赵丽艳, 陈笑艳, 张勇, 杨汉煜, 钟大放. 液相色谱-质谱-质谱联用法测定猕猴血浆中阿德福韦液相色谱-质谱-质谱联用法测定猕猴血浆中阿德福韦J. 药学学报, 2003, 38(2): 120-123.
引用本文: 赵丽艳, 陈笑艳, 张勇, 杨汉煜, 钟大放. 液相色谱-质谱-质谱联用法测定猕猴血浆中阿德福韦液相色谱-质谱-质谱联用法测定猕猴血浆中阿德福韦J. 药学学报, 2003, 38(2): 120-123.
ZHAO Li-yan, CHEN Xiao-yan, ZHANG Yong, YANG Han-yu, ZHONG Da-fang. Determination of adefovir in monkey plasma by liquid chromatography-tandem mass spectrometryJ. Acta Pharmaceutica Sinica, 2003, 38(2): 120-123.
Citation: ZHAO Li-yan, CHEN Xiao-yan, ZHANG Yong, YANG Han-yu, ZHONG Da-fang. Determination of adefovir in monkey plasma by liquid chromatography-tandem mass spectrometryJ. Acta Pharmaceutica Sinica, 2003, 38(2): 120-123.

液相色谱-质谱-质谱联用法测定猕猴血浆中阿德福韦液相色谱-质谱-质谱联用法测定猕猴血浆中阿德福韦

Determination of adefovir in monkey plasma by liquid chromatography-tandem mass spectrometry

  • 摘要: 目的 建立测定猕猴血浆中阿德福韦(adefovir)的液相色谱-质谱-质谱联用法。方法 取血浆样品0.25 mL经甲醇沉淀蛋白后,以甲醇-水-甲酸(20∶80∶1)为流动相,用Diamonsil C18柱分离,通过电喷雾离子化四极杆串联质谱,以选择离子反应监测方式进行检测。用于定量分析的离子反应分别为m/z 274→m/z 162(阿德福韦)和m/z 288→m/z 176[内标,9-(3-膦酸甲氧基丙基)腺嘌呤]。结果阿德福韦线性范围为0.02~4.00 mg·L-1,最低定量限为20 μg·L-1,日内、日间精密度(RSD)小于5.8%,准确度(RE)在±4.5%范围内。在临床前药代动力学研究中,应用此法测试了3只猕猴po给予阿德福韦地匹福酯(adefovir dipivoxil)后血浆中阿德福韦的浓度。结论该法操作简便,准确,适用于临床前药代动力学研究。

     

    Abstract: AimTo develop a sensitive and specific liquid chromatography-tandem mass spectrometry (LC/MS/MS) method for the determination of adefovir in monkey plasma. MethodsAdefovir and internal standard 9-(3-phosphonylmethoxypropyl)adenine were isolated from plasma by protein precipitation with methanol, then chromatographed by using a Diamonsil C18 column. The mobile phase consisted of methanol-water-formic acid (20∶80∶1). Electrospray ionization (ESI) source was applied and operated in the positive ion mode. Selected reaction monitoring (SRM) mode with the transitions of m/z 274→m/z 162 and m/z 288→m/z 176 were used to quantify adefovir and the internal standard, respectively. ResultsThe linear calibration curve was obtained in the concentration range of 0.02-4.00 mg·L-1. The lower limit of quantitation was 20 μg·L-1. The inter- and intra-day precision (RSD) was less than 5.8%, and the accuracy (relative error) was within ±4.5%. The method was successfully used in a pharmacokinetic study of adefovir dipivoxil in monkeys. ConclusionThe method is proved to be suitable for pre-clinical investigation of adefovir dipivoxil pharmacokinetics, which offers advantages of specificity and simple sample preparation compared with the previously reported methods.

     

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