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Chiral Pyclen-Based Heptadentate Chelates as Highly Stable MRI Contrast Agents.

Yong JianGengshen MoWeiyuan XuYao LiuZhichao ZhangYinghui DingRuonan GaoJiao XuJiang ZhuKun ShuZhihan YanFabio CarniatoCarlos Platas-IglesiasFangfu YeMauro BottaLixiong Dai
Published in: Inorganic chemistry (2024)
In recent years, pyclen-based complexes have attracted a great deal of interest as magnetic resonance imaging (MRI) contrast agents (CAs) and luminescent materials, as well as radiopharmaceuticals. Remarkably, gadopiclenol, a Gd(III) bishydrated complex featuring a pyclen-based heptadentate ligand, received approval as a novel contrast agent for clinical MRI application in 2022. To maximize stability and efficiency, two novel chiral pyclen-based chelators and their complexes were developed in this study. Gd-X-PCTA-2 showed significant enhancements in both thermodynamic and kinetic stabilities compared to those of the achiral parent derivative Gd-PCTA . 1 H NMRD profiles reveal that both chiral gadolinium complexes ( Gd-X-PCTA-1 and Gd-X-PCTA-2 ) have a higher relaxivity than Gd-PCTA , while variable-temperature 17 O NMR studies show that the two inner-sphere water molecules have distinct residence times τ M a and τ M b . Furthermore, in vivo imaging demonstrates that Gd-X-PCTA-2 enhances the signal in the heart and kidneys of the mice, and the chiral Gd complexes exhibit the ability to distinguish between tumors and normal tissues in a 4T1 mouse model more efficiently than that of the clinical agent gadobutrol. Biodistribution studies show that Gd-PCTA and Gd-X-PCTA-2 are primarily cleared by a renal pathway, with 24 h residues of Gd-X-PCTA-2 in the liver and kidney being lower than those of Gd-PCTA .
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