Method for extracting ginsenoside from American ginseng
A technology of ginsenoside and American ginseng, which is applied in the field of medicine, can solve problems such as cumbersome process, long extraction time, and loss of active ingredients, and achieve the effects of improving extraction efficiency, shortening extraction time, and promoting release
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Embodiment 1
[0013] Superfine American ginseng, pass through a 100-400 mesh drug sieve, take 1kg of American ginseng powder, add 15L of 80U / mL peroxidase, enzymatically hydrolyze at 65°C for 1h, filter, add 25L of 80% ethanol to the residue, and dissolve it at 90 Extract at ℃ for 0.5 hours, extract twice under this condition, filter and concentrate the filtrate under reduced pressure, and dry to obtain the crude ginsenoside. The content of ginsenoside Rb1 was measured by HPLC, and the extraction rate of ginsenoside Rb1 was 1.43%.
Embodiment 2
[0015] Superfine American ginseng, pass through a 100-400 mesh drug sieve, take 1kg of American ginseng powder, add 25L of 50U / mL peroxidase, enzymatically hydrolyze at 60°C for 1h, filter, add 30L of 75% ethanol to the residue, and dissolve at 90 Extract at ℃ for 0.5 hours, extract twice under this condition, filter and concentrate the filtrate under reduced pressure, and dry to obtain the crude ginsenoside. The content of ginsenoside Rb1 was measured by HPLC, and the extraction rate of ginsenoside Rb1 was 1.40%.
Embodiment 3
[0017] Grind American ginseng ultrafinely, pass through a 100-400-mesh drug sieve, take 1kg of American ginseng powder, add 20L of 70U / mL fungal laccase, enzymatically hydrolyze at 55°C for 1.5h, filter, add 30L of 75% ethanol to the residue, and dissolve it at 85 Extract at ℃ for 1 hour, extract 3 times under this condition, filter and concentrate the obtained filtrate under reduced pressure, and obtain crude ginsenoside after drying. The content of ginsenoside Rb1 was measured by HPLC, and the extraction rate of ginsenoside Rb1 was 1.41%.
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