Abstract
The signal enhancement provided by the hyperpolarization of nuclear spins of metabolites is a promising technique for diagnostic magnetic resonance imaging (MRI). To date, most13C-contrast agents are hyperpolarized utilizing a complex or cost-intensive polarizer. Recently, thein situ parahydrogen-induced13C hyperpolarization was demonstrated. Hydrogenation, spin order transfer (SOT) by a pulsed NMR sequence,in vivoadministration, and detection was achieved within the magnet bore of a 7 Tesla MRI system. So far, the hyperpolarization of the xenobiotic molecule 1-13C-hydroxyethylpropionate (HEP) and the biomolecule 1-13C-succinate (SUC) through the PH-INEPT+ sequence and a SOT scheme proposed by Goldmanet al., respectively, was shown. Here, we investigate further the hyperpolarization of SUC at 7 Tesla and study the performance of two additional SOT sequences. Moreover, we present first results of the hyperpolarization at high magnetic field of 1-13C-phospholactate (PLAC), a derivate to obtain the metabolite lactate, employing the PH-INEPT+ sequence. For SUC and PLAC,13C polarizations of about 1-2% were achieved within seconds and with minimal equipment. Effects that potentially may explain loss of13C polarization have been identified,i.e.low hydrogenation yield, fastT1/T2relaxation and the rarely considered13C isotope labeling effect.
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CITATION STYLE
Berner, S., Schmidt, A. B., Ellermann, F., Korchak, S., Chekmenev, E. Y., Glöggler, S., … Hövener, J. B. (2021). High fieldparahydrogen induced polarization of succinate and phospholactate. Physical Chemistry Chemical Physics, 23(3), 2320–2330. https://doi.org/10.1039/d0cp06281b
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