Procyanidine extraction method
An extraction method and proanthocyanidin technology, applied in the direction of organic chemistry and the like, can solve the problems that cannot be widely applied, the price of beauty products is high, and the extraction rate is not high, and the effects of not easy to be oxidized, less impurities, and high extraction efficiency are achieved.
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Embodiment 1
[0014] A method for extracting proanthocyanidins, comprising the following steps:
[0015] (1) Take the washed and dried grape seeds and grape skins, mix them evenly at a ratio of 14:4, and crush them into powder;
[0016] ⑵, step ⑴ powder, add to the mixed extraction solution, the mixed extraction solution is composed of ethanol, ethyl acetate and water with a volume ratio of 14:8:4; stir evenly;
[0017] (3) Step (2) Mix the material, extract it with 3.2MHz ultrasonic waves for 35 minutes at 9MPa and 19°C in a carbon dioxide environment, quickly cool to room temperature, filter, and vacuum-dry the filtrate.
[0018] The product is detected by liquid chromatography, and the relative content is 80%.
Embodiment 2
[0020] A method for extracting proanthocyanidins, comprising the following steps:
[0021] (1) Take the grape seeds and grape skins after washing and drying, mix them evenly in a ratio of 12:6, and crush them into powder;
[0022] (2) Step (1) powder is added to the mixed extract, which is composed of ethanol, ethyl acetate and water with a volume ratio of 12:9:3; stir evenly;
[0023] (3) Step (2) The mixed material is extracted at 10MPa and 15°C in a helium environment with a 3.5MHz ultrasonic wave for 30 minutes, rapidly cooled to room temperature, filtered, and the filtrate is vacuum-dried.
[0024] The product is detected by liquid chromatography, and the relative content is 82%.
Embodiment 3
[0026] A method for extracting proanthocyanidins, comprising the following steps:
[0027] (1) Take the washed and dried grape seeds and grape skins, mix them evenly at a ratio of 15:2, and crush them into powder;
[0028] (2) Step (1) powder is added to the mixed extract, which is composed of ethanol, ethyl acetate and water with a volume ratio of 16:6:5; stir evenly;
[0029] (3) Step (2) Mix the material, extract it with 3MHz ultrasonic waves for 50 minutes at 8MPa, 22°C, and isolate oxygen for 50 minutes, quickly cool to room temperature, filter, and vacuum-dry the filtrate.
[0030] The product is detected by liquid chromatography, and the relative content is 83%.
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