Background: Hepatic fibrosis is a progressive disease, which is reversible in the early stages. The current monitoring methods have notable limitations that pose a challenge to early detection. In this study, we evaluated the utility of [18F]AlF-ND-bisFAPI positron emission tomography imaging of fibroblast activation protein (FAP) to monitor the progression of liver fibrosis.
View Article and Find Full Text PDFRecently, we developed a bivalent prostate-specific membrane antigen (PSMA) radioligand ([F]AlF-Bi-PSMA), which showed higher tumor uptake and retention in PSMA-positive mouse models than the clinically used radioligands, [Ga]Ga-PSMA-11 and [F]PSMA-1007. Here, we developed two Lu-labeled bivalent PSMA ligands with (DOTA-Alb-Bi-PSMA) or without an albumin-binding motif (DOTA-Bi-PSMA) to enhance radiotherapeutic efficacy with minimal toxicity. The results demonstrated that both Lu-labeled bivalent radioligands showed good stability, high binding affinity, and PSMA-targeting specificity in vitro.
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