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
相关论文
共 50 条
  • [1] Synthesis and 18F-labeling of the analogues of Omecamtiv Mecarbil as a potential cardiac myosin imaging agent with PET
    Zhang Mingru
    Mou Tiantian
    Zhao Zuoquan
    Peng Cheng
    Ma Yunchuan
    Zhang Xianzhong
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2013, 56 : S135 - S135
  • [2] Synthesis of [18F]fluorocholine analogues as a potential Imaging agent for PET studies
    Yu, KH
    Park, JH
    Yang, SD
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2004, 25 (04): : 506 - 510
  • [3] Synthesis of Precursors for 18F-Labeling of Folic Acid for PET Application
    Groehn, Viola
    Moser, Rudolf
    Ross, Tobias L.
    Betzel, Thomas
    Mueller, Cristina
    Schibli, Roger
    Ametamey, Simon
    SYNTHESIS-STUTTGART, 2011, (22): : 3639 - 3648
  • [4] Synthesis of [18F]Fluoroclofilium as a potential cardiac imaging agent for PET studies
    Yu, KH
    Kim, YS
    Kim, SW
    Park, SW
    Park, JH
    Yang, SD
    Herdering, W
    Knoechel, A
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2003, 46 (12): : 1151 - 1160
  • [5] One step 18F-Labeling of Complex Peptides for Functional PET Imaging
    Li, Ying
    Liu, Zhibo
    Wang, May
    Lozada, Jerome
    Lin, Kuo-Shyan
    Yapp, Donald
    Benard, Francois
    Perrin, David
    BIOPOLYMERS, 2013, 100 (03) : 242 - 242
  • [6] Pretargeted PET imaging using a dual click 18F-labeling strategy
    Steen, Johanna
    Denk, Christoph
    Jorgensen, Jesper
    Norregard, Kamilla
    Rossin, Raffaella
    Wilkovitsch, Martin
    Svatunek, Dennis
    Edem, Patricia
    Kuntner, Claudia
    Wanek, Thomas
    Robillard, Marc
    Kristensen, Jesper
    Kjaer, Andreas
    Mikula, Hannes
    Herth, Matthias
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2019, 62 : S22 - S23
  • [7] Rapid, one step aqueous 18F-labeling of peptides for PET imaging
    Perrin, David M.
    Li, Ying
    Ting, Richard
    Harwig, Curtis W.
    Keller, Ulrich Auf Dem
    Bellac, Caroline L.
    Lange, Philipp F.
    Inkster, James A. H.
    Schaffer, Paul
    Adam, Michael J.
    Ruth, Thomas J.
    Overall, Christopher M.
    Benard, Francois
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
  • [8] Arylfluoroborates and alkylfluorosilicates as potential PET imaging agents:: High-yielding aqueous biomolecular 18F-labeling
    Ting, R
    Adam, MJ
    Ruth, TJ
    Perrin, DM
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (38) : 13094 - 13095
  • [9] Kit-like 18F-labeling of an estradiol derivative as a potential PET imaging agent for estrogen receptor-positive breast cancer
    Guiqing Liu
    Wei Wang
    Jianguo Lin
    Ke Li
    Gaochao Lv
    Xueyu Zhao
    Shanshan Wang
    Shineng Luo
    Ling Qiu
    Journal of Radioanalytical and Nuclear Chemistry, 2017, 312 : 599 - 607
  • [10] Kit-like 18F-labeling of an estradiol derivative as a potential PET imaging agent for estrogen receptor-positive breast cancer
    Liu, Guiqing
    Wang, Wei
    Lin, Jianguo
    Li, Ke
    Lv, Gaochao
    Zhao, Xueyu
    Wang, Shanshan
    Luo, Shineng
    Qiu, Ling
    JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY, 2017, 312 (03) : 599 - 607