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Sensitivity enhancement for detection of hyperpolarized 13 C MRI probes with 1 H spin coupling introduced by enzymatic transformation in vivo
Author(s) -
Morze Cornelius,
Tropp James,
Chen Albert P.,
MarcoRius Irene,
Criekinge Mark,
Skloss Timothy W.,
Mammoli Daniele,
Kurhanewicz John,
Vigneron Daniel B.,
Ohliger Michael A.,
Merritt Matthew E.
Publication year - 2018
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.27000
Subject(s) - in vivo , decoupling (probability) , nuclear magnetic resonance , chemistry , glycerol , physics , biochemistry , biology , engineering , microbiology and biotechnology , control engineering
Purpose Although 1 H spin coupling is generally avoided in probes for hyperpolarized (HP) 13 C MRI, enzymatic transformations of biological interest can introduce large 13 C‐ 1 H couplings in vivo. The purpose of this study was to develop and investigate the application of 1 H decoupling for enhancing the sensitivity for detection of affected HP 13 C metabolic products. Methods A standalone 1 H decoupler system and custom concentric 13 C/ 1 H paddle coil setup were integrated with a clinical 3T MRI scanner for in vivo 13 C MR studies using HP [2‐ 13 C]dihydroxyacetone, a novel sensor of hepatic energy status. Major 13 C‐ 1 H coupling [1][Ardenkjaer‐Larsen JH, 2003] J CH = ∼150 Hz) is introduced after adenosine triphosphate–dependent enzymatic transformation of HP [2‐ 13 C]dihydroxyacetone to [2‐ 13 C]glycerol‐3‐phosphate in vivo. Application of WALTZ‐16 1 H decoupling for elimination of large 13 C‐ 1 H couplings was first tested in thermally polarized glycerol phantoms and then for in vivo HP MR studies in three rats, scanned both with and without decoupling. Results As configured, 1 H‐decoupled 13 C MR of thermally polarized glycerol and the HP metabolic product [2‐ 13 C]glycerol‐3‐phosphate was achieved at forward power of approximately 15 W. High‐quality 3‐s dynamic in vivo HP 13 C MR scans were acquired with decoupling duty cycle of 5%. Application of 1 H decoupling resulted in sensitivity enhancement of 1.7‐fold for detection of metabolic conversion of [2‐ 13 C]dihydroxyacetone to HP [2‐ 13 C]glycerol‐3‐phosphate in vivo. Conclusions Application of 1 H decoupling provides significant sensitivity enhancement for detection of HP 13 C metabolic products with large 1 H spin couplings, and is therefore expected to be useful for preclinical and potentially clinical HP 13 C MR studies. Magn Reson Med 80:36–41, 2018. © 2017 International Society for Magnetic Resonance in Medicine.