Dioscin preparation method
A technology of diosgenin and diosgenin, which is applied in the field of diosgenin preparation, can solve the problems of unstable product quality, large amount of acid, and long time consumption, and achieve high content of active ingredients in the solution, strong oxidation resistance, and avoid heating. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0020] Prepare Dioscorea scutellaria, pulverize it, grind it into powder, add citric acid-disodium hydrogen phosphate buffer solution with a pH value of 4.5 at a material-to-liquid ratio of 1:5, add 15% cellulase by mass after uniformity, and heat at 55°C After enzymatic hydrolysis for 1 h, centrifuge at 4000 r / min for 10 min, collect the supernatant, take an appropriate amount of enzymatically broken wall sediment, and add warm water (30°C), 50% absolute ethanol, 0.05 mol / L citric acid-sodium hydrogen phosphate buffer solution with a pH value of 3.7, extracted for 30 min, and placed the material in a 30KHz ultrasonic device for extraction under the same conditions. After the extraction, centrifuged at 4000 r / min for 10 min, and took the The supernatants were combined and dried at 60°C to obtain diosgenin, with an extraction rate of 85.28%. According to UV detection, the content of diosgenin was 83.5%.
Embodiment 2
[0022] Prepare Dioscorea scutellaria, pulverize it, grind it into powder, add citric acid-disodium hydrogen phosphate buffer solution with a pH value of 4.5 at a material-to-liquid ratio of 1:5, add 15% cellulase by mass after uniformity, and heat at 55°C After enzymatic hydrolysis for 1 h, centrifuge at 4000 r / min for 10 min, collect the supernatant, take an appropriate amount of enzyme-broken sediment, add warm water (45°C), 55% absolute ethanol, 0.05 mol / L citric acid-disodium hydrogen phosphate buffer solution with a pH value of 3.7, extract for 35 min, and extract the material in a 30KHz ultrasonic device under the same conditions. After the extraction, centrifuge at 4000 r / min for 10 min, and take the The supernatants were combined twice and dried at 60°C to obtain diosgenin, with an extraction rate of 87.35%. According to UV detection, the content of dioscin was 85.8%.
Embodiment 3
[0024] Prepare Dioscorea scutellaria, pulverize it, grind it into powder, add citric acid-disodium hydrogen phosphate buffer solution with a pH value of 4.5 at a material-to-liquid ratio of 1:5, add 15% cellulase by mass after uniformity, and heat at 55°C After enzymatic hydrolysis for 1 h, centrifuge at 4000 r / min for 10 min, collect the supernatant, take an appropriate amount of enzyme-broken wall sediment, add warm water (50°C), 60% absolute ethanol, 0.05 mol / L citric acid-disodium hydrogen phosphate buffer solution with a pH value of 3.7 was extracted for 40 min, and the material was extracted in a 30KHz ultrasonic device under the same conditions. After the extraction was completed, centrifuged at 4000 r / min for 10 min, and the The supernatants were combined twice and dried at 60°C to obtain diosgenin, with an extraction rate of 88.21%. According to UV detection, the content of dioscin was 90.2%.
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