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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8309178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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