液相色谱-质谱联用法测定人参皂苷Re在健康人血浆的浓度  

Determination of ginsenoside Re in human plasma by LC/MS/MS

作　　者：刘奕明[1] 杨柳[1] 曾星[1] 邓远辉[1] 冯怡[1] 梁伟雄[1] 

机构地区：[1]广州中医药大学附属广东省中医院临床药理室,广东广州510120

出　　处：《中国临床药理学杂志》2005年第5期381-383,共3页The Chinese Journal of Clinical Pharmacology

基　　金：国家863基金资助项目(2002AA22341B)

摘　　要：目的建立液相色谱-质谱联用法测定人参皂苷Re在健康人血浆中浓 度的方法。方法血浆样品用固相萃取法处理。用电喷雾离子化和正离子多 离子反应监测方式检测人参皂苷Re。结果该方法人参皂苷Re线性范围为 1．05～1 050 ng·mL-1;定量下限为1．05 ng·mL-1;方法回收率在99．3％～ 104．3％;日内、日间变异系数(RSD)均<15％。结论该法准确、灵敏、特异, 适用于健康人血浆人参皂苷Re浓度测定。Objective To develop a HPLC/MS/MS method for the determination of ginsenoside Re in healthy human plasma. Methods Plasma samples were pretreated by solid phase extraction . Ginsenoside Re was detected by the positive electrospray ionization -MS method under multiple reaction monitoring mode. Results The calibration curve of ginsenoside Re in plasma was linear over the range of 1.05 ～ 1 050 ng · mL^-1 , the limit of quantitation was 1.05 ng · mL^-1. The relative recovery was 99.3% 104. 3%. The within - day and between - day RSDs were less than 15%. Conclusion This assay method is accurate, sensitive, and specific, it is suitable for the measurement of plasma ginsenoside Re concentration.

关 键 词：人参皂苷RE 液相色谱-质谱联用法 血药浓度 

分 类 号：R969.1[医药卫生—药理学] R977[医药卫生—药学]