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XeNA: An automated ‘open-source’ 129Xe hyperpolarizer for clinical use

Nikolaou, Panayiotis; Coffey, Aaron M.; Walkup, Laura L.; Gust, Brogan M.; Whiting, Nicholas; Newton, Hayley; Muradyan, Iga; Dabaghyan, Mikayel; Ranta, Kaili; Moroz, Gregory D.; Rosen, Matthew S.; Patz, Samuel; Barlow, Michael J.; Chekmenev, Eduard Y.; Goodson, Boyd M.

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Authors

Panayiotis Nikolaou

Aaron M. Coffey

Laura L. Walkup

Brogan M. Gust

Nicholas Whiting

Hayley Newton

Iga Muradyan

Mikayel Dabaghyan

Kaili Ranta

Gregory D. Moroz

Matthew S. Rosen

Samuel Patz

Michael J. Barlow

Eduard Y. Chekmenev

Boyd M. Goodson



Abstract

Here we provide a full report on the construction, components, and capabilities of our consortium’s “open-source” large-scale (~ 1 L/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 1800 Torr Xe in 0.5 L) 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 ~ 300–1600 Torr. Typical 129Xe polarization build-up and T1 relaxation time constants were ~ 8.5 min and ~ 1.9 h 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 ~ 200 W), 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 6 h) were observed in Tedlar bags following transport to a clinical 3 T 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.

Journal Article Type Article
Acceptance Date Feb 2, 2014
Online Publication Date Feb 10, 2014
Publication Date 2014-06
Deposit Date Aug 10, 2018
Publicly Available Date Aug 10, 2018
Journal Magnetic Resonance Imaging
Print ISSN 0730-725X
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 32
Issue 5
Pages 541-550
DOI https://doi.org/10.1016/j.mri.2014.02.002
Keywords Hyperpolarization; MRI; Laser-polarized xenon; Optical pumping; Lung imaging
Publisher URL https://www.sciencedirect.com/science/article/pii/S0730725X14000459?via%3Dihub

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