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Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting

Atherosclerosis is a chronic progressive disease involving inflammatory events, such as the overexpression of adhesion molecules including the endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1). VCAM-1 is rapidly overexpressed in the first stages of atherosclerosis, thus representing a promising...

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Autores principales: Pastorino, Sara, Baldassari, Sara, Ailuno, Giorgia, Zuccari, Guendalina, Drava, Giuliana, Petretto, Andrea, Cossu, Vanessa, Marini, Cecilia, Alfei, Silvana, Florio, Tullio, Sambuceti, Gianmario, Caviglioli, Gabriele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8309178/
https://www.ncbi.nlm.nih.gov/pubmed/34371717
http://dx.doi.org/10.3390/pharmaceutics13071025
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author Pastorino, Sara
Baldassari, Sara
Ailuno, Giorgia
Zuccari, Guendalina
Drava, Giuliana
Petretto, Andrea
Cossu, Vanessa
Marini, Cecilia
Alfei, Silvana
Florio, Tullio
Sambuceti, Gianmario
Caviglioli, Gabriele
author_facet Pastorino, Sara
Baldassari, Sara
Ailuno, Giorgia
Zuccari, Guendalina
Drava, Giuliana
Petretto, Andrea
Cossu, Vanessa
Marini, Cecilia
Alfei, Silvana
Florio, Tullio
Sambuceti, Gianmario
Caviglioli, Gabriele
author_sort Pastorino, Sara
collection PubMed
description Atherosclerosis is a chronic progressive disease involving inflammatory events, such as the overexpression of adhesion molecules including the endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1). VCAM-1 is rapidly overexpressed in the first stages of atherosclerosis, thus representing a promising target for early atheroma detection. Two novel Positron Emission Tomography (PET) radiopharmaceuticals (MacroP and NAMP), based on the VCAM-1-binding peptide having sequence VHPKQHRGGSKGC, were synthesized and characterized. MacroP is derived from the direct conjugation of a DOTA derivative with the peptide, while NAMP is a biotin derivative conceived to be employed in a three-step pretargeting system, involving the use of a double-chelating derivative of DOTA. The identity of the newly synthesized radiopharmaceuticals was confirmed by mass spectrometry and, after radiolabeling with (68)Ga, both showed high radiochemical purity; in vitro tests on human umbilical vein endothelial cells evidenced their VCAM-1 binding ability, with higher radioactive uptake in the case of NAMP. Moreover, NAMP might also be employed in a theranostic approach in association with functionalized biotinylated nanoparticles.
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spelling pubmed-83091782021-07-25 Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting Pastorino, Sara Baldassari, Sara Ailuno, Giorgia Zuccari, Guendalina Drava, Giuliana Petretto, Andrea Cossu, Vanessa Marini, Cecilia Alfei, Silvana Florio, Tullio Sambuceti, Gianmario Caviglioli, Gabriele Pharmaceutics Article Atherosclerosis is a chronic progressive disease involving inflammatory events, such as the overexpression of adhesion molecules including the endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1). VCAM-1 is rapidly overexpressed in the first stages of atherosclerosis, thus representing a promising target for early atheroma detection. Two novel Positron Emission Tomography (PET) radiopharmaceuticals (MacroP and NAMP), based on the VCAM-1-binding peptide having sequence VHPKQHRGGSKGC, were synthesized and characterized. MacroP is derived from the direct conjugation of a DOTA derivative with the peptide, while NAMP is a biotin derivative conceived to be employed in a three-step pretargeting system, involving the use of a double-chelating derivative of DOTA. The identity of the newly synthesized radiopharmaceuticals was confirmed by mass spectrometry and, after radiolabeling with (68)Ga, both showed high radiochemical purity; in vitro tests on human umbilical vein endothelial cells evidenced their VCAM-1 binding ability, with higher radioactive uptake in the case of NAMP. Moreover, NAMP might also be employed in a theranostic approach in association with functionalized biotinylated nanoparticles. MDPI 2021-07-06 /pmc/articles/PMC8309178/ /pubmed/34371717 http://dx.doi.org/10.3390/pharmaceutics13071025 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pastorino, Sara
Baldassari, Sara
Ailuno, Giorgia
Zuccari, Guendalina
Drava, Giuliana
Petretto, Andrea
Cossu, Vanessa
Marini, Cecilia
Alfei, Silvana
Florio, Tullio
Sambuceti, Gianmario
Caviglioli, Gabriele
Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting
title Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting
title_full Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting
title_fullStr Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting
title_full_unstemmed Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting
title_short Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting
title_sort two novel pet radiopharmaceuticals for endothelial vascular cell adhesion molecule-1 (vcam-1) targeting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8309178/
https://www.ncbi.nlm.nih.gov/pubmed/34371717
http://dx.doi.org/10.3390/pharmaceutics13071025
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