A versatile fluorinated azamacrocyclic chelator enabling 18 F PET or 19 F MRI: a first step towards new multimodal and smart contrast agents.

Macrocyclic chelators play a central role in medical imaging and nuclear medicine owing to their unparalleled metal cation coordination abilities. Their functionalization by fluorinated groups is an attractive design, to combine their properties with those of ¹⁸ F for Positron Emission Tomography (PET) or natural ¹⁹ F for Magnetic Resonance Imaging (MRI), and access potential theranostic or smart medical imaging probes. For the first time, a compact fluorinated macrocyclic architecture has been synthesized, based on a cyclen chelator bearing additional pyridine coordinating units and simple methyltrifluoroborate prosthetic groups. This ligand and its corresponding model Zn(ii) complex were investigated to evaluate the ¹⁸ F-PET or ¹⁹ F MRI abilities provided by this novel molecular structure. The chelator and the complex were obtained via a simple and high-yielding synthetic route, present excellent solvolytic stability of the trifluoroborate groups at various pH, and provide facile late-stage ¹⁸ F-radiolabeling (up to 68% radiochemical yield with high activity) as well as a satisfying detection limit for ¹⁹ F MRI imaging (low mM range).
Competing Interests: There are no conflicts to declare.
(This journal is © The Royal Society of Chemistry.)