【摘要】 目的建立测定人血浆中阿立哌唑浓度的反相高效液相串联质谱电喷雾检测法(LC-ESI-MS/MS)。方法以迪马C18反相柱(4.6mm×150mm,5μm)为色谱柱,流动相为甲醇-5mmol·L-1甲酸铵(90∶10),流速为1mL·min-1,柱温:25℃,以醋酸乙酯-二氯甲烷(4∶1)为提取剂。样品经电喷雾离子源正离子化后,通过三重四级杆串联质谱仪,采用选择反应监测(SRM)对阿立哌唑(m/z448.3→285.0)和内标替米沙坦(m/z515.3→497.3)进行测定。并用此法测定30例患者稳态血药浓度。结果阿立哌唑的高(400μg·L-1)、中(125μg·L-1)、低(10μg·L-1)3个质量浓度的平均回收率分别为94.27%、102.58%和97.97%,日内(n=5)、日间(n=3)RSD均小于15%;分析方法的最低定量限为1μg·L-1。线性范围为:5～500μg·L-1,回归方程为F=0.5469ρ+0.0714,r=0.999(n=7)。结论该方法灵敏、准确、简单、快速,可用于临床血浓监测和药动学研究。更多还原

【Abstract】 OBJECTIVE To develop a LC-ESI-MS/MS method for aripiprazole assay in plasma. METHODS Aripiprazole was extracted with ethyl acetate- dichiloromethane (4∶1). The residues were separated on a Dikma diamonsilTM C18 column (4.6 mm×150 mm,5 μm) with the mobile phase consisting of methanol:water with 5 mmol·L-1 ammonium formate (90∶10). A agilent 6410 triple quad mass spectrometer system equipped with an electrospray ionization ion-trap source was used as the detector and operated in the positive ion mode. Selected reaction monitoring(SRM) using the precursor to product ion combinations of m/z 448.3→285.0 and m/z 515.3→497.3 was performed to detect aripiprazole and the internal standard, respectively. The method was used to evaluate clinical application for 30 patients after multiple oral doses aripiprazole tablets. RESULTS The average recoveries for aripiprazole were 94.27%, 102.58% and 97.97%,respectively. The within-day (n=5) and between-day (n=3) precision of variation were less than 15%. The calibration curves for aripiprazole had good linearity , (r = 0.999,n=7) over the range of 5-500 μg·L-1 . The limits of quantitation for aripiprazole was 1 μg·L-1 . CONCLUSION The method provides a sensitive, accurate, precise and reliable analytical procedure for clinical monitoring of aripiprazole plasma and its phamacokinetic studies.更多还原