Article ID Journal Published Year Pages File Type
2153892 Nuclear Medicine and Biology 2012 6 Pages PDF
Abstract

IntroductionEstablished radiotracers for positron emission tomography (PET) myocardial perfusion study are commonly labeled with short-lived radio-isotopes that limit their widespread clinical use. Thus, we synthesized (2-(2-[18F]fluoroethoxy)ethyl)tris(4-methoxyphenyl)phosphonium salt ([18F]FETMP) as a novel myocardial perfusion agent that penetrates the hydrophobic barriers of the plasma and mitochondrial membranes and accumulate in mitochondria of cardiomyocytes in response to the negative inner-transmembrane potentials.MethodsThe [18F]FETMP was synthesized via two-step nucleophilic substitution reactions of no-carrier-added [18F]fluoride with the precursor 2,2′-oxybis(ethane-2,1-diyl)bis(4-methylbenzenesulfonate) in the presence of Kryptofix 2.2.2 and K2CO3. The [18F]FETMP accumulation was measured in cell culture with rat embryonic cardiomyoblast (H9c2) and mouse normal fibroblast (NIH/3T3) cell lines. The mitochondrial membrane potential-dependent cellular uptake of [18F]FETMP was further assessed using the H9c2 cells treated with carbonyl cyanide m-chlorophenylhydrazone (CCCP) which is a protonophore that selectively abolishes the mitochondrial membrane potential. Biodistribution and micro-PET studies were performed in normal BALB/c mice to test and optimize the kinetics for radiolabeled phosphonium cation.ResultsThe radiolabeled compound was synthesized with 10%–20% yield. The radiochemical purity was > 98% by analytical HPLC, and the specific activity was > 5.92 TBq/μmol. The cellular uptake assay showed preferential uptake of [18F]FETMP in cardiomyocytes. The results of biodistribution and micro-PET imaging studies of [18F]FETMP in mice and rats showed preferential accumulation in the myocardium.ConclusionsThe results suggest that [18F]FETMP would be a promising candidate for myocardial imaging and might be useful for clinical cardiac PET/CT applications.

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