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作 者:张清[1] 陈豪[2] 王晋朝[2] 陈尧[2] 谭志荣[2]
机构地区:[1]长沙市中心医院药剂科,长沙410004 [2]中南大学临床药理研究所,长沙410078
出 处:《中南药学》2010年第4期282-285,共4页Central South Pharmacy
摘 要:目的建立HPLC-MS/MS法同时测定人血浆中的安非他酮及其代谢产物4-OH-安非他酮的浓度。方法血浆样品经乙腈沉淀蛋白后,采用Hypurity C18柱(150mm×2.1mm,5μm)以乙腈-0.1%甲酸-10mm01.L。甲酸铵缓冲液(65:10:25)为流动相,流速为0.2mL·min,通过电喷雾离子化离子阱质谱,以二级质谱选择离子反应监测(SRM)方式进行检测。结果安非他酮线性范围为1.172~1200ng·mL^-1,4-OH-安非他酮线性范围为0.42-430ng·mL^-1,安非他酮和4-OH-安非他酮最低检测浓度分别低于1.0ng·mL^-1和0.21ng·mL^-1结论本法特异性强、灵敏度高,操作简便快速,测定结果可靠,可以准确地测定人体血浆安非他酮和4-OH-安非他酮的浓度。Objective To establish an HPLC-MS/MS method for the simultaneous determination of amfebutamone and 4-OH-amfebutamone in human plasma. Methods After precipitation with acetonitrile, plasma sample was separated on a Hypurity C18 column ( 150 mm×2.1 mm, 5μm ), with acetonitrile-0.1% formate acid -10 mmol ·mL^-1 ammonium formate (65 : 10 : 25) as the mobile phase, the flow rate was 0. 2 mL·min^-1. The eletronspray ion trap mass spectrum in the positive mode and selected reaction monitor ( SRM ) were used to detect the concentration of roxithromycin. Results The linear range of amfebutarnone and 4-OH- amfebutamone was 1. 172-1 200 ng·mL^-1 and 0. 42--430 ng·mL^-1. The limitation of detection for amfebutamone and 4 OH amfebutamone were 1.0 ng·mL^-1 and 0.21 ng·mL^-1, respectively. Conclusion This method is accurate, sensitive and simple, and suitable for the determination of amfebutamone and 4-OH amfebutamone.
关 键 词:高效液相色谱串联质谱 安非他酮 4-OH-安非他酮 电喷雾 药物代谢动力学
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