Refining method of ginkgo flavone
A technology of ginkgo flavonoids and ginkgo leaves, which is applied in chemical instruments and methods, preparation of sugar derivatives, sugar derivatives, etc. It can solve the problems of high investment in supercritical extraction equipment, restrictions on production and application of flavonoids, and residual organic solvents in products, etc. problems, achieve the effects of saving organic and inorganic reagents, increasing the content, and shortening the production cycle
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0017] 20g ginkgo biloba extract (GBE) was dissolved in 5000mL ethanol-water with ethanol mass fraction of 60%. The solution was subjected to the first ultrafiltration at a pressure of 0.15 MPa and a temperature of 30°C. A polyvinylidene fluoride (PVDF) ultrafiltration membrane with a molecular weight cut-off of 10,000 dalton was selected (provided by Shanghai Xinya Purification Device Factory, the same below). Collect permeate. The collected permeate was evaporated to dryness, and then 1 part by mass of the evaporated powder was dissolved in 50 parts by mass of absolute ethanol. Gradually add methylated β-cyclodextrin, so that the ratio of flavonoids and methylated β-cyclodextrin in the solution is 1:3. First react in a 60°C water bath for 2h, and then react at room temperature for 4h. The reacted product was subjected to a second ultrafiltration at a pressure of 0.15 MPa and a temperature of 30°C. A PVDF ultrafiltration membrane with a molecular weight cut-off of 5000dal...
Embodiment 2
[0019] 20g ginkgo biloba extract (GBE) was dissolved in 5000mL ethanol-water with ethanol mass fraction of 60%. The solution was subjected to the first ultrafiltration at a pressure of 0.15 MPa and a temperature of 30°C. Choose a PVDF ultrafiltration membrane with a molecular weight cut-off of 10,000dalton. Collect permeate. The collected permeate was evaporated to dryness, and then the evaporated powder was dissolved in absolute ethanol. Add methylated β-cyclodextrin gradually, so that the ratio of flavonoids and methylated β-cyclodextrin in the solution is 1:9. First react in a 60°C water bath for 2h, and then react at room temperature for 4h. The reacted product was subjected to a second ultrafiltration at a pressure of 0.15 MPa and a temperature of 30°C. A PVDF ultrafiltration membrane with a molecular weight cut-off of 5000dalton was selected. The concentrated liquid is collected to obtain the final product. It is determined that the percentage content of flavonoids...
Embodiment 3
[0021] 20g ginkgo biloba extract (GBE) was dissolved in 5000mL ethanol-water with ethanol mass fraction of 60%. The solution was subjected to the first ultrafiltration at a pressure of 0.15 MPa and a temperature of 30°C. Choose a PVDF ultrafiltration membrane with a molecular weight cut-off of 10,000dalton. Collect permeate. The collected permeate was evaporated to dryness, and then the evaporated powder was dissolved in absolute ethanol. Add methylated β-cyclodextrin gradually, so that the ratio of flavonoids and methylated β-cyclodextrin in the solution is 1:6. First react in a 60°C water bath for 2h, and then react at room temperature for 4h. The reacted product was subjected to a second ultrafiltration at a pressure of 0.15 MPa and a temperature of 30°C. A PVDF ultrafiltration membrane with a molecular weight cut-off of 5000dalton was selected. The concentrated liquid is collected to obtain the final product. It is determined that the percentage content of flavonoids...
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