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Selecting optimal spectral bands for improved detection of autofluorescent biomarkers in multiphoton microscopy

Significance: In multiphoton microscopy, two-photon excited fluorescence (TPEF) spectra carry valuable information on morphological and functional biological features. For measuring these biomarkers, separation of different parts of the fluorescence spectrum into channels is typically achieved by th...

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Autores principales: Meyer, Björn-Ole, Stella, M. Pilar J., Holst, Bjørn, Nielsen, Boye S., Holmstrøm, Kim, Andersen, Peter E., Marti, Dominik
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/PMC7338838/
https://www.ncbi.nlm.nih.gov/pubmed/32638570
http://dx.doi.org/10.1117/1.JBO.25.7.071206
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author Meyer, Björn-Ole
Stella, M. Pilar J.
Holst, Bjørn
Nielsen, Boye S.
Holmstrøm, Kim
Andersen, Peter E.
Marti, Dominik
author_facet Meyer, Björn-Ole
Stella, M. Pilar J.
Holst, Bjørn
Nielsen, Boye S.
Holmstrøm, Kim
Andersen, Peter E.
Marti, Dominik
author_sort Meyer, Björn-Ole
collection PubMed
description Significance: In multiphoton microscopy, two-photon excited fluorescence (TPEF) spectra carry valuable information on morphological and functional biological features. For measuring these biomarkers, separation of different parts of the fluorescence spectrum into channels is typically achieved by the use of optical band pass filters. However, spectra from different biomarkers can be unknown or overlapping, creating a crosstalk in between the channels. Previously, establishing these channels relied on prior knowledge or heuristic testing. Aim: The presented method aims to provide spectral bands with optimal separation between groups of specimens expressing different biomarkers. Approach: We have developed a system capable of resolving TPEF with high spectral resolution for the characterization of biomarkers. In addition, an algorithm is created to simulate and optimize optical band pass filters for fluorescence detection channels. To demonstrate the potential improvements in cell and tissue classification using these optimized channels, we recorded spectrally resolved images of cancerous (HT29) and normal epithelial colon cells (FHC), cultivated in 2D layers and in 3D to form spheroids. To provide an example of an application, we relate the results with the widely used redox ratio. Results: We show that in the case of two detection channels, our system and algorithm enable the selection of optimized band pass filters without the need of knowing involved fluorophores. An improvement of 31,5% in separating different 2D cell cultures is achieved, compared to using established spectral bands that assume NAD(P)H and FAD as main contributors of autofluorescence. The compromise is a reduced SNR in the images. Conclusions: We show that the presented method has the ability to improve imaging contrast and can be used to tailor a given label-free optical imaging system using optical band pass filters targeting a specific biomarker or application.
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spelling pubmed-73388382020-07-14 Selecting optimal spectral bands for improved detection of autofluorescent biomarkers in multiphoton microscopy Meyer, Björn-Ole Stella, M. Pilar J. Holst, Bjørn Nielsen, Boye S. Holmstrøm, Kim Andersen, Peter E. Marti, Dominik J Biomed Opt Special Section on Selected Topics in Biophotonics: Fluorescence Lifetime Imaging and Optical Micromechanics Significance: In multiphoton microscopy, two-photon excited fluorescence (TPEF) spectra carry valuable information on morphological and functional biological features. For measuring these biomarkers, separation of different parts of the fluorescence spectrum into channels is typically achieved by the use of optical band pass filters. However, spectra from different biomarkers can be unknown or overlapping, creating a crosstalk in between the channels. Previously, establishing these channels relied on prior knowledge or heuristic testing. Aim: The presented method aims to provide spectral bands with optimal separation between groups of specimens expressing different biomarkers. Approach: We have developed a system capable of resolving TPEF with high spectral resolution for the characterization of biomarkers. In addition, an algorithm is created to simulate and optimize optical band pass filters for fluorescence detection channels. To demonstrate the potential improvements in cell and tissue classification using these optimized channels, we recorded spectrally resolved images of cancerous (HT29) and normal epithelial colon cells (FHC), cultivated in 2D layers and in 3D to form spheroids. To provide an example of an application, we relate the results with the widely used redox ratio. Results: We show that in the case of two detection channels, our system and algorithm enable the selection of optimized band pass filters without the need of knowing involved fluorophores. An improvement of 31,5% in separating different 2D cell cultures is achieved, compared to using established spectral bands that assume NAD(P)H and FAD as main contributors of autofluorescence. The compromise is a reduced SNR in the images. Conclusions: We show that the presented method has the ability to improve imaging contrast and can be used to tailor a given label-free optical imaging system using optical band pass filters targeting a specific biomarker or application. Society of Photo-Optical Instrumentation Engineers 2020-07-07 2020-07 /pmc/articles/PMC7338838/ /pubmed/32638570 http://dx.doi.org/10.1117/1.JBO.25.7.071206 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 on Selected Topics in Biophotonics: Fluorescence Lifetime Imaging and Optical Micromechanics
Meyer, Björn-Ole
Stella, M. Pilar J.
Holst, Bjørn
Nielsen, Boye S.
Holmstrøm, Kim
Andersen, Peter E.
Marti, Dominik
Selecting optimal spectral bands for improved detection of autofluorescent biomarkers in multiphoton microscopy
title Selecting optimal spectral bands for improved detection of autofluorescent biomarkers in multiphoton microscopy
title_full Selecting optimal spectral bands for improved detection of autofluorescent biomarkers in multiphoton microscopy
title_fullStr Selecting optimal spectral bands for improved detection of autofluorescent biomarkers in multiphoton microscopy
title_full_unstemmed Selecting optimal spectral bands for improved detection of autofluorescent biomarkers in multiphoton microscopy
title_short Selecting optimal spectral bands for improved detection of autofluorescent biomarkers in multiphoton microscopy
title_sort selecting optimal spectral bands for improved detection of autofluorescent biomarkers in multiphoton microscopy
topic Special Section on Selected Topics in Biophotonics: Fluorescence Lifetime Imaging and Optical Micromechanics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338838/
https://www.ncbi.nlm.nih.gov/pubmed/32638570
http://dx.doi.org/10.1117/1.JBO.25.7.071206
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