Pyrazolyl conjugates of bombesin: a new tridentate ligand framework for the stabilization of fac-[M(CO)₃]⁺ moiety

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• 作者：Susana Alves ; Joao D.G. Correia ; Isabel Santos ; Bhadrasetty Veerendra ; Gary L. Sieckman ; Timothy J. Hoffman ; Tammy L. Rold ; Said Daibes Figueroa ; Lauren Retzloff ; Joseph McCrate et al.
• 关键词：Technetium ; Carbonyl ; Bombesin ; Conjugates
• 刊名：Nuclear Medicine and Biology
• 出版年：2006
• 出版时间：July 2006
• 年：2006
• 卷：33
• 期：5
• 页码：625-634
• 全文大小：478 K

文摘

We have described the synthesis of tridentate pyrazolyl ligand frameworks for coordination to the fac-[*M(CO)₃]⁺ metal fragment (*M=^186/188Re or ^99mTc). These ligands impart a degree of kinetic inertness on the metal center, warranting their study in biological systems. We herein report in vitro/in vivo radiolabeling investigations of a new series of pyrazolyl bombesin (BBN) conjugates radiolabeled via the Isolink kit. These new conjugates are based on the general structure [^99mTc-pyrazolyl-X-BBN[7–14]NH₂], where X=β-alanine, serylserylserine or glycylglycylglycine. The pyrazolyl ligand is a tridentate ligand framework that coordinates the metal center through nitrogen donor atoms. The results of these investigations demonstrate the ability of these new conjugates to specifically target the gastrin-releasing peptide receptor subtype 2, which is overexpressed on human prostate PC-3 cancerous tissues. Therefore, these studies suggest the tridentate pyrazolyl ligand framework to be an ideal candidate for the design and development of low-valent ^99mTc-based diagnostic radiopharmaceuticals based on BBN or other targeting vectors.