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Contrast enhanced high-resolution diffuse optical tomography of the human brain using ICG

Non-invasive diffuse optical tomography (DOT) of the adult brain has recently been shown to improve the spatial resolution for functional brain imaging applications. Here we show that high-resolution (HR) DOT is also advantageous for clinical perfusion imaging using an optical contrast agent. We pre...

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Detalles Bibliográficos
Autores principales: Habermehl, Christina, Schmitz, Christoph H., Steinbrink, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482886/
https://www.ncbi.nlm.nih.gov/pubmed/21935232
http://dx.doi.org/10.1364/OE.19.018636
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author Habermehl, Christina
Schmitz, Christoph H.
Steinbrink, Jens
author_facet Habermehl, Christina
Schmitz, Christoph H.
Steinbrink, Jens
author_sort Habermehl, Christina
collection PubMed
description Non-invasive diffuse optical tomography (DOT) of the adult brain has recently been shown to improve the spatial resolution for functional brain imaging applications. Here we show that high-resolution (HR) DOT is also advantageous for clinical perfusion imaging using an optical contrast agent. We present the first HR-DOT results with a continuous wave near infrared spectroscopy setup using a dense grid of optical fibers and indocyanine green (ICG) as an exogenic contrast agent. We find an early arrival of the ICG bolus in the intracerebral tissue and a delayed arrival of the bolus in the extracerebral tissue, achieving the separation of both layers. This demonstrates the method’s potential for brain perfusion monitoring in neurointensive care patients.
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spelling pubmed-34828862012-10-30 Contrast enhanced high-resolution diffuse optical tomography of the human brain using ICG Habermehl, Christina Schmitz, Christoph H. Steinbrink, Jens Opt Express Research-Article Non-invasive diffuse optical tomography (DOT) of the adult brain has recently been shown to improve the spatial resolution for functional brain imaging applications. Here we show that high-resolution (HR) DOT is also advantageous for clinical perfusion imaging using an optical contrast agent. We present the first HR-DOT results with a continuous wave near infrared spectroscopy setup using a dense grid of optical fibers and indocyanine green (ICG) as an exogenic contrast agent. We find an early arrival of the ICG bolus in the intracerebral tissue and a delayed arrival of the bolus in the extracerebral tissue, achieving the separation of both layers. This demonstrates the method’s potential for brain perfusion monitoring in neurointensive care patients. Optical Society of America 2011-09-08 /pmc/articles/PMC3482886/ /pubmed/21935232 http://dx.doi.org/10.1364/OE.19.018636 Text en ©2011 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.
spellingShingle Research-Article
Habermehl, Christina
Schmitz, Christoph H.
Steinbrink, Jens
Contrast enhanced high-resolution diffuse optical tomography of the human brain using ICG
title Contrast enhanced high-resolution diffuse optical tomography of the human brain using ICG
title_full Contrast enhanced high-resolution diffuse optical tomography of the human brain using ICG
title_fullStr Contrast enhanced high-resolution diffuse optical tomography of the human brain using ICG
title_full_unstemmed Contrast enhanced high-resolution diffuse optical tomography of the human brain using ICG
title_short Contrast enhanced high-resolution diffuse optical tomography of the human brain using ICG
title_sort contrast enhanced high-resolution diffuse optical tomography of the human brain using icg
topic Research-Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482886/
https://www.ncbi.nlm.nih.gov/pubmed/21935232
http://dx.doi.org/10.1364/OE.19.018636
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