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血小板活化因子 C-18及其乙酰水解酶的液质联用检测方法

刘维 熊歆 宋福鱼 杨丽 翟所迪

中国临床药理学杂志Issue(12):1191-1193,1201,4.
中国临床药理学杂志Issue(12):1191-1193,1201,4.DOI:10.13699/j.cnki.1001-6821.2015.12.033

血小板活化因子 C-18及其乙酰水解酶的液质联用检测方法

LC-MS/MS method for the detection of platelet-activating factor C-18 and its acetylhydrolase

刘维 1熊歆 2宋福鱼 1杨丽 2翟所迪3

作者信息

  • 1. 北京大学第三医院药剂科,北京 100191
  • 2. 北京大学,治疗药物监测和临床毒理中心,北京 100191
  • 3. 北京大学临床研究所,北京 100191
  • 折叠

摘要

Abstract

Objective To establish a liquid chromatography -mass spectrometry ( LC-MS/MS) method for the analysis of platelet-activa-ting factor C-18(PAF C-18)and its acetylhydrolase in human plasma. Methods A convenient extraction procedure using trichloromethane, methanol and water as the extract solvent was used.The separation was carried out on Agilent XDB C -18 analytical column.Mobile phase A consisted of methanol -ammonium acetate(1 mmol・ L-1 )-acetonitrile ( 57 ∶23 ∶20 ) , and mobile phase B was methanol containing 1 mmol・ L-1 ammonium acetate.Gradient elution was used.The speci-ficity, linearity and limit of quantification, precision and recovery, ma-trix effect and stability were assessed.Results The assay was reproduci-ble within the linearity range from 0.5-25.0 ng・ mL-1 ( r=0.998 4 ) . The relative standard deviation( RSD) of intra-day precision were below 10%, with recovery rate ranged from 67.0% to 82.1% and the matrix effect ranged from 115.3%to 116.9%.PAF C-18 was fully degraded over 90 min at room temperature.Conclusion This method provides a sensitive, special and convenient approach for the clinical analysis of PAF C-18, as well as the indirect measurement of PAF-acetylhydrolase activity by analyzing the concentration decrease of an exogenous PAF.

关键词

血小板活化因子/液质联用/血小板活化因子乙酰水解酶

Key words

platelet-activating factor/LC-MS/MS/platelet-activating factor-acetylhydrolase

分类

医药卫生

引用本文复制引用

刘维,熊歆,宋福鱼,杨丽,翟所迪..血小板活化因子 C-18及其乙酰水解酶的液质联用检测方法[J].中国临床药理学杂志,2015,(12):1191-1193,1201,4.

中国临床药理学杂志

OA北大核心CSCDCSTPCD

1001-6821

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