Department of Chemistry, Portland State University, 1719 SW 10th Ave, Portland, OR, 97201, USA.
Dipartimento di Scienze e Innovazione Tecnologica, Università del Piemonte Orientale "Amedeo Avogadro", Alessandria I-15121, Italy.
Chem Commun (Camb). 2024 Mar 7;60(21):2898-2901. doi: 10.1039/d3cc05989h.
Enhancing the performance of Gd chelates as relaxation agents for MRI has the potential to lower doses, improving safety and mitigating the environmental impact on our surface waters. More than three decades of research into manipulating the properties of Gd have failed to develop a chelate that simultaneously optimizes all relevant parameters and affords maximal relaxivity. Introducing aryl substituents into the α-position of the pendant arms of a GdDOTA chelate affords chelates that, for the first time, simultaneously optimize all physico-chemical properties. Slowing tumbling by binding to human serum albumin affords a relaxivity of 110 ± 5 mM s, close to the maximum possible. As discrete chelates, these α-aryl substituted GdDOTA chelates exhibit relaxivities that are 2-3 times higher than those of currently used agents, even at the higher fields (1.5 & 3.0 T) used in modern clinical MRI.
增强 Gd 螯合物作为 MRI 弛豫剂的性能有可能降低剂量,提高安全性,并减轻对我们地表水的环境影响。三十多年来,人们一直在研究如何改变 Gd 的性质,但仍未能开发出一种同时优化所有相关参数并提供最大弛豫率的螯合物。在 GdDOTA 螯合物的侧臂的α-位置引入芳基取代基,可得到首次同时优化所有物理化学性质的螯合物。通过与人血清白蛋白结合来减缓旋转,可提供 110 ± 5 mM s 的弛豫率,接近可能的最大值。作为离散的螯合物,这些α-芳基取代的 GdDOTA 螯合物的弛豫率比目前使用的药物高 2-3 倍,即使在现代临床 MRI 中使用的更高磁场(1.5 和 3.0 T)也是如此。