Extraction process of effective ingredients of gynostemma pentaphylla
A technology of active ingredients and extraction process, applied to medical preparations containing active ingredients, plant/algae/fungus/moss ingredients, plant raw materials, etc., can solve the problems of small production scale, difficult operation, and low extraction rate , to improve work efficiency, facilitate preservation and eliminate oxygen
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Embodiment 1
[0017] Embodiment 1: Gynostemma pentaphyllum is broken to 80 orders, add the Na that pH value is 7.5 2 CO 3 Leach in weakly alkaline solution, the weight ratio of weakly alkaline solution to Gynostemma pentaphyllum is 1.5:1, leaching for 30 minutes under heating and boiling, adding citric acid to adjust the pH to 4.5, and then adding 0.1% of the solution weight CTS flocculant After standing for 2 hours, precipitate and filter to obtain the supernatant containing the active ingredient of Gynostemma pentaphyllum.
Embodiment 2
[0018] Example 2: Break Gynostemma pentaphyllum to 150 mesh, add NaOH weak alkaline solution with a pH value of 8 for extraction, the weight ratio of weak alkaline solution to Gynostemma pentaphyllum is 2:1, and extract for 60 minutes under heating and boiling. Add malic acid to adjust the pH to 5, then add 0.5% PACS synergistic flocculant by weight of the solution, let it stand for 2 hours, precipitate and filter, and obtain the supernatant containing the active ingredient of Gynostemma pentaphyllum.
Embodiment 3
[0019] Embodiment 3: Gynostemma pentaphyllum is broken to 80 orders, add the Na that pH value is 8.5 2 CO 3 Leach in weakly alkaline solution, the weight ratio of weakly alkaline solution to Gynostemma pentaphyllum is 3:1, leaching for 100 minutes under heating and boiling, adding citric acid to adjust the pH to 4.7, and then adding 1% diatoms by weight of the solution The soil precipitation filter aid is left to stand for 2 hours, precipitated and filtered to obtain a supernatant liquid containing the active ingredient of Gynostemma pentaphyllum.
[0020] The extraction results of the above process of the present invention and the existing water decoction method and alcohol extraction method are shown in the table below. The results show that the saponin amount and dissolution rate extracted by the process of the present invention are the highest, the alcohol extraction method is second, and the water decoction method is the lowest.
[0021] Extract comparison table:
[002...
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