Cavity Plasmon Resonance Biosensing

被引:0
|
作者
Razansky, Daniel [1 ]
Einziger, Pinchas D. [2 ]
Adam, Dan [3 ]
机构
[1] Harvard Univ, Sch Med, Lab Bioopt & Mol Imaging, Ctr Mol Imaging Res, Boston, MA 02115 USA
[2] Technion Israel Inst Technol, Dept Elect Engn, IL-32000 Haifa, Israel
[3] Technion Israel Inst Technol, Dept Biomed Engn, IL-32000 Haifa, Israel
关键词
DNA hybridization; immunosensing; optical spectroscopy; surface plasmon resonance (SPR);
D O I
10.1109/TNANO.2008.926446
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Surface plasmon resonance (SPR) spectroscopy has demonstrated unprecedented performance in label-free real-time probing of various biopolymer, ligand, protein, and DNA interactions. Since its inception in the late sixties, the basic physical phenomenon underlying the SPR biosensing remained unchanged, namely, resonant absorption of TM-polarized light incident upon a metallic nanofilm above the critical total internal reflection angle. Since the SPR field is strictly confined to the metal-analyte interface, the measurements are usually limited to molecular adsorbates located in an immediate vicinity of this surface. Herein, we propose a novel biosensing method utilizing cavity plasmon resonance (CPR) excitation in nanofilms. As opposed to the classical TM-polarized SPR, the CPR is applicable for both TE and TM polarizations and does not require complicated evanescent field excitation conditions. It holds a promise for highly sensitive real-time probing of scalable amounts of analytes in a variety of frequency bands.
引用
收藏
页码:580 / 585
页数:6
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