Two-step phase-shifting fluorescence incoherent holographic microscopy

被引:22
作者
Qin, Wan [1 ,2 ]
Yang, Xiaoqi [1 ,2 ]
Li, Yingying [3 ]
Peng, Xiang [3 ]
Yao, Hai [1 ,2 ]
Qu, Xinghua [4 ]
Gao, Bruce Z. [1 ,2 ]
机构
[1] Clemson Univ, Dept Bioengn, Clemson, SC 29634 USA
[2] Clemson Univ, COMSET, Clemson, SC 29634 USA
[3] Shenzhen Univ, Inst Optoelect, Shenzhen 518060, Guangdong, Peoples R China
[4] Tianjin Univ, State Key Lab Precis Measuring Technol & Instrume, Tianjin 300072, Peoples R China
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Fresnel incoherent correlation holography; fluorescence holographic microscope; two-step phase-shifting interferometry; spatial light modulator; INTERFEROMETRY; RESOLUTION;
D O I
10.1117/1.JBO.19.6.060503
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescence holographic microscope (FINCHSCOPE) is a motionless fluorescence holographic imaging technique based on Fresnel incoherent correlation holography (FINCH) that shows promise in reconstructing three-dimensional fluorescence images of biological specimens with three holograms. We report a developing two-step phase-shifting method that reduces the required number of holograms from three to two. Using this method, we resolved microscopic fluorescent beads that were three-dimensionally distributed at different depths with two interferograms captured by a CCD camera. The method enables the FINCHSCOPE to work in conjunction with the frame-straddling technique and significantly enhance imaging speed. (C) The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License.
引用
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页数:3
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