| Literature DB >> 18581406 |
Bastiaan Driehuys1, Jim Pollaro, Gary P Cofer.
Abstract
MR imaging of hyperpolarized (HP) nuclei is challenging because they are typically delivered in a single dose of nonrenewable magnetization, from which the entire image must be derived. This problem can be overcome with HP (129)Xe, which can be produced sufficiently rapidly to deliver in dilute form (1%) continuously and on-demand. We demonstrate a real-time in vivo delivery of HP (129)Xe mixture to rats, a capability we now routinely use for setting frequency, transmitter gain, shimming, testing pulse sequences, scout imaging, and spectroscopy. Compared to images acquired using conventional fully concentrated (129)Xe, real-time (129)Xe images have 26-fold less signal, but clearly depict ventilation abnormalities. Real-time (129)Xe MRI could be useful for time-course studies involving acute injury or response to treatment. Ultimately, real-time (129)Xe MRI could be done with more highly concentrated (129)Xe, which could increase the signal-to-noise ratio by 100 relative to these results to enable a new class of gas imaging applications. (c) 2008 Wiley-Liss, Inc.Entities:
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Year: 2008 PMID: 18581406 PMCID: PMC2548276 DOI: 10.1002/mrm.21651
Source DB: PubMed Journal: Magn Reson Med ISSN: 0740-3194 Impact factor: 4.668