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手性 Pyclen 基七齿螯合剂作为高稳定性 MRI 造影剂。

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

机构信息

Joint Centre of Translational Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, People's Republic of China 325035.

Joint Centre of Translational Medicine, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, People's Republic of China 325000.

出版信息

Inorg Chem. 2024 May 6;63(18):8462-8475. doi: 10.1021/acs.inorgchem.4c01028. Epub 2024 Apr 20.

Abstract

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. showed significant enhancements in both thermodynamic and kinetic stabilities compared to those of the achiral parent derivative . H NMRD profiles reveal that both chiral gadolinium complexes ( and ) have a higher relaxivity than , while variable-temperature O NMR studies show that the two inner-sphere water molecules have distinct residence times τ and τ. Furthermore, imaging demonstrates that 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 and are primarily cleared by a renal pathway, with 24 h residues of in the liver and kidney being lower than those of .

摘要

近年来,基于 pyclen 的配合物作为磁共振成像(MRI)造影剂(CA)和发光材料以及放射性药物引起了极大的关注。值得注意的是,gadopiclenol 是一种基于 pyclen 的七齿配位体的 Gd(III)双水合配合物,于 2022 年被批准为临床 MRI 应用的新型造影剂。为了最大限度地提高稳定性和效率,本研究开发了两种新型手性 pyclen 基螯合剂及其配合物。与非手性母体衍生物相比,它们显示出热力学和动力学稳定性的显著提高。H NMRD 谱表明,两种手性镧系元素配合物(和)的弛豫率均高于,而变温 O NMR 研究表明,两个内球水分子具有不同的停留时间 τ 和 τ。此外,MRI 成像表明,可增强小鼠心脏和肾脏的信号,并且手性 Gd 配合物在 4T1 小鼠模型中比临床试剂 gadobutrol 更有效地区分肿瘤和正常组织。生物分布研究表明,和主要通过肾脏途径清除,肝脏和肾脏中 24 h 的残留量低于。

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