首页> 美国卫生研究院文献>Molecules >An Efficient Method for the Preparative Isolation and Purification of Flavonoid Glycosides and Caffeoylquinic Acid Derivatives from Leaves of Lonicera japonica Thunb. Using High Speed Counter-Current Chromatography (HSCCC) and Prep-HPLC Guided by DPPH-HPLC Experiments
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An Efficient Method for the Preparative Isolation and Purification of Flavonoid Glycosides and Caffeoylquinic Acid Derivatives from Leaves of Lonicera japonica Thunb. Using High Speed Counter-Current Chromatography (HSCCC) and Prep-HPLC Guided by DPPH-HPLC Experiments

机译:忍冬叶中黄酮苷和咖啡酰奎尼酸衍生物的制备分离和纯化工艺在DPPH-HPLC实验指导下使用高速逆流色谱(HSCCC)和Prep-HPLC

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摘要

In this work, the n-butanol extract from leaves of Lonicera japonica Thunb. (L. japonica) was reacted with DPPH and subjected to a HPLC analysis for the guided screening antioxidants (DPPH-HPLC experiments). Then, nine antioxidants, including flavonoid glycosides and caffeoylquinic acid derivatives, were isolated and purified from leaves of L. japonica using high speed counter-current chromatography (HSCCC) and prep-HPLC. The n-butanol extract was firstly isolated by HSCCC using methyl tert-butyl ether-butanol/acetonitrile/water (0.5% acetic acid) (2:2:1:5, v/v), yielding five fractions F1, F2 (rhoifolin), F3 (luteoloside), F4 and F5 (collected from the column after the separation). The sub-fractions F1, F4 and F5 were successfully separated by prep-HPLC. Finally, nine compounds, including chlorogenic acid (>1), lonicerin (>2), rutin (>3), rhoifolin (>4), luteoloside (>5), 3,4-O-dicaffeoylquinic acid (>6), hyperoside (>7), 3,5-O-dicaffeoylquinic acid (>8), and 4,5-O-dicaffeoylquinic acid (>9) were obtained, respectively, with the purities over 94% as determined by HPLC. The structures were identified by electrospray ionization mass spectrometry (ESI-MS), 1H- and 13C-NMR. Antioxidant activities were tested, and the isolated compounds showed strong antioxidant activities.
机译:在这项工作中,从忍冬的叶子中提取正丁醇。 (日本粳稻)与DPPH反应,并进行HPLC分析以指导筛选抗氧化剂(DPPH-HPLC实验)。然后,使用高速逆流色谱(HSCCC)和高压液相色谱(HPLC),从粳稻叶片中分离并纯化了9种抗氧化剂,包括类黄酮苷和咖啡酰奎尼酸衍生物。首先通过HSCCC使用甲基叔丁基醚/正丁醇/乙腈/水(0.5%乙酸)(2:2:1:5,v / v)分离正丁醇提取物,得到五个馏分F1,F2 (rhoifolin),F3(黄体苷),F4和F5(分离后从色谱柱中收集)。通过制备型HPLC成功分离出亚组分F1,F4和F5。最后,有9种化合物,包括绿原酸(> 1 ),lonicerin(> 2 ),芦丁(> 3 ),rhoifolin(> 4 < / strong>),黄体甙(> 5 ),3,4-O-二咖啡酰奎尼酸(> 6 ),高甙(> 7 ),3,分别获得了5-O-二咖啡酰奎尼酸(> 8 )和4,5-O-二咖啡酰奎尼酸(> 9 ),其纯度超过94%。 HPLC。通过电喷雾电离质谱(ESI-MS), 1 H-和 13 C-NMR鉴定结构。测试了抗氧化活性,分离出的化合物显示出很强的抗氧化活性。

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