Method for separation and purification of homoarbutin and hyperoside from P. calliantha H Andr
A high arbutin, separation and purification technology, applied in the field of separation and purification of high arbutin and hypericin, can solve the problems of increased cost, long time consumption, large loss of target compounds, etc. Repeatability and high product yield
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0023] Weigh 500g of crushed wintergreen whole plant, add 10 times the volume of 85% ethanol, and carry out ultrasonic-assisted extraction. The extraction time is 40min, the temperature is 40-50°C, and the power is 36KHz. The above process was performed twice, and the three extracts were combined and concentrated under reduced pressure to a density of 1.15. Prepare 89.3 g of the solid matter obtained by extraction and concentration with water to prepare a suspension drug solution with a feed concentration of 15 mg / ml. The sample volume is 0.6 times the column volume, and the AB-8 macroporous adsorption is carried out under the condition of an elution flow rate of 7 ml / min. Resin, after adsorption, wash impurities with 2 times column volume of water, and then use 6 times column volume in turn, and carry out gradient elution and desorption with solvent systems with ethanol concentrations of 10%, 30%, 50% and 70% respectively, and collect each gradient Combine the eluents with et...
Embodiment 2
[0027]Weigh 300g of crushed wintergreen whole plant, add 15 times the volume of 75% ethanol, and carry out ultrasonic-assisted extraction. The extraction time is 50min, the temperature is 40-50°C, and the power is 32KHz. The above process was performed twice, and the three extracts were combined and concentrated under reduced pressure to a density of 1.20. Prepare 57.1 g of the solid matter obtained by extraction and concentration with water to prepare a suspension drug solution with a feed concentration of 20 mg / ml. The sample volume is 0.8 times the column volume, and the NKA-9 macroporous adsorption is carried out under the condition of an elution flow rate of 8 ml / min. Resin, after adsorption, wash impurities with 2 times column volume of water, then use 5 times column volume, solvent system with ethanol concentration of 10%, 30%, 50% and 70% respectively for gradient elution and desorption, collect each gradient Combine the eluents with ethanol concentrations of 30-50% an...
Embodiment 3
[0031] Weigh 1000g of crushed wintergreen whole plant, add 12 times the volume of 70% ethanol, and carry out hot reflux extraction, extraction time is 50min, temperature is 75°C, after extraction, the extract is filtered out, and the above process is repeated twice, The three extracts were combined and concentrated under reduced pressure to a density of 1.20. The solid matter 182.4g obtained by extracting and concentrating is formulated with water to prepare a suspension liquid with a feed concentration of 25mg / ml, and the loading amount is 1 times the column volume, and the D101 type macroporous adsorption resin is passed under the condition of an elution flow rate of 10ml / min. After adsorption, wash the impurities with 2 times the column volume of water, and then use 6 times the column volume and solvent systems with ethanol concentrations of 10%, 30%, 50% and 70% for gradient elution and desorption, and collect the washes of each gradient respectively. Remove the liquid, co...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 