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Siderophores for molecular imaging applications

This review covers publications on siderophores applied for molecular imaging applications, mainly for radionuclide-based imaging. Siderophores are low molecular weight chelators produced by bacteria and fungi to scavenge essential iron. Research on these molecules has a continuing history over the...

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Autores principales: Petrik, Milos, Zhai, Chuangyan, Haas, Hubertus, Decristoforo, Clemens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269471/
https://www.ncbi.nlm.nih.gov/pubmed/28138436
http://dx.doi.org/10.1007/s40336-016-0211-x
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author Petrik, Milos
Zhai, Chuangyan
Haas, Hubertus
Decristoforo, Clemens
author_facet Petrik, Milos
Zhai, Chuangyan
Haas, Hubertus
Decristoforo, Clemens
author_sort Petrik, Milos
collection PubMed
description This review covers publications on siderophores applied for molecular imaging applications, mainly for radionuclide-based imaging. Siderophores are low molecular weight chelators produced by bacteria and fungi to scavenge essential iron. Research on these molecules has a continuing history over the past 50 years. Many biomedical applications have been developed, most prominently the use of the siderophore desferrioxamine (DFO) to tackle iron overload related diseases. Recent research described the upregulation of siderophore production and transport systems during infection. Replacing iron in siderophores by radionuclides, the most prominent Ga-68 for PET, opens approaches for targeted imaging of infection; the proof of principle has been reported for fungal infections using (68)Ga-triacetylfusarinine C (TAFC). Additionally, fluorescent siderophores and therapeutic conjugates have been described and may be translated to optical imaging and theranostic applications. Siderophores have also been applied as bifunctional chelators, initially DFO as chelator for Ga-67 and more recently for Zr-89 where it has become the standard chelator in Immuno-PET. Improved DFO constructs and bifunctional chelators based on cyclic siderophores have recently been developed for Ga-68 and Zr-89 and show promising properties for radiopharmaceutical development in PET. A huge potential from basic biomedical research on siderophores still awaits to be utilized for clinical and translational imaging.
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spelling pubmed-52694712017-02-01 Siderophores for molecular imaging applications Petrik, Milos Zhai, Chuangyan Haas, Hubertus Decristoforo, Clemens Clin Transl Imaging Review Article This review covers publications on siderophores applied for molecular imaging applications, mainly for radionuclide-based imaging. Siderophores are low molecular weight chelators produced by bacteria and fungi to scavenge essential iron. Research on these molecules has a continuing history over the past 50 years. Many biomedical applications have been developed, most prominently the use of the siderophore desferrioxamine (DFO) to tackle iron overload related diseases. Recent research described the upregulation of siderophore production and transport systems during infection. Replacing iron in siderophores by radionuclides, the most prominent Ga-68 for PET, opens approaches for targeted imaging of infection; the proof of principle has been reported for fungal infections using (68)Ga-triacetylfusarinine C (TAFC). Additionally, fluorescent siderophores and therapeutic conjugates have been described and may be translated to optical imaging and theranostic applications. Siderophores have also been applied as bifunctional chelators, initially DFO as chelator for Ga-67 and more recently for Zr-89 where it has become the standard chelator in Immuno-PET. Improved DFO constructs and bifunctional chelators based on cyclic siderophores have recently been developed for Ga-68 and Zr-89 and show promising properties for radiopharmaceutical development in PET. A huge potential from basic biomedical research on siderophores still awaits to be utilized for clinical and translational imaging. Springer Milan 2016-10-11 2017 /pmc/articles/PMC5269471/ /pubmed/28138436 http://dx.doi.org/10.1007/s40336-016-0211-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Review Article
Petrik, Milos
Zhai, Chuangyan
Haas, Hubertus
Decristoforo, Clemens
Siderophores for molecular imaging applications
title Siderophores for molecular imaging applications
title_full Siderophores for molecular imaging applications
title_fullStr Siderophores for molecular imaging applications
title_full_unstemmed Siderophores for molecular imaging applications
title_short Siderophores for molecular imaging applications
title_sort siderophores for molecular imaging applications
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269471/
https://www.ncbi.nlm.nih.gov/pubmed/28138436
http://dx.doi.org/10.1007/s40336-016-0211-x
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