Hyperpolarization (HP) of nuclear spins is critical for ultrasensitive nuclear magnetic resonance (NMR) and magnetic resonance imaging (MRI). We demonstrate an approach for >1500-fold enhancement of key small-molecule metabolites: 1-(13)C-pyruvic acid, 1-(13)C-sodium lactate, and 1-(13)C-acetic acid. The (13)C solution NMR signal of pyruvic acid was enhanced 1600-fold at B = 1 T and 40 degrees C by pre-polarizing at 14 T and approximately 2.3 K. This "brute-force" approach uses only field and temperature to generate HP. The noted 1 T observation field is appropriate for benchtop NMR and near the typical 1.5 T of MRI, whereas high-field observation scales enhancement as 1/B. Our brute-force process ejects the frozen, solid sample from the low-T, high-B polarizer, passing it through low field (B < 100 G) to facilitate "thermal mixing". That equilibrates (1)H and (13)C in hundreds of milliseconds, providing (13)C HP from (1)H Boltzmann polarization attained at high B/T. The ejected sample arrives at a room-temperature, permanent magnet array, where rapid dissolution with 40 degrees C water yields HP solute. Transfer to a 1 T NMR system yields (13)C signals with enhancements at 80% of ideal for noted polarizing conditions. High-resolution NMR of the same product at 9.4 T had consistent enhancement plus resolution of (13)C shifts and J-couplings for pyruvic acid and its hydrate. Comparable HP was achieved with frozen aqueous lactate, plus notable enhancement of acetic acid, demonstrating broader applicability for small-molecule NMR and metabolic MRI. Brute-force avoids co-solvated free-radicals and microwaves that are essential to competing methods. Here, unadulterated samples obviate concerns about downstream purity and also exhibit slow solid-state spin relaxation, favorable for transporting HP samples.
Brute-Force Hyperpolarization for NMR and MRI
Brute-Force Hyperpolarization for NMR and MRI
Matthew L. Hirsch, Neal Kalechofsky, Avrum Belzer, Melanie Rosay and James G. Kempf
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.5b01252/20150629/images/medium/ja-2015-01252r_0007.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.5b01252
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/jacsat/~4/j9sb5gEVc1k
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06-29-2015 07:21 PM
NMR hyperpolarization techniques for biomedicine
From The DNP-NMR Blog:
NMR hyperpolarization techniques for biomedicine
Nikolaou, P., B.M. Goodson, and E.Y. Chekmenev, NMR hyperpolarization techniques for biomedicine. Chemistry, 2015. 21(8): p. 3156-66.
http://www.ncbi.nlm.nih.gov/pubmed/25470566
[NMR paper] Recommendations of the wwPDB NMR Validation Task Force.
Recommendations of the wwPDB NMR Validation Task Force.
Recommendations of the wwPDB NMR Validation Task Force.
Structure. 2013 Sep 3;21(9):1563-70
Authors: Montelione GT, Nilges M, Bax A, Güntert P, Herrmann T, Richardson JS, Schwieters CD, Vranken WF, Vuister GW, Wishart DS, Berman HM, Kleywegt GJ, Markley JL
Abstract
As methods for analysis of biomolecular structure and dynamics using nuclear magnetic resonance spectroscopy (NMR) continue to advance, the resulting 3D structures, chemical shifts, and other NMR data are broadly impacting...
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09-10-2013 08:44 PM
Hyperpolarization Methods and Applications in NMR
From The DNP-NMR Blog:
Hyperpolarization Methods and Applications in NMR
Köckenberger, W. and J. Matysik, Hyperpolarization Methods and Applications in NMR, in Encyclopedia of Spectroscopy and Spectrometry (Second Edition), L. Editor-in-Chief: John, Editor. 2010, Academic Press: Oxford. p. 963-970.
http://dx.doi.org/10.1016/B978-0-12-374413-5.00054-3
[NMR thesis] Theoretical and experimental investigations in MEMS-based force detected NMR
Theoretical and experimental investigations in MEMS-based force detected NMR
Elgammal, Ramez Ahmed (2005) Theoretical and experimental investigations in MEMS-based force detected NMR. Dissertation (Ph.D.), California Institute of Technology. http://resolver.caltech.edu/CaltechETD:etd-02182006-145814
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