Paper
7 September 2018 An adaptive optics 3D STED microscope for super-resolution imaging of thick samples with background noise suppression using digital image processing
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Proceedings Volume 10834, Speckle 2018: VII International Conference on Speckle Metrology; 108342G (2018) https://doi.org/10.1117/12.2324145
Event: SPECKLE 2018: VII International Conference on Speckle Metrology, 2018, Janów Podlaski, Poland
Abstract
The emerge of super-resolution (SR) microscopy enabled imaging below the diffraction barrier. One of the SR techniques, Stimulated Emission Depletion (STED) microscopy, has shown promise in super-resolution imaging of thick specimen. Imaging such structures is a non-trivial task due to the increased aberrations introduced by the sample. Adaptive optics provides the solution to this problem. AO can correct the aberrations by modulation of the phase. Although STED microscopy is theoretically a diffraction unlimited technique, the resolution limiting factor is noise. Modern filtering techniques, such as block matching and 3D filtering (BM3D), can increase the signal-to-noise ratio of the STED images. This work presents an AO 3D STED microscope with aberration correction and background noise filtering using BM3D algorithm. We show the super-resolution images of thick samples and emphasize the importance of image processing for recovering of object high spatial frequencies.
© (2018) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Piotr Zdańkowski, Maciej Trusiak, Maria Cywińska, and Jason R. Swedlow "An adaptive optics 3D STED microscope for super-resolution imaging of thick samples with background noise suppression using digital image processing", Proc. SPIE 10834, Speckle 2018: VII International Conference on Speckle Metrology, 108342G (7 September 2018); https://doi.org/10.1117/12.2324145
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KEYWORDS
Stimulated emission depletion microscopy

3D image processing

Image filtering

Microscopes

Adaptive optics

Image resolution

Confocal microscopy

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