Abstract

This study presents an efficient strategy for large-scale preparation of low polarity gingerols directly from ginger crude extract by high-speed countercurrent chromatography with different rotation mode. The ultrasonic-assisted extraction conditions were optimized by response surface methodology and the results showed the major low polarity gingerols could be well enriched under the optimized extraction conditions. Then the crude extract without any pretreatment was directly separated by high-speed countercurrent chromatography with different rotation mode using n-hexane/ethyl acetate/methanol/water (6:4:6:4, v/v/v/v) as the solvent system. In about 400min, five major gingerols including 150mg of [6]-gingerol, 50mg of [8]-gingerol, 20mg of [6]-shogaol, 43mg of [6]-dehydrogingerdione, and 40mg of [10]-gingerol were obtained from 1.2g of crude extract in a single run with repeated injection. Their structures were identified by 1 H-NMR spectroscopy.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call