Au@SiO2 core/shell nanoparticle assemblage used for highly sensitive SERS-based determination of glucose and uric acid

被引:60
作者
Tran Thi Bich Quyen [1 ]
Su, Wei-Nien [2 ]
Chen, Kuan-Jung [1 ]
Pan, Chun-Jern [1 ]
Rick, John [1 ]
Chang, Chun-Chao [3 ]
Hwang, Bing-Joe [1 ,4 ]
机构
[1] Natl Taiwan Univ Sci & Technol, Dept Chem Engn, Nanoelectrochem Lab, Taipei 106, Taiwan
[2] Natl Taiwan Univ Sci & Technol, Grad Inst Appl Sci & Technol, Taipei 106, Taiwan
[3] Taipei Med Univ, Taipei 250, Taiwan
[4] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
关键词
SERS; Au@SiO2 core; shell nanoparticles (Au@SiO2 NPs); Rhodamine 6G (R6G); glucose; uric acid; ENHANCED RAMAN-SPECTROSCOPY; GOLD NANOPARTICLES; BLOOD-GLUCOSE; SCATTERING; SHAPE; SIZE; IMMUNOASSAY; FABRICATION; ABSORPTION; DEPENDENCE;
D O I
10.1002/jrs.4400
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The use of Au@SiO2 core/shell nanoparticle (NP) assemblage with highly sensitive surface-enhanced Raman scattering (SERS) was investigated for the determination of glucose and uric acid in this study. Rhodamine 6G dye molecules were used to evaluate the SERS enhancement factor for the synthesized Au@SiO2 core/shell NPs with various silica shell thicknesses. The enhancement of SERS signal from Rhodamine 6G was found to increase with a decrease in the shell thickness. The core/shell assemblage with silica layer of 1-2nm over a Au NP of 36nm showed the highest SERS signal. Our results show that the SERS technique is able to detect glucose and uric acid within wide concentration ranges, i.e. 20ng/dL to 20mg/dL (10(-12)-10(-3)M) and 16.8ng/dL to 2.9mg/dL (10(-11)-1.72x10(-4)M), respectively, with associated lower detection limits of 20ng/dL (1.0x10(-12)M) and 16.8ng/dL (1.0x10(-11)M). Our work offers a low-cost route to the fabrication of agile sensing devices applicable to the monitoring of disease progression. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:1671 / 1677
页数:7
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