ContinuousDelivery of Hyperpolarized Xenon-129 GasUsing a “Stopped-Flow” Clinical-Scale Cryogen-Free Hyperpolarizer
In 2022, the FDA approved hyperpolarized (HP) <sup>129</sup>Xe gas as an inhalable contrast agent for functional lung imaging. For clinical imaging, HP <sup>129</sup>Xe is usually given as a bolus inhalation. However, for preclinical applications (e.g., pulmonary imaging in small rodents), the continuous delivery of HP <sup>129</sup>Xe is greatly desired to enable MRI scanning under conditions of physiological continuous animal breathing patterns. Moreover, HP <sup>129</sup>Xe gas can be utilized for other applications including materials science and bioanalytical chemistry, where a continuous flow of hyperpolarized gas through an NMR sample over several minutes is also desired for sensing of <sup>129</sup>Xe inside an NMR spectrometer. <sup>129</sup>Xe is often hyperpolarized using continuous-flow spin-exchange optical pumping, which employs a lean (1–2%) mixture of Xe and a carrier gas (e.g., He and N<sub>2</sub>). The low Xe concentration in the produced output reduces the NMR detection sensitivity, and thus, Xe cryo-collection is typically employed to achieve near-100% pure gas-phase Xe before administration to the sample or subject. However, the need for cryo-collection undermines a key advantage of continuous-flow production, i.e., the continuous flowing in a hyperpolarizer HP <sup>129</sup>Xe gas is trapped inside the hyperpolarizer, and the produced HP <sup>129</sup>Xe gas is released at once when the production cycle (30–60 min) is completed. An alternative HP <sup>129</sup>Xe production technology employs a “stopped-flow” approach, where a batch of HP gas is hyperpolarized over time and quickly released from a hyperpolarizer. Here, a clinical-scale “stopped-flow” <sup>129</sup>Xe hyperpolarizer was employed to hyperpolarize a 1.3 L-atm batch of 50:50 Xe:N<sub>2</sub> gas mixture inside a glass cell with an ultralong lifetime of the HP <sup>129</sup>Xe state (<i>T</i><sub>1</sub> > 2 h). The produced HP <sup>129</sup>Xe gas was slowly delivered into a 5 mm NMR tube via PEEK tubing under a wide range of gas flow rates: 3–180 standard cubic centimeters per minute (sccm). The polarization of the gas ejected from the hyperpolarizer was quantified using <i>in situ</i> low-field NMR polarimetry and additionally verified using a 0.35 T clinical MRI scanner. Continuous-flow delivery of HP <sup>129</sup>Xe was demonstrated for up to 15 min with a gas flow rate of 45–150 sccm over a 2.5-m length of PEEK tubing, suffering only small losses in <sup>129</sup>Xe polarization. These observations are additionally supported by <sup>129</sup>Xe relaxation measurements inside the PEEK tubing employed for gas delivery and the 5 mm NMR tube employed for polarimetry. <sup>129</sup>Xe polarization of 16–19% was obtained in the delivered gas, starting with an “in-polarizer” <sup>129</sup>Xe polarization of 19%. We envision that this method can be employed for on-demand cryogen-free delivery of hyperpolarized gas using “stopped-flow” <sup>129</sup>Xe hyperpolarizers for a broad range of applications, from preclinical imaging to biosensors, and to spectroscopy of materials surfaces.
Publication Details
- Journal
- Figshare
- Published
- 2025-02-04
- DOI
- https://doi.org/10.1021/acs.analchem.4c05372.s001
- Primary Topic
- Atomic and Subatomic Physics Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00