| Literature DB >> 34813142 |
Isaiah Adelabu1, Patrick TomHon2, Mohammad S H Kabir1, Shiraz Nantogma1, Mustapha Abdulmojeed2, Iuliia Mandzhieva2, Jessica Ettedgui3, Rolf E Swenson3, Murali C Krishna4, Thomas Theis2, Boyd M Goodson5, Eduard Y Chekmenev1,6.
Abstract
Signal Amplification By Reversible Exchange in SHield Enabled Alignment Transfer (SABRE-SHEATH) is investigated to achieve rapid hyperpolarization of 13 C1 spins of [1-13 C]pyruvate, using parahydrogen as the source of nuclear spin order. Pyruvate exchange with an iridium polarization transfer complex can be modulated via a sensitive interplay between temperature and co-ligation of DMSO and H2 O. Order-unity 13 C (>50 %) polarization of catalyst-bound [1-13 C]pyruvate is achieved in less than 30 s by restricting the chemical exchange of [1-13 C]pyruvate at lower temperatures. On the catalyst bound pyruvate, 39 % polarization is measured using a 1.4 T NMR spectrometer, and extrapolated to >50 % at the end of build-up in situ. The highest measured polarization of a 30-mM pyruvate sample, including free and bound pyruvate is 13 % when using 20 mM DMSO and 0.5 M water in CD3 OD. Efficient 13 C polarization is also enabled by favorable relaxation dynamics in sub-microtesla magnetic fields, as indicated by fast polarization buildup rates compared to the T1 spin-relaxation rates (e. g., ∼0.2 s-1 versus ∼0.1 s-1 , respectively, for a 6 mM catalyst-[1-13 C]pyruvate sample). Finally, the catalyst-bound hyperpolarized [1-13 C]pyruvate can be released rapidly by cycling the temperature and/or by optimizing the amount of water, paving the way to future biomedical applications of hyperpolarized [1-13 C]pyruvate produced via comparatively fast and simple SABRE-SHEATH-based approaches.Entities:
Keywords: 13C; NMR spectroscopy; hyperpolarization; parahydrogen; pyruvate
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Year: 2021 PMID: 34813142 PMCID: PMC8770613 DOI: 10.1002/cphc.202100839
Source DB: PubMed Journal: Chemphyschem ISSN: 1439-4235 Impact factor: 3.102