Ishikawa Aline Akemi, da Silva Rodrigo Moreira, Santos Mauro Sérgio Ferreira, da Costa Eric Tavares, Sakamoto Americo Ceiki, Carrilho Emanuel, de Gaitani Cristiane Masetto, Garcia Carlos D
Department of Chemistry, Clemson University, Clemson, SC, USA.
Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brazil.
Electrophoresis. 2018 Oct;39(20):2598-2604. doi: 10.1002/elps.201800046. Epub 2018 Apr 25.
Topiramate (TPM) is the main antiepileptic drug used for the control of partial and generalized seizures in both adults and children. In association with clinical observations, the analysis of plasmatic concentration of TPM is of utmost importance for the individual adjustment of the administered dose to the patient. In the present work, a bioanalytical method was developed and validated for TPM analysis in plasma samples by capillary electrophoresis with capacitively-coupled contactless conductivity detection (CE-C D). A simple background electrolyte composed of 15 mmol/L triethylamine, hydrodynamic injections (0.8 psi for 5 s) and a moderate separation voltage (20 kV) were used, rendering relatively short analysis times (<3 min). The sample pre-treatment was carried out by liquid-liquid extraction using methyl terc-butyl ether as solvent and 200 μL of plasma. The method was validated according to the official guidelines from the European Medicine Agency and showed linearity in plasmatic concentration range from 1 to 30 μg/mL, which covers the clinically-relevant interval. The lower limit of quantification of 1 μg/mL obtained also allows following patients with low dosage of the drug. The method was successfully applied to analysis of plasma samples and allowed the identification of 80% under-medicated patients in the analyzed patient pool.
托吡酯(TPM)是用于控制成人和儿童部分性及全身性癫痫发作的主要抗癫痫药物。结合临床观察,分析TPM的血浆浓度对于根据患者个体情况调整给药剂量至关重要。在本研究中,开发并验证了一种采用毛细管电泳-电容耦合非接触电导检测(CE-C D)法分析血浆样品中TPM的生物分析方法。使用由15 mmol/L三乙胺组成的简单背景电解质、液压进样(0.8 psi,持续5 s)和中等分离电压(20 kV),分析时间相对较短(<3分钟)。样品预处理采用液-液萃取法,以甲基叔丁基醚为溶剂,取200 μL血浆。该方法根据欧洲药品管理局的官方指南进行了验证,在1至30 μg/mL的血浆浓度范围内呈线性,涵盖了临床相关区间。所获得的1 μg/mL的定量下限也能够对低剂量用药患者进行跟踪。该方法成功应用于血浆样品分析,并在分析的患者群体中识别出80%用药不足的患者。