Laboratory of Pharmaco-Toxicological Analysis, Department of Pharmaceutical Sciences, Faculty of Pharmacy, Alma Mater Studiorum - University of Bologna, Via Belmeloro 6, I-40126 Bologna, Italy.
J Pharm Biomed Anal. 2010 Dec 15;53(5):1319-23. doi: 10.1016/j.jpba.2010.03.007. Epub 2010 Mar 11.
A rapid capillary zone electrophoresis method with indirect UV detection for the determination of topiramate in human plasma was developed and validated. The analyses were carried out with a background electrolyte composed of 10mM sulfamethoxazole as chromophore in phosphate buffer (25 mM, pH 12.0); gabapentin was selected as the internal standard. Application of a voltage of +15 kV led to an analysis time shorter than 5 min; indirect UV detection was operated at 256 nm. Isolation of topiramate from plasma was accomplished by a carefully implemented solid-phase extraction procedure on C18 cartridges. The method provided a linear response over the concentration range of 2-60 microg of topiramate per mL of plasma. The limit of detection (LOD) was 0.8 microg mL(-1) and the limit of quantitation (LOQ) was 2.0 microg mL(-1). Precision, expressed as relative standard deviation, was always lower than 7.3%, extraction yields were always greater than 92%. The results obtained analysing plasma samples from epileptic patients undergoing therapy with topiramate were satisfactory in terms of precision and selectivity.
建立并验证了一种快速毛细管区带电泳-间接紫外检测法,用于测定人血浆中的托吡酯。分析在由磷酸缓冲液(25 mM,pH 值 12.0)中的 10mM 磺胺甲恶唑作为生色团组成的背景电解质中进行;加巴喷丁被选为内标。施加+15 kV 的电压可使分析时间短于 5 分钟;间接紫外检测在 256nm 下进行。通过 C18 小柱上精心实施的固相萃取程序从血浆中分离托吡酯。该方法在 2-60μg/mL 血浆的浓度范围内提供了线性响应。检测限(LOD)为 0.8μg/mL,定量限(LOQ)为 2.0μg/mL。精密度(表示为相对标准偏差)始终低于 7.3%,提取回收率始终大于 92%。对接受托吡酯治疗的癫痫患者的血浆样品进行分析,结果在精密度和选择性方面令人满意。