Coordination Chemistry of Bifunctional Chemical Agents Designed for Applications in 64Cu PET Imaging for Alzheimer's Disease

被引:44
|
作者
Sharma, Anuj K. [1 ,3 ]
Schultz, Jason W. [1 ]
Prior, John T. [1 ]
Rath, Nigam P. [2 ]
Mirica, Liviu M. [1 ]
机构
[1] Washington Univ, Dept Chem, One Brookings Dr, St Louis, MO 63130 USA
[2] Univ Missouri, Dept Chem & Biochem, One Univ Blvd, St Louis, MO 63121 USA
[3] Cent Univ Rajasthan, Dept Chem, NH-8, Bandar Sindri 305801, Ajmer, India
关键词
POSITRON-EMISSION-TOMOGRAPHY; BETA-AMYLOID PLAQUES; IN-VIVO STABILITY; COPPER-64; RADIOPHARMACEUTICALS; TETRAAZAMACROCYCLIC COMPLEXES; ELECTRONIC-PROPERTIES; PEPTIDE AGGREGATION; A-BETA(42) PEPTIDE; CELLULAR TOXICITY; PENDANT ARMS;
D O I
10.1021/acs.inorgchem.7b01883
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Positron emission tomography (PET) is emerging as one of the most important diagnostic tools for brain imaging, yet the most commonly used radioisotopes in PET imaging, C-11 and F-18, have short half-lives, and their usage is thus somewhat limited. By comparison, the Cu-11 radionuclide has a half-life of 12.7 h, which is ideal for administering and imaging purposes. In spite of appreciable research efforts, high-affinity copper chelators suitable for brain imaging applications are still lacking. Herein, we present the synthesis and characterization of a series of bifunctional compounds (BFCs) based on macrocyclic 1,4,7-triazacyclononane and 2,11-diaza[3.3](2,6)pyridinOphane ligand frameworks that exhibit a high affinity for Cu2+ ions. In addition, these BFCs contain a 2-phenylbenzothiazole fragment that is known to interact tightly with amyloid,6 fibrillar aggregates. Determination of the protonation constants (plc values) and stability constants (log beta values) of these BFCs, as well as characterization of the isolated copper complexes using X-ray crystallography, electron paramagnetic resonance spectroscopy, and electrochemical studies, suggests that these BFCs exhibit desirable properties for the development of novel Cu-64 PET imaging agents for Alzheimer's disease.
引用
收藏
页码:13801 / 13814
页数:14
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