XeNA: An automated ‘open-source’ 129Xe hyperpolarizer for clinical use
Here we provide a full report on the construction, components, and capabilities of our consortium’s “open-source” large-scale (~1L/h) 129Xe hyperpolarizer for clinical, pre-clinical, and materials NMR/MRI (Nikolaou et al., Proc. Natl. Acad. Sci. USA, 110, 14150 (2013)). The ‘hyperpolarizer’ is autom...
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Published in | Magnetic resonance imaging Vol. 32; no. 5; pp. 541 - 550 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.06.2014
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Subjects | |
Online Access | Get full text |
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Summary: | Here we provide a full report on the construction, components, and capabilities of our consortium’s “open-source” large-scale (~1L/h) 129Xe hyperpolarizer for clinical, pre-clinical, and materials NMR/MRI (Nikolaou et al., Proc. Natl. Acad. Sci. USA, 110, 14150 (2013)). The ‘hyperpolarizer’ is automated and built mostly of off-the-shelf components; moreover, it is designed to be cost-effective and installed in both research laboratories and clinical settings with materials costing less than $125,000. The device runs in the xenon-rich regime (up to 1800Torr Xe in 0.5L) in either stopped-flow or single-batch mode—making cryo-collection of the hyperpolarized gas unnecessary for many applications. In-cell 129Xe nuclear spin polarization values of ~30%–90% have been measured for Xe loadings of ~300–1600Torr. Typical 129Xe polarization build-up and T1 relaxation time constants were ~8.5min and ~1.9h respectively under our spin-exchange optical pumping conditions; such ratios, combined with near-unity Rb electron spin polarizations enabled by the high resonant laser power (up to ~200W), permit such high PXe values to be achieved despite the high in-cell Xe densities. Importantly, most of the polarization is maintained during efficient HP gas transfer to other containers, and ultra-long 129Xe relaxation times (up to nearly 6h) were observed in Tedlar bags following transport to a clinical 3T scanner for MR spectroscopy and imaging as a prelude to in vivo experiments. The device has received FDA IND approval for a clinical study of chronic obstructive pulmonary disease subjects. The primary focus of this paper is on the technical/engineering development of the polarizer, with the explicit goals of facilitating the adaptation of design features and operative modes into other laboratories, and of spurring the further advancement of HP-gas MR applications in biomedicine. |
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Bibliography: | Present address: Cincinnati Children’s Hospital Medical Center, Cincinnati, OH Present address: MD Anderson Cancer Center, Houston, TX |
ISSN: | 0730-725X 1873-5894 |
DOI: | 10.1016/j.mri.2014.02.002 |