Image scanning microscopy with a long depth of focus generated by an annular radially polarized beam

被引:19
作者
Wang, Weibo [1 ,2 ,3 ]
Zhang, Baoyuan [1 ,2 ]
Wu, Biwei [1 ,2 ]
Li, Xiaojun [1 ,2 ]
Ma, Jie [1 ,2 ]
Sun, Pengyu [1 ,2 ]
Zheng, Shenghao [1 ,2 ]
Tan, Jiubin [1 ,2 ]
机构
[1] Harbin Inst Technol, Inst Ultraprecis Optoelect Instrument Engn, Harbin 150001, Peoples R China
[2] Harbin Inst Technol, Minist Ind & Informat Technol, Key Lab Ultraprecis Intelligent Instrumentat, Harbin 150001, Peoples R China
[3] Harbin Inst Technol, Postdoctoral Res Stn Opt Engn, Harbin 150001, Peoples R China
来源
OPTICS EXPRESS | 2020年 / 28卷 / 26期
基金
中国博士后科学基金;
关键词
RESOLUTION; SPOT; SUPERRESOLUTION; FIELD;
D O I
10.1364/OE.413292
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Image scanning microscopy (ISM) is a promising tool for bioimaging owing to its integration of signal to noise ratio (SNR) and super resolution superior to that obtained in confocal scanning microscopy. In this paper, we introduce the annular radially polarized beam to the ISM, which yields an axially extended excitation focus and enhanced resolution, providing a new possibility to obtain the whole information of thick specimen with a single scan. We present the basic principle and a rigorous theoretical model for ISM with annular radially polarized beam (ISM-aRP). Results show that the resolution of ISM-aRP can be enhanced by 4% compared with that in conventional ISM, and the axial extent of the focus is longer than 6k. The projected view of the simulated fluorescent beads suspension specimen demonstrates the validity of ISM-aRP to obtain the whole information of volume sample. Moreover, this simple method can be easily integrated into the commercial laser scanning microscopy systems. (C) 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:39288 / 39298
页数:11
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