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High-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria

We present a dual-color laser scanning endomicroscope capable of fluorescence lifetime endomicroscopy at one frame per second (FPS). The scanning system uses a coherent imaging fiber with 30,000 cores. High-speed lifetime imaging is achieved by distributing the signal over an array of 1024 parallel...

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Autores principales: Pedretti, Ettore, Tanner, Michael G., Choudhary, Tushar R., Krstajić, Nikola, Megia-Fernandez, Alicia, Henderson, Robert K., Bradley, Mark, Thomson, Robert R., Girkin, John M., Dhaliwal, Kevin, Dalgarno, Paul A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363193/
https://www.ncbi.nlm.nih.gov/pubmed/30775092
http://dx.doi.org/10.1364/BOE.10.000181
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author Pedretti, Ettore
Tanner, Michael G.
Choudhary, Tushar R.
Krstajić, Nikola
Megia-Fernandez, Alicia
Henderson, Robert K.
Bradley, Mark
Thomson, Robert R.
Girkin, John M.
Dhaliwal, Kevin
Dalgarno, Paul A.
author_facet Pedretti, Ettore
Tanner, Michael G.
Choudhary, Tushar R.
Krstajić, Nikola
Megia-Fernandez, Alicia
Henderson, Robert K.
Bradley, Mark
Thomson, Robert R.
Girkin, John M.
Dhaliwal, Kevin
Dalgarno, Paul A.
author_sort Pedretti, Ettore
collection PubMed
description We present a dual-color laser scanning endomicroscope capable of fluorescence lifetime endomicroscopy at one frame per second (FPS). The scanning system uses a coherent imaging fiber with 30,000 cores. High-speed lifetime imaging is achieved by distributing the signal over an array of 1024 parallel single-photon avalanche diode detectors (SPADs), minimizing detection dead-time maximizing the number of photons detected per excitation pulse without photon pile-up to achieve the high frame rate. This also enables dual color fluorescence imaging by temporally shifting the dual excitation lasers, with respect to each other, to separate the two spectrally distinct fluorescent decays in time. Combining the temporal encoding, to provide spectral separation, with lifetime measurements we show a one FPS, multi-channel endomicroscopy platform for clinical applications and diagnosis. We demonstrate the potential of the system by imaging SmartProbe labeled bacteria in ex vivo samples of human lung using lifetime to differentiate bacterial fluorescence from the strong background lung autofluorescence which was used to provide structural information.
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spelling pubmed-63631932019-02-15 High-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria Pedretti, Ettore Tanner, Michael G. Choudhary, Tushar R. Krstajić, Nikola Megia-Fernandez, Alicia Henderson, Robert K. Bradley, Mark Thomson, Robert R. Girkin, John M. Dhaliwal, Kevin Dalgarno, Paul A. Biomed Opt Express Article We present a dual-color laser scanning endomicroscope capable of fluorescence lifetime endomicroscopy at one frame per second (FPS). The scanning system uses a coherent imaging fiber with 30,000 cores. High-speed lifetime imaging is achieved by distributing the signal over an array of 1024 parallel single-photon avalanche diode detectors (SPADs), minimizing detection dead-time maximizing the number of photons detected per excitation pulse without photon pile-up to achieve the high frame rate. This also enables dual color fluorescence imaging by temporally shifting the dual excitation lasers, with respect to each other, to separate the two spectrally distinct fluorescent decays in time. Combining the temporal encoding, to provide spectral separation, with lifetime measurements we show a one FPS, multi-channel endomicroscopy platform for clinical applications and diagnosis. We demonstrate the potential of the system by imaging SmartProbe labeled bacteria in ex vivo samples of human lung using lifetime to differentiate bacterial fluorescence from the strong background lung autofluorescence which was used to provide structural information. Optical Society of America 2018-12-12 /pmc/articles/PMC6363193/ /pubmed/30775092 http://dx.doi.org/10.1364/BOE.10.000181 Text en Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI. Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) . Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI.
spellingShingle Article
Pedretti, Ettore
Tanner, Michael G.
Choudhary, Tushar R.
Krstajić, Nikola
Megia-Fernandez, Alicia
Henderson, Robert K.
Bradley, Mark
Thomson, Robert R.
Girkin, John M.
Dhaliwal, Kevin
Dalgarno, Paul A.
High-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria
title High-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria
title_full High-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria
title_fullStr High-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria
title_full_unstemmed High-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria
title_short High-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria
title_sort high-speed dual color fluorescence lifetime endomicroscopy for highly-multiplexed pulmonary diagnostic applications and detection of labeled bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363193/
https://www.ncbi.nlm.nih.gov/pubmed/30775092
http://dx.doi.org/10.1364/BOE.10.000181
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