Method for separating and purifying Impatiens pritzellii var. hupehensis triterpenoid saponin monomers by using dynamic axial compression column
A technology of seven triterpenoid saponins and axial compression, which is applied in the field of biochemistry, can solve the problems of low purity of triterpenoid saponins, cumbersome separation steps, and large solvent consumption, and achieve low equipment performance requirements, high preparation efficiency, and simple operation Effect
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Embodiment 1
[0037] Dry the seven rhizomes in cold water, crush them, put them into a multifunctional extraction tank, add pure water to extract three times, each time for 3 hours, and the temperature is 80-95°C. After the extraction is completed, adjust the pH of the extract to 8, and combine the three extracts. Settled for 24 hours. After the settling is completed, take the supernatant for coarse filtration, pump the clean supernatant into the high level tank, enter the resin column filled with D101 resin for adsorption, wash the column with water after the adsorption is completed, and wash until the pH test paper is neutral . Then 4 times the resin volume of 30% ethanol was used to elute to remove impurities, and then 4 times the resin volume of 78% ethanol was used for analysis at a flow rate of 100 L / h. The ethanol was recovered from the analysis solution under vacuum and reduced pressure to obtain cold water seven total saponins fluid extract.
[0038] Dissolve the cold water hepta...
Embodiment 2
[0049] Dry the seven rhizomes in cold water, crush them, put them into a multi-functional extraction tank, add pure water to extract three times, each time for 4 hours, and the temperature is 80-95°C. After the extraction, adjust the pH of the extract to 9, combine the three extracts, and settle 24 hours. After the settling is completed, take the supernatant for coarse filtration, pump the clean supernatant into the high level tank, enter the resin column filled with D101 resin for adsorption, wash the column with water after the adsorption is completed, and wash until the pH test paper is neutral . Then 4 times the resin volume of 30% ethanol was used to elute to remove impurities, and then 4 times the resin volume of 80% ethanol was used for analysis at a flow rate of 100 L / h. The ethanol was recovered from the analysis solution under vacuum and reduced pressure to obtain cold water seven total saponins fluid extract.
[0050] Dissolve the cold water heptasaponin fluid ext...
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