Triton X-100 to modify AuNPs and clarify possible interaction mechanisms to improve detection performance. The dynamic changes of surface plasmon resonance absorption peaks in the dispersed and aggregated states of AuNPs were skillfully utilized to match the emission of multicolor gold nanoclusters to trigger the multi-inner filter effect. Accompanied by the addition of MEL-induced AuNPs to change from dispersed to aggregated state, the fluorescence of green-emitting and red-emitting gradually turned on and turned off, respectively. The fluorescence turn-on mode detection limit was 10 times higher than the colorimetric method and as low as 5.5 ng/mL; the detection took only 10 min. The sensor detected MEL in spiked milk samples with a good recovery in the range of 81.2-111.0 % with a coefficient of variation less than 11.4 % and achieved a good correlation with commercial kits. The proposed sensor integrates numerous merits of label-free, multi-signal readout, self-calibration, simple operations, and economical, which provides a promising tool for convenient on-site detection of MEL.
引用
收藏
页数:10
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