摘要
目的:建立同时测定拉莫三嗪(LTG)、卡马西平(CBZ)、苯巴比妥(PB)血药浓度的高效液相色谱(HPLC)法。方法:色谱柱:SunFire^TM C18(250mm×4.6mm,5μm);流动相:水-乙腈-三乙胺(64.5:35:0.5),磷酸调节pH6.5;流速1.0mL/min,检测波长237nm;血浆样品经乙酸乙酯-二氯甲烷(75:25)提取,以布洛芬为内标。结果:LTG、CBZ在0.625~40.000Fg/mL、PB在1.5625~100.0000μg/mL的血药浓度范围内,其相应峰面积和内标峰面积的比值与浓度呈良好线性关系,相对回收率91%~101%,日内和日间RSD均〈8%。结论:该方法专属性强、准确灵敏、操作简便,适用于LTG、CBZ、PB血药浓度监测和药动学研究。
Objective: To establish a simultaneous determination method of lamotrigine, carbamazepine, and phenobarbital in human plasma by high-performance liquid chromatography. Methods: The analytical column was packed with SunFire^TM C18 (250 mm×4.6 mm, 5 μm). An isocratic elution was applied at a flow rate of 1.0 mL/min with a mobile phase composed of water-acetonitrile-TEA (64.5 : 35 : 0. 5 ) adjusted at pH 6.5 with phosphoric acid. The wavelength detection was set at 237 nm. Plasma samples were extracted with ethylacetate-dichloromethane (75 : 25 ). Results: Calibration curves were linear with regression coefficients greater than 0. 9991 over the concentration ranges 0.625 - 40.000 μg/mL for LTG and CBZ, 1. 562 5 - 100. 000 0 μg/mL for PB, and the relative recovery was 91% - 101%. Both the relative standard deviations of interday and intraday were less than 8%. Conclusions: This bioanalytical method is rapid, sensitive and suitable for clinical therapeutic drug monitoring and also for supporting other clinical pharmacokinetic -based studies.
出处
《儿科药学杂志》
CAS
2014年第4期42-45,共4页
Journal of Pediatric Pharmacy