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Fast spectrally encoded Mueller optical scanning microscopy
Mueller microscopes enable imaging of the optical anisotropic properties of biological or non-biological samples, in phase and amplitude, at sub-micrometre scale. However, the development of Mueller microscopes poses an instrumental challenge: the production of polarimetric parameters must be suffic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408429/ https://www.ncbi.nlm.nih.gov/pubmed/30850680 http://dx.doi.org/10.1038/s41598-019-40467-z |
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author | Rivet, Sylvain Dubreuil, Matthieu Bradu, Adrian Le Grand, Yann |
author_facet | Rivet, Sylvain Dubreuil, Matthieu Bradu, Adrian Le Grand, Yann |
author_sort | Rivet, Sylvain |
collection | PubMed |
description | Mueller microscopes enable imaging of the optical anisotropic properties of biological or non-biological samples, in phase and amplitude, at sub-micrometre scale. However, the development of Mueller microscopes poses an instrumental challenge: the production of polarimetric parameters must be sufficiently quick to ensure fast imaging, so that the evolution of these parameters can be visualised in real-time, allowing the operator to adjust the microscope while constantly monitoring them. In this report, a full Mueller scanning microscope based on spectral encoding of polarization is presented. The spectrum, collected every 10 μs for each position of the optical beam on the specimen, incorporates all the information needed to produce the full Mueller matrix, which allows simultaneous display of all the polarimetric parameters, at the unequalled rate of 1.5 Hz (for an image of 256 × 256 pixels). The design of the optical blocks allows for the real-time display of linear birefringent images which serve as guidance for the operator. In addition, the instrument has the capability to easily switch its functionality from a Mueller to a Second Harmonic Generation (SHG) microscope, providing a pixel-to-pixel matching of the images produced by the two modalities. The device performance is illustrated by imaging various unstained biological specimens. |
format | Online Article Text |
id | pubmed-6408429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64084292019-03-12 Fast spectrally encoded Mueller optical scanning microscopy Rivet, Sylvain Dubreuil, Matthieu Bradu, Adrian Le Grand, Yann Sci Rep Article Mueller microscopes enable imaging of the optical anisotropic properties of biological or non-biological samples, in phase and amplitude, at sub-micrometre scale. However, the development of Mueller microscopes poses an instrumental challenge: the production of polarimetric parameters must be sufficiently quick to ensure fast imaging, so that the evolution of these parameters can be visualised in real-time, allowing the operator to adjust the microscope while constantly monitoring them. In this report, a full Mueller scanning microscope based on spectral encoding of polarization is presented. The spectrum, collected every 10 μs for each position of the optical beam on the specimen, incorporates all the information needed to produce the full Mueller matrix, which allows simultaneous display of all the polarimetric parameters, at the unequalled rate of 1.5 Hz (for an image of 256 × 256 pixels). The design of the optical blocks allows for the real-time display of linear birefringent images which serve as guidance for the operator. In addition, the instrument has the capability to easily switch its functionality from a Mueller to a Second Harmonic Generation (SHG) microscope, providing a pixel-to-pixel matching of the images produced by the two modalities. The device performance is illustrated by imaging various unstained biological specimens. Nature Publishing Group UK 2019-03-08 /pmc/articles/PMC6408429/ /pubmed/30850680 http://dx.doi.org/10.1038/s41598-019-40467-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Rivet, Sylvain Dubreuil, Matthieu Bradu, Adrian Le Grand, Yann Fast spectrally encoded Mueller optical scanning microscopy |
title | Fast spectrally encoded Mueller optical scanning microscopy |
title_full | Fast spectrally encoded Mueller optical scanning microscopy |
title_fullStr | Fast spectrally encoded Mueller optical scanning microscopy |
title_full_unstemmed | Fast spectrally encoded Mueller optical scanning microscopy |
title_short | Fast spectrally encoded Mueller optical scanning microscopy |
title_sort | fast spectrally encoded mueller optical scanning microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408429/ https://www.ncbi.nlm.nih.gov/pubmed/30850680 http://dx.doi.org/10.1038/s41598-019-40467-z |
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