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
  • [31] CLICK CHEMISTRY BASED 18F-LABELING AND GLYCOSYLATION OF AN RGD PEPTIDE FOR PET IMAGING OF αvβ3 INTEGRIN EXPRESSION
    Maschauer, S.
    Haubner, R.
    Hocke, C.
    Ocker, M.
    Kuwert, T.
    Prante, O.
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2009, 52 : S199 - S199
  • [32] Synthesis, 18F-labeling and radiopharmacological characterization of a claudin-targeting peptide
    Loeser, Reik
    Bader, Miriam
    Kuchar, Manuela
    Wodtke, Robert
    Bergmann, Ralf
    Lenk, Jens
    Haase-Kohn, Cathleen
    Pufe, Johanna
    Steinbach, Joerg
    Pietzsch, Jens
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2015, 58 : S205 - S205
  • [33] Synthesis and biological evaluation of 18F labeled tryptophan analogues as potential PET agents for tumor imaging
    Chiotellis, A.
    Mu, L.
    Selivanova, S.
    Mueller, A.
    Siebeneicher, H.
    Graham, K.
    Kraemer, S. D.
    Schibli, R.
    Ametamey, S. M.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2012, 39 : S169 - S169
  • [34] Synthesis of F-18 labelled 2,2-difluoroglucose as a potential imaging agent for PET
    Adam, MJ
    JOURNAL OF NUCLEAR MEDICINE, 1998, 39 (05) : 231P - 231P
  • [35] Direct 18F-labeling of peptides for imaging gastrin releasing peptide receptor expression
    Srinivasan, Ananth
    Borkowski, Sandra
    Graham, Keith
    Stellfeld, Timo
    AMINO ACIDS, 2009, 37 (01) : 38 - 38
  • [36] 18F-Talazoparib: A novel potential PET imaging agent of PARP
    Muzzioli, Riccardo
    Pisaneschi, Federica
    Rao, Yi
    Gammon, Seth
    Piwnica-Worms, David
    CANCER RESEARCH, 2022, 82 (12)
  • [37] [18F]Talazoparib: a novel potential PET imaging agent of PARP
    Muzzioli, Riccardo
    Pisaneschi, Federica
    Gammon, Seth
    Rao, Yi
    Piwnica-Worms, David
    NUCLEAR MEDICINE AND BIOLOGY, 2021, 96-97 : S7 - S8
  • [38] ONE-STEP 18F-LABELING OF BOMBESIN ANALOGS FOR PROSTATE CANCER IMAGING
    Mu, L.
    Becaud, J.
    Martic, M.
    Honer, M.
    Schubiger, P. A.
    Ametamey, S. M.
    Graham, K.
    Stellfeld, T.
    Lehmann, L.
    Suelzle, D.
    Dinkelborg, L.
    Srinivasan, A.
    JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2009, 52 : S150 - S150
  • [39] 2-Nitroimidazole-Furanoside Derivatives for Hypoxia Imaging-Investigation of Nucleoside Transporter Interaction, 18F-Labeling and Preclinical PET Imaging
    Maier, Florian C.
    Schweifer, Anna
    Damaraju, Vijaya L.
    Cass, Carol E.
    Bowden, Gregory D.
    Ehrlichmann, Walter
    Kneilling, Manfred
    Pichler, Bernd J.
    Hammerschmidt, Friedrich
    Reischl, Gerald
    PHARMACEUTICALS, 2019, 12 (01)
  • [40] Translating the concept of peptide labeling with 5-deoxy-5-[18F] fluororibose into preclinical practice: 18F-labeling of Siglec-9 peptide for PET imaging of inflammation
    Li, Xiang-Guo
    Autio, Anu
    Ahtinen, Helena
    Helariutta, Kerttuli
    Liljenback, Heidi
    Jalkanen, Sirpa
    Roivainen, Anne
    Airaksinen, Anu J.
    CHEMICAL COMMUNICATIONS, 2013, 49 (35) : 3682 - 3684