阮邹荣, 程源深, 丁德云. 高效液相色谱法测定尿中美芬妥英及代谢产物4'-羟基美芬妥英J. 药学学报, 1994, 29(8): 621-628.
引用本文: 阮邹荣, 程源深, 丁德云. 高效液相色谱法测定尿中美芬妥英及代谢产物4'-羟基美芬妥英J. 药学学报, 1994, 29(8): 621-628.
ZR Ruan, YS Cheng , DY Ding, . DETERMINATION OF MEPHENYTOIN AND 4'-HYDROXYMEPHENYTOIN IN URINE BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHYJ. Acta Pharmaceutica Sinica, 1994, 29(8): 621-628.
Citation: ZR Ruan, YS Cheng , DY Ding, . DETERMINATION OF MEPHENYTOIN AND 4'-HYDROXYMEPHENYTOIN IN URINE BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHYJ. Acta Pharmaceutica Sinica, 1994, 29(8): 621-628.

高效液相色谱法测定尿中美芬妥英及代谢产物4'-羟基美芬妥英

DETERMINATION OF MEPHENYTOIN AND 4'-HYDROXYMEPHENYTOIN IN URINE BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY

  • Abstract: A simple, sensitive and reproducible HPLC assay is described for the determination of mephenytoin and 4'-hydroxymephenytoin in human urine. Phenobarbital was used as an internal standard.The compounds were separated on a U-Bondapack RP-C18 column using a mobile phase of and the UV detectou was set at 210 nm. Calibration curves in the range 0.05~1.00ug/ml for mephenytoin and 0.5~100.0ug/ml for 4'-hydroxymephenytoin were linear (r=0.9998and r=0.9992,respectivesy). The average recovery was 95.10±2。95%,and the relative standard devia- tion within day and day to day was less than 10%。The detection limit for mephenytoin was 25mg/ml and 4‘-hydroxymephenytoin was 50mg。ml。The method was used to study the metabolism of S-mephenytoin 4'-hydroxylatoin in 10healthy volunteers.The 12 h urinary metabolic ratio (MR)and hydroxylation index(HI)were calculated to express interindividual variation in metabolism. Two of them exhibited defective 4'-hydroxylation of S-mephenytoin as poor metabllizers (HI:1349.18 and 409.57;MR:105.29 and 8.25).In the remaining 8 subjects, the ranged from 1.68 to 6.71 and the MR ranged from 0.002 to 0.014,as extensive metabolizers of S-mephenytoin.

     

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