Abstract
The bioactive iridoid component catalpol was successfully separated by high-speed countercurrent chromatography with high purity from the partially purified crude extract of Rehmannia glutinosa. A polar two-phase solvent system composed of ethyl acetate-n-butanol-water (2:1:3, v/v/v) was selected by thin-layer chromatography and run on a preparative scale where the lower aqueous phase was used as the mobile phase with a head-to-tail elution mode. A 105 mg quantity of the partially purified sample containing 39.2% catalpol was loaded on a 270-mL capacity high-speed countercurrent separation column, yielding 35 mg of catalpol at 95.6% purity. The chemical structure of catalpol was determined by comparison with the high-performance liquid chromatography retention time of standard substance as well as the 1H NMR spectrum.
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CITATION STYLE
Tong, S., Chen, L., Zhang, Q., Liu, J., Yan, J., & Ito, Y. (2015). Separation of catalpol from rehmannia glutinosa libosch. by High-speed countercurrent chromatography. Journal of Chromatographic Science, 53(5), 725–729. https://doi.org/10.1093/chromsci/bmu114
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