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

  • Pharmaceutics. 2021 Jul 6;13(7):1025. doi: 10.3390/pharmaceutics13071025.
Sara Pastorino  1 Sara Baldassari  2 Giorgia Ailuno  2 Guendalina Zuccari  2 Giuliana Drava  2 Andrea Petretto  3 Vanessa Cossu  4  5 Cecilia Marini  4  5  6 Silvana Alfei  2 Tullio Florio  5  7 Gianmario Sambuceti  4  5 Gabriele Caviglioli  2
Affiliations
  • 1. Nuclear Medicine Unit, S. Andrea Hospital, via Vittorio Veneto 197, 19124 La Spezia, Italy.
  • 2. Department of Pharmacy, University of Genova, viale Cembrano 4, 16148 Genova, Italy.
  • 3. Core Facilities-Clinical Proteomics and Metabolomics, IRCCS Istituto Giannina Gaslini, via Gerolamo Gaslini 5, 16147 Genova, Italy.
  • 4. Department of Health Science, University of Genova-Nuclear Medicine Unit, via A. Pastore 1, 16132 Genova, Italy.
  • 5. IRCCS Ospedale Policlinico San Martino, Largo R. Benzi 10, 16132 Genova, Italy.
  • 6. CNR Institute of Bioimages and Molecular Physiology, via Fratelli Cervi 93, 20090 Segrate, Italy.
  • 7. Department of Internal Medicine, University of Genova, viale Benedetto XV 2, 16136 Genova, Italy.
Abstract

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 68Ga, 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.

Keywords
Gallium-68; PET; VCAM-1; avidin–biotin complex; imaging; inflammation; peptide; pretargeting; radiopharmaceuticals.
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