Department of Chemistry, Punjabi University, Patiala, India.
J Sep Sci. 2012 Nov;35(21):2970-7. doi: 10.1002/jssc.201200439. Epub 2012 Sep 20.
A simple, accurate, and sensitive microextraction by packed sorbent-gas chromatography-mass spectrometry method has been developed for the simultaneous quantification of four antiepileptic drugs; oxcarbazepine, carbamazepine, phenytoin, and alprazolam in human plasma and urine as a tool for drug monitoring. Caffeine was used as internal standards for the electron ionization mode. An original pretreatment procedure on biological samples, based on microextraction in packed syringe using C(18) as packing material gave high extraction yields (69.92-99.38%), satisfactory precision (RSD < 4.7%) and good selectivity. Linearity was found in the 0.1-500 ng/mL range for these drugs with limits of detection (LODs) between 0.0018 and 0.0036 ng/mL. Therefore, the method has been found to be suitable for the therapeutic drug monitoring of patients treated with oxcarbazepine, carbamazepine, phenytoin, and alprazolam. After validation, the method was successfully applied to some plasma samples from patients undergoing therapy with one or more of these drugs. A comparison of the detection limit with similar methods indicates high sensitivity of the present method over the earlier reported methods. The present method is applied for the analysis of these drugs in the real urine and plasma samples of the epileptic patients.
一种简单、准确、灵敏的微萃取-填充固相萃取-气相色谱-质谱联用方法已被开发出来,用于同时定量检测人血浆和尿液中的四种抗癫痫药物;奥卡西平、卡马西平、苯妥英和阿普唑仑,作为药物监测的工具。咖啡因被用作电子电离模式的内标。一种基于 C(18)填充的微萃取填充注射器的原始预处理方法,可获得高萃取产率(69.92-99.38%)、令人满意的精密度(RSD < 4.7%)和良好的选择性。这些药物在 0.1-500 ng/mL 范围内具有线性关系,检测限(LOD)在 0.0018 和 0.0036 ng/mL 之间。因此,该方法已被发现适用于奥卡西平、卡马西平、苯妥英和阿普唑仑治疗患者的治疗药物监测。经过验证,该方法已成功应用于一些接受这些药物之一或多种药物治疗的患者的血浆样本。与类似方法的检测限比较表明,本方法的灵敏度明显高于早期报道的方法。本方法应用于分析癫痫患者的真实尿液和血浆样本中的这些药物。