4.7 Article

Physico-Chemical Characterization of a Highly Rigid Gd(III) Complex Formed with a Phenanthroline Derivative Ligand

期刊

INORGANIC CHEMISTRY
卷 61, 期 34, 页码 13497-13509

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.2c02050

关键词

-

资金

  1. Hungarian National Research, Development and Innovation Office [PD-135169, FK-134551, K-128201, K-139140]
  2. bilateral Hungarian-Spanish Science and Technology Cooperation Program [2019-2.1.11-TET-2019-00084]
  3. New National Excellence Program [UNKP-21-5, UNKP-21-4-II]
  4. Ministerio de Ciencia e Innovacion [PID2019-104626GB-I00]
  5. Janos Bolyai Research Scholarship of the Hungarian Academy of Sciences
  6. Gedeon Richter's Talentum Foundation by Gedeon Richter Plc (GedeonRichter Ph.D. Fellowship)
  7. Ministry of Innovation and Technology from the National Research, Development and Innovation Fund (NKFIH)
  8. National Research, Development and Innovation Fund of Hungary [TKP2020-NKA-04]

向作者/读者索取更多资源

This article introduces a stable Gd(III) complex designed using a phenanthroline ligand, which exhibits high relaxivity and fluorescence lifetime in MRI imaging. This ligand has the potential to be used in the design of safer Gd(III) contrast agents.
The discovery of the nephrogenic systemic fibrosis (NSF) and its link with the in vivo dissociation of certain Gd(III)-based contrast agents (CAs) applied in the magnetic resonance imaging (MRI) induced a still growing research to replace the compromised agents with safer alternatives. In recent years, several ligands were designed to exploit the luminescence properties of the lanthanides, containing structurally constrained aromatic moieties, which may form rigid Gd(III) complexes. One of these ligands is (1,10-phenanthroline-2,9-diyl)bis(methyliminodiacetic acid) (H4FENTA) de-signed and synthesized to sensitize Eu(III) and Tb(III) luminescence. Our results show that the conditional stability of the [Gd(FENTA)]- chelate calculated for physiological pH (pGd = 19.7) is similar to those determined for [Gd(DTPA)]2- (pGd = 19.4) and [Gd(DOTA)]- (pGd = 20.1), routinely used in the clinical practice. The [Gd(FENTA)]- complex is remarkably inert with respect to its dissociation (t1/2 = 872 days at pH = 7 and 25 ?); furthermore, its relaxivity values determined at different field strengths and temperatures (e.g., r1p = 4.3 mM-1s-1at 60 MHz and 37 ?) are ca. one unit higher than those of [Gd(DTPA)]2- (r1p = 3.4 mM-1 s-1) and [Gd(DOTA)]- (r1p = 3.1 mM-1 s-1) under the same conditions. Moreover, significant improvement on the relaxivity was observed in the presence of serum proteins (r1p = 6.9 mM-1 s-1 at 60 MHz and 37 & DEG;C). The luminescence lifetimes recorded in H2O and D2O solutions indicate the presence of a water molecule (q = 1) in the inner sphere of the complex directly coordinated to the metal ion, possessing a relatively high water exchange rate (kex298 = 29(2) x 106 s(-1)). The acceleration of the water exchange can be explained by the steric compression around the water binding site due to the rigid structure of the complex, which was supported by DFT calculations. On the basis of these results, ligands containing a phenanthroline platform have great potential in the design of safer Gd(III) agents for MRI.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据