High gastrin releasing peptide receptor (GRPR) expression is associated with numerous cancers including prostate and breast cancer. The aim of the current study was to develop a Co-labeled PET agent based on GRPR antagonist RM26 for visualization of GRPR-expressing tumors. Labeling with Co and Co, stability, binding specificity, and in vitro and in vivo characteristics of Co-NOTA-PEG-RM26 were studied. NOTA-PEG-RM26 was successfully radiolabeled with Co and Co with high yields and demonstrated high stability. The radiopeptide showed retained binding specificity to GRPR in vitro and in vivo. Co-NOTA-PEG-RM26 biodistribution in mice was characterized by rapid clearance of radioactivity from blood and normal non-GRPR-expressing organs and low hepatic uptake. The clearance was predominantly renal with a low degree of radioactivity reabsorption. Tumor-to-blood ratios were approximately 200 (3 h pi) and 1000 (24 h pi). The favorable biodistribution of cobalt-labeled NOTA-PEG-RM26 translated into high contrast preclinical PET/CT (using Co) and SPECT/CT (using Co) images of PC-3 xenografts. The initial biological results suggest that Co-NOTA-PEG-RM26 is a promising tracer for PET visualization of GRPR-expressing tumors.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612608 | PMC |
http://dx.doi.org/10.1155/2017/6873684 | DOI Listing |
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