Analysis of the surface plasmon resonance interferometric imaging performance of scanning confocal surface plasmon microscopy

被引:5
|
作者
Tontarawongsa, Sorawit [1 ]
Visitsattapongse, Sarinporn [1 ]
Pechprasarn, Suejit [2 ]
机构
[1] King Mongkuts Inst Technol, Sch Engn, Dept Biomed Engn, Bangkok 10520, Thailand
[2] Rangsit Univ, Coll Biomed Engn, Pathum Thani 12000, Thailand
来源
BIOMEDICAL OPTICS EXPRESS | 2022年 / 13卷 / 01期
关键词
RESOLUTION; SENSITIVITY; SENSOR; CELLS;
D O I
10.1364/BOE.448085
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here, we apply rigorous coupled-wave theory to analyze the optical phase imaging performance of scanning confocal surface plasmon microscope. The scanning confocal surface plasmon resonance microscope is an embedded interferometric microscope interfering between two integrated optical beams. One beam is provided by the central part around the normal incident angle of the back focal plane, and the other beam is the incident angles beyond the critical angle, exciting the surface plasmon. Furthermore, the two beams can form an interference signal inside a confocal pinhole in the image plane, which provides a well-defined path for the surface plasmon propagation. The scanning confocal surface plasmon resonance microscope operates by scanning the sample along the optical axis z, so-called V(z). The study investigates two imaging modes: non-quantitative imaging and quantitative imaging modes. We also propose a theoretical framework to analyze the scanning confocal surface plasmon resonance microscope compared to non-interferometric surface plasmon microscopes and quantify quantitative performance parameters including spatial resolution and optical contrast for non-quantitative imaging; sensitivity and crosstalk for quantitative imaging. The scanning confocal SPR microscope can provide a higher spatial resolution, better sensitivity, and lower crosstalk measurement. The confocal SPR microscope configuration is a strong candidate for high throughput measurements since it requires a smaller sensing channel than the other SPR microscopes. (c) 2021 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement
引用
收藏
页码:485 / 501
页数:17
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