Department of Chemistry, KU Leuven, Celestijnlaan 200F, Heverlee 3001, Belgium.
Chem Commun (Camb). 2018 Nov 15;54(92):12986-12989. doi: 10.1039/c8cc07092j.
A novel, reversible redox-active MRI probe, GdNR1, has been developed for the study of redox changes associated with diseased states. This system exhibits switching in relaxivity upon reduction and oxidation of the appended nicotinimidium. Relaxivity studies and cyclic voltammetry confirmed the impressive reversibility of this system, at a biologically-relevant reduction potential. A 2.5-fold increase in relaxivity was observed upon reduction of the complex, which corresponds to a change in the number of inner-sphere water molecules, as confirmed by luminescence lifetimes of the Eu(iii) analogue and NMRD studies. This is the first example of a redox-responsive MRI probe utilising the biologically-inspired nicotinimidium redox switch. In the future this strategy could enable the non-invasive identification of hypoxic tissue and related cardiovascular disease.
一种新型的、可还原的磁共振成像(MRI)探针 GdNR1 已经被开发出来,用于研究与疾病状态相关的氧化还原变化。该系统在附加的烟酰胺亚硝鎓还原和氧化时表现出弛豫率的切换。弛豫率研究和循环伏安法证实了该系统在生物学相关还原电位下的显著可逆性。复合物还原时,弛豫率增加了 2.5 倍,这对应于内球水分子数量的变化,Eu(iii)类似物的荧光寿命和 NMRD 研究证实了这一点。这是第一个利用生物启发的烟酰胺亚硝鎓氧化还原开关的氧化还原响应 MRI 探针的例子。在未来,这种策略可以实现对缺氧组织和相关心血管疾病的非侵入性识别。