Electrochemiluminescence Energy Resonance Transfer System between RuSi Nanoparticles and Hollow Au Nanocages for Nucleic Acid Detection

被引:88
作者
Lu, Hai-Jie [1 ,2 ]
Pan, Jian-Bin [1 ,2 ]
Wang, Yin-Zhu [1 ,2 ]
Ji, Si-Yuan [1 ,2 ]
Zhao, Wei [1 ,2 ]
Luo, Xi-Liang [3 ]
Xu, Jing-Juan [1 ,2 ]
Chen, Hong-Yuan [1 ,2 ]
机构
[1] Nanjing Univ, State Key Lab Analyt Chem Life Sci, Sch Chem & Chem Engn, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Univ, Collaborat Innovat Ctr Chem Life Sci, Sch Chem & Chem Engn, Nanjing 210023, Jiangsu, Peoples R China
[3] Qingdao Univ Sci & Technol, Key Lab Sensor Anal Tumor Marker, Minist Educ, Coll Chem & Mol Engn, Qingdao 266042, 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
SURFACE-PLASMON RESONANCE; ULTRASENSITIVE DNA DETECTION; PROSTATE-SPECIFIC ANTIGEN; METAL-ORGANIC FRAMEWORK; GOLD NANOCAGES; OPTICAL-PROPERTIES; ENHANCED ELECTROCHEMILUMINESCENCE; BIOMEDICAL APPLICATIONS; MICRORNA DETECTION; BIPOLAR ELECTRODE;
D O I
10.1021/acs.analchem.8b02347
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper describes an electrochemiluminescence resonance energy transfer (ECL-RET) system using Ru(bpy)(3)(2+)-doped silica nanoparticles (RuSi NPs) as the ECL donor and hollow Au nanocages as the ECL acceptor. Tetrahedron DNA (TD) was used to construct the biosensing interface and control the distance (4.8 nm) between the ECL donor-acceptor pairs. The surface plasmon resonance (SPR) nanostructures, Au nanocages were assembled via the hairpin based sandwich assay. Due to the well overlap between the plasmon absorption spectrum of Au nanocages (628 nm) and the ECL emission spectrum of RuSi NPs (620 nm), high efficient energy transfer could occur. Subsequent cyclic DNA amplification further increased the binding amount of Au nanocages. Since the ECL inhibition is closely related with the binding amount of Au nanocages, a general "signal-off" ECL bioassay could thus be tailored with high sensitivity. At the optimized conditions, this ECL-RET system performed well with great stability and repeatability for nucleic acid detection in the range from 1.0 fM to 10 pM. This work manifested the great promise of hollow Au nanocages for an ECL-RET biosensor that to the best of our knowledge has not been reported. We believe that it could inspire more interest in the design and development of numerous other SPR nanostructures for advanced ECL-RET biosensors.
引用
收藏
页码:10434 / 10441
页数:8
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