Stimulated emission depletion microscopy with array detection and photon reassignment

被引:4
|
作者
Wang, Wensheng [1 ]
Zhang, Zhimin [1 ]
Liu, Shaocong [1 ]
Chen, Yuchen [1 ]
Xu, Liang [1 ]
Kuang, Cuifang [1 ,2 ,3 ]
Hao, Xiang [1 ]
Liu, Xu [1 ,3 ]
机构
[1] Zhejiang Univ, Coll Opt Sci & Engn, State Key Lab Modern Opt Instrumentat, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Ningbo Res Inst, Ningbo 315100, Peoples R China
[3] Shanxi Univ, Collaborat Innovat Ctr Extreme Opt, Taiyuan 030006, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescence microscopy; Superresolution; Imaging system; FLUORESCENCE MICROSCOPY; STED MICROSCOPY; RESOLUTION; SUPERRESOLUTION; LIMIT;
D O I
10.1016/j.optlaseng.2020.106061
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
ISM can effectively enhance the signal strength and spatial resolution of traditional confocal microscopy. How ever, its maximum resolution is limited to root 2 times higher than confocal. On the other hand, stimulated emission depletion (STED) microscopy has been proven to be able to greatly improve the spatial resolution of confocal and has been widely used in practical applications. In this article, we present the implementation of STED with array detection and photon reassignment, and for convenient engineering applications, we also implement an integrated and practical array detection and photon reassignment module. We give a brief explanation of theoretical basis of array detection and photon reassignment, and make a comparison of these two methods. In practical applications, we tested the imaging characteristics of the system with a variety of samples. The results show that array detection can effectively improve the imaging signal-to-noise ratio (SNR); meanwhile, photon reassignment can also improve SNR and resolution to some extent under different depletion intensity. We believe that our research will provide effective inspiration and reference for subsequent research and can be widely applied to actual imaging observations.
引用
收藏
页数:7
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