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LC-ESI-MS/MS 快速测定人血浆中奥氮平的浓度及临床应用
引用本文:温预关,廖日房,王伟华.LC-ESI-MS/MS 快速测定人血浆中奥氮平的浓度及临床应用[J].中国药学杂志,2009,44(23):1815-1817.
作者姓名:温预关  廖日房  王伟华
摘    要: 目的 建立快速测定人血浆中奥氮平浓度的高效液相色谱串联质谱电喷雾检测法 (LC-ESI-MS/MS) 。 方法 以 Dikma diamonsilTM C18 反相柱( 4.6 mm × 150 mm , 5 μm )为色谱柱,流动相为甲醇 -5 mmol·L-1 甲酸铵( 90 ∶ 10 ),流速为 1 mL·min-1 ,柱温: 25 ℃ ,以乙酸乙酯 - 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 )对奥氮平( <> m/z 313 → 256 )和内标替米沙坦( <> m/z 515.3 → 497.3 )进行测定,并用此法测定 36 例患者稳态血药浓度。 结果 奥氮平的高( 50 μg · L-1 )、中( 25 μg · L-1 )、低( 1 μg·L-1 ) 3 个浓度的平均回收率分别为 100.14% 、 100.33% 和 100.21% ,日内( <> n =5 )、日间( <> n =3 ) RSD 均小于 15% ;分析方法的最低定量限为 0.5 μg · L-1 。线性范围为: 0.5~100 μg · L-1 ,回归方程为 <> F =1.529 5 <> ρ - 0.014 3 , <> r =0.999 ( <> n =8 ),权重系数为 1/ <> ρ 。 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。

关 键 词:奥氮平  血药浓度  高效液相色谱串联质谱电喷雾法
收稿时间:2000-01-01;

Rapid Determination of Olanzapine in Plasma by LC-ESI-MS/MS and Its Clinical Application
WEN Yu-guan,LIAO Ri-fang,WANG Wei-hua.Rapid Determination of Olanzapine in Plasma by LC-ESI-MS/MS and Its Clinical Application[J].Chinese Pharmaceutical Journal,2009,44(23):1815-1817.
Authors:WEN Yu-guan  LIAO Ri-fang  WANG Wei-hua
Institution:(1. <>Department of Clinical Pharmacology, Guangzhou Brain Hospital, Guangzhou 510370 , <> China ; 2. <>Department of Pharmacy, Second Affiliated Hospital of Sun Yat-sen University,<> Guangzhou 510120, <>China
Abstract:OBJECTIVE To develop a LC-ESI-MS/MS method for olanzapine assay in plasma. METHODS Olanzapine was extracted with hexane-isoamyl alcohol. The residues were analyzed with a LC-ESI-MS/MS system (Dikma DiamonsilTM C18 column , 4.6 mm×150 mm,5 μm) with the mobile phase consisted of methanol:water with 5 mmol·L-1 ammonium formate (90∶10). A Agilent 6 410 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 313→256 and m/z 515.3→497.3 was performed to detect olanzapine and the internal standard, respectively. The method was used to evaluate clinical application for 36 patients after multiple oral doses of olanzapine tablets. RESULTS The average recoveries for olanzapine were 100.14%, 100.33% and 100.21%,respectively. The within-day (n=5) and between-day (n=3) precision of variation was less than 15%. The calibration curves for olanzapine had good linearity (r=0.999, n=8) within the range of 0.5~100 μg·L-1 . The limits of quantitation for olanzapine was 0.5 μg·L-1 . CONCLUSION The method provides a sensitive, accurate, precise and reliable analytical procedure for clinical monitoring of olanzapine plasma and its pharmacokinetic studies.
Keywords:olanzapine  plasma concentration  LC-ESI-MS/MS
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