Use of Nuclear Magnetic Resonance Spectroscopy and Selective ^<13>C-Labeling for Pharmacokinetic Research in Man : Detection of Benzoic Acid Conversion to Hippuric Acid

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This paper demonstrates that the stable isotope tracer technique using NMR spectroscopy and the selective ^<13>C labeling of protonated carbons can provide a relatively sensitive method to investigate pharmacokinetic problems in man. The urinary excreted [1,3,5-^<13>C_3] hippuric acid ([^<13>C] HA) formed from orally administered [1,3,5-^<13>C_3] benzoic acid ([^<13>C] BA) as a model substrate was successfully quantitated without any separation procedures by proton-decoupled ^<13>C-NMR spectroscopy of 10-fold concentrated urine in a 10 min accumulation time. In spite of the low dosage (10mg BA), the C3,5 resonances of [^<13>C] HA were detected with favorable signal-to-noise ratios to quantitate [^<13>C] HA concentration. The administered [^<13>C] BA was found to be quantitatively biotransformed to HA and excreted in urine within 4h. The lower limit of detection was estimated to be 50 nmol in an NMR tube, which was improved about one order of magnitude over that of BA labeled in the quaternary carbon (C7). The potential of an inverse detection experiment using heteronuclear multiple quantum coherence was also investigated in order to detect [^<13>C] HA in urine with a higher sensitivity. The inverse experiment improved the sensitivity by a factor of 2-3 over ^<13>C{^1H}-NMR, although the specificity of detection was relatively poor.
公益社団法人日本薬学会の論文
1995-05-15