Dual-channel biosensor for Hg2+ sensing in food using Au@Ag/graphene-upconversion nanohybrids as metal-enhanced fluorescence and SERS indicators

被引:35
作者
Li, Huanhuan [1 ]
Huang, Xiaoqian [1 ]
Hassan, Md Mehedi [1 ]
Zuo, Min [2 ,3 ]
Wu, Xiangyang [4 ]
Chen, Yiping [5 ,6 ,7 ]
Chen, Quansheng [1 ]
机构
[1] Jiangsu Univ, Sch Food & Biol Engn, Zhenjiang 212013, Peoples R China
[2] Beijing Technol & Business Univ, Beijing Key Lab Big Data Technol Food Safety, Beijing 100048, Peoples R China
[3] Beijing Technol & Business Univ, Sch Comp & Informat Engn, Beijing 100048, Peoples R China
[4] Jiangsu Univ, Sch Environm & Safety Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[5] Huazhong Agr Univ, Coll Food Sci & Technol, Wuhan 430070, Peoples R China
[6] Natl Ctr NanoSci & Technol, Beijing Engn Res Ctr BioNanotechnol, Beijing 100190, Peoples R China
[7] Natl Ctr NanoSci & Technol, CAS Key Lab Biol Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Hg2+; Graphene; Upconversion nanoparticles; SERS; Fluorescence; Dual-channel; GOLD NANOPARTICLES; HYBRID MATERIALS; GRAPHENE; AG; MERCURY; SILVER; NANOSTRUCTURES;
D O I
10.1016/j.microc.2019.104563
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Here, we proposed a novel dual-channel biosensor for rapid and sensitive detection of Hg2+. Compared with the previous biosensors, the Au@Ag/graphene-upconversion (Au@Ag-GU) was prepared via a facile method and acted as a versatile signal indicator that can simultaneously readout surface-enhanced Raman spectroscopy (SERS) and fluorescence signals for Hg2+ detection. In this strategy, the core shell magnetite colloid nanocrystal clusters-polymethacrylic acid magnetic beads (MCNCs/PMAA MBs) were synthesized and conjugated with aptamer to specific capture the Hg2+. The dual-channel biosensor was thus fabricated by immobilizing the Au@Ag-GU onto the surface of MBs through the complementary pairing of aptamer and complementary DNA (cDNA). Upon Hg2+ incubation, Hg2+ preferably bound to the MBs-aptamer, resulting in the subsequent release of preloaded cDNA-Au@Ag-GU into supernatants. Under magnetic attraction, the MBs-aptamer was accumulated immediately, resulting in the concentration of Hg2+ become homodromous proportional to the dual channel intensity of the supernatants. Under the optimized conditions, the dual channel biosensor achieved excellent performances for Hg2+ with limits of detection (LOD) of 0.33 and 1 ppb, respectively. Furthermore, the feasibility of the biosensor to qualify Hg2+ was also established in spiked tap water and milk samples. This strategy may provide a bridge between a highly sensitive fluorescence assay and a rapid SERS assay, it can broaden the applicability of Hg2+ detection, which can be easy to detect Hg2+ in real samples by coupling with SERS or fluorescence assay.
引用
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页数:9
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