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Miniaturized structured illumination microscopy using two 3-axis MEMS micromirrors
We present the development and performance characterisation of a novel structured illumination microscope (SIM) in which the grating pattern is generated using two optical beams controlled via 2 micro-electro-mechanical system (MEMS) three-axis scanning micromirrors. The implementation of MEMS micro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Optica Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9774859/ https://www.ncbi.nlm.nih.gov/pubmed/36589569 http://dx.doi.org/10.1364/BOE.475811 |
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author | Tinning, Peter Donnachie, Mark Christopher, Jay Uttamchandani, Deepak Bauer, Ralf |
author_facet | Tinning, Peter Donnachie, Mark Christopher, Jay Uttamchandani, Deepak Bauer, Ralf |
author_sort | Tinning, Peter |
collection | PubMed |
description | We present the development and performance characterisation of a novel structured illumination microscope (SIM) in which the grating pattern is generated using two optical beams controlled via 2 micro-electro-mechanical system (MEMS) three-axis scanning micromirrors. The implementation of MEMS micromirrors to accurately and repeatably control angular, radial and phase positioning delivers flexible control of the fluorescence excitation illumination, with achromatic beam delivery through the same optical path, reduced spatial footprint and cost-efficient integration being further benefits. Our SIM architecture enables the direct implementation of multi-color imaging in a compact and adaptable package. The two-dimensional SIM system approach is enabled by a pair of 2 mm aperture electrostatically actuated three-axis micromirrors having static angular tilt motion along the x- and y-axes and static piston motion along the z-axis. This allows precise angular, radial and phase positioning of two optical beams, generating a fully controllable spatial interference pattern at the focal plane by adjusting the positions of the beam in the back-aperture of a microscope objective. This MEMS-SIM system was applied to fluorescent bead samples and cell specimens, and was able to obtain a variable lateral resolution improvement between 1.3 and 1.8 times the diffraction limited resolution. |
format | Online Article Text |
id | pubmed-9774859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Optica Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-97748592022-12-29 Miniaturized structured illumination microscopy using two 3-axis MEMS micromirrors Tinning, Peter Donnachie, Mark Christopher, Jay Uttamchandani, Deepak Bauer, Ralf Biomed Opt Express Article We present the development and performance characterisation of a novel structured illumination microscope (SIM) in which the grating pattern is generated using two optical beams controlled via 2 micro-electro-mechanical system (MEMS) three-axis scanning micromirrors. The implementation of MEMS micromirrors to accurately and repeatably control angular, radial and phase positioning delivers flexible control of the fluorescence excitation illumination, with achromatic beam delivery through the same optical path, reduced spatial footprint and cost-efficient integration being further benefits. Our SIM architecture enables the direct implementation of multi-color imaging in a compact and adaptable package. The two-dimensional SIM system approach is enabled by a pair of 2 mm aperture electrostatically actuated three-axis micromirrors having static angular tilt motion along the x- and y-axes and static piston motion along the z-axis. This allows precise angular, radial and phase positioning of two optical beams, generating a fully controllable spatial interference pattern at the focal plane by adjusting the positions of the beam in the back-aperture of a microscope objective. This MEMS-SIM system was applied to fluorescent bead samples and cell specimens, and was able to obtain a variable lateral resolution improvement between 1.3 and 1.8 times the diffraction limited resolution. Optica Publishing Group 2022-11-15 /pmc/articles/PMC9774859/ /pubmed/36589569 http://dx.doi.org/10.1364/BOE.475811 Text en Published by Optica Publishing Group under the terms of the Creative Commons Attribution 4.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI. https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Tinning, Peter Donnachie, Mark Christopher, Jay Uttamchandani, Deepak Bauer, Ralf Miniaturized structured illumination microscopy using two 3-axis MEMS micromirrors |
title | Miniaturized structured illumination microscopy using two
3-axis MEMS micromirrors |
title_full | Miniaturized structured illumination microscopy using two
3-axis MEMS micromirrors |
title_fullStr | Miniaturized structured illumination microscopy using two
3-axis MEMS micromirrors |
title_full_unstemmed | Miniaturized structured illumination microscopy using two
3-axis MEMS micromirrors |
title_short | Miniaturized structured illumination microscopy using two
3-axis MEMS micromirrors |
title_sort | miniaturized structured illumination microscopy using two
3-axis mems micromirrors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9774859/ https://www.ncbi.nlm.nih.gov/pubmed/36589569 http://dx.doi.org/10.1364/BOE.475811 |
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