Gleditsia delavayi total saponins extracting and purifying method
A technology for total saponins and acacia, which is applied in the field of extraction and purification of total saponins from Acacia yunnanensis, can solve the problems of high industrial production cost, reduced total saponin purity, large single solvent consumption, etc., achieves complete extraction, realizes pollution-free discharge, and shortens extraction time. effect of time
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0020] Example 1: Dried acacia yunnanensis in an oven at 60°C, peeled, and crushed to 10 meshes, took 20Kg of fruit shell powder and put it into a pressurized solvent extractor, added 200L of distilled water, at a temperature of 80°C, and a pressure of 2.5 Kg / cm 2 Extract under pressure for 30 min, extract 3 times, combine extracts and centrifuge. The extract was cooled to room temperature, and 1% Rhodococcus erythropolis ( Rhodococcusery thropolis ), cultured at 35°C for 5 days, centrifuged, and the supernatant was taken. Use membranes with molecular weight cut-offs of 15000 and 5000Da for separation, and membrane filtration working pressure: 0.1~0.2Mpa. After the permeate passed through a 2000Da membrane, the extract was concentrated and then spray-dried to obtain 8.2Kg of total saponin powder from Dian saponins. The extraction rate of total saponins was 32.8%, and the purity of total saponins was 80.2%.
Embodiment 2
[0021] Example 2: Dian saponica shells were dried in an oven at 60°C, peeled, and crushed to 20 meshes. Take 20Kg of fruit shell powder and put it into a pressurized solvent extractor, add 100L of distilled water, and set the temperature at 100°C and the pressure at 4.0 Kg / cm 2 Extract under pressure for 30 min, extract 4 times, combine extracts and centrifuge. The extract was cooled to room temperature, and 3% Rhodococcus erythropolis ( Rhodococcusery thropolis ), cultured at 20°C for 8 days, centrifuged, and the supernatant was taken. Use membranes with molecular weight cut-offs of 15000 and 5000Da for separation, and membrane filtration working pressure: 0.1~0.2Mpa. After the permeated liquid passed through a 2000Da membrane, the extract was concentrated and then spray-dried to obtain 8.5Kg of total saponins powder from Acacia saponins. The extraction rate of total saponins was 35.0%, and the purity of total saponins was 82.3%.
Embodiment 3
[0022] Example 3, Dian saponica shells were dried in an oven at 60°C, peeled, and crushed to 10 meshes. Take 20Kg of fruit shell powder and put it into a pressurized solvent extractor, add 160L of distilled water, and heat at a temperature of 100°C and a pressure of 3.5 Kg / cm 2 Extract under pressure for 45 minutes, extract 6 times, combine the extracts and centrifuge. The extract was cooled to room temperature, and 7% Rhodococcus erythropolis ( Rhodococcusery thropolis ), cultured at 20°C for 10 days, centrifuged, and the supernatant was taken. Use membranes with molecular weight cut-offs of 15000 and 5000Da for separation, and membrane filtration working pressure: 0.1~0.2Mpa. After the permeate passed through a 2000Da membrane, the extract was concentrated and then spray-dried to obtain 8.3Kg of total saponins powder from Acacia saponins. The extraction rate of total saponins was 34.6%, and the purity of total saponins was 81.3%.
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