Super-resolution differential interference contrast microscopy by structured illumination
Author(s) -
Jianling Chen,
Xu Yan,
Xiaohua Lv,
Xiaomin Lai,
Shaoqun Zeng
Publication year - 2013
Publication title -
optics express
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.394
H-Index - 271
ISSN - 1094-4087
DOI - 10.1364/oe.21.000112
Subject(s) - differential interference contrast microscopy , optics , microscopy , resolution (logic) , materials science , diffraction , image resolution , numerical aperture , interference microscopy , optical microscope , condenser (optics) , interference (communication) , light sheet fluorescence microscopy , scanning confocal electron microscopy , physics , scanning electron microscope , computer science , wavelength , telecommunications , light source , channel (broadcasting) , artificial intelligence
We propose a structured illumination differential interference contrast (SI-DIC) microscopy, breaking the diffraction resolution limit of differential interference contrast (DIC) microscopy. SI-DIC extends the bandwidth of coherent transfer function of the DIC imaging system, thus the resolution is improved. With 0.8 numerical aperture condenser and objective, the reconstructed SI-DIC image of 53 nm polystyrene beads reveals lateral resolution of approximately 190 nm, doubling that of the conventional DIC image. We also demonstrate biological observations of label-free cells with improved spatial resolution. The SI-DIC microscopy can provide sub-diffraction resolution and high contrast images with marker-free specimens, and has the potential for achieving sub-diffraction resolution quantitative phase imaging.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom