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Novel Design and Application of High-NA Fiber Imaging Bundles for In Vivo Brain Imaging with Two-Photon Scanning Fluorescence Microscopy
[Image: see text] Here, we provide experimental verification supporting the use of short-section imaging bundles for two-photon microscopy imaging of the mouse brain. The 8 mm long bundle is made of a pair of heavy-metal oxide glasses with a refractive index contrast of 0.38 to ensure a high numeric...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020965/ https://www.ncbi.nlm.nih.gov/pubmed/36880640 http://dx.doi.org/10.1021/acsami.2c22985 |
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author | Bijoch, Łukasz Włodkowska, Urszula Kasztelanic, Rafał Pawłowska, Monika Pysz, Dariusz Kaczmarek, Leszek Lapkiewicz, Radek Buczyński, Ryszard Czajkowski, Rafał |
author_facet | Bijoch, Łukasz Włodkowska, Urszula Kasztelanic, Rafał Pawłowska, Monika Pysz, Dariusz Kaczmarek, Leszek Lapkiewicz, Radek Buczyński, Ryszard Czajkowski, Rafał |
author_sort | Bijoch, Łukasz |
collection | PubMed |
description | [Image: see text] Here, we provide experimental verification supporting the use of short-section imaging bundles for two-photon microscopy imaging of the mouse brain. The 8 mm long bundle is made of a pair of heavy-metal oxide glasses with a refractive index contrast of 0.38 to ensure a high numerical aperture NA = 1.15. The bundle is composed of 825 multimode cores, ordered in a hexagonal lattice with a pixel size of 14 μm and a total diameter of 914 μm. We demonstrate successful imaging through custom-made bundles with 14 μm resolution. As the input, we used a 910 nm Ti-sapphire laser with 140 fs pulse and a peak power of 9 × 10(4) W. The excitation beam and fluorescent image were transferred through the fiber imaging bundle. As test samples, we used 1 μm green fluorescent latex beads, ex vivo hippocampal neurons expressing green fluorescent protein and cortical neurons in vivo expressing the fluorescent reporter GCaMP6s or immediate early gene Fos fluorescent reporter. This system can be used for minimal-invasive in vivo imaging of the cerebral cortex, hippocampus, or deep brain areas as a part of a tabletop system or an implantable setup. It is a low-cost solution, easy to integrate and operate for high-throughput experiments. |
format | Online Article Text |
id | pubmed-10020965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100209652023-03-18 Novel Design and Application of High-NA Fiber Imaging Bundles for In Vivo Brain Imaging with Two-Photon Scanning Fluorescence Microscopy Bijoch, Łukasz Włodkowska, Urszula Kasztelanic, Rafał Pawłowska, Monika Pysz, Dariusz Kaczmarek, Leszek Lapkiewicz, Radek Buczyński, Ryszard Czajkowski, Rafał ACS Appl Mater Interfaces [Image: see text] Here, we provide experimental verification supporting the use of short-section imaging bundles for two-photon microscopy imaging of the mouse brain. The 8 mm long bundle is made of a pair of heavy-metal oxide glasses with a refractive index contrast of 0.38 to ensure a high numerical aperture NA = 1.15. The bundle is composed of 825 multimode cores, ordered in a hexagonal lattice with a pixel size of 14 μm and a total diameter of 914 μm. We demonstrate successful imaging through custom-made bundles with 14 μm resolution. As the input, we used a 910 nm Ti-sapphire laser with 140 fs pulse and a peak power of 9 × 10(4) W. The excitation beam and fluorescent image were transferred through the fiber imaging bundle. As test samples, we used 1 μm green fluorescent latex beads, ex vivo hippocampal neurons expressing green fluorescent protein and cortical neurons in vivo expressing the fluorescent reporter GCaMP6s or immediate early gene Fos fluorescent reporter. This system can be used for minimal-invasive in vivo imaging of the cerebral cortex, hippocampus, or deep brain areas as a part of a tabletop system or an implantable setup. It is a low-cost solution, easy to integrate and operate for high-throughput experiments. American Chemical Society 2023-03-07 /pmc/articles/PMC10020965/ /pubmed/36880640 http://dx.doi.org/10.1021/acsami.2c22985 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Bijoch, Łukasz Włodkowska, Urszula Kasztelanic, Rafał Pawłowska, Monika Pysz, Dariusz Kaczmarek, Leszek Lapkiewicz, Radek Buczyński, Ryszard Czajkowski, Rafał Novel Design and Application of High-NA Fiber Imaging Bundles for In Vivo Brain Imaging with Two-Photon Scanning Fluorescence Microscopy |
title | Novel Design and
Application of High-NA Fiber Imaging
Bundles for In Vivo Brain Imaging with Two-Photon Scanning Fluorescence
Microscopy |
title_full | Novel Design and
Application of High-NA Fiber Imaging
Bundles for In Vivo Brain Imaging with Two-Photon Scanning Fluorescence
Microscopy |
title_fullStr | Novel Design and
Application of High-NA Fiber Imaging
Bundles for In Vivo Brain Imaging with Two-Photon Scanning Fluorescence
Microscopy |
title_full_unstemmed | Novel Design and
Application of High-NA Fiber Imaging
Bundles for In Vivo Brain Imaging with Two-Photon Scanning Fluorescence
Microscopy |
title_short | Novel Design and
Application of High-NA Fiber Imaging
Bundles for In Vivo Brain Imaging with Two-Photon Scanning Fluorescence
Microscopy |
title_sort | novel design and
application of high-na fiber imaging
bundles for in vivo brain imaging with two-photon scanning fluorescence
microscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020965/ https://www.ncbi.nlm.nih.gov/pubmed/36880640 http://dx.doi.org/10.1021/acsami.2c22985 |
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