4.6 Article

Simultaneous determination by UPLC-MS/MS of seven bioactive compounds in rat plasma after oral administration of Ginkgo biloba tablets: application to a pharmacokinetic study

期刊

JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B
卷 15, 期 11, 页码 929-939

出版社

ZHEJIANG UNIV
DOI: 10.1631/jzus.B1400035

关键词

Ginkgo biloba tablet; Ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS); Pharmacokinetics

资金

  1. National Basic Research Program (973) of China [2012CB724001]
  2. National Natural Science Foundation of China [81473365]
  3. Beijing Natural Science Foundation of China [7132172]
  4. Independent Project of Beijing University of Chinese Medicine [2014-JYBZZ-XS-106]
  5. Innovative Research Team of Beijing University of Chinese Medicine, China [2011-CXTD-13]

向作者/读者索取更多资源

A rapid, reliable, and sensitive method was developed using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) with an electrospray ionization (ESI) source for determination of seven bioactive compounds in rat plasma after oral administration of Ginkgo biloba tablets (GBTs). The method simultaneously detects bilobalide (BB), ginkgolide A (GA), ginkgolide B (GB), ginkgolide C (GC), quercetin (QCT), kaempferol (KMF), and isorhamnetin (ISR) for pharmacokinetic study. The analytes and internal standard (IS) were extracted from rat plasma by acetidin. An MS/MS detection was conducted using multiple reaction monitoring (MRM) and operating in the negative ionization mode. The calibration curve ranges were 5-500, 5-500, 2.5-250, 1-100, 1-100, 1-100, and 1-100 ng/ml for BB, GA, GB, GC, QCT, KMF, and ISR, respectively. The mean recovery of the analytes ranged from 68.11% to 84.42%. The intra-and inter-day precisions were in the range of 2.33%-9.86% and the accuracies were between 87.67% and 108.37%. The method was used successfully in a pharmacokinetic study of GBTs. The pharmacokinetic parameters of seven compounds were analyzed using a non-compartment model. Plasma concentrations of the seven compounds were determined up to 48 h after administration, and their pharmacokinetic parameters were in agreement with previous studies.

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