Srivastava Kriti, Weitz Evan A, Peterson Katie L, Marjańska Małgorzata, Pierre Valérie C
Department of Chemistry and ‡Center for Magnetic Resonance Research and Department of Radiology, University of Minnesota , Minneapolis, Minnesota 55455, United States.
Inorg Chem. 2017 Feb 6;56(3):1546-1557. doi: 10.1021/acs.inorgchem.6b02631. Epub 2017 Jan 17.
A series of fluorinated macrocyclic complexes, M-DOTAm-F12, where M is La, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Fe, was synthesized, and their potential as fluorine magnetic resonance imaging (MRI) contrast agents was evaluated. The high water solubility of these complexes and the presence of a single fluorine NMR signal, two necessary parameters for in vivo MRI, are substantial advantages over currently used organic polyfluorocarbons and other reported paramagnetic F probes. Importantly, the sensitivity of the paramagnetic probes on a per fluorine basis is at least 1 order of magnitude higher than that of diamagnetic organic probes. This increased sensitivity is due to a substantial-up to 100-fold-decrease in the longitudinal relaxation time (T) of the fluorine nuclei. The shorter T allows for a greater number of scans to be obtained in an equivalent time frame. The sensitivity of the fluorine probes is proportional to the T/T ratio. In water, the optimal metal complexes for imaging applications are those containing Ho and Fe, and to a lesser extent Tm and Yb. Whereas T of the lanthanide complexes are little affected by blood, the T are notably shorter in blood than in water. The sensitivity of Ln-DOTAm-F12 complexes is lower in blood than in water, such that the most sensitive complex in water, Ho-DOTAm-F12, could not be detected in blood. Tm yielded the most sensitive lanthanide fluorine probe in blood. Notably, the relaxation times of the fluorine nuclei of Fe-DOTAm-F12 are similar in water and in blood. That complex has the highest T/T ratio (0.57) and the lowest limit of detection (300 μM) in blood. The combination of high water solubility, single fluorine signal, and high T/T of M-DOTAm-F12 facilitates the acquisition of three-dimensional magnetic resonance images.
合成了一系列氟化大环配合物M-DOTAm-F12,其中M为La、Eu、Gd、Tb、Dy、Ho、Er、Tm、Yb和Fe,并评估了它们作为氟磁共振成像(MRI)造影剂的潜力。这些配合物的高水溶性以及单一氟核磁共振信号的存在,这是体内MRI的两个必要参数,相对于目前使用的有机多氟碳化合物和其他报道的顺磁性氟探针具有显著优势。重要的是,顺磁性探针基于每个氟的灵敏度比抗磁性有机探针至少高1个数量级。这种灵敏度的提高是由于氟原子核的纵向弛豫时间(T)大幅降低,降幅高达100倍。较短的T使得在相同时间框架内能够获得更多的扫描次数。氟探针的灵敏度与T/T比率成正比。在水中,用于成像应用的最佳金属配合物是含有Ho和Fe的那些,其次是Tm和Yb。镧系配合物的T受血液影响较小,而T在血液中明显比在水中短。Ln-DOTAm-F12配合物在血液中的灵敏度低于在水中,以至于在水中最敏感的配合物Ho-DOTAm-F12在血液中无法检测到。Tm在血液中产生了最敏感的镧系氟探针。值得注意的是,Fe-DOTAm-F12的氟原子核弛豫时间在水和血液中相似。该配合物在血液中具有最高的T/T比率(0.57)和最低的检测限(300μM)。M-DOTAm-F12的高水溶性、单一氟信号和高T/T的组合有助于获取三维磁共振图像。