Improved Redox-Responsive Cobalt(II) 19F Magnetic Resonance Imaging Agents through Addition of Hydrogen Bond Donors

被引：0

作者：

Scott, Kathleen M. ^{[1
]}

Davenport, Brooke L. ^{[1
]}

Vasylevskyi, Serhii ^{[1
]}

Que, Emily L. ^{[1
]}

机构：

[1] Univ Texas Austin, Dept Chem, Austin, TX 78712 USA

来源：

INORGANIC CHEMISTRY | 2025年 / 64卷 / 22期

基金：

美国国家科学基金会;

关键词：

MRI CONTRAST; MACROCYCLIC COMPLEXES; METAL-COMPLEXES; CHEMICAL-SHIFT; COORDINATION; TEMPERATURE; RELAXIVITY; MECHANISM; TRACKING; IRON(II);

D O I：

10.1021/acs.inorgchem.5c01465

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Redox regulation through reactive oxygen species (ROS) is an essential component of the inflammatory response. ROS can be sensed by 19F magnetic resonance spectroscopy and imaging using redox-active cobalt macrocycles with an appended fluorine tag. The sensitivity of these cobalt complexes was investigated by altering the identity of the oxygen donor (hydroxypropyl, carboxylate, dimethyl amide, and acetamide) attached to the triazacyclononane scaffold. A distinct shift in the 19F MR frequency between the Co2+ and Co3+ states (6-10 ppm) allows for robust imaging of the probes before and after oxidation using selective pulse sequences. Of these complexes, [Co(II)HP] 2+ exhibited an enhanced sensitivity to ROS when comparing burst kinetics and steady state oxidation through the glucose oxidase enzyme (GOX). This sensitivity corresponded with an increased fractional q value and enhanced interactions between Co2+ and 17O nuclei, which are indicative of a strong hydrogen bonding network in the secondary coordination sphere.

引用

页码：11130 / 11138

页数：9

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