4.6 Article

Multicomponent Characterization of the Flower Bud of Panax notoginseng and Its Metabolites in Rat Plasma by Ultra-High Performance Liquid Chromatography/Ion Mobility Quadrupole Time-of-Flight Mass Spectrometry

期刊

MOLECULES
卷 27, 期 24, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27249049

关键词

Panax notoginseng; flower bud; saponin; multicomponent identification; metabolism

资金

  1. Tianjin Committee of Science and Technology of China
  2. Science & Technology Program of Haihe Laboratory of Modern Chinese Medicine
  3. National Natural Science Foundation of China
  4. [22ZYJDSS00040]
  5. [22HHZYJC00002]
  6. [81872996]

向作者/读者索取更多资源

The flower bud of Panax notoginseng has shown potential in the prevention and treatment of cardiovascular diseases. This study used advanced analytical techniques to comprehensively identify the components and metabolites of Panax notoginseng, revealing its potential therapeutic effects. The findings contribute to a better understanding of the medicinal properties of Panax notoginseng and its further development.
The flower bud of Panax notoginseng (PNF) consumed as a tonic shows potential in the prevention and treatment of cardiovascular diseases. To identify the contained multi-components and, in particular, to clarify which components can be absorbed and what metabolites are transformed, unveiling the effective substances of PNF is of vital significance. A unique ultrahigh-performance liquid chromatography/ion mobility quadrupole time-of-flight mass spectrometry (UHPLC/IM-QTOF-MS) profiling approach and efficient data processing by the UNIFITM bioinformatics platform were employed to comprehensively identify the multi-components of PNF and the related metabolites in the plasma of rats after oral administration (at a dose of 3.6 g/kg). Two MS2 data acquisition modes operating in the negative electrospray ionization mode, involving high-definition MSE (HDMSE) and data-dependent acquisition (DDA), were utilized aimed to extend the coverage and simultaneously ensure the quality of the MS2 spectra. As a result, 219 components from PNF were identified or tentatively characterized, and 40 thereof could be absorbed. Moreover, 11 metabolites were characterized from the rat plasma. The metabolic pathways mainly included the phase I (deglycosylation and oxidation). To the best of our knowledge, this is the first report that systematically studies the in vivo metabolites of PNF, which can assist in better understanding its tonifying effects and benefit its further development.

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