Abstract

Deuterium Magnetic Resonance Spectroscopy (DMRS) is a non-invasive technique that allows the detection of deuterated compounds in vivo. DMRS has a large potential to analyze uptake, perfusion, washout or metabolism, since deuterium is a stable isotope and therefore does not decay during biologic processing of a deuterium labelled substance. Moreover, DMRS allows the distinction between different deuterated substances. In this work, we performed DMRS of deuterated 3-O-Methylglucose (OMG). OMG is a non-metabolizable glucose analog which is transported similar to D-glucose. DMRS of OMG was performed in phantom and in vivo measurements using a preclinical 7 Tesla MRI system. The chemical shift (3.51 ± 0.1 ppm) and relaxation times were determined. OMG was injected intravenously and spectra were acquired over a period of one hour to monitor the time evolution of the deuterium signal in tumor-bearing rats. The increase and washout of OMG could be observed. Three different exponential functions were compared in terms of how well they describe the OMG washout. A mono-exponential model with offset seems to describe the observed time course best with a time constant of 1910 ± 770 s and an offset of 2.5 ± 1.2 mmol/l (mean ± std, N = 3). Chemical shift imaging could be performed with a voxel size of 7.1 mm x 7.1 mm x 7.9 mm. The feasibility of DMRS with deuterium labelled OMG could be demonstrated. These data might serve as basis for future studies that aim to characterize glucose transport using DMRS.

Highlights

  • Some diseases, such as cancer, are characterized by an increased glucose uptake [1]

  • We investigated deuterated OMG as potential tracer for Deuterium Magnetic Resonance Spectroscopy (DMRS)

  • Spectrum B was recorded at t = 370 s, about 115 s after the end of the injection

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Summary

Introduction

Some diseases, such as cancer, are characterized by an increased glucose uptake [1]. A widely used technique for molecular imaging of glucose is positron emission tomography (PET). One of the most frequently used PET tracers is the radioactively labeled glucose analog 2-18Ffluoro-2-deoxy-D-glucose (FDG). FDG spreads in the body and accumulates in tissue with high glucose uptake [2].

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