Lanças Fernando M, Sozza Marlene A, Queiroz Maria E C
University of São Paulo, Institute of Chemistry of São Carlos, São Carlos, Brazil.
J Anal Toxicol. 2003 Jul-Aug;27(5):304-8. doi: 10.1093/jat/27.5.304.
The determination of lamotrigine (LTG) simultaneously with carbamazepine (CBZ), carbamazepine 10,11 epoxide (CBZ-E), primidone (PRM), phenytoin (PHT), phenobarbital (PB), and 2-phenyl-2-ethyl-malonamide (PEMA) in human plasma was developed using micellar electrokinetic capillary chromatography (MECC) with a diode-array detector. The reproducibility of both separation and quantitation with MECC analysis were appropriate for the intra- and interassay coefficients. The evaluated drugs concentration intervals of LTG, 0.5-10.0 micro g/mL; CBZ, 1.0-16.0 micro g/mL; PEMA, 1.0-20.0 micro g/mL; PB, 1.0-60.0 micro g/mL; PRM, 1.0-20.0 micro g/mL; PHT, 0.7-40.0 micro g/mL; and CBZ-E, 1.0-14.0 micro g/mL were linear with correlation coefficients higher than 0.987 and coefficients of the variation of the points of the calibration curve lower than 10%. The limit of quantitation of the investigated drugs in plasma varied from 0.5 to 1.0 micro g/mL, depending upon the drug. The MECC technique was sensitive enough to work with microsamples into the subtherapeutic, therapeutic, and toxic concentrations, as well as showed to be simple and efficient when applied to monitoring therapeutic drugs in patients treated with a combination of lamotrigine and other antiepileptic drugs such as hepatic enzyme-inducing agents.
采用胶束电动毛细管色谱法(MECC)结合二极管阵列检测器,建立了同时测定人血浆中拉莫三嗪(LTG)与卡马西平(CBZ)、卡马西平10,11-环氧化物(CBZ-E)、扑米酮(PRM)、苯妥英(PHT)、苯巴比妥(PB)和2-苯基-2-乙基丙二酰胺(PEMA)的方法。MECC分析的分离和定量重现性适用于批内和批间系数。所评估的拉莫三嗪、卡马西平、2-苯基-2-乙基丙二酰胺、苯巴比妥、扑米酮、苯妥英和卡马西平10,11-环氧化物的药物浓度区间分别为0.5 - 10.0μg/mL、1.0 - 16.0μg/mL、1.0 - 20.0μg/mL、1.0 - 60.0μg/mL、1.0 - 20.0μg/mL、0.7 - 40.0μg/mL和1.0 - 14.0μg/mL,呈线性关系,相关系数高于0.987,校准曲线各点的变异系数低于10%。血浆中所研究药物的定量限为0.5至1.0μg/mL,具体取决于药物。MECC技术灵敏度足以处理亚治疗、治疗和中毒浓度的微量样品,并且在应用于监测接受拉莫三嗪与其他抗癫痫药物(如肝酶诱导剂)联合治疗的患者的治疗药物时,显示出简单高效的特点。