## Abstract Chemical‐shift artifact correction methods for multislice F‐19 imaging with perfluorooctyl bromide are described and results obtained with physical phantoms presented. Utilization of the two long‐T2 spectral peaks of PFOB in multislice imaging enhances the imaging efficiency considerabl
Application of 19F chemical shift imaging in studies of mice with orally administered 5-fluorouracil
✍ Scribed by Hideto Kuribayashi; Yoshihiro Doi; Yoko Kanazawa
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 185 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0740-3194
- DOI
- 10.1002/mrm.1270
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
In vivo quantitative metabolic mapping is an ideal tool for pharmacokinetic studies. Oral 5‐fluorouracil (5‐FU) and its metabolites in mice were imaged simultaneously by the ^19^F fast spin echo (FSE) sequence using interleaved frequency selection at 9.4T. However, 5‐FU images in the small intestine have never been obtained regardless of concentration. The reason for the discrepancy between image intensity and concentration was T~2~. At a pH above 6, a dramatic decrease in T~2~ of a ^19^F 5‐FU signal in an aqueous solution was found; T~2~ was shorter in the small intestine (14 ms) than in the stomach (52 ms). The ^19^F CSI sequence in FID sampling mode was employed for detecting short T~2~ signals. With a 13‐min resolution time, the detection of the 5‐FU signals in the region of the small intestine (0.6 mmol/kg) was successful with a 5 × 5 mm^2^ in‐plane resolution. Furthermore, two signals separated by 2 ppm were clearly distinguishable, but failed to be separately detectable with the ^19^F FSE sequence. For quantitative simultaneous monitoring of 5‐FU and its metabolites of varying T~2~, the ^19^F CSI sequence in FID sampling mode was found to be superior to the ^19^F FSE sequence. Magn Reson Med 46:864–869, 2001. © 2001 Wiley‐Liss, Inc.
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