Rapid reconstruction algorithm for multifocal structured illumination microscopy

被引:1
|
作者
Chen, Zhiqi [1 ]
He, Haozhen [1 ]
Ai, Qi [1 ]
Liu, Penghuan [1 ]
机构
[1] China Jiliang Univ, Lab Modern Measurement Technol & Instruments Zheji, Hangzhou 310018, Peoples R China
关键词
Multifocal SIM; Super-resolution; Rapid reconstruction; IMAGE SCANNING MICROSCOPY; FLUORESCENCE MICROSCOPY; RESOLUTION; SUPERRESOLUTION; LIVE;
D O I
10.1016/j.optcom.2023.129807
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Multifocal structured illumination microscopy (MSIM) could surpass the diffraction limit by illuminating the sample with multiple-spot grid patterns. Developed as a parallel version of image scanning microscopy (ISM) to enhance data acquisition speed, MSIM can also be viewed as a variation of structured illumination microscopy (SIM) in which the conventional sinusoidal illumination is substituted with a lattice array of spots. This method outperforms regular SIM when imaging samples that are thick or highly scattered. In this study, we present a rapid reconstruction algorithm for MSIM in the spatial domain and demonstrate that the radius of its equivalent optical transfer function (OTF) support is twice that of a general wide-field microscopy in the epi-illumination geometry. Numerical simulations and experimental results have validated the effectiveness of the proposed algorithm.
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页数:4
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