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Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting

Two-photon microscopy (2PM) has revolutionized biomedical imaging by allowing thin optical sectioning in relatively thick biological specimens. Because dispersive microscope components in 2PM, such as objective lens, can alter temporal laser pulse width (typically being broader at the sample plane),...

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Autores principales: Kim, Youngchan, Vogel, Steven S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Photo-Optical Instrumentation Engineers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987257/
https://www.ncbi.nlm.nih.gov/pubmed/31994362
http://dx.doi.org/10.1117/1.JBO.25.1.014516
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author Kim, Youngchan
Vogel, Steven S.
author_facet Kim, Youngchan
Vogel, Steven S.
author_sort Kim, Youngchan
collection PubMed
description Two-photon microscopy (2PM) has revolutionized biomedical imaging by allowing thin optical sectioning in relatively thick biological specimens. Because dispersive microscope components in 2PM, such as objective lens, can alter temporal laser pulse width (typically being broader at the sample plane), for accurate measurements of two-photon absorption properties, it is important to characterize pulse duration at the sample plane. We present a simple modification to a two-photon microscope light path that allows for second-harmonic-generation-based interferometric autocorrelation measurements to characterize ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting (TCSPC). We show that TCSPC can be used as a simple and versatile method to estimate the zero time delay step value between two adjacent ultrafast laser pulses for these measurements. To demonstrate the utility of this modification, we measured the Coherent Chameleon-Ultra II Ti:sapphire laser pulse width at the sample plane using a [Formula: see text] air, [Formula: see text] air, or [Formula: see text] water-immersion objective lens. At 950-nm two-photon excitation, the measured pulse width was [Formula: see text] , [Formula: see text] , and [Formula: see text] ([Formula: see text] , [Formula: see text]), respectively.
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spelling pubmed-69872572020-02-03 Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting Kim, Youngchan Vogel, Steven S. J Biomed Opt Special Section Celebrating Thirty Years of Multiphoton Microscopy in the Biomedical Sciences Two-photon microscopy (2PM) has revolutionized biomedical imaging by allowing thin optical sectioning in relatively thick biological specimens. Because dispersive microscope components in 2PM, such as objective lens, can alter temporal laser pulse width (typically being broader at the sample plane), for accurate measurements of two-photon absorption properties, it is important to characterize pulse duration at the sample plane. We present a simple modification to a two-photon microscope light path that allows for second-harmonic-generation-based interferometric autocorrelation measurements to characterize ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting (TCSPC). We show that TCSPC can be used as a simple and versatile method to estimate the zero time delay step value between two adjacent ultrafast laser pulses for these measurements. To demonstrate the utility of this modification, we measured the Coherent Chameleon-Ultra II Ti:sapphire laser pulse width at the sample plane using a [Formula: see text] air, [Formula: see text] air, or [Formula: see text] water-immersion objective lens. At 950-nm two-photon excitation, the measured pulse width was [Formula: see text] , [Formula: see text] , and [Formula: see text] ([Formula: see text] , [Formula: see text]), respectively. Society of Photo-Optical Instrumentation Engineers 2020-01-29 2020-01 /pmc/articles/PMC6987257/ /pubmed/31994362 http://dx.doi.org/10.1117/1.JBO.25.1.014516 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/ Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
spellingShingle Special Section Celebrating Thirty Years of Multiphoton Microscopy in the Biomedical Sciences
Kim, Youngchan
Vogel, Steven S.
Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting
title Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting
title_full Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting
title_fullStr Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting
title_full_unstemmed Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting
title_short Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting
title_sort measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting
topic Special Section Celebrating Thirty Years of Multiphoton Microscopy in the Biomedical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987257/
https://www.ncbi.nlm.nih.gov/pubmed/31994362
http://dx.doi.org/10.1117/1.JBO.25.1.014516
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