Journal
ANALYTICAL CHEMISTRY
Volume 93, Issue 8, Pages 3883-3888Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.0c04545
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Funding
- DOD CDMRP [W81XWH-15-10271, W81XWH-15-1-0272, W81XWH-20-10576, W81XWH-20-10578]
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This study utilizes NMR and NIR technologies to analyze the Xe-129 hyperpolarization process in detail, aiming to improve production efficiency and stability. Mapping the dynamics of Xe-129 polarization and relaxation at different SEOP temperatures enables systematic optimization of the batch-mode SEOP process.
We present on the utility of in situ nuclear magnetic resonance (NMR) and near-infrared (NIR) spectroscopic techniques for automated advanced analysis of the Xe-129 hyperpolarization process during spin-exchange optical pumping (SEOP). The developed software protocol, written in the MATLAB programming language, facilitates detailed characterization of hyperpolarized contrast agent production efficiency based on determination of key performance indicators, including the maximum achievable Xe-129 polarization, steady-state Rb-Xe-129 spin-exchange and Xe-129 polarization build-up rates, Xe-129 spin-relaxation rates, and estimates of steady-state Rb electron polarization. Mapping the dynamics of Xe-129 polarization and relaxation as a function of SEOP temperature enables systematic optimization of the batch- mode SEOP process. The automated analysis of a typical experimental data set, encompassing similar to 300 raw NMR and NIR spectra combined across six different SEOP temperatures, can be performed in under 5 min on a laptop computer. The protocol is designed to be robust in operation on any batch-mode SEOP hyperpolarizer device. In particular, we demonstrate the implementation of a combination of low-cost NIR and low-frequency NMR spectrometers (similar to$1,100 and similar to$300 respectively, ca. 2020) for use in the described protocols. The demonstrated methodology will aid in the characterization of NMR hyperpolarization hardware in the context of SEOP and other hyperpolarization techniques for more robust and less expensive clinical production of HP Xe-129 and other contrast agents.
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