Contin Manuela, Balboni Monica, Callegati Erica, Candela Carmina, Albani Fiorenzo, Riva Roberto, Baruzzi Agostino
Laboratory of Clinical Neuropharmacology, Neurology Clinic, Department of Neurological Sciences, University of Bologna, Via Foscolo 7, 40123 Bologna, Italy.
J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Dec 15;828(1-2):113-7. doi: 10.1016/j.jchromb.2005.09.009. Epub 2005 Sep 22.
A very simple and fast method has been developed and validated for simultaneous determination of the new generation antiepileptic drugs (AEDs) lamotrigine (LTG), oxcarbazepine's (OXC) main active metabolite monohydroxycarbamazepine and felbamate in plasma of patients with epilepsy using high-performance liquid chromatography (HPLC) with spectrophotometric detection. Plasma sample (500 microL) pre-treatment was based on simple deproteinization by acetonitrile. Liquid chromatographic analysis was carried out on a Synergi 4 microm Hydro-RP, 150 mm x 4 mm I.D. column, using a mixture of potassium dihydrogen phosphate buffer (50mM, pH 4.5) and acetonitrile/methanol (3/1) (65:35, v/v) as the mobile phase, at a flow rate of 1.0 mL/min. The UV detector was set at 210 nm. Calibration curves were linear (mean correlation coefficient >0.999 for all the three analytes) over a range of 1-20 mg/mL for lamotrigine, 2-40 microg/mL for monohydroxycarbamazepine and 10-120 microg/mL for felbamate. Both intra and interassay precision and accuracy were lower than 7.5% for all three analytes. Absolute recoveries ranged between 100 and 104%. The present procedure describes for the first time the simultaneous determination of these three new antiepileptic drugs. The simple sample pre-treatment, combined with the fast chromatographic run permit rapid processing of a large series of patient samples.
已开发并验证了一种非常简单快速的方法,用于使用高效液相色谱(HPLC)和分光光度检测法同时测定癫痫患者血浆中的新一代抗癫痫药物(AEDs)拉莫三嗪(LTG)、奥卡西平(OXC)的主要活性代谢物单羟基卡马西平和非氨酯。血浆样品(500微升)的预处理基于用乙腈进行简单的脱蛋白处理。液相色谱分析在Synergi 4微米Hydro-RP,150毫米×4毫米内径的色谱柱上进行,使用磷酸二氢钾缓冲液(50mM,pH 4.5)与乙腈/甲醇(3/1)(65:35,v/v)的混合物作为流动相,流速为1.0毫升/分钟。紫外检测器设置在210纳米。校准曲线在拉莫三嗪1-20毫克/毫升、单羟基卡马西平2-40微克/毫升和非氨酯10-120微克/毫升的范围内呈线性(所有三种分析物的平均相关系数>0.999)。所有三种分析物的批内和批间精密度和准确度均低于7.5%。绝对回收率在100%至104%之间。本方法首次描述了同时测定这三种新型抗癫痫药物。简单的样品预处理与快速的色谱运行相结合,允许对大量患者样品进行快速处理。