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作 者:朱加银[1] 程晶晶[2] 王贤亲[3] 李翔[1] 陈锡文[1]
机构地区:[1]温州医学院实验动物中心,浙江温州325035 [2]温州医学院附属口腔医院,浙江温州325000 [3]温州医学院分析测试中心,浙江温州325035
出 处:《中国卫生检验杂志》2010年第3期516-518,共3页Chinese Journal of Health Laboratory Technology
摘 要:目的:建立LC-MS/MS法测定大鼠血浆中的阿托品。方法:血浆样品经乙腈沉淀蛋白提取。采用C18色谱柱,以乙腈-0.1%甲酸(60:40,v/v)为流动相,氯氮平为内标,采用电喷雾电离源(ESI),选择正离子多离子反应监测(MRM),质核比(m/z)为290.0→123.9(阿托品)和m/z 327.1→269.9(氯氮平)。结果:阿托品在5~1000 ng/ml浓度范围内线性关系良好。方法回收率大于97%,提取回收率大于85%,日内和日间RSD小于8%。结论:方法简便、快速、准确,可满足临床药动学研究的要求。Objective:A LC-MS/MS method was established for the determination of atropine in rat plasma.Method:Plasma samples were treated with acetonitrile to deposit proteins.A C18 column was used with the mobile phase of acetonitrile-0.1%formic acid(60:40,v/v).Clozapine was used as internal standard.ESI was applied in positive ion mode.Multiple reaction monitoring(MRM)mode was used.The detected ions were m/z 290.0→123.9 for atropine and m/z 327.1→269.9 for clozapine.Results:The calibration curve was linear in the concentration of 5~1000 ng/ml.The average recovery was more than 97% and the average extraction recovery was above 85%.The inter-and intra-day RSD were less than 8%.Conclusion:The method is simple,convenient and accurate,which may be suitable for the pharmacokinetic study of atropine.
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