## Abstract The magnetic polarization of the stable ^129^Xe isotope may be enhanced dramatically by means of optical techniques and, in principle, hyperpolarized ^129^Xe MRI should allow quantitative mapping of cerebral blood flow with better spatial resolution than scintigraphic techniques. A para
B0 dependence of the on-resonance longitudinal relaxation time in the rotating frame (T1ρ) in protein phantoms and rat brain in vivo
✍ Scribed by Heidi I. Mäkelä; Enrico De Vita; Olli H.J. Gröhn; Mikko I. Kettunen; Martin Kavec; Mark Lythgoe; Michael Garwood; Roger Ordidge; Risto A. Kauppinen
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 102 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
On‐resonance longitudinal relaxation time in the rotating frame (T~1ρ~) has been shown to provide unique information during the early minutes of acute stroke. In the present study, the contributions of the different relaxation mechanisms to on‐resonance T~1ρ~ relaxation were assessed by determining relaxation rates (R~1ρ~) in both protein phantoms and in rat brain at 2.35, 4.7, and 9.4 T. Similar to transverse relaxation rate (R~2~), R~1ρ~ increased substantially with increasing magnetic field strength (B~0~). The B~0~ dependence was more pronounced at weak spin‐lock fields. In contrast to R~1ρ~, longitudinal relaxation rate (R~1~) decreased as a function of increasing B~0~ field. The present data argue that dipole–dipole interaction forms only one pathway for T~1ρ~ relaxation and the contributions from other physicochemical factors need to be considered. Magn Reson Med 51:4–8, 2004. © 2003 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES