## Abstract Simultaneous acquisition of ^1^H‐decoupled ^31^P and ^19^F 3D CSI is demonstrated in the liver of a patient undergoing 5‐fluorouracil chemotherapy. Both ^31^P and ^19^F shared the same voxel size (64 or 27 ml), bi‐level ^1^H‐decoupling and 0.35 s __TR.__ The measurements were done in a
Simultaneous 3D NMR spectroscopy of fluorine and phosphorus in human liver during 5-fluorouracil chemotherapy
✍ Scribed by Chun-Wei Li; Oded Gonen
- Book ID
- 102953709
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 716 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Simultaneous multivoxel ^31^P and ^19^F 3D localized NMR spec‐troscopy is demonstrated on a phantom and in the liver of patients undergoing bolus‐infusion 5‐fluorouracil chemotherapy. The ^19^F and ^31^P spectra were localized with 8 × 8 × 8 3D chemical‐shift imaging, with both nuclei sharing the same field of view and voxel size (27 and 64 ml in phantom and liver, respectively) using a 1.5‐Tesla clinical imager with two RF channels and a dual‐tuned surface coil. The repetition time (TR = 0.26 s) and Ernst nutation angles (θ~E~ = 32° for ^19^F, 28° for ^31^P) were chosen to optimize the signal‐to‐noise ratio (SNR) per‐untt time for the 0.5‐ to 2‐s T~1~ range of the ^19^F and ^31^P metabolites of interest The overall examination time, including tuning, imaging, shimming and dual‐nuclear spectroscopy, was under 90 min. Simultaneous acquisition of ^31^P and ^19^F spectra will permit the study of the influence of hepatic and/or tumor metabolism on the uptake and catabolism of fluoropyrimidine drugs with no extra measurement time.
📜 SIMILAR VOLUMES