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Synthesis, radiolabeling, and evaluation of gastrin releasing peptide receptor antagonist 68 Ga‐HBED‐CC‐RM26
Author(s) -
Satpati Drishty,
Vats Kusum,
Sharma Rohit,
Kameswaran Mythili,
Sarma Haladhar Dev,
Dash Ashutosh
Publication year - 2019
Publication title -
journal of labelled compounds and radiopharmaceuticals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 47
eISSN - 1099-1344
pISSN - 0362-4803
DOI - 10.1002/jlcr.3795
Subject(s) - chemistry , biodistribution , peptide , chelation , in vitro , peg ratio , gastrin , radiochemistry , in vivo , ligand (biochemistry) , clearance , antagonist , combinatorial chemistry , pharmacology , receptor , biochemistry , organic chemistry , medicine , microbiology and biotechnology , finance , secretion , economics , urology , biology
The acyclic chelator HBED‐CC has attained huge clinical significance owing to high thermodynamic and kinetic stability of 68 Ga‐HBED‐CC chelate. It provides an excellent platform for quick preparation of 68 Ga‐based radiotracers in high yield. Thus, the present study aimed at conjugation of gastrin releasing peptide receptor (GRPr) antagonist, RM26, with HBED‐CC chelator for 68 Ga‐labeling. In vitro and vivo behavior of the peptide tracer, 68 Ga‐HBED‐CC‐PEG 2 ‐RM26, was assessed and compared with 68 Ga‐NODAGA‐PEG 2 ‐RM26. The peptide tracers, 68 Ga‐HBED‐CC‐PEG 2 ‐RM26 and 68 Ga‐NODAGA‐PEG 2 ‐RM26, prepared either by wet chemistry or formulated using freeze‐dried kits exhibited excellent radiochemical yield and in vitro stability. The two peptide tracers cleared rapidly from the blood. Biodistribution studies in normal mice demonstrated slightly higher or comparable uptake of 68 Ga‐HBED‐CC‐PEG 2 ‐RM26 in GRPr‐expressing organs pancreas, stomach, and intestine. The preliminary studies suggest high potential of 68 Ga‐HBED‐CC‐PEG 2 ‐RM26 for further investigation as a GRPr imaging agent and the wide scope of HBED‐CC chelator in development of 68 Ga‐based peptide tracers.