• 首页期刊简介编委会刊物订阅专栏专刊电子刊学术动态联系我们English
引用本文:邹尚荣1,温预关2,林琼英3.LC-MS/MS测定人血浆中阿米舒必利的浓度[J].中国现代应用药学,2009,(6):483-486.
ZOU Shangrong1,WEN Yuguan2,LIN Qiongying3.Determination of Amisulpride in Plasma by LC-MS/MS[J].Chin J Mod Appl Pharm(中国现代应用药学),2009,(6):483-486.
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  【EndNote】   【RefMan】   【BibTex】
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 2182次   下载 1542 本文二维码信息
码上扫一扫!
分享到: 微信 更多
LC-MS/MS测定人血浆中阿米舒必利的浓度
邹尚荣1,温预关2,林琼英3
作者单位
邹尚荣1,温预关2,林琼英3  
摘要:
目的建立测定人血浆中阿米舒必利浓度的高效液相色谱串联质谱电喷雾检测法(LC-MS/MS)。方法以Welch Materials XB-C18(2.1 mm×150 mm,3 μm)为色谱柱,流动相为甲醇-水(95∶5,含5 mmol·L-1甲酸铵),流速为0.3 mL·min-1,柱温:40 ℃,以乙酸乙酯-二氯甲烷(4∶1)为提取溶剂。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)对阿米舒必利(m/z370.3→242.1)和内标舒必利(m/z324.2→112.1)进行测定。结果阿米舒必利高(400 μg·L-1)、中(250 μg·L-1)、低(1.25 μg·L-1)3个浓度的平均方法回收率分别为104.44%、104.74%和95.65%,日内(n=5)、日间(n=3)RSD均小于15%;分析方法的最低定量限为0.52 μg·L-1。线性范围为:0.5~500 μg·L-1。结论该方法灵敏、准确、简单、快速,可用于阿米舒必利临床血浓监测和药动学研究。
关键词:  阿米舒必利  血药浓度  高效液相色谱串联质谱电喷雾法
DOI:
分类号:
基金项目:
Determination of Amisulpride in Plasma by LC-MS/MS
ZOU Shangrong1,WEN Yuguan2,LIN Qiongying3
Abstract:
OBJECTIVE To establish an LC-MS/MS method for the determination of amisulpride in human plasma. METHODS The sample extraction was performed by ethyl acetate-dichloromethane(4∶1). Separation was achieved on a Welch Materials XB-C18(2.1 mm×150 mm,3 μm) column with the mobile phase consisted of methanol-water with 5 mmol·L-1 ammonium formate (95:5). An 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) was used as the precursor to product ion combinations of m/z 370.3→242.1 and m/z 324.2→112.1 to detect amisulpride and the internal standard, respectively. The method was used to evaluate clinical application for 10 healthy volunteer after oral dose of 200 mg amisulpride tablet. RESULTS The average recoveries for amisulpride were 104.44%,104.74% and 95.65%,respectively. The method was accurate with intra-day(n=5) and inter-day (n=3) RSD within 15%. The calibration curves for amisulpride had good linearity, over the concentration range of 0.5-500 μg·L-1. The limits of quantitation for amisulpride was 0.52 μg·L-1. CONCLUSION The method provides a sensitive, accurate, precise and reliable analytical procedure for clinical monitoring of amisulpride plasma and its phamacokinetic studies.
Key words:  amisulpride  plasma concentration  LC-ESI-MS/MS
扫一扫关注本刊微信