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机构地区:[1]同济大学化学系,上海200092 [2]中国科学院上海有机化学研究所,上海200032
出 处:《分析测试学报》2008年第8期901-903,共3页Journal of Instrumental Analysis
摘 要:建立了一种直接进样HPLC法测定血清中苯妥因的方法。采用混合型苯基浸透限进柱(CAPCELL PAK MF Ph.1,20mm×4.6mm i.d.,5μm),以乙腈-磷酸盐缓冲液(pH6.9,50mmol/L,体积比5:100)为流动相,流速1.0mL/min,210nm紫外检测。苯妥因在1.0~40mg/L间线性良好(r=0.9998),日内、日间相对标准偏差(RSD)为3.6%~6.0%。检出限为0.3mg/L,回收率在98%~104%。该方法不需样品预处理,血清样品用量少,快速简便,适用于临床治疗药物监测。A direct injection high-performance liquid chromatographh method was described for the determination of phenytoin in human serum. The HPLC column (CAPCELL PAK MF Ph-1,20 mm× 4.6 mm i. d. , 5μm) has restricted access material consisting of mixed functional groups covalently bound to silica beads. The method used acetonitrile -phosphate buffer (pH 6.9, 50 retool/L) (5 : 100, by volume) as mobile phase with a flow-rate of 1.0 mL/min and UV detection at 210 nm. The linear range of calibration curve for phenytoin was 1.0 - 40 mg/L with a correlation coefficient of 0. 999 8. The intra- and inter-day variations were between 3.6% and 6.0%. The limit of detection was 0. 3 mg/L. The recoveries were 98% - 104% . The method can be applied to determine phenytoin concentration in clinical serum sample as it was rapid, convenient and reliable.
关 键 词:苯妥因 血清 浸透限进柱 高效液相色谱(HPLC)
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