## Abstract The ^1^H CW off‐resonance decoupled ^13^C NMR spectra of pheromones and unsaturated fatty acids were measured for the determination of the configuration of double bonds of the type CH~2~CH CHCH~2~. The decoupling frequency corresponded to the resonance frequency of the CH~2~ proto
Sensitivity enhancement in whole-body natural abundance 13C spectroscopy using 13C/1H double-resonance techniques at 4 tesla
✍ Scribed by H. Bomsdorf; P. Röschmann; J. Wieland
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 708 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0740-3194
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✦ Synopsis
Abstract
In vivo ^13^C spectroscopy experiments were performed using a whole‐body MR system at a static field of 4 T. The main goal of the investigations was to evaluate the sensitivity increase achievable by means of ^13^C/^1^H double‐resonance techniques at 4 T. Spectra from subcutaneous fat as well as muscle glycogen from the lower leg were acquired using frequency selective proton decoupling and the polarization transfer method SINEPT. With respect to measurements on subcutaneous fat, polarization transfer turned out to be more efficient than selective decoupling. About a fourfold enhancement in spectral peak intensity for the CC line doublet of the unsaturated fatty acid chain was obtained. Combining polarization transfer with decoupling yielded a factor of 6 in signal amplitude. In contrast to that, the signal enhancement observed in measurements on the glycogen C‐1 resonance was only around twofold. The lower efficiency is explained by fast T~2~ relaxation of the proton transition. A T~2~ value of about 3 ms was derived from the experimental data. Acquisition times as low as 3 min were realized for normal level glycogen in human calf muscle, enabling a time resolution adequate for dynamic studies on muscle glycogen depletion. Aspects of RF power absorption in tissue and the generally higher efficiency make polarization transfer methods preferable to selective decoupling in whole‐body ^13^C spectroscopy at 4 T. © 1991 Academic Press, Inc.
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