New Tris(hydroxypyridinone) Bifunctional Chelators Containing Isothiocyanate Groups Provide a Versatile Platform for Rapid One Step Labeling and PET Imaging with 68Ga3+

被引:53
作者
Ma, Michelle T. [1 ]
Cullinane, Carleen [2 ,3 ]
Imberti, Cinzia [1 ]
Baguna Torres, Julia [1 ]
Terry, Samantha Y. A. [1 ]
Roselt, Peter [2 ]
Hicks, Rodney J. [2 ,3 ]
Blower, Philip J. [1 ]
机构
[1] St Thomas Hosp, Kings Coll London, Div Imaging Sci & Biomed Engn, Fourth Floor Lambeth Wing, London SE1 7EH, England
[2] Peter MacCallum Canc Ctr, East Melbourne, Vic 3002, Australia
[3] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic 3010, Australia
基金
英国工程与自然科学研究理事会; 英国惠康基金;
关键词
ALPHA(V)BETA(3) INTEGRIN EXPRESSION; NEUROENDOCRINE TUMORS; RGD PEPTIDE; RADIOPHARMACEUTICALS; LIGANDS; GALLIUM; RADIOSYNTHESIS; RADIOMETALS; ANTAGONISTS; COMPLEXES;
D O I
10.1021/acs.bioconjchem.5b00335
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Two new bifunctional tris(hydroxypyridinone) (THP) chelators designed specifically for rapid labeling with Ga-68 have been synthesized, each with pendant isothiocyanate groups and three 1,6-dimethyl-3-hydroxypyridin-4-one groups. Both compounds have been conjugated with the primary amine group of a cyclic integrin targeting peptide, RGD. Each conjugate can be radiolabeled and formulated by treatment with generator-produced Ga-68(3+) in over 95% radiochemical yield under ambient conditions in less than 5 min, with specific activities of 60-80 MBq nmol(-1). Competitive binding assays and in vivo biodistribution in mice bearing U87MG tumors demonstrate that the new Ga-68(3+)-labeled THP peptide conjugates retain affinity for the alpha(v)beta(3) integrin receptor, clear within 1-2 h from circulation, and undergo receptor mediated tumor uptake in vivo. We conclude that bifunctional THP chelators can be used for simple, efficient labeling of 68Ga biomolecules under mild conditions suitable for peptides and proteins.
引用
收藏
页码:309 / 318
页数:10
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