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通过高效液相色谱-电喷雾电离串联四极杆-飞行时间质谱联用技术,从青葙子中进行去重复导向的新型保肝三萜皂苷的分离。

Dereplication-guided isolation of novel hepatoprotective triterpenoid saponins from Celosiae Semen by high-performance liquid chromatography coupled with electrospray ionization tandem quadrupole-time-of-flight mass spectrometry.

作者信息

Jiang Yan, Liu Feng-Jie, Wang Yu-Mei, Li Hui-Jun

机构信息

Nanjing Forestry University, Nanjing 210037, China.

State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China.

出版信息

J Pharm Biomed Anal. 2017 Jan 5;132:148-155. doi: 10.1016/j.jpba.2016.10.001. Epub 2016 Oct 3.

DOI:10.1016/j.jpba.2016.10.001
PMID:27721071
Abstract

Although natural products (NPs) from ethnomedical plants have played a vital role in modern drug discovery, separation and purification of bioactive compounds from plant extract is still challenging. In this study, a dereplication strategy using HPLC-QTOF-MS was employed to rapidly discover and highly targeted isolate the novel hepatoprotective triterpenoid saponins from the methanol extract of Celosiae Semen. Firstly, four known saponins, i.e. celosin H, celosin I, celosin J, and pseudoginsenoside RT1 were selected as model compounds, and their fragmentation patterns in ESI-QTOF-MS/MS were characterized. Secondly, an HPLC-QTOF-MS/MS method was applied to chemically screen the saponins of interest, and thereby to guide the subsequent fraction and isolation procedure. Thirdly, the targeted isolation of desired compounds afforded two new triterpenoid saponins namely celosin K (1) and celosin L (2), which were structurally elucidated by combination of extensive NMR spectroscopic and chemical analyses. Finally, the protective effects of compounds 1 and 2 against APAP-induced hepatotoxicity in HepG2 cells were evaluated. These results indicate that the HPLC-QTOF-MS-guided isolation is an efficient methodology for isolating new NPs from medicinal plants through improving selectivity in separation and purification process.

摘要

尽管来自民族药用植物的天然产物(NPs)在现代药物发现中发挥了至关重要的作用,但从植物提取物中分离和纯化生物活性化合物仍然具有挑战性。在本研究中,采用了一种使用HPLC-QTOF-MS的去重复策略,以快速发现并高度靶向地从青葙子甲醇提取物中分离新型保肝三萜皂苷。首先,选择了四种已知皂苷,即青葙皂苷H、青葙皂苷I、青葙皂苷J和伪人参皂苷RT1作为模型化合物,并对它们在ESI-QTOF-MS/MS中的碎裂模式进行了表征。其次,应用HPLC-QTOF-MS/MS方法对感兴趣的皂苷进行化学筛选,从而指导后续的分馏和分离过程。第三,对所需化合物进行靶向分离,得到了两种新的三萜皂苷,即青葙皂苷K(1)和青葙皂苷L(2),通过广泛的核磁共振光谱和化学分析相结合对其结构进行了阐明。最后,评估了化合物1和2对乙酰氨基酚诱导的HepG2细胞肝毒性的保护作用。这些结果表明,HPLC-QTOF-MS引导的分离是一种通过提高分离和纯化过程中的选择性从药用植物中分离新NPs的有效方法。

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