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High resolution, high speed, long working distance, large field of view confocal fluorescence microscope
Confocal fluorescence microscopy is often used in brain imaging experiments, however conventional confocal microscopes are limited in their field of view, working distance, and speed for high resolution imaging. We report here the development of a novel high resolution, high speed, long working dist...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645379/ https://www.ncbi.nlm.nih.gov/pubmed/29042677 http://dx.doi.org/10.1038/s41598-017-13778-2 |
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author | Pacheco, Shaun Wang, Chengliang Chawla, Monica K. Nguyen, Minhkhoi Baggett, Brend K. Utzinger, Urs Barnes, Carol A. Liang, Rongguang |
author_facet | Pacheco, Shaun Wang, Chengliang Chawla, Monica K. Nguyen, Minhkhoi Baggett, Brend K. Utzinger, Urs Barnes, Carol A. Liang, Rongguang |
author_sort | Pacheco, Shaun |
collection | PubMed |
description | Confocal fluorescence microscopy is often used in brain imaging experiments, however conventional confocal microscopes are limited in their field of view, working distance, and speed for high resolution imaging. We report here the development of a novel high resolution, high speed, long working distance, and large field of view confocal fluorescence microscope (H(2)L(2)-CFM) with the capability of multi-region and multifocal imaging. To demonstrate the concept, a 0.5 numerical aperture (NA) confocal fluorescence microscope is prototyped with a 3 mm × 3 mm field of view and 12 mm working distance, an array of 9 beams is scanned over the field of view in 9 different regions to speed up the acquisition time by a factor of 9. We test this custom designed confocal fluorescence microscope for future use with brain clarification methods to image large volumes of the brain at subcellular resolution. This multi-region and multi-spot imaging method can be used in other imaging modalities, such as multiphoton microscopes, and the field of view can be extended well beyond 12 mm × 12 mm. |
format | Online Article Text |
id | pubmed-5645379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56453792017-10-26 High resolution, high speed, long working distance, large field of view confocal fluorescence microscope Pacheco, Shaun Wang, Chengliang Chawla, Monica K. Nguyen, Minhkhoi Baggett, Brend K. Utzinger, Urs Barnes, Carol A. Liang, Rongguang Sci Rep Article Confocal fluorescence microscopy is often used in brain imaging experiments, however conventional confocal microscopes are limited in their field of view, working distance, and speed for high resolution imaging. We report here the development of a novel high resolution, high speed, long working distance, and large field of view confocal fluorescence microscope (H(2)L(2)-CFM) with the capability of multi-region and multifocal imaging. To demonstrate the concept, a 0.5 numerical aperture (NA) confocal fluorescence microscope is prototyped with a 3 mm × 3 mm field of view and 12 mm working distance, an array of 9 beams is scanned over the field of view in 9 different regions to speed up the acquisition time by a factor of 9. We test this custom designed confocal fluorescence microscope for future use with brain clarification methods to image large volumes of the brain at subcellular resolution. This multi-region and multi-spot imaging method can be used in other imaging modalities, such as multiphoton microscopes, and the field of view can be extended well beyond 12 mm × 12 mm. Nature Publishing Group UK 2017-10-17 /pmc/articles/PMC5645379/ /pubmed/29042677 http://dx.doi.org/10.1038/s41598-017-13778-2 Text en © The Author(s) 2017 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 Pacheco, Shaun Wang, Chengliang Chawla, Monica K. Nguyen, Minhkhoi Baggett, Brend K. Utzinger, Urs Barnes, Carol A. Liang, Rongguang High resolution, high speed, long working distance, large field of view confocal fluorescence microscope |
title | High resolution, high speed, long working distance, large field of view confocal fluorescence microscope |
title_full | High resolution, high speed, long working distance, large field of view confocal fluorescence microscope |
title_fullStr | High resolution, high speed, long working distance, large field of view confocal fluorescence microscope |
title_full_unstemmed | High resolution, high speed, long working distance, large field of view confocal fluorescence microscope |
title_short | High resolution, high speed, long working distance, large field of view confocal fluorescence microscope |
title_sort | high resolution, high speed, long working distance, large field of view confocal fluorescence microscope |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645379/ https://www.ncbi.nlm.nih.gov/pubmed/29042677 http://dx.doi.org/10.1038/s41598-017-13778-2 |
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