Transferrin conjugates of triazacyclononane-based bifunctional NE3TA chelates for PET imaging: Synthesis, Cu-64 radiolabeling, and in vitro and in vivo evaluation

• Published in: Journal of inorganic biochemistry Vol. 154; pp. 60 - 66
• Main Authors: Kang, Chi Soo, Wu, Ningjie, Chen, Yunwei, Sun, Xiang, Bandara, Nilantha, Liu, Dijie, Lewis, Michael R., Rogers, Buck E., Chong, Hyun-Soon
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2016
• Subjects: Animals; Aza Compounds - chemical synthesis; Aza Compounds - pharmacokinetics; Bifunctional chelator; Biodistribution; Cell Line, Tumor; Chelating Agents - chemical synthesis; Chelating Agents - pharmacokinetics; Copper 64; Copper Radioisotopes - chemistry; Copper Radioisotopes - pharmacokinetics; Drug Stability; Female; Half-Life; Male; Mice, SCID; Neoplasm Transplantation; Piperidines - chemical synthesis; Piperidines - pharmacokinetics; Positron-Emission Tomography; Prostatic Neoplasms - diagnostic imaging; Radiolabeling; Radiopharmaceuticals - chemical synthesis; Radiopharmaceuticals - pharmacokinetics; Serum stability; Tissue Distribution; Transferrin; Transferrin - analogs & derivatives; Transferrin - pharmacokinetics; Radiolabeling; Copper 64; Transferrin; Serum stability; Bifunctional chelator; Biodistribution
• ISSN: 0162-0134; 1873-3344
• DOI: 10.1016/j.jinorgbio.2015.10.012

Three different polyaminocarboxylate-based bifunctional NE3TA (7-[2-[carboxymethyl)amino]ethyl]-1,4,7-triazacyclononane-1,4-diacetic acid) chelating agents were synthesized for potential use in copper 64-PET imaging applications. The bifunctional chelates were comparatively evaluated using transferrin (Tf) as a model targeting vector that binds to the transferrin receptor overexpressed in many different cancer cells. The transferrin conjugates of the NE3TA-based bifunctional chelates were evaluated for radiolabeling with 64Cu. In vitro stability and cellular uptake of 64Cu-radiolabeled conjugates were evaluated in human serum and prostate (PC-3) cancer cells, respectively. Among the three NE3TA–Tf conjugates tested, N-NE3TA–Tf was identified as the best conjugate for radiolabeling with 64Cu. N-NE3TA–Tf rapidly bound to 64Cu (>98% radiolabeling efficiency, 1min, RT), and 64Cu–N-NE3TA–Tf remained stable in human serum for 2days and demonstrated high uptake in PC-3 cancer cells. 64Cu–N-NE3TA–Tf was shown to have rapid blood clearance and increasing tumor uptake in PC-3 tumor bearing mice over a 24h period. This bifunctional chelate presents highly efficient chelation chemistry with 64Cu under mild condition that can be applied for radiolabeling of various tumor-specific biomolecules with 64Cu for potential use in PET imaging applications. Three different NE3TA (7-[2-[carboxymethyl)amino]ethyl]-1,4,7-triazacyclononane-1,4-diacetic acid)-based bifunctional chelating agents were comparatively evaluated for potential use in copper 64-PET imaging applications using transferrin as a model targeting vector. The biological data indicate that N-NE3TA attached to transferrin more rapidly and stably bound with 64Cu than the other NE3TA chelating agents. [Display omitted] •Synthesis of three triazacyclononane-based bifunctional chelates (NE3TAs) for potential use in Cu-64-PET imaging.•Rapid Cu-64 radiolabeling of NE3TA-transferrin (Tf) conjugates at room temperature.•Excellent complex stability of 64Cu-NE3TA-Tf conjugates in human serum.•Rapid blood clearance and increasing tumor uptake of 64Cu-N-NE3TA-Tf in tumor-bearing mice.