Virtual single-pixel imaging-based deconvolution method for spatial resolution improvement in wide-field fluorescence microscopy

被引:7
作者
Zhang, Wei [1 ,2 ]
Li, Siwei [1 ,2 ]
Yang, Zhigang [1 ,2 ]
Yu, Bin [1 ,2 ]
Lin, Danying [1 ,2 ]
Xiong, Jia [1 ,2 ]
Qu, Junle [1 ,2 ]
机构
[1] Shenzhen Univ, Ctr Biomed Photon, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Coll Phys & Optoelect Engn, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
ILLUMINATION; LIVE; CELL;
D O I
10.1364/BOE.396336
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Deconvolution technique has been widely used in fluorescence microscopy to restore tine structures of biological samples. However, conventional deconvolution methods usually achieve little contrast enhancement in dense structures that have the intervals close to the Rayleigh criterion. Herein, we developed a novel deconvolution method, termed virtual single-pixel imaging (v-SPI). Differing from existing deconvolution methods, v-SPI aims to retrieve the less blurred image directly, not the sample distribution which cannot be actually obtained. And the result can be retrieved simply by solving a linear matrix in spatial domain. In addition, the proposed method has no requirement of calibrating parameters of microscope system. Simulation and experimental results demonstrated that the proposed v-SPI method can enhance the contrast of dense structures significantly and acquire a 24% increase in resolution. (C) 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:3648 / 3658
页数:11
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