Coreopsis tinctoria nutt extract extraction method
An extraction method and extract technology, which is applied in the field of snow chrysanthemum extract, can solve the problems of low purity of chemical components, little research on Kunlun snow chrysanthemum, and can not meet the needs of scientific research and clinical needs, so as to achieve high purity and wide application Prospect, effect of promoting effective separation
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Embodiment 1
[0021] Embodiment 1: the preparation of snow chrysanthemum extract
[0022] 1. Soaking: Weigh 100 grams of snow chrysanthemum powder, soak in 60% ethanol solution at a ratio of 1:15, and soak overnight.
[0023] 2. Ultrasonic and suction filtration: Ultrasonic the snow chrysanthemum ethanol solution soaked overnight, the temperature is 70°C, the time is 30min, and then the first suction filtration is performed. The snow chrysanthemum solid after the first suction filtration was soaked in 70% ethanol solution at a ratio of 1:15 and ultrasonicated again at a temperature of 70°C for 30 minutes, and then the second suction filtration was performed. The liquids after two suction filtrations were all poured into a flask for rotary evaporation to make an extract. Rotary evaporator (RE-3000 type, Zhengzhou Yarong Instrument Co., Ltd.), the temperature is 40°C and the speed is 100r / min (revolutions / minute). The final pH of the extract was 7.2-7.4.
Embodiment 2
[0024] Embodiment 2: The content of flavonoids in snow chrysanthemum is determined by high performance liquid chromatography
[0025] Precisely weigh 7 mg of the extract sample of Snow Chrysanthemum, put it in a 25 mL measuring bottle, add methanol to the mark, filter through a 0.45 μm microporous membrane, and perform high performance liquid chromatography detection. Chromatography using LC-20 AB Shimadzu high performance liquid chromatography (Shimadzu, Japan). Chromatographic column Inertsil ODS-SP column (4.6 mm × 150 mm, 5 μm); mobile phase is methanol-0.05% phosphoric acid aqueous solution; flow rate 0.6 mL min -1 , column temperature 25 ℃, detection wavelength 330nm, injection volume 10 μL, external standard method.
Embodiment 3
[0026] Embodiment 3: the content of chlorogenic acid in snow chrysanthemum is determined by chromatographic analysis
[0027] Precisely weigh 7 mg of the extract sample of Snow Chrysanthemum, put it in a 25 mL measuring bottle, add methanol to the mark, filter through a 0.45 μm microporous membrane, and perform high performance liquid chromatography detection. Chromatography using LC-20 AB Shimadzu high performance liquid chromatography (Shimadzu, Japan). Chromatographic column Inertsil ODS-SP column (4.6 mm × 150 mm, 5 μm); mobile phase is methanol-0.05% phosphoric acid aqueous solution; flow rate 0. 6 mL min -1 , column temperature 25 ℃, detection wavelength 330nm, injection volume 10 μL, external standard method.
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