Wu Shihua, Yang Lu, Gao Yuan, Liu Xiaoyue, Liu Feiyan
Zhejiang University, Research Center of Siyuan Natural Pharmacy and Biotoxicology, College of Life Sciences, Zijinggang Campus, Hangzhou 310058, China.
J Chromatogr A. 2008 Feb 8;1180(1-2):99-107. doi: 10.1016/j.chroma.2007.12.024. Epub 2007 Dec 31.
A multi-channel counter-current chromatography (CCC) method has been designed and fabricated for the high-throughput fractionation of natural products without complications sometimes encountered with other conventional chromatographic systems, such as irreversible adsorptive constituent losses and deactivation, tailing of solute peaks and contamination. It has multiple independent CCC channels and each channel connects independent separation column(s) by parallel flow tubes, and thus the multi-channel CCC apparatus can achieve simultaneously two or more independent chromatographic processes. Furthermore, a high-throughput CCC fractionation method for natural products has been developed by a combination of a new three-channel CCC apparatus and conventional parallel chromatographic devices including pumps, sample injectors, effluent detectors and collectors, and its performance has been displayed on the fractionation of ethyl acetate extracts of three natural materials Solidago canadensis, Suillus placidus, and Trichosanthes kirilowii, which are found to be potent cytotoxic to tumor cell lines in the course of screening the antitumor candidates. By combination of biological screening programs and preparative high-performance liquid chromatography (HPLC) purification, 22.8 mg 6 beta-angeloyloxykolavenic acid and 29.4 mg 6 beta-tigloyloxykolavenic acid for S. canadensis, 25.3mg suillin for S. placidus, and 6.8 mg 23,24-dihydrocucurbitacin B for T. Kirilowii as their major cytotoxic principles were isolated from each 1000 mg crude ethyl acetate extract. Their chemical structures were characterized by electrospray ionization mass spectrometry, one- and two-dimensional nuclear magnetic resonance. The overall results indicate the multi-channel CCC is very useful for high-throughput fractionation of natural products for drug discovery in spite of the solvent balancing requirement and the lower resolution of the shorter CCC columns.
已设计并制造了一种多通道逆流色谱(CCC)方法,用于天然产物的高通量分离,避免了其他传统色谱系统有时会遇到的复杂问题,如不可逆的吸附成分损失和失活、溶质峰拖尾和污染。它具有多个独立的CCC通道,每个通道通过平行流管连接独立的分离柱,因此多通道CCC装置可同时实现两个或更多独立的色谱过程。此外,通过将新型三通道CCC装置与包括泵、进样器、流出物检测器和收集器在内的传统平行色谱设备相结合,开发了一种用于天然产物的高通量CCC分离方法,并在三种天然材料加拿大一枝黄花、滑锈伞和栝楼的乙酸乙酯提取物的分离中展示了其性能。在筛选抗肿瘤候选物的过程中,发现这些提取物对肿瘤细胞系具有强大的细胞毒性。通过结合生物筛选程序和制备型高效液相色谱(HPLC)纯化,从每1000mg粗乙酸乙酯提取物中分离出22.8mg 6β-当归酰氧基科拉韦尼克酸和29.4mg 6β-惕各酰氧基科拉韦尼克酸作为加拿大一枝黄花的主要细胞毒性成分,25.3mg滑锈伞素作为滑锈伞的主要细胞毒性成分,6.8mg 23,24-二氢葫芦素B作为栝楼的主要细胞毒性成分。通过电喷雾电离质谱、一维和二维核磁共振对它们的化学结构进行了表征。总体结果表明,尽管存在溶剂平衡要求和较短CCC柱分辨率较低的问题,但多通道CCC对于天然产物的高通量分离以用于药物发现非常有用。