Song Kwangho, Lee Kyoung Jin, Kim Yeong Shik
College of Pharmacy, Natural Products Research Institute, Seoul National University, Seoul 08826, South Korea.
College of Pharmacy, Natural Products Research Institute, Seoul National University, Seoul 08826, South Korea.
J Chromatogr A. 2017 Mar 17;1489:107-114. doi: 10.1016/j.chroma.2017.02.005. Epub 2017 Feb 3.
A novel application of counter-current chromatography (CCC) to enrich plant extracts using direct and continuous injection (CCC-DCI) was developed to fractionate sesquiterpenoids from the buds of Tussilago farfara L. In this study, an n-hexane-acetonitrile-water (HAcW) solvent system was separately pumped into the CCC column, and an extraction solution (45% acetonitrile) was directly and continuously injected into the CCC column. Since the extraction solution was used as a mobile phase in this method, solvent consumption could be greatly reduced. To enrich the extraction solution (315.9g/5.4L), only 4.2L water, 4.6L acetonitrile, and 1.2L n-hexane were used, including the extraction step. Finally, 6.8g of a sesquiterpenoid-enriched (STE) fraction was obtained from the crude extract (315.9g) of Tussilago farfara (1kg) in a single CCC run with a separation time of 8.5h. The sample injection capacity of CCC-DCI was greater than 300g; this amount of sample could not be handled in conventional CCC or other fractionation methods with the same column volume. Moreover, three major sesquiterpenoids (1: tussilagone, 2: 14-acetoxy-7β-(3'-ethyl cis-crotonoyloxy)-1α-(2'-methylburyryloxy)-notonipetranone, and 3: 7β-(3'-ethyl cis-crotonoyloxy)-1α-(2'-methylburyryloxy)-3, 14-dehydro-Z-notonipetranone) were purified from the STE fraction by CCC, and their chemical structures were elucidated by H NMR and C NMR. A quantification study was conducted, and the contents of compounds 1-3 in the CCC-DCI fraction were higher than those of conventional multi-step fractionations performed in series: solvent partitioning and open column chromatography. Furthermore, the average CCC-DCI recoveries were 96.1% (1), 96.9% (2), and 94.6% (3), whereas the open column chromatography recoveries were 77.7% (1), 66.5% (2), and 58.4% (3). The developed method demonstrates that CCC is a useful technique for enriching target components from natural products.
开发了一种逆流色谱(CCC)的新型应用,即采用直接连续进样(CCC-DCI)来富集植物提取物,用于从款冬(Tussilago farfara L.)的花蕾中分离倍半萜类化合物。在本研究中,将正己烷-乙腈-水(HAcW)溶剂体系分别泵入CCC柱中,并将萃取液(45%乙腈)直接连续注入CCC柱。由于在该方法中萃取液用作流动相,因此可大幅降低溶剂消耗。为了富集萃取液(315.9g/5.4L),包括萃取步骤在内,仅使用了4.2L水、4.6L乙腈和1.2L正己烷。最终,在一次CCC运行中,分离时间为8.5小时,从1kg款冬的粗提物(315.9g)中获得了6.8g倍半萜富集(STE)馏分。CCC-DCI的样品进样量大于300g;在相同柱体积下,传统CCC或其他分馏方法无法处理如此大量的样品。此外,通过CCC从STE馏分中纯化出三种主要的倍半萜类化合物(1:款冬酮;2:14-乙酰氧基-7β-(3'-乙基顺式巴豆酰氧基)-1α-(2'-甲基丁酰氧基)-去甲蜂斗菜内酯;3:7β-(3'-乙基顺式巴豆酰氧基)-1α-(2'-甲基丁酰氧基)-3,14-脱氢-Z-去甲蜂斗菜内酯),并通过1H NMR和13C NMR对其化学结构进行了阐明。进行了定量研究,CCC-DCI馏分中化合物1-3的含量高于串联进行的传统多步分馏:溶剂分配和开放柱色谱法。此外,CCC-DCI的平均回收率分别为96.1%(1)、96.9%(2)和94.6%(3),而开放柱色谱法的回收率分别为77.7%(1)、66.5%(2)和58.4%(3)。所开发的方法表明,CCC是一种从天然产物中富集目标成分有用的技术。