Rigiflex Lithography-Based Nanodot Arrays for Localized Surface Plasmon Resonance Biosensors

被引:9
|
作者
Park, Dong Kyu [1 ]
Kim, Hye In [1 ]
Kim, Jun Pyo [1 ]
Park, Je Seob [2 ]
Lee, Su Yeon [3 ]
Yang, Seung-Man [3 ]
Lee, Jeewon [4 ]
Chung, Chan-Hwa [1 ]
Sim, Sang Jun [1 ]
Yoo, Pil J. [1 ,2 ]
机构
[1] Sungkyunkwan Univ, Sch Chem Engn, Suwon 440746, South Korea
[2] Sungkyunkwan Univ, SAINT, Suwon 440746, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon 305701, South Korea
[4] Korea Univ, Dept Chem & Biol Engn, Seoul 136701, South Korea
基金
新加坡国家研究基金会;
关键词
GOLD NANOPARTICLES; NANOSPHERE LITHOGRAPHY; OPTICAL-PROPERTIES; SPECTROSCOPY; SHAPE; SIZE; SENSITIVITY; SPECTRA; FILMS; MOLD;
D O I
10.1021/la100598v
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present a facile and robust means of fabricating metallic nanodot arrays for localized surface plasmon resonance (LSPR) biosensors through the strategic coupling of a polymeric template prepared with rigiflex lithography and a subsequent metallization via electrodeposition. Rigiflex lithography provides the capability to realize large-scale nanosized features as well as process flexibility during contact molding. In addition, the electrodeposition process enables wet-based nanoscale metallization with high pattern fidelity and geometric controllability. Generated metallic nanodot arrays can be used as a general platform for LSPR biosensors via the sequential binding of chemicals and biomolecules. Extinction spectra of the corresponding LSPR signal are measured with UV-vis-NIR spectroscopy, from which the pattern size and shape dependence of LSPR are readily confirmed. The feasibility of a very sensitive biosensor is demonstrated by the targeted binding of human immunoglobulin G, yielding subnanomolar detection capability with high selectivity.
引用
收藏
页码:6119 / 6126
页数:8
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