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Synthesis and Evaluation of [67Ga]-AMD3100: A Novel Imaging Agent for Targeting the Chemokine Receptor CXCR4
Authors:Ayuob Aghanejad  Amir R. Jalilian  Yousef Fazaeli  Behrouz Alirezapoor  Mehraban Pouladi  Davoud Beiki  Stephan Maus  Ali Khalaj
Affiliation:1.Research Center for Nuclear Medicine, Tehran University of Medical Sciences, Tehran, Iran.;2.Department of Nuclear Pharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.;3.Radiation Application Research School, Nuclear Science and Technology Research Institute, Tehran, 11365-3486, Iran.;4.Clinic of Nuclear Medicine, University Medical Centre Mainz, Langenbeckstr. 1, D-55131 Mainz, Germany.
Abstract:In order to develop a possible C-X-C chemokine receptor type 4 (CXCR4) imaging agent for oncological scintigraphy, [67Ga]-labeled 1,1′-[1,4-Phenylene-bis(methylene)]bis(1,4,8,11-tetraazacyclotetradecane) ([67Ga]-AMD3100) was prepared by using [67Ga]GaCl3 and AMD-3100 for 2 h at 50 °C (radiochemical purity: >95% ITLC, >99% HPLC, specific activity: 1800–2000 TBq/mmol) in acetate buffer. The stability of the complex was checked in the presence of human serum (37 °C) and in the final formulation for four days. The biodistribution of the labeled compound in the vital organs of wild type Sprague-Dawley rats was determined and compared with that of the free Ga3+ cation up to 48 h. Considering the spleen as the target organ, the best target:non target ratios were obtained 48 h post-injection (spleen:blood ratio; 14.5 and spleen:muscle ratio; 88.4). Initial SPECT images and biodistribution results in the wild type rats matched each other and demonstrated rapid washout of the tracer from the urinary tract. SPECT images in human breast carcinoma-bearing mice demonstrated a detectable tumor uptake in 48 h post-injection.
Keywords:Gallium-67   CXCR4   Biodistribution   SPECT   Breast carcinoma
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