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Isolation Purification and Quantification of Ginsenoside F5 and F3 Isomeric Compounds from Crude Extracts of Flower Buds of Panax ginseng

机译:人参花蕾粗提物中人参皂苷F5和F3异构化合物的分离纯化和定量

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摘要

In this paper, the isolation, purification and quantification of ginsenoside F5 and F3 isomeric compounds from crude extracts of flower buds of Panax ginseng (CEFBPG) was investigated by reversed-phase high-performance liquid chromatography (RP-HPLC) for the first time. The satisfied separation at analytical scale was achieved using a Zorbax Eclipse XDB C-18 column with a ternary mobile phase of acetonitrile–water–phosphoric acid (28:71:1) at a flow rate of 1.0 mL/min within 40 min. UV detection was set at 203 nm. Ginsenoside F5 and F3 was 4.21 mg and 5.13 mg in 1 g flower buds of P. ginseng (FBPG), respectively. The preparation of ginsenoside F5 and F3 at semi-preparative scale was performed by using a Daisogel C-18 column and gradient elution system of acetonitrile–water (32:68 → 28:72) at a flow rate of 10 mL/min with a sample load of 20–30 mg, and yielded ginsenosides in purity of more than 96%. Their structures were characterized by NMR and high resolution electrospray ionization mass spectrometry (HRESIMS). All the method validations showed acceptable limits. The results indicate a new source to obtain ginsenoside F5 and F3, and show that the method developed here appears to be reliable for simultaneously preparing them from CEFBPG.
机译:本文首次通过反相高效液相色谱法(RP-HPLC)对人参花蕾粗提物中人参皂苷F5和F3的异构体化合物进行分离,纯化和定量分析。使用Zorbax Eclipse XDB C-18色谱柱和乙腈-水-磷酸三元流动相(28:71:1),在40分钟内以1.0 mL / min的流速实现了满意的分离度。 UV检测设定在203nm。在1 g人参(FBPG)的花蕾中,人参皂苷F5和F3分别为4.21 mg和5.13 mg。使用Daisogel C-18色谱柱和乙腈-水(32:68→28:72)梯度洗脱系统以10 mL / min的流速用半制备规模的人参皂苷F5和F3进行制备样品负载量为20–30 mg,所产生的人参皂苷纯度超过96%。其结构通过NMR和高分辨率电喷雾电离质谱(HRESIMS)进行表征。所有方法验证均显示可接受的限值。结果表明获得人参皂苷F5和F3的新来源,并表明此处开发的方法对于从CEFBPG同时制备人参皂苷似乎是可靠的。

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