Synthesis and 18F-labeling of the analogues of Omecamtiv Mecarbil as a potential cardiac myosin imaging agent with PET

被引:3
|
作者
Zhang, Mingru [1 ]
Mou, Tiantian [1 ]
Zhao, Zuoquan [1 ]
Peng, Cheng [3 ]
Ma, Yunchuan [3 ]
Fang, Wei [4 ,5 ]
Zhang, Xianzhong [1 ,2 ]
机构
[1] Beijing Normal Univ, Coll Chem, Minist Educ, Key Lab Radiopharmaceut, Beijing 100875, Peoples R China
[2] Xiamen Univ, Sch Publ Hlth, Ctr Mol Imaging & Translat Med, Xiamen 361005, Peoples R China
[3] Capital Med Univ, PET Ctr, Xuan Wu Hosp, Beijing 100053, Peoples R China
[4] Chinese Acad Med Sci, Dept Nucl Med, Cardiovasc Inst, Beijing 100037, Peoples R China
[5] Chinese Acad Med Sci, Fu Wai Hosp, Beijing 100037, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
F-18-labeling; Positron emission tomography; Biodistribution; Cardiac myosin; Heart failure; SYSTOLIC HEART-FAILURE; POSITRON-EMISSION-TOMOGRAPHY; ANTIBODIES; ACTIVATION; EXPRESSION; DISCOVERY;
D O I
10.1016/j.nucmedbio.2013.02.013
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Introduction: Cardiac myosin is a potential molecular target for heart failure imaging since its changes can be used to assess the function of heart. In this study, two analogues of Omecamtiv Mecarbil, which is the first selective activator of cardiac myosin, were synthesized and radio-labeled with F-18. Then the radio-compounds were evaluated as potential cardiac myosin imaging agent. Methods: The labeling precursor and the nonradioactive compounds were synthesized and characterized by IR, H-1 NMR, C-13 NMR and MS analysis. By substituting bromo of precursors with F-18, the radiolabeled compounds [F-18]8 and [F-18]10 were prepared and further evaluated for their in vitro physicochemical properties, stabilities, protein binding assay and ex vivo biodistribution. Results: Starting with [F-18]F- Kryptofix 2.2.2./K2CO3 solution, the total reaction time for [F-18]8 and [F-18]10 was about 40 min respectively, with final high-performance liquid chromatography purification included. Typical decay-corrected radiochemical yield stayed at 12.47% +/- 3.30% (n = 8), the radiochemical purity, 98% or more. Their specific activity was estimated as 50 GBq/mu mol. Both [F-18]8 and [F-18]10 could be stable after incubation in water at room temperature and in serum or binding buffer at 37 degrees C for 3 h. Biodistribution in normal mice showed that both [F-18]8 and [F-18]10 have good heart uptake at 2 min post-injection time. Compound [F-18]10 has better heart retention and higher heart to background ratios than those of [F-18]8. In vitro protein binding assay demonstrates that [F-18]10 may have high affinity with myosin from bovine heart. Conclusion: [F-18]8 and [F-18]10 were synthesized with good radiochemical yield and high radiochemical purity (>98%). One of the compounds ([F-18]10) has higher bovine heart myosin binding affinity and better heart/liver ratio. It will be further evaluated as a potent cardiac myosin imaging agent in normal and systolic heart failure model with positron emission tomography in the future. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:689 / 696
页数:8
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