Highly sensitive and stable Ag@SiO2 nanocubes for label-free SERS-photoluminescence detection of biomolecules

被引:27
|
作者
Nguyen, Minh-Kha [1 ]
Su, Wei-Nien [2 ]
Chen, Ching-Hsiang [1 ]
Rick, John [2 ]
Hwang, Bing-Joe [1 ,3 ]
机构
[1] Natl Taiwan Univ Sci & Technol, Dept Chem Engn, Taipei 106, Taiwan
[2] Natl Taiwan Univ Sci & Technol, Grad Inst Appl Sci & Technol, Taipei 106, Taiwan
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu, Taiwan
关键词
SERS; Photoluminescence; Ag@SiO2 nanocubes; Dual functionality; Biomolecule detection; RAMAN-SCATTERING; QUANTUM DOTS; LIVE CELLS; FLUORESCENCE; DNA; NANORODS; ADENINE; LIGHT;
D O I
10.1016/j.saa.2016.12.024
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Surface-enhanced Raman scattering (SERS) and fluorescence microscopy are a widely used biological and chemical characterization techniques. However, the peak overlapping in multiplexed experiments and rapid photobleaching of fluorescent organic dyes is still the limitations. When compared to Ag nanocubes (NCs), higher SERS sensitivities can be obtained with thin shelled silica Ag@SiO2 NCs, in contrast metal-enhanced photoluminescence (MEPL) is only found with NCs that have thicker silica shells. A 'dual functionality' represented by the simultaneous strengthening of SERS and MEPL signals can be achieved by mixing Ag@SiO2 NCs, with a silica shell thickness of similar to 1.5 nm and similar to 4.4 nm. This approach allows both the Ag@SiO2 NCs SERS and MEPL sensitivities to be maintained at similar to 90% after 12 weeks of storage. Based on the distinguished detection of creatinine and flavin adenine dinucleotide in the mixture, the integration of SERS and MEPL together on a stable single plasmonic nanoparticle platform offers an opportunity to enhance both biomarker detection sensitivity and specificity. (C) 2016 Published by Elsevier B.V.
引用
收藏
页码:239 / 245
页数:7
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