A method for the separation and purification of harpagoside and zalongoside a by using high-speed countercurrent chromatography
A technology of high-speed countercurrent chromatography and zalongin, which is applied in the field of separation of natural medicines, can solve problems such as time-consuming and labor-intensive pollution, environmental pollution, irreversible adsorption, etc., and achieve good separation effect, less solvent consumption, and easy operation.
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Embodiment 1
[0035] 1. Take 50g of Radix Scrophulariae and crush it into a coarse powder, add 500mL of ethanol with a volume fraction of 50% and heat and reflux for extraction for 3 times, extracting for 1 hour each time, combine the extracts and filter, cool to room temperature, and depressurize the filtrate in a rotary evaporator to Without alcohol, the ethanol extract is obtained, and its high-performance liquid chromatogram is as follows figure 1 shown.
[0036] 2. After dispersing 4.1g ethanol extract with 30mL water, add it to AB-8 macroporous adsorption resin column chromatography. After the adsorption is completed, use 5 times the column volume of water → 30% ethanol → 50% ethanol → 70% ethanol →Elute with 95% ethanol solution, collect the ethanol eluate containing the target products harpagoside and sapagoside A, concentrate under reduced pressure to no alcohol, and dry to obtain the mixed crude extract of harpagoside and sapagoside A , see HPLC diagram figure 2 . (% means vol...
Embodiment 2
[0044] 1. Take 50g of Radix Scrophulariae and crush it into a coarse powder, add 500mL of ethanol with a volume fraction of 50% and heat and reflux for extraction for 3 times, each extraction for 1h, combine the extracts, filter, and cool to room temperature. The filtrate was reduced to alcohol-free with a rotary evaporator to obtain ethanol extract and ethanol extract.
[0045] 2. After dispersing 10.2g ethanol extract with 40mL water, add it to AB-8 macroporous adsorption resin column chromatography. After the adsorption is completed, use 5 times the column volume of water → 30% ethanol → 40% ethanol → 50% ethanol → 60% ethanol → 70% ethanol → 95% ethanol solution for elution, collect the ethanol eluate containing the target products harpagoside and zalongoside A, concentrate under reduced pressure to no alcohol, and dry to obtain harpagoside and zalongoside Mixed crude extracts of glucoside A.
[0046] 3. Apply high-speed countercurrent chromatography to separate and purif...
Embodiment 3
[0050] 1. Scrophulariaceae medicinal material extraction is the same as embodiment 1.
[0051] 2. After dispersing 10.3g ethanol extract with 40mL water, add it to AB-8 macroporous adsorption resin column chromatography. After the adsorption is completed, use 5 times the column volume of water → 10% ethanol → 30% ethanol → 40% ethanol → 60% ethanol → 95% ethanol solution for elution, collect the ethanol eluate containing the target products harpagoside and zalongoside A, concentrate under reduced pressure to no alcohol, and dry to obtain harpagoside and zalongoside A. Combine the crude extracts.
[0052] 3. Apply high-speed countercurrent chromatography to separate and purify the crude extract. Take n-butanol, ethyl acetate and water, mix them at a volume ratio of 1:9:10, mix well and let stand, separate the upper and lower phases, remove the upper phase as the stationary phase, and the lower phase as the mobile phase, fill the stationary phase with high-speed For the multi-...
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