Exploiting multimode waveguides for pure fibre-based imaging

There has been an immense drive in modern microscopy towards miniaturization and fibre-based technology. This has been necessitated by the need to access hostile or difficult environments in situ and in vivo. Strategies to date have included the use of specialist fibres and miniaturized scanning sys...

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Main Authors: Čižmár, Tomáš, Dholakia, Kishan
Format: Online
Language:English
Published: Nature Pub. Group 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432471/
id pubmed-3432471
recordtype oai_dc
spelling pubmed-34324712012-09-05 Exploiting multimode waveguides for pure fibre-based imaging Čižmár, Tomáš Dholakia, Kishan Article There has been an immense drive in modern microscopy towards miniaturization and fibre-based technology. This has been necessitated by the need to access hostile or difficult environments in situ and in vivo. Strategies to date have included the use of specialist fibres and miniaturized scanning systems accompanied by ingenious microfabricated lenses. Here we present a novel approach for this field by utilizing disordered light within a standard multimode optical fibre for lensless microscopy and optical mode conversion. We demonstrate the modalities of bright- and dark-field imaging and scanning fluorescence microscopy at acquisition rates that allow observation of dynamic processes such as Brownian motion of mesoscopic particles. Furthermore, we show how such control can realize a new form of mode converter and generate various types of advanced light fields such as propagation-invariant beams and optical vortices. These may be useful for future fibre-based implementations of super-resolution or light-sheet microscopy. Nature Pub. Group 2012-08-28 /pmc/articles/PMC3432471/ /pubmed/22929784 http://dx.doi.org/10.1038/ncomms2024 Text en Copyright © 2012, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Čižmár, Tomáš
Dholakia, Kishan
spellingShingle Čižmár, Tomáš
Dholakia, Kishan
Exploiting multimode waveguides for pure fibre-based imaging
author_facet Čižmár, Tomáš
Dholakia, Kishan
author_sort Čižmár, Tomáš
title Exploiting multimode waveguides for pure fibre-based imaging
title_short Exploiting multimode waveguides for pure fibre-based imaging
title_full Exploiting multimode waveguides for pure fibre-based imaging
title_fullStr Exploiting multimode waveguides for pure fibre-based imaging
title_full_unstemmed Exploiting multimode waveguides for pure fibre-based imaging
title_sort exploiting multimode waveguides for pure fibre-based imaging
description There has been an immense drive in modern microscopy towards miniaturization and fibre-based technology. This has been necessitated by the need to access hostile or difficult environments in situ and in vivo. Strategies to date have included the use of specialist fibres and miniaturized scanning systems accompanied by ingenious microfabricated lenses. Here we present a novel approach for this field by utilizing disordered light within a standard multimode optical fibre for lensless microscopy and optical mode conversion. We demonstrate the modalities of bright- and dark-field imaging and scanning fluorescence microscopy at acquisition rates that allow observation of dynamic processes such as Brownian motion of mesoscopic particles. Furthermore, we show how such control can realize a new form of mode converter and generate various types of advanced light fields such as propagation-invariant beams and optical vortices. These may be useful for future fibre-based implementations of super-resolution or light-sheet microscopy.
publisher Nature Pub. Group
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432471/
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