4.5 Article

Simultaneous determination of eight bioactive constituents of Zhi-Zi-Hou-Po decoction in rat plasma by ultra high performance liquid chromatography with tandem mass spectrometry and its application to a pharmacokinetic study

Journal

JOURNAL OF SEPARATION SCIENCE
Volume 43, Issue 2, Pages 406-417

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jssc.201900670

Keywords

active constituents; pharmacokinetics; tandem mass spectrometry; traditional Chinese medicine; ultra high performance liquid chromatography

Funding

  1. National Natural Science Foundation of China [81703683, 81773692, 81673396, 81872831]
  2. Science and Technology Project from the Department of Education of Jilin Province [JJKH20191071KJ]
  3. Scientific Research Foundation of Administration of Traditional Chinese Medicine of Jilin Province of China [2017250, 2018124]
  4. Scientific Research Foundation of Department of Health and Family Planning Commission [2017Q048]
  5. young talent training plan from Jilin Science and Technology Bureau [20166029, 20166031]

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Zhi-Zi-Hou-Po Decoction, consisting of Gardenia jasminoides Ellis, Magnolia officinalis Rehd. et Wils., and Citrus aurantium L, is a classical Traditional Chinese Medicine formula for the treatment of depression. In order to make good and rational use of this formula in the future, a sensitive, selective, and reliable ultra high performance liquid chromatography with tandem mass spectrometry method was developed for simultaneous determination of two iridoid glycosides (geniposide and genipin gentiobioside), two lignans (honokiol and magnolol), four flavonoid glycosides (isonaringin, naringin, hesperidin, and neohesperidin), the major bioactive constituents of Zhi-Zi-Hou-Po Decoction, in rat plasma using paeoniflorin as internal standard. Plasma samples were pretreated by a simple protein precipitation with acetonitrile. Chromatographic separation was performed on a shim-pack XR-ODS C-18 column (75 x 3.0 mm, 2.2 mu m) using gradient elution with mobile phase consisting of 0.1% formic acid aqueous solution and acetonitrile at a flow rate of 0.5 mL/min. Mass spectrometric detection was conducted on a 3200 QTRAP mass spectrometry equipped with electrospray ionization source in negative ionization mode. Quantification was performed using multiple reactions monitoring mode. Calibration curves exhibited good linearity (r > 0.9947) over a wide concentration range for all analytes, and the lower limits of quantification were 10, 5, 1, 5, 1, 5, 1, and 5 ng/mL for geniposide, genipin gentiobioside, honokiol, magnolol, isonaringin, naringin, hesperidin, and neohesperidin, respectively. The intraday and interday precisions at three quality control levels were less than 12.3% and the accuracies ranged from -11.2 to 10.7%. Extraction recovery, matrix effect, and stability were satisfactory in rat plasma. The validated method was successfully applied to a pharmacokinetic study of the eight analytes after oral administration of Zhi-Zi-Hou-Po decoction to rats.

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