2. Academic Validation
  3. A novel and effective chromatographic approach to the separation of isoflavone derivatives from Pueraria lobata

A novel and effective chromatographic approach to the separation of isoflavone derivatives from Pueraria lobata

  • Molecules. 2015 Mar 5;20(3):4238-53. doi: 10.3390/molecules20034238.
Jiang Fu 1 2,  Wenguang Jing 3,  Weihao Wang 4,  Sha Chen 5,  Jun Zhang 6,  An Liu 7
Affiliations

Affiliations

  • 1 Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China. [email protected].
  • 2 College of Pharmacy, Jiang Xi University of Traditional Chinese Medicine, Nanchang 330006, China. [email protected].
  • 3 Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China. [email protected].
  • 4 Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China. [email protected].
  • 5 Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China. [email protected].
  • 6 Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China. [email protected].
  • 7 Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China. [email protected].
PMID: 25751785 DOI: 10.3390/molecules20034238
Abstract

A novel and effective chromatographic approach to the separation and purification of isoflavone compounds from Pueraria lobata is described. The method is based on flash chromatography (FC), coupled to preparative high performance liquid chromatography (prep-HPLC) via a six-way valve. The FC step comprised tandem reversed phase columns, pre-packed with MCI gel (Mitsubishi Chemical Corp., Tokyo, Japan) and C18 (Fuji Silysia Chemical Ltd, Osaka, Japan) resin, respectively, and was designed to separate a crude Pueraria lobata extract into several preliminary fractions. Fractions containing the target compounds were then directly injected via the six-way valve into prep-HPLC columns, without further treatment, for final isolation and purification. Nine isoflavonoids were successfully isolated, three through an online mode and the Other six through an offline mode. The purities of all compounds exceeded 95.0%, as determined by HPLC with an UV-vis photodiode array detector. The convenience, low solvent consumption, and time-saving advantages of this method offer an attractive and promising approach to the isolation of natural products.

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