4.5 Article

Chemical characterisation and quantification of the major constituents in the Chinese herbal formula Jian-Pi-Yi-Shen pill by UPLC-Q-TOF-MS/MS and HPLC-QQQ-MS/MS

期刊

PHYTOCHEMICAL ANALYSIS
卷 31, 期 6, 页码 915-929

出版社

WILEY
DOI: 10.1002/pca.2963

关键词

HPLC-QQQ-MS; MS; Jian-Pi-Yi-Shen pill; qualitative and quantitative analysis; UPLC-Q-TOF-MS; MS

资金

  1. Shenzhen Science and Technology Plan Project [JCYJ20170817094838619, JCYJ20160428182041577, ZDSYS201606081515458, JCYJ20170818094033689]
  2. Traditional Chinese Medicine Bureau of Guangdong Province [20201320]
  3. Natural Science Foundation of Guangdong Province [2018A030313305]
  4. Natural Science Foundation of China [81973602, 81804052]

向作者/读者索取更多资源

Introduction Jian-Pi-Yi-Shen pill (JPYSP) is a Chinese medicine formula developed for the treatment of anaemic patients with chronic kidney disease (CKD). Objective To investigate the chemical profile of JPYSP in the treatment of renal anaemia. Methods A method coupling ultra-performance liquid chromatography with quadrupole time-of-flight tandem mass spectrometry (UPLC-Q-TOF-MS/MS) was established to characterise the chemical constituents present in JPYSP. Subsequently, a high-performance liquid chromatography method coupled with triple-quadrupole tandem mass spectrometry (HPLC-QQQ-MS/MS) was developed to quantify the major constituents from the identified compounds related to the treatment of CKD and anaemia. Results A total of 71 compounds were tentatively identified from JPYSP, including saponins, flavonoids, sesquiterpenoids, coumarins, phenylpropanoids, anthranones, anthraquinones, tannins, phenolic acids and others. Amongst them, 12 compounds (i.e. astragaloside IV, calycosin, calycosin 7-O-glucoside, salvianolic acid A, rosmarinic acid, rhein, liquiritin, formononetin, atractylenolide I, dioscin, tanshinone IIA, and acteoside) were further quantified simultaneously by HPLC-QQQ-MS/MS. Conclusion The newly developed approach is suitable for the chemical profiling analysis and quality control of JPYSP, and could lead to additional pharmacodynamic studies involving the components of JPYSP.

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