Radiosynthesis and biodistribution studies of [62Zn/62Cu]-plerixafor complex as a novel in vivo PET generator for chemokine receptor imaging

被引:39
作者
Aghanejad, Ayuob [1 ,2 ]
Jalilian, Amir R. [3 ]
Fazaeli, Yousef [3 ]
Beiki, Davood [1 ]
Fateh, Behrooz [4 ]
Khalaj, Ali [5 ]
机构
[1] Univ Tehran Med Sci, Res Ctr Nucl Med, Tehran, Iran
[2] Univ Tehran Med Sci, Dept Radiopharm, Fac Pharm, Tehran, Iran
[3] Nucl Sci & Technol Res Inst, Tehran 113653486, Iran
[4] Swinburne Univ Technol, Fac Engn & Ind Sci H38, Hawthorn, Vic 3122, Australia
[5] Univ Tehran Med Sci, Dept Med Chem, Fac Pharm, Tehran, Iran
关键词
Zn-62; Production; AMD-3100; Radiolabeling; Biodistribution; Co-incidence imaging; EXCITATION-FUNCTIONS; PROTON-BOMBARDMENT; CXCR4; CANCER; ZN-62; XENOGRAFTS; EXPRESSION; AMD3100; COPPER;
D O I
10.1007/s10967-013-2822-2
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In order to develop a possible C-X-C chemokine receptor type 4 (CXCR4) imaging agent for oncological scintigraphy, [Zn-62]labeled 1,1'-[1,4-phenylenebis(methylene)]bis-1,4,8,11-tetraazacyclotetradecane ([Zn-62]-AMD3100) was prepared using in-house made [Zn-62]ZnCl2 and AMD-3100 for 1 h at 50 degrees C (radiochemical purity: >97 % ITLC, >96 % HPLC, specific activity: 20-22 GBq/mmol) in acetate buffer. The complex showed highly hydrophilic properties (log P = -1.114). Stability of the complex was checked in presence of human serum (37 degrees C) and in final formulation for 1 day. The biodistribution of the labeled compound in vital organs of wild-type Sprague-Dawdley rats were determined and compared with that of free Zn2+ cation up to 6 h. Co-incidence imaging of the complex was consistent with the distribution data up to 3 h. The complex can be a possible in vivo generator compound for PET imaging in CXCR4 positive tumors.
引用
收藏
页码:1635 / 1644
页数:10
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