68 Ga-DOTA-D-Alanine-BoroPro Radiotracer for Imaging of the Fibroblast Activation Protein in Malignant and Non-Malignant Diseases.
Diana Trujillo-BenítezMyrna Luna-GutiérrezJosé G Aguirre-De PazPedro Cruz-NovaGerardo Bravo-VillegasJoel E Vargas-AhumadaPaola Vallejo-ArmentaEnrique Morales-ÁvilaNallely Jiménez-MancillaRigoberto Oros-PantojaClara Leticia Santos CuevasErika Azorín-VegaBlanca Ocampo-GarciaGuillermina Ferro-FloresPublished in: Pharmaceutics (2024)
Recently, we reported a new fibroblast activation protein (FAP) inhibitor radiopharmaceutical based on the 99m Tc-((R)-1-((6-hydrazinylnicotinoyl)-D-alanyl) pyrrolidin-2-yl) boronic acid ( 99m Tc-HYNIC-D-Alanine-BoroPro)( 99m Tc-HYNIC-iFAP) structure for tumor microenvironment SPECT imaging. This research aimed to synthesize 68 Ga-[2,2',2″,2‴-(2-(4-(2-(5-(((S)-1-((S)-2-boronopyrrolidin-1-yl)-1-oxopropan-2-yl)carbamoyl)pyridin-2-yl)hydrazine-1-carbothioamido)benzyl)-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetrayl)tetraacetic acid] ( 68 Ga-DOTA-D-Alanine-BoroPro)( 68 Ga-iFAP) as a novel radiotracer for PET imaging and evaluate its usefulness for FAP expression in malignant and non-malignant tissues. The coupling of p-SCN-benzene DOTA with HYNIC-iFAP was used for the chemical synthesis and further labeling with 68 Ga. Radiochemical purity was verified by radio-HPLC. The specificity of 68 Ga-iFAP was evaluated in HCT116 cells, in which FAP expression was verified by immunofluorescence and Western blot. Biodistribution and biokinetic studies were performed in murine models. 68 Ga-iFAP uptake at the myocardial level was assessed in mice with induced infarction. First-in-human images of 68 Ga-iFAP in healthy subjects and patients with myocardial infarction, glioblastoma, prostate cancer, and breast cancer were also obtained. DOTA-D-Alanine BoroPro was prepared with a chemical purity of 98% and was characterized by UPLC mass spectroscopy, FT-IR, and UV-vis. The 68 Ga-iFAP was obtained with a radiochemical purity of >95%. In vitro and in vivo studies demonstrated 68 Ga-iFAP-specific recognition for FAP, rapid renal elimination, and adequate visualization of the glioblastoma, breast tumor, prostate cancer, and myocardial infarction sites. The results of this research justify further dosimetry and clinical trials to establish the specificity and sensitivity of 68 Ga-iFAP PET for FAP expression imaging.
Keyphrases
- pet ct
- pet imaging
- prostate cancer
- positron emission tomography
- poor prognosis
- clinical trial
- high resolution
- left ventricular
- heart failure
- radical prostatectomy
- binding protein
- type diabetes
- computed tomography
- young adults
- gene expression
- metabolic syndrome
- convolutional neural network
- cell proliferation
- endothelial cells
- single molecule
- atrial fibrillation
- induced apoptosis
- machine learning
- amino acid
- ionic liquid
- open label
- adipose tissue
- case control
- fluorescence imaging
- stress induced