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arXiv · 2205.15709

Radio-Frequency Sweeps at {\mu}T Fields for Parahydrogen-Induced Polarization of Biomolecules

Alastair Marshall·Alon Salhov·Martin Gierse·Christoph Müller·Michael Keim·Sebastian Lucas·Anna Parker·Jochen Scheuer·Christophoros Vassiliou·Philipp Neumann·Fedor Jelezko·Alex Retzker·John W. Blanchard·Ilai Schwartz·Stephan Knecht
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Abstract

Magnetic resonance imaging of $^{13}$C-labeled metabolites enhanced by parahydrogen-induced polarization (PHIP) can enable real-time monitoring of processes within the body. We introduce a robust, easily implementable technique for transferring parahydrogen-derived singlet order into 13C magnetization using adiabatic radio-frequency sweeps at $\mu$T fields. We experimentally demonstrate the applicability of this technique to several molecules, including some molecules relevant for metabolic imaging, where we show significant improvements in the achievable polarization, in some cases reaching above 60%. Furthermore, we introduce a site-selective deuteration scheme, where deuterium is included in the coupling network of a pyruvate ester to enhance the efficiency of the polarization transfer. These improvements are enabled by the fact that the transfer protocol avoids relaxation induced by strongly coupled quadrupolar nuclei.

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Alastair Marshall, Alon Salhov, Martin Gierse, Christoph Müller, Michael Keim, Sebastian Lucas, Anna Parker, Jochen Scheuer, Christophoros Vassiliou, Philipp Neumann, Fedor Jelezko, Alex Retzker, John W. Blanchard, Ilai Schwartz, Stephan Knecht. 2022-05-31. Radio-Frequency Sweeps at {\mu}T Fields for Parahydrogen-Induced Polarization of Biomolecules. https://doi.org/10.1021/acs.jpclett.2c03785

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