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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
来源:
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.
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页数:6
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