Main content area

Isolation and purification of series bioactive components from Hypericum perforatum L. by counter-current chromatography

Cao, Xueli, Wang, Qiaoe, Li, Yan, Bai, Ge, Ren, Hong, Xu, Chunming, Ito, Yoichiro
Journal of chromatography 2011 v.879 no.7-8 pp. 480-488
Hypericum perforatum, acetonitrile, bioactive properties, butanol, countercurrent chromatography, electrospray ionization mass spectrometry, ethyl acetate, hexane, high performance liquid chromatography, hyperforin, hypericin, methanol, plant extracts, rutin, solvents
Counter-current chromatography (CCC) combined with pre-separation by ultrasonic solvent extraction was successively used for the separation of series bioactive compounds from the crude extract of Hypericum perforatum L. The petroleum ether extract was separated by the solvent system of n-heptane–methanol–acetonitrile (1.5:0.5:0.5, v/v) and n-heptane–methanol (1.5:1, v/v) in gradient elution, yielding a phloroglucinol compound, hyperforin with HPLC purity over 98%. The ethyl acetate extract was separated by using the solvent system composed of hexane–ethyl acetate–methanol–water (1:1:1:1 and 1:3:1:3, v/v) in gradient through both reverse phase and normal phase elution mode, yielding a naphthodianthrone compound, hypericin with HPLC purity about 95%. The n-butanol extract was separated with the solvent system composed of n-butanol–ethyl acetate–water (1:4:5 and 1.5:3.5:5, v/v) in elution and back-extrusion mode, yielding two of flavones, rutin and hyperoside, with HPLC purity over 95%. HPLC–MS, reference sample and UV spectrum were selectively used in separation to search for target compounds from HPLC-DAD profiles of different sub-extracts. The structures of isolated compounds were further identified by ESI-MS, ¹HNMR and ¹³CNMR.