Preparation method of astragaloside
A technology of astragaloside IV and astragalus, which is applied in the field of preparation of astragaloside IV, can solve the problems of unstable product quality, large amount of acid, long time consumption, etc., and achieves a solution with high content of active ingredients, strong anti-oxidation, and avoidance of damage. Effect
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Embodiment 1
[0020] Prepare Astragalus membranaceus, 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 17% cellulase by mass after uniformity, and enzymolyze at 55°C After 1h, centrifuge at 4000r / min for 10min, collect the supernatant, take an appropriate amount of enzyme-broken wall sediment, and add warm water (30°C), 50% absolute ethanol, 0.05mol / LPH value 3.7 at a material-to-liquid ratio of 1:5 citric acid-disodium hydrogen phosphate buffer solution, extract for 30min, and extract the material in a 30KHz ultrasonic device under the same conditions. , dried at 60°C to obtain astragaloside IV, and the content of astragaloside IV was 99.4% as detected by HPLC.
Embodiment 2
[0022] Prepare Astragalus membranaceus, 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 17% cellulase by mass after uniformity, and enzymolyze at 55°C After 1h, centrifuge at 4000r / min for 10min, collect the supernatant, take an appropriate amount of enzyme-broken wall sediment, and add warm water (45°C), 55% absolute ethanol, 0.05mol / LPH value 3.7 at a material-to-liquid ratio of 1:5 citric acid-disodium hydrogen phosphate buffer solution, extracted for 35min, and the material was extracted in a 30KHz ultrasonic device under the same conditions. , dried at 60°C to obtain astragaloside IV, and the content of astragaloside IV was 99.6% as detected by HPLC.
Embodiment 3
[0024] Prepare Astragalus membranaceus, 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 17% cellulase by mass after uniformity, and enzymolyze at 55°C After 1h, centrifuge at 4000r / min for 10min, collect the supernatant, take an appropriate amount of enzymatically broken wall sediment, and add warm water (50°C), 60% absolute ethanol, 0.05mol / LPH value 3.7 at a material-to-liquid ratio of 1:5 citric acid-disodium hydrogen phosphate buffer solution, extracted for 40min, and placed the material in a 30KHz ultrasonic device for extraction under the same conditions. After the extraction, centrifuged at 4000r / min for 10min, took the supernatant, and combined the two supernatants , dried at 60°C to obtain astragaloside IV, and the content of astragaloside IV was 99.8% as detected by HPLC.
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