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
Summary
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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