3D localized 1H-13C heteronuclear single-quantum coherence correlation spectroscopy in vivo

A method for spatially three‐dimensional (3D) localized two‐dimensional (2D) 1H‐13C correlation spectroscopy, localized HSQC, is proposed. This method has the following special feature in the preparation period. The 180°(13C) and 180°(1H) pulses are separated in time, and the 180°(13C) pulse is appl...

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Published inMagnetic resonance in medicine Vol. 43; no. 2; pp. 200 - 210
Main Authors Watanabe, H., Ishihara, Y., Okamoto, K., Oshio, K., Kanamatsu, T., Tsukada, Y.
Format Journal Article
LanguageEnglish
Published New York John Wiley & Sons, Inc 01.02.2000
Williams & Wilkins
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Summary:A method for spatially three‐dimensional (3D) localized two‐dimensional (2D) 1H‐13C correlation spectroscopy, localized HSQC, is proposed. This method has the following special feature in the preparation period. The 180°(13C) and 180°(1H) pulses are separated in time, and the 180°(13C) pulse is applied at 1/(4 1JCH) before the 90°(1H) polarization transfer pulse. The preparation (echo) period 2τ can then be set substantially longer than 1/(2 1JCH), so that even in a whole‐body system, slice‐selective 90°(1H) pulses and gradient pulses can be applied in that period. The localization capabilities of this method were confirmed in a phantom experiment. The 3D localized 2D 1H‐13C correlation spectra from a monkey brain in vivo were obtained after [1‐13C]glucose injection, and amino acid metabolism was detected; that is, [4‐13C]glutamate appeared immediately after the injection, followed by the appearance of [2‐13C]glutamate, [3‐13C]glutamate, and [4‐13C]glutamine. Magn Reson Med 43:200–210, 2000. © 2000 Wiley‐Liss, Inc.
Bibliography:ArticleID:MRM6
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istex:2397FD1CB22F89FA05ACB23F76ABF3B33A6E41D5
This work was presented in part at the 4th Annual Meeting of the International Society for Magnetic Resonance, New York, May, 1996
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ISSN:0740-3194
1522-2594
DOI:10.1002/(SICI)1522-2594(200002)43:2<200::AID-MRM6>3.0.CO;2-H