Abstract

Since long-chain fatty acids work as the primary energy source for the myocardium, radiolabeled long-chain fatty acids play an important role as imaging agents to diagnose metabolic heart dysfunction and heart diseases. With the aim of developing radiogallium-labeled fatty acids, herein four fatty acid-based tracers, [67Ga]Ga-HBED-CC-PDA, [67Ga]Ga-HBED-CC-MHDA, [67Ga]Ga-DOTA-PDA, and [67Ga]Ga-DOTA-MHDA, which are [67Ga]Ga-HBED-CC and [67Ga]Ga-DOTA conjugated with pentadecanoic acid (PDA) and 3-methylhexadecanoic acid (MHDA), were synthesized, and their potential for myocardial metabolic imaging was evaluated. Those tracers were found to be chemically stable in 0.1 M phosphate buffered saline. Initial [67Ga]Ga-HBED-CC-PDA, [67Ga]Ga-HBED-CC-MHDA, [67Ga]Ga-DOTA-PDA, and [67Ga]Ga-DOTA-MHDA uptakes in the heart at 0.5 min postinjection were 5.01 ± 0.30%ID/g, 5.74 ± 1.02%ID/g, 5.67 ± 0.22%ID/g, and 5.29 ± 0.10%ID/g, respectively. These values were significantly lower than that of [123I]BMIPP (21.36 ± 2.73%ID/g). For their clinical application as myocardial metabolic imaging agents, further structural modifications are required to increase their uptake in the heart.

Highlights

  • Long-chain fatty acids are the predominant energy substrate for the healthy myocardium and are metabolized by β-oxidation in the heart [1]

  • Alteration in fatty acid metabolism has been identified as a biomarker for ischemia and myocardial damage [2,3,4]

  • Proton nuclear magnetic resonance (1H-NMR) spectra was recorded on JEOL JNM-ECS400 (JEOL Ltd, Tokyo, Japan)

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Summary

Introduction

Long-chain fatty acids are the predominant energy substrate for the healthy myocardium and are metabolized by β-oxidation in the heart [1]. With myocardial abnormalities, such as ischemic disease and cardiomyopathy, the alteration of cardiac fuel metabolism is mostly observed. Glycolysis and glycogen metabolism become the primary energy source, whereas fatty acid oxidation is suppressed. Alteration in fatty acid metabolism has been identified as a biomarker for ischemia and myocardial damage [2,3,4]. Either single-photon emission computed tomography (SPECT) or positron emission tomography (PET) imaging with radiolabeled long-.

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