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Towards Whole-Body Fluorescence Imaging in Humans
Dynamic near-infrared fluorescence (DNIF) whole-body imaging of small animals has become a popular tool in experimental biomedical research. In humans, however, the field of view has been limited to body parts, such as rheumatoid hands, diabetic feet or sentinel lymph nodes. Here we present a new wh...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877082/ https://www.ncbi.nlm.nih.gov/pubmed/24391820 http://dx.doi.org/10.1371/journal.pone.0083749 |
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author | Piper, Sophie K. Habermehl, Christina Schmitz, Christoph H. Kuebler, Wolfgang M. Obrig, Hellmuth Steinbrink, Jens Mehnert, Jan |
author_facet | Piper, Sophie K. Habermehl, Christina Schmitz, Christoph H. Kuebler, Wolfgang M. Obrig, Hellmuth Steinbrink, Jens Mehnert, Jan |
author_sort | Piper, Sophie K. |
collection | PubMed |
description | Dynamic near-infrared fluorescence (DNIF) whole-body imaging of small animals has become a popular tool in experimental biomedical research. In humans, however, the field of view has been limited to body parts, such as rheumatoid hands, diabetic feet or sentinel lymph nodes. Here we present a new whole-body DNIF-system suitable for adult subjects. We explored whether this system (i) allows dynamic whole-body fluorescence imaging and (ii) can detect modulations in skin perfusion. The non-specific fluorescent probe indocyanine green (ICG) was injected intravenously into two subjects, and fluorescence images were obtained at 5 Hz. The in- and out-flow kinetics of ICG have been shown to correlate with tissue perfusion. To validate the system, skin perfusion was modulated by warming and cooling distinct areas on the chest and the abdomen. Movies of fluorescence images show a bolus passage first in the face, then in the chest, abdomen and finally in the periphery (∼10, 15, 20 and 30 seconds, respectively). When skin perfusion is augmented by warming, bolus arrives about 5 seconds earlier than when the skin is cooled and perfusion decreased. Calculating bolus arrival times and spatial fitting of basis time courses extracted from different regions of interest allowed a mapping of local differences in subcutaneous skin perfusion. This experiment is the first to demonstrate the feasibility of whole-body dynamic fluorescence imaging in humans. Since the whole-body approach demonstrates sensitivity to circumscribed alterations in skinperfusion, it may be used to target autonomous changes in polyneuropathy and to screen for peripheral vascular diseases. |
format | Online Article Text |
id | pubmed-3877082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38770822014-01-03 Towards Whole-Body Fluorescence Imaging in Humans Piper, Sophie K. Habermehl, Christina Schmitz, Christoph H. Kuebler, Wolfgang M. Obrig, Hellmuth Steinbrink, Jens Mehnert, Jan PLoS One Research Article Dynamic near-infrared fluorescence (DNIF) whole-body imaging of small animals has become a popular tool in experimental biomedical research. In humans, however, the field of view has been limited to body parts, such as rheumatoid hands, diabetic feet or sentinel lymph nodes. Here we present a new whole-body DNIF-system suitable for adult subjects. We explored whether this system (i) allows dynamic whole-body fluorescence imaging and (ii) can detect modulations in skin perfusion. The non-specific fluorescent probe indocyanine green (ICG) was injected intravenously into two subjects, and fluorescence images were obtained at 5 Hz. The in- and out-flow kinetics of ICG have been shown to correlate with tissue perfusion. To validate the system, skin perfusion was modulated by warming and cooling distinct areas on the chest and the abdomen. Movies of fluorescence images show a bolus passage first in the face, then in the chest, abdomen and finally in the periphery (∼10, 15, 20 and 30 seconds, respectively). When skin perfusion is augmented by warming, bolus arrives about 5 seconds earlier than when the skin is cooled and perfusion decreased. Calculating bolus arrival times and spatial fitting of basis time courses extracted from different regions of interest allowed a mapping of local differences in subcutaneous skin perfusion. This experiment is the first to demonstrate the feasibility of whole-body dynamic fluorescence imaging in humans. Since the whole-body approach demonstrates sensitivity to circumscribed alterations in skinperfusion, it may be used to target autonomous changes in polyneuropathy and to screen for peripheral vascular diseases. Public Library of Science 2013-12-31 /pmc/articles/PMC3877082/ /pubmed/24391820 http://dx.doi.org/10.1371/journal.pone.0083749 Text en © 2013 Piper et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Piper, Sophie K. Habermehl, Christina Schmitz, Christoph H. Kuebler, Wolfgang M. Obrig, Hellmuth Steinbrink, Jens Mehnert, Jan Towards Whole-Body Fluorescence Imaging in Humans |
title | Towards Whole-Body Fluorescence Imaging in Humans |
title_full | Towards Whole-Body Fluorescence Imaging in Humans |
title_fullStr | Towards Whole-Body Fluorescence Imaging in Humans |
title_full_unstemmed | Towards Whole-Body Fluorescence Imaging in Humans |
title_short | Towards Whole-Body Fluorescence Imaging in Humans |
title_sort | towards whole-body fluorescence imaging in humans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877082/ https://www.ncbi.nlm.nih.gov/pubmed/24391820 http://dx.doi.org/10.1371/journal.pone.0083749 |
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