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中国精品科技期刊2020
宋道光,陈志. 高速逆流色谱法从小叶金钱草中分离四种黄酮苷类化合物[J]. 华体会体育,2022,43(24):93−101. doi: 10.13386/j.issn1002-0306.2022030223.
引用本文: 宋道光,陈志. 高速逆流色谱法从小叶金钱草中分离四种黄酮苷类化合物[J]. 华体会体育,2022,43(24):93−101. doi: 10.13386/j.issn1002-0306.2022030223.
SONG Daoguang, CHEN Zhi. Separation of Four Flavonoid Glycosides from Hydrocotyle sibthorpioides Lam. by High-speed Counter-current Chromatography[J]. Science and Technology of Food Industry, 2022, 43(24): 93−101. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022030223.
Citation: SONG Daoguang, CHEN Zhi. Separation of Four Flavonoid Glycosides from Hydrocotyle sibthorpioides Lam. by High-speed Counter-current Chromatography[J]. Science and Technology of Food Industry, 2022, 43(24): 93−101. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022030223.

高速逆流色谱法从小叶金钱草中分离四种黄酮苷类化合物

Separation of Four Flavonoid Glycosides from Hydrocotyle sibthorpioides Lam. by High-speed Counter-current Chromatography

  • 摘要: 为研究小叶金钱草中大极性黄酮苷类化合物,采用正丁醇萃取、DM 301大孔吸附树脂、葡聚糖凝胶、反相硅胶柱层析纯化,得到大极性黄酮苷类组分。结合离线二维高速逆流色谱,分别以正己烷/正丁醇/水/冰乙酸(系统I:1:2:1:0.1,v/v/v/v和系统II:1:1:1:0.1,v/v/v/v)为溶剂系统,在主机转速900 r/min、流速2 mL/min、254 nm检测波长条件下进行分离。结果表明,从小叶金钱草正丁醇组分中分离得到四种黄酮苷类化合物,经1H、13C NMR鉴定为杨梅素3,3'-二-α-L-鼠李糖苷(1)、木犀草素-7-O-β-D-葡萄糖醛酸苷(2)、槲皮素3,3'-二-α-L-鼠李糖苷(3)和芹菜素-7-O-β-D-葡萄糖醛酸苷(4),高效液相色谱分析其纯度均大于95%。化合物3为首次从小叶金钱草中分离得到,本研究为小叶金钱草的化学成分研究提供依据。

     

    Abstract: For an improved study of flavonoid glycosides of great polarity from Hydrocotyle sibthorpioides Lam (HSL), the large polar flavonoid glycosides were extracted with n-BuOH, purified by DM 301 macroporous resin, Sephadex LH-20 and reversed-phase silica gel (ODS/RP-18). Combined with offline two-dimensional high-speed counter-current chromatography (HSCCC), the fraction with the target compounds was purified by HSCCC adopting a two-phase solvent system consisting of n-hexane/n-BuOH/water/glacial acetic acid (system I: 1:2:1:0.1, v/v/v/v and system II: 1:1:1:0.1, v/v/v/v). Additionally, the rotation velocity, and flow rate in conjunction with detection wavelength were adjusted to 2.0 mL/min, 900 r/min, and 254 nm respectively. The results demonstrated that four compounds were isolated from HSL, whose structures were determined as myricetin 3,3'-di-α-L-rhamnopyranoside (1), luteolin-7-O-β-D-glucuronide (2), quercetin 3,3'-di-α-L-rhamnopyranoside (3) and apigenin 7-O-β-D-glucuronide (4) operating 1H NMR and 13C NMR spectroscopy. The purity of the four compounds were above 95% by HPLC analysis, and compound 3 was isolated from the HSL for the first time. Thus, this work would provide a basis for the study of the chemical constituents of HSL.

     

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