Simultaneous HPLC Determination of Acetaminophen and Four of Its Major Metabolites in Small-Volume Biologic Fluids.
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概要
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An HPLC method for quantifying acetaminophen (APAP) and four of its major metabolites: glucuronide, cysteine, sulfate, and mercapturate conjugates in biologic fluids has been developed. Proteinous samples (25μl) were deproteinized with ZnSO<SUB>4</SUB>-saturated acetonitrile, and urine (100μl) was extracted under alkaline conditions with chloroform-isopropanol (95: 5, v/v) followed by N<SUB>2</SUB> evaporation. The separations were resolved on a 250mm×4.6mm ID, Phenomenex-ODS reverse-phase column with a simple isocratic mobile phase composed of 0.73 M acetic acid in water (pH 2.44) methanol (90: 10, v/v, plus 15μl/L n-octylamine for serum/plasma; 80: 20, v/v, for saliva and 92: 8, v/v, plus 30μl/L n-octylamine for urine). All compounds were simultaneously detected at a wavelength of 260 nm using the structural analog of APAP, 3-acetamidophenol, as an internal standard. Analysis was achieved within 9 min (for serum/plasma) and 4.5 min (for saliva) or 13.8 min (for urine) per run at a flow rate of 1.5 ml/min. The limits of detection ranged between 6 and 16 ng/ml, while limits of quantitation were 11-103 ng/ml for the compounds. The relationship between peak areas and concentration was linear over the range of 0.088 and 70.00μg/ml for APAP, 0.074 and 14.75μg/ml for APAP cysteine, 0.123 and 197.30μg/ml for APAP glucuronide, 0.205 and 390.21μg/ml for APAP sulfate, and 0.124 and 12.40μg/ml for APAP mercapturate. The resolution chromatograms showed no interfering peaks from endogenous components of biologic fluids. Accuracy of the method ranged from -9.0 to 11.1%, and intra-day and inter-day coefficient of variation ranged from 0.2 to 9.3% and 0.1 to 5.7% for all compounds. Extraction efficiencies of urine samples were between 90.1% and 111.6%. Applicability of the method was examined by a pharmacokinetic study in men and male rats that received one dose of 10 mg/kg of APAP.
- 一般社団法人 日本臨床薬理学会の論文
著者
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Qi Jin
Department Of Complex Prescription Of Tcm China Pharmaceutical University
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Honda Yumiko
Department Of Physics Faculty Of Science Ochanomizu University
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MINESHITA Satoru
Department of Clinical Pharmacology, Medical Research Institute, Tokyo Medical and Dental University
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QI Jin
Department of Pathopharmacokinetics Graduate School, Tokyo Medical and Dental University
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MINESHITA Satoru
Department of Pathopharmacokinetics Graduate School, Tokyo Medical and Dental University
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HONDA Yumiko
Department of Medicine, Aoyama Kyosai Hospital
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HONDA Yumiko
Department of Pathopharmacokinetics Graduate School, Tokyo Medical and Dental University
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