Glucose sensing using 3 D array of reproducible Surface Enhanced Raman Scattering substrates

被引:0
作者
Dinish, U. S. [1 ]
Fu, Chit Yaw [1 ]
Agarwal, Ajay [2 ]
Thoniyot, Praveen [1 ]
Olivo, Malini [1 ,3 ,4 ]
机构
[1] ASTAR, Singapore Bioimaging Consortium, Bio Opt Imaging Grp, 11 Biopolis Way, Singapore 138667, Singapore
[2] ASTAR, Inst Microelect, Singapore 117685, Singapore
[3] Natl Canc Ctr Singapore, Div Med Sci, Singapore 169610, Singapore
[4] Natl Univ Singapore, Dept Pharm, Singapore 117543, Singapore
来源
BIOSENSING II | 2009年 / 7397卷
关键词
Surface Enhanced Raman Scattering; deep UV lithography; self assembled monolayer; glucose sensing; SILVER ELECTRODE; PARTITION LAYER; SPECTROSCOPY; SERS; STABILITY; AU;
D O I
10.1117/12.827228
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Surface Enhanced Raman Scattering (SERS) technique is used as an indispensable and sensitive modality for bio-sensing due to its ability to distinguish the analyte molecules based on their distinct `fingerprint' spectra. One of the most promising SERS substrates for biosensing was fabricated by coating noble metal film over orderly packed nanospheres. However, the major challenge in developing such a sensor is to achieve reproducible SERS substrate. Here, we report a new class of SERS substrate with ordered 3D nanostructures fabricated on silicon wafer by deep UV lithography technique followed by bi-metallic coating of silver and gold. Compared to the substrate fabricated by conventional nanosphere lithography, this approach allows better control of the nanostructures, which in turn gives uniform surface roughness for the metal film to provide adequate SERS enhancement with high reproducibility. Significance of this substrate for biomedical application was demonstrated by glucose sensing under physiologically relevant conditions. Partitioning and localization of glucose molecules within the first few nanometers of active SERS substrate was achieved by a self assembled monolayer (SAM) on the surface of substrate.
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页数:10
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