Kuang T Y, Zhang J M, Zou A Q, Lou Y Q
Department of Pharmacology, Beijing Medical University.
Yao Xue Xue Bao. 1993;28(4):307-11.
A gas chromatographic method equipped with nitrogen-phosphorus detector was developed for the determination of the S- and R-enantiomers of the anticonvulsant, mephenytoin (MP) in human urine. Dichloromethane (4 ml) was added to 1 ml urine, the mixture was shaken and centrifuged. The organic phase was transferred to another tube and blown to dryness under nitrogen on water bath (37 degrees C). The residue was dissolved in 10 microliters ethylacetate and 1-2 microliters was injected into the GC. Our results showed that direct enantiomeric separation of mephenytoin was obtained by using a chiral capillary column, the retention times for S- and R-mephenytoin were 25.5 and 26.2 min respectively, with a detection limit less than 50 ng/ml of mephenytoin. Similar linear and reproducible standard curves were obtained over the concentration range of 53.2 to 2128.0 ng/ml (for S-MP, r = 0.9914 +/- 0.0070, n = 6; and for R-MP, r = 0.9939 +/- 0.0070, n = 6), and the mean recoveries of S- and R-MP were 95.4% and 95.8% respectively. The within-day relative standard deviations were less than 8.8% for both S- and R-MP, and that of between-days were less than 14.3%. There was a good reproducibility of the urine S/R mephenytoin determined in China and in Sweden by using similar method in 107 Chinese volunteers after a single oral dose of 100 mg racemic mephenytoin (r = 0.9091, P < 0.001).
建立了一种配备氮磷检测器的气相色谱法,用于测定人尿中抗惊厥药美芬妥英(MP)的S-和R-对映体。向1 ml尿液中加入4 ml二氯甲烷,混合液振荡并离心。将有机相转移至另一试管,在37℃水浴中用氮气吹干。残渣溶于10 μl乙酸乙酯,取1 - 2 μl注入气相色谱仪。结果表明,使用手性毛细管柱可实现美芬妥英对映体的直接分离,S-和R-美芬妥英的保留时间分别为25.5和26.2分钟,美芬妥英的检测限小于50 ng/ml。在53.2至2128.0 ng/ml浓度范围内获得了相似的线性且可重现的标准曲线(对于S-MP,r = 0.9914±0.0070,n = 6;对于R-MP,r = 0.9939±0.0070,n = 6),S-和R-MP的平均回收率分别为95.4%和95.8%。S-和R-MP日内相对标准偏差均小于8.8%,日间相对标准偏差小于14.3%。107名中国志愿者单次口服100 mg消旋美芬妥英后,采用相似方法在中国和瑞典测定的尿中美芬妥英S/R具有良好的重现性(r = 0.9091,P < 0.001)。