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Aza-BODIPY: A New Vector for Enhanced Theranostic Boron Neutron Capture Therapy Applications
Boron neutron capture therapy (BNCT) is a radiotherapeutic modality based on the nuclear capture of slow neutrons by stable (10)B atoms followed by charged particle emission that inducing extensive damage on a very localized level (<10 μm). To be efficient, a sufficient amount of (10)B should acc...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565158/ https://www.ncbi.nlm.nih.gov/pubmed/32854219 http://dx.doi.org/10.3390/cells9091953 |
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author | Kalot, Ghadir Godard, Amélie Busser, Benoît Pliquett, Jacques Broekgaarden, Mans Motto-Ros, Vincent Wegner, Karl David Resch-Genger, Ute Köster, Ulli Denat, Franck Coll, Jean-Luc Bodio, Ewen Goze, Christine Sancey, Lucie |
author_facet | Kalot, Ghadir Godard, Amélie Busser, Benoît Pliquett, Jacques Broekgaarden, Mans Motto-Ros, Vincent Wegner, Karl David Resch-Genger, Ute Köster, Ulli Denat, Franck Coll, Jean-Luc Bodio, Ewen Goze, Christine Sancey, Lucie |
author_sort | Kalot, Ghadir |
collection | PubMed |
description | Boron neutron capture therapy (BNCT) is a radiotherapeutic modality based on the nuclear capture of slow neutrons by stable (10)B atoms followed by charged particle emission that inducing extensive damage on a very localized level (<10 μm). To be efficient, a sufficient amount of (10)B should accumulate in the tumor area while being almost cleared from the normal surroundings. A water-soluble aza-boron-dipyrromethene dyes (BODIPY) fluorophore was reported to strongly accumulate in the tumor area with high and BNCT compatible Tumor/Healthy Tissue ratios. The clinically used (10)B-BSH (sodium borocaptate) was coupled to the water-soluble aza-BODIPY platform for enhanced (10)B-BSH tumor vectorization. We demonstrated a strong uptake of the compound in tumor cells and determined its biodistribution in mice-bearing tumors. A model of chorioallantoic membrane-bearing glioblastoma xenograft was developed to evidence the BNCT potential of such compound, by subjecting it to slow neutrons. We demonstrated the tumor accumulation of the compound in real-time using optical imaging and ex vivo using elemental imaging based on laser-induced breakdown spectroscopy. The tumor growth was significantly reduced as compared to BNCT with (10)B-BSH. Altogether, the fluorescent aza-BODIPY/(10)B-BSH compound is able to vectorize and image the (10)B-BSH in the tumor area, increasing its theranostic potential for efficient approach of BNCT. |
format | Online Article Text |
id | pubmed-7565158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75651582020-10-26 Aza-BODIPY: A New Vector for Enhanced Theranostic Boron Neutron Capture Therapy Applications Kalot, Ghadir Godard, Amélie Busser, Benoît Pliquett, Jacques Broekgaarden, Mans Motto-Ros, Vincent Wegner, Karl David Resch-Genger, Ute Köster, Ulli Denat, Franck Coll, Jean-Luc Bodio, Ewen Goze, Christine Sancey, Lucie Cells Article Boron neutron capture therapy (BNCT) is a radiotherapeutic modality based on the nuclear capture of slow neutrons by stable (10)B atoms followed by charged particle emission that inducing extensive damage on a very localized level (<10 μm). To be efficient, a sufficient amount of (10)B should accumulate in the tumor area while being almost cleared from the normal surroundings. A water-soluble aza-boron-dipyrromethene dyes (BODIPY) fluorophore was reported to strongly accumulate in the tumor area with high and BNCT compatible Tumor/Healthy Tissue ratios. The clinically used (10)B-BSH (sodium borocaptate) was coupled to the water-soluble aza-BODIPY platform for enhanced (10)B-BSH tumor vectorization. We demonstrated a strong uptake of the compound in tumor cells and determined its biodistribution in mice-bearing tumors. A model of chorioallantoic membrane-bearing glioblastoma xenograft was developed to evidence the BNCT potential of such compound, by subjecting it to slow neutrons. We demonstrated the tumor accumulation of the compound in real-time using optical imaging and ex vivo using elemental imaging based on laser-induced breakdown spectroscopy. The tumor growth was significantly reduced as compared to BNCT with (10)B-BSH. Altogether, the fluorescent aza-BODIPY/(10)B-BSH compound is able to vectorize and image the (10)B-BSH in the tumor area, increasing its theranostic potential for efficient approach of BNCT. MDPI 2020-08-25 /pmc/articles/PMC7565158/ /pubmed/32854219 http://dx.doi.org/10.3390/cells9091953 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kalot, Ghadir Godard, Amélie Busser, Benoît Pliquett, Jacques Broekgaarden, Mans Motto-Ros, Vincent Wegner, Karl David Resch-Genger, Ute Köster, Ulli Denat, Franck Coll, Jean-Luc Bodio, Ewen Goze, Christine Sancey, Lucie Aza-BODIPY: A New Vector for Enhanced Theranostic Boron Neutron Capture Therapy Applications |
title | Aza-BODIPY: A New Vector for Enhanced Theranostic Boron Neutron Capture Therapy Applications |
title_full | Aza-BODIPY: A New Vector for Enhanced Theranostic Boron Neutron Capture Therapy Applications |
title_fullStr | Aza-BODIPY: A New Vector for Enhanced Theranostic Boron Neutron Capture Therapy Applications |
title_full_unstemmed | Aza-BODIPY: A New Vector for Enhanced Theranostic Boron Neutron Capture Therapy Applications |
title_short | Aza-BODIPY: A New Vector for Enhanced Theranostic Boron Neutron Capture Therapy Applications |
title_sort | aza-bodipy: a new vector for enhanced theranostic boron neutron capture therapy applications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565158/ https://www.ncbi.nlm.nih.gov/pubmed/32854219 http://dx.doi.org/10.3390/cells9091953 |
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