Extraction separation method of bracken amylose
A separation method and bracken technology are applied in the field of extraction and separation of bracken polysaccharides, which can solve the problems of poor water solubility, low purity and low extraction rate of bracken crude polysaccharides, and achieve good water solubility, high extraction rate, and simple and reasonable method. Effect
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Embodiment 1
[0019] 1. Preparation of Bracken Crude Polysaccharide
[0020] Take 100 g of dried bracken powder, crush it and pass it through a 40-mesh sieve, add 100 ml of 90% ethanol and extract it under reflux at 90° C. for 1 hour. After removing the ethanol, add 2000ml of water, and extract twice on a 65°C water bath, each time for 3 hours. After centrifugation, take the supernatant, add an equal volume of chloroform-n-butanol, the volume ratio of chloroform and n-butanol is 4:1, shake fully, let stand for 10 minutes, and centrifuge at 4500 rpm for 10 minutes. Repeat the above steps until there is no precipitation. The supernatant was concentrated by distillation under reduced pressure at 55°C, and the supernatant was collected, and then precipitated with 2.5 times the volume of ethanol until no precipitate was precipitated. Finally, the precipitate was vacuum freeze-dried at -60°C for 10 hours to obtain crude polysaccharide. Then use the phenol-sulfuric acid method to detect the pol...
Embodiment 2
[0024] 1. Preparation of Bracken Crude Polysaccharide
[0025] Take 100g of dried bracken powder, crush it and pass it through an 80-mesh sieve, add 100ml of 90% ethanol and extract it under reflux at 100°C for 2 hours. After removing the ethanol, add 2500ml of water, and extract 3 times on a 90°C water bath, each time for 4 hours. After centrifugation, take the supernatant, add an equal volume of chloroform-n-butanol, the volume ratio of chloroform and n-butanol is 4:1, shake fully, let stand for 10 minutes, and centrifuge at 4500 rpm for 10 minutes. Repeat the above steps until there is no precipitation. The supernatant was concentrated by distillation under reduced pressure at 50°C, and the supernatant was taken, and then precipitated with 2 times the volume of ethanol until no precipitate was precipitated. Finally, the precipitate was vacuum freeze-dried at -60°C for 12 hours to obtain crude polysaccharide. Then use the phenol-sulfuric acid method to detect the polysacc...
Embodiment 3
[0029] 1. Preparation of Bracken Crude Polysaccharide
[0030] Take 100g of dried bracken powder, crush it and pass it through a 60-mesh sieve, add 100ml of 90% ethanol and extract it under reflux at 80°C for 0.5 hours. After removing the ethanol, add 1500ml of water, and extract twice on a 75°C water bath, each time for 3.5 hours. After centrifugation, take the supernatant, add an equal volume of chloroform-n-butanol, the volume ratio of chloroform and n-butanol is 4:1, shake fully, let stand for 10 minutes, and centrifuge at 4500 rpm for 10 minutes. Repeat the above steps until there is no precipitation. The supernatant was concentrated by distillation under reduced pressure at 60°C, and the supernatant was taken, and then precipitated with 3 times the volume of ethanol until no precipitate was precipitated. Finally, the precipitate was vacuum freeze-dried at -60°C for 8 hours to obtain crude polysaccharide. Then use the phenol-sulfuric acid method to detect the polysacch...
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Abstract
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