Method for extracting platycodin
An extraction method and a technology for platycodon saponins are applied in the field of purifying platycodon saponins and extraction, which can solve the problems of low purity and low extraction rate of platycodon saponins, and achieve the effects of high extraction efficiency, easy industrial production and simple operation.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0023] Get fresh platycodon grandiflorum, dry, pulverize, and pass through a 20-mesh sieve. Weigh 50 grams of bellflower powder and put it into an extractor, add 25 milliliters of water to soak for 20 minutes, then add 0.25 grams of pectinase reagent, and enzymolyze it for 2 minutes at a temperature of 30 ° C, collect the raw materials for enzymolysis, and then Add 250 milliliters of 60% ethanol aqueous solution for reflux extraction, extract the filter residue twice, combine the filtrate for 3 times, concentrate under reduced pressure to form an extract, dissolve the gained extract, and pour the solution into the X-5 macroporous adsorption resin column, First wash away the sugar with 2 times column volume of water, then wash away some impurities with 2 times column volume and 10% ethanol, and finally elute with 2 times column volume and 60% ethanol, collect the ethanol eluate, concentrate under reduced pressure, and dry, that is Total saponins were obtained. The content of t...
Embodiment 2
[0025] Get fresh platycodon grandiflorum, dry, pulverize, and pass through a 40-mesh sieve. Weigh 50 grams of bellflower powder and put it into an extractor, add 30 ml of water to soak for 40 minutes, then add 0.5 grams of pectinase, and enzymolyze it for 3 minutes at a temperature of 40°C, collect the raw materials for enzymolysis, and then add 250 milliliters of 60% ethanol aqueous solution was refluxed and extracted, the filter residue was extracted twice, the filtrate was combined for three times, concentrated under reduced pressure and concentrated under reduced pressure to form an extract, the gained extract was dissolved, and the solution was poured into a D3520 macroporous adsorption resin column, First use 3 times the column volume to wash away the sugar, then use 4 times the column volume and 15% ethanol to wash away some impurities, and finally use 4 times the column volume and 65% ethanol to elute, collect the ethanol eluate, concentrate it under reduced pressure, a...
Embodiment 3
[0027] Get fresh platycodon grandiflorum, dry, pulverize, and pass through a 60-mesh sieve. Weigh 50 grams of bellflower powder and put it into the extractor, add 50 ml of water to soak for 60 minutes, then add 1 g of biological enzyme reagent, and enzymolyze it for 4 minutes at a temperature of 45 ° C, collect the raw materials for enzymolysis, and then add 250 milliliters of 60% ethanol aqueous solution was refluxed and extracted, and the filter residue was extracted 3 times, and the filtrate was combined for 4 times, concentrated under reduced pressure to become an extract, and the gained extract was dissolved, and the solution was poured into an AB-8 macroporous adsorption resin column. Wash away the sugar with 4 times column volume of water, then wash away some impurities with 5 times column volume and 20% ethanol, and finally elute with 5 times column volume and 70% ethanol, collect the ethanol eluate, concentrate under reduced pressure, and dry, that is Total saponins w...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com