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Ga-DOTA-D-Alanine-BoroPro Radiotracer for Imaging of the Fibroblast Activation Protein in Malignant and Non-Malignant Diseases
Recently, we reported a new fibroblast activation protein (FAP) inhibitor radiopharmaceutical based on the [sup.99m]Tc-((R)-1-((6-hydrazinylnicotinoyl)-D-alanyl) pyrrolidin-2-yl) boronic acid ([sup.99m]Tc-HYNIC-D-Alanine-BoroPro)([sup.99m]Tc-HYNIC-iFAP) structure for tumor microenvironment SPECT ima...
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Published in: | Pharmaceutics 2024-04, Vol.16 (4) |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Recently, we reported a new fibroblast activation protein (FAP) inhibitor radiopharmaceutical based on the [sup.99m]Tc-((R)-1-((6-hydrazinylnicotinoyl)-D-alanyl) pyrrolidin-2-yl) boronic acid ([sup.99m]Tc-HYNIC-D-Alanine-BoroPro)([sup.99m]Tc-HYNIC-iFAP) structure for tumor microenvironment SPECT imaging. This research aimed to synthesize [sup.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] ([sup.68]Ga-DOTA-D-Alanine-BoroPro)([sup.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 [sup.68]Ga. Radiochemical purity was verified by radio-HPLC. The specificity of [sup.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. [sup.68]Ga-iFAP uptake at the myocardial level was assessed in mice with induced infarction. First-in-human images of [sup.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 [sup.68]Ga-iFAP was obtained with a radiochemical purity of >95%. In vitro and in vivo studies demonstrated [sup.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 [sup.68]Ga-iFAP PET for FAP expression imaging. |
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ISSN: | 1999-4923 1999-4923 |
DOI: | 10.3390/pharmaceutics16040532 |