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超高压技术与高速逆流色谱法从乳香中提取和纯化五种萜类化合物。

Extraction and purification of five terpenoids from olibanum by ultrahigh pressure technique and high-speed countercurrent chromatography.

机构信息

Shandong Key Laboratory of TCM Quality Control Technology, Shandong Analysis and Test Center, Jinan, P.R. China.

Reyoung Pharmaceutical Co., Ltd., Jinan, P.R. China.

出版信息

J Sep Sci. 2017 Jul;40(13):2732-2740. doi: 10.1002/jssc.201700215. Epub 2017 Jun 9.

DOI:10.1002/jssc.201700215
PMID:28544633
Abstract

Five terpenoids, including two new ones, 3,7-dioxo-tirucalla-8,24-dien-21-oic acid (2) and 3α-acetoxyl-7-oxo-tirucalla-8,24-dien-21-oic acid (3), and three known ones, boscartol A (1), 11-keto-β-boswellic acid (4), and acetyl-11-keto-boswellic acid (5), have been extracted by the ultrapressure extraction and purified by pH-zone-refining countercurrent chromatography and high-speed countercurrent chromatography from olibanum. For ultrapressure extraction, the optimal condition including 200 MPa of extraction pressure, ethyl acetate of extraction solvent, 1:20 (g/mL) of solid/liquid ratio, and 2 min of extraction time were obtained. For the separation, from 1.5 g of the terpenoid extract, 220.1 mg of 4, 255.5 mg of 5, and 212.3 mg of the mixture of 1, 2, and 3 were obtained by pH-zone-refining countercurrent chromatography under the solvent system of chloroform/ethyl acetate/methanol/water (3:1:3:2, v/v/v/v) with aqueous ammonia and trifluoroacetic acid as retention and eluter agents. The enriched mixture (210 mg) was further separated by conventional high-speed countercurrent chromatography with petroleum ether/ethyl acetate/methanol/water (1:0.8:1.1:0.6, v/v/v/v), yielding 30.1 mg of 1, 35.5 mg of 2, 12.3 mg of 3. The structures of these five terpenoids were elucidated by extensive spectroscopic methods.

摘要

从乳香中通过超高压提取和 pH 区带精制逆流色谱和高速逆流色谱提取并分离出 5 种三萜类化合物,包括 2 个新化合物 3,7-二氧代齐墩果-8,24-二烯-21-酸(2)和 3α-乙酰氧基-7-氧代齐墩果-8,24-二烯-21-酸(3),以及 3 个已知化合物 boscartol A(1)、11-酮-β-乳香酸(4)和乙酰-11-酮-β-乳香酸(5)。对于超高压提取,得到了最佳条件,包括 200 MPa 的提取压力、乙酸乙酯作为提取溶剂、1:20(g/mL)的固液比和 2 分钟的提取时间。对于分离,在氯仿/乙酸乙酯/甲醇/水(3:1:3:2,v/v/v/v)中用氨水和三氟乙酸作为保留和洗脱剂的溶剂系统下,通过 pH 区带精制逆流色谱从 1.5 g 三萜提取物中获得 4 的 220.1 mg、5 的 255.5 mg 和 1、2 和 3 的混合物的 212.3 mg。用石油醚/乙酸乙酯/甲醇/水(1:0.8:1.1:0.6,v/v/v/v)进一步分离富集的混合物(210 mg),得到 30.1 mg 的 1、35.5 mg 的 2 和 12.3 mg 的 3。通过广泛的光谱方法阐明了这 5 种三萜类化合物的结构。

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