Synthesis and Characterization of a Stable Copper(I) Complex for Radiopharmaceutical Applications

被引:10
|
作者
Bodio, Ewen [1 ,2 ]
Boujtita, Mohammed [1 ]
Julienne, Karine [1 ]
Le Saec, Patricia [3 ]
Gouin, Sebastien G. [1 ]
Hamon, Jonathan [4 ]
Renault, Eric [1 ]
Deniaud, David [1 ]
机构
[1] LUNAM Univ, UMR CNRS 6230, UFR Sci & Tech, F-44322 Nantes 3, France
[2] Univ Bourgogne, UMR CNRS 6302, Inst Chim Mol, F-21078 Dijon, France
[3] Univ Nantes, Inst Rech Therapeut, INSERM U892, Ctr Rech Cancerol Nantes Angers,UMR CNRS 6299, F-44093 Nantes 1, France
[4] IMN, Inst Mat Jean Rouxel, UMR CNRS 6502, UFR Sci & Tech, F-44322 Nantes 3, France
来源
CHEMPLUSCHEM | 2014年 / 79卷 / 09期
关键词
chelates; copper; density functional calculations; ligand design; radiopharmaceuticals; BIFUNCTIONAL CHELATORS; AGENTS; RADIONUCLIDES; NANOPARTICLES; CONJUGATION; STABILITY; LIGANDS; PEPTIDE; MODELS; CANCER;
D O I
10.1002/cplu.201402031
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A highly stable copper(I) complex was obtained starting from a copper(II) salt. This compound was characterized by a combination of several analytical techniques (UV/Vis spectroscopy, energy-dispersive X-ray spectroscopy, electrochemistry, and X-ray photoelectron spectroscopy) and was shown to present an N4Cu structure. These results were confirmed by a density functional calculations study of the binding energy and the electronic structure of model ligand and copper complexes. Preliminary tests of complexation showed a high ability of the corresponding ligand to chelate Cu-64 in very diluted medium, which is of interest for developing new positron emission tomography imaging agents. The stability and the kinetic inertness of the complex are promising. In particular, it displayed good redox stability, which is important because in vivo reduction or oxidation of the copper of Cu complexes can lead to demetalation. The rapid microwave-assisted strategy used to synthesize the ligand was applied to the synthesis of more than ten ligands. One of these was functionalized by an amino group to form a bifunctional chelate for a future bioconjugation for applications in nuclear medicine.
引用
收藏
页码:1284 / 1293
页数:10
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