High-speed wide-field optical-sectioning fluorescence microscopy based on one-shot structured illumination

被引:0
|
作者
Zheng, Zhong [1 ]
Shi, Ruheng [1 ]
Kong, Lingjie [1 ]
机构
[1] Tsinghua Univ, Dept Precis Instruments, State Key Lab Precis Measurement Technol & Instru, Beijing 100084, Peoples R China
关键词
optical-sectioning; fluorescence microscopy; one-shot; Hilbert transform; empirical mode decomposition; 2-DIMENSIONAL FRINGE PATTERNS; NATURAL DEMODULATION; SPECKLE;
D O I
10.1117/12.2575172
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Wide-field fluorescence microscopy (WFFM) is widely adopted in biomedical studies. However, axial resolution in most WFFM is poor due to the absence of optical-sectioning capability. To achieve wide-field optical-sectioning, several methods have been proposed, most of which need at least two images to reconstruct one optical sectioning image. So, the frame rate of current wide-field optical sectioning microscopy is no more than half of that of conventional WFFM, which may not meet the speed requirement of fast biodynamic studies. We introduce a novel high-speed, wide-field optical sectioning method based on local contrast weighting function and two-dimensional Hilbert-Huang transform, in which only one structured image is required to reconstruct an optical sectioning image. In this way, the loss of temporal resolution in conventional wide-field optical sectioning microscopy is compensated. We validated this method with the imaging of mouse brain slices.
引用
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页数:6
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