Enhancing the isotropy of lateral resolution in coherent structured illumination microscopy

被引:7
|
作者
Park, Joo Hyun [1 ]
Lee, Jae Yong [1 ,2 ]
Lee, Eun Seong [3 ]
机构
[1] Univ Sci & Technol, Taejon 305350, South Korea
[2] Korea Res Inst Stand & Sci, Ctr Length, Taejon 304340, South Korea
[3] Korea Res Inst Stand & Sci, Ctr Nanometrol, Taejon 304340, South Korea
来源
BIOMEDICAL OPTICS EXPRESS | 2014年 / 5卷 / 06期
基金
新加坡国家研究基金会;
关键词
FLUORESCENCE MICROSCOPY; EXCITATION MICROSCOPY; OPTICAL RESOLUTION; LIMIT; SUPERRESOLUTION;
D O I
10.1364/BOE.5.001895
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We present a method to improve the isotropy of spatial resolution in a structured illumination microscopy (SIM) implemented for imaging non-fluorescent samples. To alleviate the problem of anisotropic resolution involved with the previous scheme of coherent SIM that employs the two orthogonal standing-wave illumination, referred to as the orthogonal SIM, we introduce a hexagonal-lattice illumination that incorporates three standing-wave fields simultaneously superimposed at the orientations equally divided in the lateral plane. A theoretical formulation is worked out rigorously for the coherent image formation with such a simultaneous multiple-beam illumination and an explicit Fourier-domain framework is derived for reconstructing an image with enhanced resolution. Using a computer-synthesized resolution target as a 2D coherent sample, we perform numerical simulations to examine the imaging characteristics of our three-angle SIM compared with the orthogonal SIM. The investigation on the 2D resolving power with the various test patterns of different periods and orientations reveal that the orientation-dependent undulation of lateral resolution can be reduced from 27% to 8% by using the three-angle SIM while the best resolution (0.54 times the resolution limit of conventional coherent imaging) in the directions of structured illumination is slightly deteriorated by 4.6% from that of the orthogonal SIM. (C) 2014 Optical Society of America
引用
收藏
页码:1895 / 1912
页数:18
相关论文
共 50 条
  • [31] Structured Illumination Microscopy and Super-resolution Image Reconstruction
    Bi, Ying
    Qian, Jiaming
    Cao, Yu
    TWELFTH INTERNATIONAL CONFERENCE ON INFORMATION OPTICS AND PHOTONICS (CIOP 2021), 2021, 12057
  • [32] Resolution doubling using confocal microscopy via analogy with structured illumination microscopy
    Hayashi, Shinichi
    JAPANESE JOURNAL OF APPLIED PHYSICS, 2016, 55 (08)
  • [33] Structured illumination microscopy for super-resolution and optical sectioning
    Dan Dan
    Baoli Yao
    Ming Lei
    Science Bulletin, 2014, (12) : 1291 - 1307
  • [34] Method for assessing the spatiotemporal resolution of structured illumination microscopy (SIM)
    Boualam, Abderrahim
    Rowlands, Christopher J.
    BIOMEDICAL OPTICS EXPRESS, 2021, 12 (02) : 790 - 801
  • [35] Super-resolution scanning microscopy with virtually structured illumination
    Zhang, Su
    Li, Jingtao
    Zou, Limin
    Ding, Xuemei
    TENTH INTERNATIONAL SYMPOSIUM ON PRECISION ENGINEERING MEASUREMENTS AND INSTRUMENTATION, 2019, 11053
  • [36] Structured illumination for resolution enhancement and autofocusing in digital holographic microscopy
    Gao, Peng
    Pedrini, Giancarlo
    Osten, Wolfgang
    OPTICS LETTERS, 2013, 38 (08) : 1328 - 1330
  • [37] Structured illumination microscopy for super-resolution and optical sectioning
    Dan Dan
    Baoli Yao
    Ming Lei
    Chinese Science Bulletin, 2014, 59 (12) : 1291 - 1307
  • [38] Structured illumination microscopy
    Saxena, Manish
    Eluru, Gangadhar
    Gorthi, Sai Siva
    ADVANCES IN OPTICS AND PHOTONICS, 2015, 7 (02): : 241 - 275
  • [39] Enhancing resolution in coherent microscopy using deep learning
    Liu, Tairan
    de Haan, Kevin
    Rivenson, Yair
    Wei, Zhensong
    Zeng, Xin
    Zhang, Yibo
    Ozcan, Aydogan
    2019 CONFERENCE ON LASERS AND ELECTRO-OPTICS (CLEO), 2019,
  • [40] A reconstruction method for linear sensor microscopy based on improvement of lateral resolution isotropy
    Macedo, M. P.
    Correia, C. M. B. A.
    ADVANCED MICROSCOPY TECHNIQUES II, 2011, 8086