Medicine composition of Panax notoginseng saponins
A technology of Panax notoginseng saponins and Panax notoginseng saponins, which is applied in the direction of drug combinations, pharmaceutical formulas, plant raw materials, etc., and can solve the problems of not selecting saponin components with different pertinence and insufficient research
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Embodiment 1
[0020] Macroporous Adsorption Resin Column for Group Separation
[0021] Grind 1000g of Sanqi raw medicinal material into coarse powder, reflux extract with 2, 1.5, 1.5 times the amount of ethanol respectively for 3 times, each time for 1.5h, filter, combine the filtrate, recover the ethanol until dry; or add the notoginseng coarse powder to Add 2.3 times the amount of 90% ethanol to the multi-functional heat reflux extraction concentrator, heat and reflux extraction and concentration for 10 hours, then move the concentrated solution to a single-effect external circulation concentrator and concentrate under reduced pressure until there is no alcohol smell. The residue was dissolved with an appropriate amount of methanol. Through the macroporous adsorption resin column, it was sequentially eluted with 25%, 40%, 80% and 95% (volume ratio) ethanol gradient, the flow rate was 10ml / min, and each part was collected in 500ml. The eluate was analyzed by silica gel H thin-layer chroma...
Embodiment 2
[0023] Notoginsenoside R 1 , Ginsenoside Rg 1 , Ginsenoside Rb 1 , Ginsenoside Re, Ginsenoside Rd, Ginsenoside Rb 3 and ginsenoside Rb 2 separation and extraction.
[0024] The concentrated solution containing the above-mentioned components separated by the macroporous adsorption resin in Example 1 was respectively put on the chromatographic silica gel column, and the "chloroform-methanol-water" was used successively as 83:16:1, 76:22:2, 68.5:27.5 :4, 65:30:5, 61:33:6, 54:38.5:7.5 solvent elution, flow rate 10ml / min, collected in 500ml each. The eluate was analyzed by silica gel H thin-layer chromatography, and the developing solvent was the same as above. The same components of the chromatographic spots were combined, and the solvent was recovered under reduced pressure to obtain the above-mentioned components with high purity.
[0025] Elution with acetonitrile-water binary gradient, acetonitrile: 0-30min, 18%-19% (volume ratio); 30-35min, 19-35% (volume ratio); 35-60m...
Embodiment 3
[0034] Preparation of the composition
[0035] Take the above-mentioned separated components, mix them in proportion, dissolve them in an appropriate amount with water for injection, decolorize them with activated carbon for injection, filter, add water for injection to the total amount, adjust the pH value to 6.5-7.0, filter, and freeze-dry to obtain .
[0036] According to the above method, the following composition is prepared:
[0037] Composition 1-1: 7 parts of R 1 , 31 parts of Rg 1 , 31 parts of Rb 1 , 3 parts of Re, 6 parts of Rd and 0.05 parts of Rb 3 . And in the above composition, the total content of the above components is 96.53%.
[0038] Compositions 1-2: 9 parts of R1 , 39 parts of Rg 1 , 35 parts of Rb 1 , 6 parts of Re, 11 parts of Rd and 1.0 parts of Rb 3 . And in the above composition, the total content of the above components is 96.40%.
[0039] Composition 2-1: R 1 :Rg 1 :Rb 1 :Re:Rd:Rb 2 It is 7:31:31:3:6:15, and in the above composition,...
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