Validated LC-ESI-MS/MS Method for the Quantitation of Neopanaxadiol: a Novel Neuroprotective Agent from Panax ginseng and Its Application to a Pharmacokinetic Study in Rat Plasma
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  • 作者:Cong Geng (1)
    Jihua Liu (1)
    Qingxiang Guan (1)
    Ying Zhang (1)
    Qin Meng (1)
    Deya Sun (1)
    Yuequan Sun (2)
    Jianwei Wang (2)
    Yihan Zhou (2)
    Jianyuan Yin (1)
  • 关键词:UPLC ; ESI ; MS/MS ; Neopanaxadiol ; Ginsenoside ; Pharmacokinetics ; Rat plasma
  • 刊名:Chromatographia
  • 出版年:2013
  • 出版时间:10 - May 2013
  • 年:2013
  • 卷:76
  • 期:9
  • 页码:509-514
  • 全文大小:291KB
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  • 作者单位:Cong Geng (1)
    Jihua Liu (1)
    Qingxiang Guan (1)
    Ying Zhang (1)
    Qin Meng (1)
    Deya Sun (1)
    Yuequan Sun (2)
    Jianwei Wang (2)
    Yihan Zhou (2)
    Jianyuan Yin (1)

    1. Department of Natural Products Chemistry, College of Pharmacy, Jilin University, 1266 Fujin Road, Changchun, 130021, China
    2. National Analytical Research Center of Electrochemistry and Spectroscopy, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun, 130022, China
  • ISSN:1612-1112
文摘
Neopanaxadiol (NPD), a new panaxadiol first obtained from the acid hydrolysate of the total ginsenosides of Panax ginseng C. A. Meyer (Araliaceae) in our laboratory, showed neuroprotective effect against glutamate-induced neurotoxicity in primary cultures of rat cortical cells (Tao et al. Chin Chem Lett 20:687-89, 2009). In this research, a sensitive and specifical method of ultra-performance liquid chromatography–electrospray mass spectrometry (UPLC-ESI-MS/MS) for the quantitative analysis of NPD in rat plasma was developed. The NPD and internal standard of panaxadiol were extracted from 200?μL of rat plasma samples with methanol, then the samples were injected in an UPLC (Waters BEH) with C18 column (50?mm?×?2.1?mm i.d., 1.7?μm) and eluted with the mobile phase consisting of methanol–water–formic acid (80:20:0.2, v/v/v). Excellent linearity was found between 5 and 160?ng?mL? with a limit of quantitation of 4?ng?mL?. Intra- and inter-day precision values (RSD) of QC samples were both below 7?%. This study was successfully utilized for the pharmacokinetic profiles of NPD in rats after oral administration and provided an experimental basis for the further pharmacology and clinical application of ginseng products.

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