99mTc-labeling experiments on CCK4 by a direct method

被引:14
作者
Rossin, R
Blok, D
Visentin, R
Feitsma, RIJ
Giron, MC
Pauwels, EKJ [1 ]
Mazzi, U
机构
[1] Leiden Univ, Med Ctr, Dept Nucl Med, NL-2333 ZA Leiden, Netherlands
[2] Univ Padua, Dept Pharmaceut Sci, I-35131 Padua, Italy
[3] Univ Bari, CIRCMSB, I-70125 Bari, Italy
关键词
D O I
10.1016/S0969-8051(01)00254-2
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
Tc-99m-labeling studies have been performed on CCK, fragment of cholecystokinin, starting from Tc-99m-pertechnetate, by using tin(II)pyrophosphate or tin(II)gluconate as reducing agents, together with NaBH4 acting as a stabilizing agent of tin(II). Gluconate has been used as exchange ligand in the carrier added experiments and in the syntheses of Tc-99-CCK4 and Re-CCK4 complexes to be able to reproduce at macroscopic level the same chemical reactions occurring at non carrier added conditions. 99mTc-labeling yields higher than 95% have been achieved depending on Sn(II) concentration, CCK4/gluconate ratio, reaction time and applied temperature. The species produced with Tc-99m, Tc-99, and cold rhenium nuclides have been compared by means of HPLC measurements, which showed similar retention times and thus probably the same species in the three situations. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:865 / 873
页数:9
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