4.6 Article

Nuclear hyperpolarization of (1-13C)-pyruvate in aqueous solution by proton-relayed side-arm hydrogenation

期刊

ANALYST
卷 146, 期 5, 页码 1772-1778

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0an02389b

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资金

  1. Marie Sklodowska-Curie program of the European Union [766402]
  2. Max Planck Society
  3. German Research Foundation (DFG) [DFG418416679]
  4. Marie Curie Actions (MSCA) [766402] Funding Source: Marie Curie Actions (MSCA)
  5. EPSRC [EP/P009980/1, EP/K00509X/1, EP/P030491/1] Funding Source: UKRI

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The study introduces a new method, PR-SAH, which reduces the cost and effort needed to prepare the precursor by using an intermediate proton to transfer polarization from the side-arm to the C-13-labelled site of the pyruvate. This method shows promise in hyperpolarizing C-13-labelled metabolites in solution, conducted entirely in high magnetic field.
We employ Parahydrogen Induced Polarization with Side-Arm Hydrogenation (PHIP-SAH) to polarize (1-C-13)-pyruvate. We introduce a new method called proton-relayed side-arm hydrogenation (PR-SAH) in which an intermediate proton is used to transfer polarization from the side-arm to the C-13-labelled site of the pyruvate before hydrolysis. This significantly reduces the cost and effort needed to prepare the precursor for radio-frequency transfer experiments while still maintaining acceptable polarization transfer efficiency. Experimentally we have attained on average 4.33% C-13 polarization in an aqueous solution of (1-C-13)-pyruvate after about 10 seconds of cleavage and extraction. PR-SAH is a promising pulsed NMR method for hyperpolarizing C-13-labelled metabolites in solution, conducted entirely in high magnetic field.

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