Literature DB >> 29266425

Simple and robust referencing system enables identification of dissolved-phase xenon spectral frequencies.

Michael A Antonacci1,2, Le Zhang2,3, Alex Burant1,2, Drew McCallister1,2, Rosa T Branca1,2.   

Abstract

PURPOSE: To assess the effect of macroscopic susceptibility gradients on the gas-phase referenced dissolved-phase 129 Xe (DPXe) chemical shift (CS) and to establish the robustness of a water-based referencing system for in vivo DPXe spectra.
METHODS: Frequency shifts induced by spatially varying magnetic susceptibility are calculated by finite-element analysis for the human head and chest. Their effect on traditional gas-phase referenced DPXe CS is then assessed theoretically and experimentally. A water-based referencing system for the DPXe resonances that uses the local water protons as reference is proposed and demonstrated in vivo in rats.
RESULTS: Across the human brain, macroscopic susceptibility gradients can induce an apparent variation in the DPXe CS of up to 2.5 ppm. An additional frequency shift as large as 6.5 ppm can exist between DPXe and gas-phase resonances. By using nearby water protons as reference for the DPXe CS, the effect of macroscopic susceptibility gradients is eliminated and consistent CS values are obtained in vivo, regardless of shimming conditions, region of interest analyzed, animal orientation, or lung inflation. Combining in vitro and in vivo spectroscopic measurements finally enables confident assignment of some of the DPXe peaks observed in vivo.
CONCLUSION: To use hyperpolarized xenon as a biological probe in tissues, the DPXe CS in specific organs/tissues must be reliably measured. When the gas-phase is used as reference, variable CS values are obtained for DPXe resonances. Reliable peak assignments in DPXe spectra can be obtained by using local water protons as reference. Magn Reson Med 80:431-441, 2018.
© 2017 International Society for Magnetic Resonance in Medicine. © 2017 International Society for Magnetic Resonance in Medicine.

Entities:  

Keywords:  chemical shift; hyperpolarized xenon; magnetic resonance spectroscopy; susceptibility gradients; xenon spectroscopy

Mesh:

Substances:

Year:  2017        PMID: 29266425      PMCID: PMC5910273          DOI: 10.1002/mrm.27042

Source DB:  PubMed          Journal:  Magn Reson Med        ISSN: 0740-3194            Impact factor:   4.668


  35 in total

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3.  Dynamic NMR spectroscopy of hyperpolarized (129)Xe in human brain analyzed by an uptake model.

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4.  Magnetic resonance spectra of hyperpolarized (129)xe in human blood and living rat chest.

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7.  Detection of brown adipose tissue and thermogenic activity in mice by hyperpolarized xenon MRI.

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8.  Distribution of hyperpolarized xenon in the brain following sensory stimulation: preliminary MRI findings.

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9.  High resolution spectroscopy and chemical shift imaging of hyperpolarized (129) Xe dissolved in the human brain in vivo at 1.5 tesla.

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1.  Calibration of methylene-referenced lipid-dissolved xenon frequency for absolute MR temperature measurements.

Authors:  Michael A Antonacci; Le Zhang; Simone Degan; Detlev Erdmann; Rosa T Branca
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2.  Direct detection of brown adipose tissue thermogenesis in UCP1-/- mice by hyperpolarized 129Xe MR thermometry.

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3.  Dissolved hyperpolarized xenon-129 MRI in human kidneys.

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Review 4.  In vivo methods and applications of xenon-129 magnetic resonance.

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Review 5.  Hyperpolarized 129 Xe imaging of the brain: Achievements and future challenges.

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