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Fluorescence lifetime imaging ophthalmoscopy

Imaging techniques based on retinal autofluorescence have found broad applications in ophthalmology because they are extremely sensitive and noninvasive. Conventional fundus autofluorescence imaging measures fluorescence intensity of endogenous retinal fluorophores. It mainly derives its signal from...

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Autores principales: Dysli, Chantal, Wolf, Sebastian, Berezin, Mikhail Y., Sauer, Lydia, Hammer, Martin, Zinkernagel, Martin S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396320/
https://www.ncbi.nlm.nih.gov/pubmed/28673870
http://dx.doi.org/10.1016/j.preteyeres.2017.06.005
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author Dysli, Chantal
Wolf, Sebastian
Berezin, Mikhail Y.
Sauer, Lydia
Hammer, Martin
Zinkernagel, Martin S.
author_facet Dysli, Chantal
Wolf, Sebastian
Berezin, Mikhail Y.
Sauer, Lydia
Hammer, Martin
Zinkernagel, Martin S.
author_sort Dysli, Chantal
collection PubMed
description Imaging techniques based on retinal autofluorescence have found broad applications in ophthalmology because they are extremely sensitive and noninvasive. Conventional fundus autofluorescence imaging measures fluorescence intensity of endogenous retinal fluorophores. It mainly derives its signal from lipofuscin at the level of the retinal pigment epithelium. Fundus autofluorescence, however, can not only be characterized by the spatial distribution of the fluorescence intensity or emission spectrum, but also by a characteristic fluorescence lifetime function. The fluorescence lifetime is the average amount of time a fluorophore remains in the excited state following excitation. Fluorescence lifetime imaging ophthalmoscopy (FLIO) is an emerging imaging modality for in vivo measurement of lifetimes of endogenous retinal fluorophores. Recent reports in this field have contributed to our understanding of the pathophysiology of various macular and retinal diseases. Within this review, the basic concept of fluorescence lifetime imaging is provided. It includes technical background information and correlation with in vitro measurements of individual retinal metabolites. In a second part, clinical applications of fluorescence lifetime imaging and fluorescence lifetime features of selected retinal diseases such as Stargardt disease, age-related macular degeneration, choroideremia, central serous chorioretinopathy, macular holes, diabetic retinopathy, and retinal artery occlusion are discussed. Potential areas of use for fluorescence lifetime imaging ophthalmoscopy will be outlined at the end of this review.
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spelling pubmed-73963202020-08-03 Fluorescence lifetime imaging ophthalmoscopy Dysli, Chantal Wolf, Sebastian Berezin, Mikhail Y. Sauer, Lydia Hammer, Martin Zinkernagel, Martin S. Prog Retin Eye Res Article Imaging techniques based on retinal autofluorescence have found broad applications in ophthalmology because they are extremely sensitive and noninvasive. Conventional fundus autofluorescence imaging measures fluorescence intensity of endogenous retinal fluorophores. It mainly derives its signal from lipofuscin at the level of the retinal pigment epithelium. Fundus autofluorescence, however, can not only be characterized by the spatial distribution of the fluorescence intensity or emission spectrum, but also by a characteristic fluorescence lifetime function. The fluorescence lifetime is the average amount of time a fluorophore remains in the excited state following excitation. Fluorescence lifetime imaging ophthalmoscopy (FLIO) is an emerging imaging modality for in vivo measurement of lifetimes of endogenous retinal fluorophores. Recent reports in this field have contributed to our understanding of the pathophysiology of various macular and retinal diseases. Within this review, the basic concept of fluorescence lifetime imaging is provided. It includes technical background information and correlation with in vitro measurements of individual retinal metabolites. In a second part, clinical applications of fluorescence lifetime imaging and fluorescence lifetime features of selected retinal diseases such as Stargardt disease, age-related macular degeneration, choroideremia, central serous chorioretinopathy, macular holes, diabetic retinopathy, and retinal artery occlusion are discussed. Potential areas of use for fluorescence lifetime imaging ophthalmoscopy will be outlined at the end of this review. 2017-06-30 2017-09 /pmc/articles/PMC7396320/ /pubmed/28673870 http://dx.doi.org/10.1016/j.preteyeres.2017.06.005 Text en This is an open access article under the CC BY-NC-ND, license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Dysli, Chantal
Wolf, Sebastian
Berezin, Mikhail Y.
Sauer, Lydia
Hammer, Martin
Zinkernagel, Martin S.
Fluorescence lifetime imaging ophthalmoscopy
title Fluorescence lifetime imaging ophthalmoscopy
title_full Fluorescence lifetime imaging ophthalmoscopy
title_fullStr Fluorescence lifetime imaging ophthalmoscopy
title_full_unstemmed Fluorescence lifetime imaging ophthalmoscopy
title_short Fluorescence lifetime imaging ophthalmoscopy
title_sort fluorescence lifetime imaging ophthalmoscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396320/
https://www.ncbi.nlm.nih.gov/pubmed/28673870
http://dx.doi.org/10.1016/j.preteyeres.2017.06.005
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