Abstract

The use of macroporous resins for the separation and purification of total flavonoids to obtain high-purity total flavonoids from Scorzonera austriaca was studied. The optimal conditions for separation and purification of total flavonoids in S. austriaca with macroporous resins were as follows: D4020 resin columns were loaded with crude flavonoid extract solution, and after reaching adsorptive saturation, the columns were eluted successively with 5 bed volumes (BV) of water, 5 BV of 5% (v/v) aqueous ethanol and 5 BV of 30% (v/v) aqueous ethanol at an elute flow rate of 2 BV·h−1. Total flavonoids were obtained from the 30% aqueous ethanol eluate by vacuum distillation recovery. The content of flavonoid compounds in the total flavonoids was 93.5%, which represents an improvement by about 150%. In addition, five flavonoid compounds in the product were identified as 2″-O-β-d-xylopyranosyl isoorientin, 6-C-α-l-arabipyranosyl orientin, orientin, isoorientin and vitexin by LC-ESI-MS analysis and internal standard methods. The results in this study could represent a method for the large-scale production of total flavonoids from S. austriaca.

Highlights

  • Scorzonera austriaca Wild, a perennial herb of the Compositae, is widely distributed in the northeast and northwest regions in China, being especially abundant in Jilin Province

  • Where Qa is the adsorption capacity at adsorption equilibrium; Qd is the desorption capacity after adsorption equilibrium; Rd is the desorption ratio (%); C0 and Ce are the initial and equilibrium concentrations of total flavonoids in the solution, respectively; Cd is the concentration of total flavonoids in the desorption solution; Vi is the volume of the initial sample solution; Vd is the volume of the desorption solution; W is the weight of resin (g)

  • A 1.40 mgmL1 crude flavonoid extract solutionfrom Scorzonera austriaca was used as the test sample

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Summary

Introduction

Scorzonera austriaca Wild, a perennial herb of the Compositae, is widely distributed in the northeast and northwest regions in China, being especially abundant in Jilin Province. It has been widely used as a traditional herbal medicine for curing fevers, carbuncles and mastitis [1]. To date many methods for flavonoid purification have been developed. These include high speed counter-current chromatography [5], solvent extraction, agarose gel media [6], supercritical carbon dioxide extraction [7], aqueous two-phase flotation and molecule imprinted solid phase extraction [8,9]

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