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Full spectrum fluorescence lifetime imaging with 0.5 nm spectral and 50 ps temporal resolution

The use of optical techniques to interrogate wide ranging samples from semiconductors to biological tissue for rapid analysis and diagnostics has gained wide adoption over the past decades. The desire to collect ever more spatially, spectrally and temporally detailed optical signatures for sample ch...

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Autores principales: Williams, Gareth O. S., Williams, Elvira, Finlayson, Neil, Erdogan, Ahmet T., Wang, Qiang, Fernandes, Susan, Akram, Ahsan R., Dhaliwal, Kev, Henderson, Robert K., Girkin, John M., Bradley, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595732/
https://www.ncbi.nlm.nih.gov/pubmed/34785666
http://dx.doi.org/10.1038/s41467-021-26837-0
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author Williams, Gareth O. S.
Williams, Elvira
Finlayson, Neil
Erdogan, Ahmet T.
Wang, Qiang
Fernandes, Susan
Akram, Ahsan R.
Dhaliwal, Kev
Henderson, Robert K.
Girkin, John M.
Bradley, Mark
author_facet Williams, Gareth O. S.
Williams, Elvira
Finlayson, Neil
Erdogan, Ahmet T.
Wang, Qiang
Fernandes, Susan
Akram, Ahsan R.
Dhaliwal, Kev
Henderson, Robert K.
Girkin, John M.
Bradley, Mark
author_sort Williams, Gareth O. S.
collection PubMed
description The use of optical techniques to interrogate wide ranging samples from semiconductors to biological tissue for rapid analysis and diagnostics has gained wide adoption over the past decades. The desire to collect ever more spatially, spectrally and temporally detailed optical signatures for sample characterization has specifically driven a sharp rise in new optical microscopy technologies. Here we present a high-speed optical scanning microscope capable of capturing time resolved images across 512 spectral and 32 time channels in a single acquisition with the potential for ~0.2 frames per second (256 × 256 image pixels). Each pixel in the resulting images contains a detailed data cube for the study of diverse time resolved light driven phenomena. This is enabled by integration of system control electronics and on-chip processing which overcomes the challenges presented by high data volume and low imaging speed, often bottlenecks in previous systems.
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spelling pubmed-85957322021-11-19 Full spectrum fluorescence lifetime imaging with 0.5 nm spectral and 50 ps temporal resolution Williams, Gareth O. S. Williams, Elvira Finlayson, Neil Erdogan, Ahmet T. Wang, Qiang Fernandes, Susan Akram, Ahsan R. Dhaliwal, Kev Henderson, Robert K. Girkin, John M. Bradley, Mark Nat Commun Article The use of optical techniques to interrogate wide ranging samples from semiconductors to biological tissue for rapid analysis and diagnostics has gained wide adoption over the past decades. The desire to collect ever more spatially, spectrally and temporally detailed optical signatures for sample characterization has specifically driven a sharp rise in new optical microscopy technologies. Here we present a high-speed optical scanning microscope capable of capturing time resolved images across 512 spectral and 32 time channels in a single acquisition with the potential for ~0.2 frames per second (256 × 256 image pixels). Each pixel in the resulting images contains a detailed data cube for the study of diverse time resolved light driven phenomena. This is enabled by integration of system control electronics and on-chip processing which overcomes the challenges presented by high data volume and low imaging speed, often bottlenecks in previous systems. Nature Publishing Group UK 2021-11-16 /pmc/articles/PMC8595732/ /pubmed/34785666 http://dx.doi.org/10.1038/s41467-021-26837-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Williams, Gareth O. S.
Williams, Elvira
Finlayson, Neil
Erdogan, Ahmet T.
Wang, Qiang
Fernandes, Susan
Akram, Ahsan R.
Dhaliwal, Kev
Henderson, Robert K.
Girkin, John M.
Bradley, Mark
Full spectrum fluorescence lifetime imaging with 0.5 nm spectral and 50 ps temporal resolution
title Full spectrum fluorescence lifetime imaging with 0.5 nm spectral and 50 ps temporal resolution
title_full Full spectrum fluorescence lifetime imaging with 0.5 nm spectral and 50 ps temporal resolution
title_fullStr Full spectrum fluorescence lifetime imaging with 0.5 nm spectral and 50 ps temporal resolution
title_full_unstemmed Full spectrum fluorescence lifetime imaging with 0.5 nm spectral and 50 ps temporal resolution
title_short Full spectrum fluorescence lifetime imaging with 0.5 nm spectral and 50 ps temporal resolution
title_sort full spectrum fluorescence lifetime imaging with 0.5 nm spectral and 50 ps temporal resolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595732/
https://www.ncbi.nlm.nih.gov/pubmed/34785666
http://dx.doi.org/10.1038/s41467-021-26837-0
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