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Simultaneous characterization of multiple Psoraleae Fructus bioactive compounds in rat plasma by ultra‐high‐performance liquid chromatography coupled with triple quadrupole mass spectrometry for application in sex‐related differences in pharmacokinetics
Author(s) -
Zhou Zhixing,
Yang Li,
Cheng Liyuan,
Yu Yingli,
Song Lei,
Zhou Kun,
Wu Yingliang,
Zhang Yue
Publication year - 2020
Publication title -
journal of separation science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.72
H-Index - 102
eISSN - 1615-9314
pISSN - 1615-9306
DOI - 10.1002/jssc.202000286
Subject(s) - chromatography , chemistry , analyte , pharmacokinetics , mass spectrometry , high performance liquid chromatography , selected reaction monitoring , calibration curve , analytical chemistry (journal) , detection limit , tandem mass spectrometry , pharmacology , medicine
A method for the simultaneous quantification of 13 bioactive compounds (psoralen, isopsoralen, isobavachin, bakuchalcone, neobabaisoflavone, bavachin, corylin, psoralidin, isobavachalcone, bavachinin, corylifol A, bavachalcone, and bakuchiol) by ultra‐high‐performance liquid chromatography coupled with triple quadrupole mass spectrometry has been developed and validated in rat plasma. Osthol was used as an internal standard and plasma samples were pretreated with one‐step liquid–liquid extraction. These analytes were separated using a gradient mobile phase system of water and acetonitrile at a flow rate of 0.2 mL/min on a reverse‐phase C18 column and analyzed in the selected multiple reactions monitoring mode. All calibration curves were linear ( r > 0.9952) over the tested ranges. The intra‐ and interday accuracy and precisions of these analytes at three different concentration levels were within the acceptable limits of <15% at all concentrations. The mean recoveries of these analytes at three concentrations were more than 60.2% and the matrix effects were in the range of 85–115%. Stability studies proved that the analytes were stable under the tested conditions. The developed method was applied to evaluating the pharmacokinetic study of 13 bioactive compounds after oral administration of Psoraleae Fructus in rat of different genders. Some active compounds in Psoraleae Fructus had sex‐related pharmacokinetics.