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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...

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Autores principales: Bijoch, Łukasz, Włodkowska, Urszula, Kasztelanic, Rafał, Pawłowska, Monika, Pysz, Dariusz, Kaczmarek, Leszek, Lapkiewicz, Radek, Buczyński, Ryszard, Czajkowski, Rafał
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
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.
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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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