Two Novel PET Radiopharmaceuticals for Endothelial Vascular Cell Adhesion Molecule-1 (VCAM-1) Targeting.
Sara PastorinoSara BaldassariGiorgia AilunoGuendalina ZuccariGiuliana DravaAndrea PetrettoVanessa CossuCecilia MariniSilvana AlfeiTullio FlorioGianmario SambucetiGabriele CaviglioliPublished in: Pharmaceutics (2021)
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.
Keyphrases
- cell adhesion
- pet ct
- positron emission tomography
- endothelial cells
- pet imaging
- computed tomography
- mass spectrometry
- cardiovascular disease
- multiple sclerosis
- liquid chromatography
- high resolution
- water soluble
- high glucose
- oxidative stress
- cell proliferation
- cancer therapy
- dna binding
- cystic fibrosis
- quantum dots
- cell migration
- oxide nanoparticles