Journal of Innovative Optical Health Sciences (Nov 2019)

Super-resolution microscopy based on parallel detection

  • Zhimin Zhang,
  • Shaocong Liu,
  • Liang Xu,
  • Yubing Han,
  • Cuifang Kuang,
  • Yong Liu,
  • Xiang Hao,
  • Hongqin Yang,
  • Xu Liu

DOI
https://doi.org/10.1142/S1793545819500238
Journal volume & issue
Vol. 12, no. 6
pp. 1950023-1 – 1950023-7

Abstract

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Image scanning microscopy based on pixel reassignment can improve the confocal resolution limit without losing the image signal-to-noise ratio (SNR) greatly [C. J. R. Sheppard, “Super-resolution in confocal imaging,” Optik 80(2) 53–54 (1988). C. B. Müller, E. Jörg, “Image scanning microscopy, “Phys. Rev. Lett. 104(19) 198101 (2010). C. J. R. Sheppard, S. B. Mehta, R. Heintzmann, “Superresolution by image scanning microscopy using pixel reassignment,” Opt. Lett. 38(15) 2889–2892 (2013)]. Here, we use a tailor-made optical fiber and 19 avalanche photodiodes (APDs) as parallel detectors to upgrade our existing confocal microscopy, termed as parallel-detection super-resolution (PDSR) microscopy. In order to obtain the correct shift value, we use the normalized 2D cross correlation to calculate the shifting value of each image. We characterized our system performance by imaging fluorescence beads and applied this system to observing the 3D structure of biological specimen.

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