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  Pulsed magnetic resonance to signal‐enhance metabolites within seconds by utilizing para‐hydrogen

Korchak, S., Yang, S., Mamone, S., & Glöggler, S. (2018). Pulsed magnetic resonance to signal‐enhance metabolites within seconds by utilizing para‐hydrogen. ChemistryOpen, 7(5), 344-348. doi:10.1002/open.201800024.

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Korchak, S.1, Author           
Yang, S.1, Author           
Mamone, S.1, Author           
Glöggler, S.1, Author           
Affiliations:
1Research Group of NMR Signal Enhancement, MPI for Biophysical Chemistry, Max Planck Society, ou_2396691              

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Free keywords: hyperpolarization; magnetic resonance; metabolite; para-hydrogen-induced polarization; sidearm hydrogenation
 Abstract: Diseases such as Alzheimer's and cancer have been linked to metabolic dysfunctions, and further understanding of metabolic pathways raises hope to develop cures for such diseases. To broaden the knowledge of metabolisms in vitro and in vivo, methods are desirable for direct probing of metabolic function. Here, we are introducing a pulsed nuclear magnetic resonance (NMR) approach to generate hyperpolarized metabolites within seconds, which act as metabolism probes. Hyperpolarization represents a magnetic resonance technique to enhance signals by over 10 000‐fold. We accomplished an efficient metabolite hyperpolarization by developing an isotopic labeling strategy for generating precursors containing a favorable nuclear spin system to add para‐hydrogen and convert its two‐spin longitudinal order into enhanced metabolite signals. The transfer is performed by an invented NMR experiment and 20 000‐fold signal enhancements are achieved. Our technique provides a fast way of generating hyperpolarized metabolites by using para‐hydrogen directly in a high magnetic field without the need for field cycling.

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Language(s): eng - English
 Dates: 2018-05-08
 Publication Status: Published online
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 Rev. Type: Peer
 Identifiers: DOI: 10.1002/open.201800024
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Title: ChemistryOpen
Source Genre: Journal
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Pages: - Volume / Issue: 7 (5) Sequence Number: - Start / End Page: 344 - 348 Identifier: -