Simultaneous determination of phenolic acids by UPLC-MS/MS in rat plasma and its application in pharmacokinetic study after oral administration of Flos Lonicerae preparations

被引:15
|
作者
Zhou, Wei [1 ,2 ,3 ]
Liu, Shijia [4 ]
Ju, Wenzheng [4 ]
Shan, Jinjun [5 ]
Meng, Minxin [6 ]
Cai, Baochang [1 ]
Di, Liuqing [1 ,2 ,3 ]
机构
[1] Nanjing Univ Chinese Med, Coll Pharm, Nanjing 210046, Peoples R China
[2] Jiangsu Engn Res Ctr Efficient Delivery Syst TCM, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Engn Res Ctr Industrializat Chinese Med P, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Univ Chinese Med, Affiliated Hosp, Dept Clin Pharmacol, Nanjing 210093, Peoples R China
[5] Nanjing Univ Chinese Med, Med Coll 1, Nanjing 210046, Peoples R China
[6] Waters Corp, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Flos Lonicerae; Phenolic acids; UPLC-MS/MS; Oral delivery; Pharmacokinetics; MASS-SPECTROMETRY; COMPONENTS; INJECTION; POWDER;
D O I
10.1016/j.jpba.2013.08.010
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The current study aims to investigate the pharmacokinetic study of five phenolic acids (neochlorogenic acid, chlorogenic acid, cryptochlorogenic acid, 3,5-dicaffeoylquinic acid and 3,4-dicaffeoylquinic acid) following oral administration of Flos Lonicerae preparations in rats. A rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed to simultaneously determine the five phenolic acids in rat plasma. After mixing with the internal standard (IS) tinidazole, plasma samples were pretreated by liquid-liquid extraction with ethyl acetate/n-hexane (9:1, v/v). The separation was performed on an Acquity UPLC BEH C18 column (100 mm x 2.1 mm, 1.7 mu m) at a flow rate of 0.4 ml min(-1), and acetonitrile/methanol (4:1, v/v)-0.4% formic acid was used as mobile phase. The detection was performed on a triple quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) via electrospray ionization (ESI) source with positive ionization mode. All calibration curves had good linearity (r > 0.991) over the concentration ranges of 0.74-378 ng ml(-1) for neochlorogenic acid, 0.50-1030 ng ml(-1) for chlorogenic acid, 1.9-250 ng ml(-1) for cryptochlorogenic acid, 0.74-380 ng ml(-1) for 3,5-dicaffeoylquinic acid, and 5.1-328 ng ml(-1) for 3,4-dicaffeoylquinic acid. The intra-and inter-day precision were within 15% and the accuracy ranged from 86.2% to 114.1%. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:189 / 197
页数:9
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