Ultrasonic-assisted method for extracting dihydroquercetin in sorghum bran
A technology of ultrasonic-assisted extraction and dihydroquercetin, which is applied in the direction of organic chemistry and the like, can solve the problems of short extraction time, destruction, hindering industrial production and application, etc. Effect
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Embodiment 1
[0017] Take 100g of sorghum bran powder that has been crushed through a 20-mesh sieve, add 1000mL of ethanol aqueous solution with a volume fraction of 10%, and conduct ultrasonic extraction for 5 minutes under the conditions of ultrasonic frequency 25KHz, power 100W, and temperature 25°C. , the filter residue was repeatedly extracted three times, the combined filtrate was concentrated under vacuum to no alcohol smell; the concentrated solution was applied to a macroporous resin chromatographic column (AB-8 macroporous adsorption resin, non-polar, glass column type is Φ3 .0*L100cm), with the same flow rate, wash the column with 2000mL distilled water; Adopt the ethanol aqueous solution elution of 30% by volume fraction, collect dihydroquercetin effective distillate liquid, detect with high performance liquid chromatography (method sees embodiment 3) Concentrate the collected effective distillates under reduced pressure until there is no alcohol smell, let stand at 0°C, precipit...
Embodiment 2
[0019] Take 100g of sorghum bran powder that has been crushed through a 200-mesh sieve, add 5000mL of ethanol aqueous solution with a volume fraction of 95%, and conduct ultrasonic extraction for 60 minutes under the conditions of ultrasonic frequency 25KHz, power 300W, and temperature 70°C. , the filter residue was repeatedly extracted three times, the combined filtrate was concentrated under vacuum and reduced pressure; the concentrated liquid was applied to a macroporous resin chromatographic column (ADS-17 macroporous adsorption resin, non-polar, glass column type Φ3.0* at a flow rate of 3 mL / min) (1100cm), with the same flow rate, wash the column with 2000mL distilled water; adopt the ethanol aqueous solution elution of 95% by volume fraction, collect dihydroquercetin effective distillate liquid, detect with high performance liquid chromatography (method sees embodiment 3); Concentrate the collected effective fractions under reduced pressure until there is no alcohol smell...
Embodiment 3
[0021] This embodiment is an embodiment of the detection method of dihydroquercetin.
[0022] Dihydroquercetin is detected by high-performance liquid chromatography, and the dihydroquercetin product is 290nm in the detection wavelength, and is separated through Agilent ZORBAX SB-C18 column (4.6 * 250mm, 5 μ m) (mobile phase: A phase is 0.1% Acetic acid aqueous solution, phase B is methanol; flow rate is 1mL / min, column temperature is 25°C, gradient elution), the chromatogram is as follows figure 1 Shown, dihydroquercetin appears chromatographic peak at 25.45min place, and under the same chromatographic condition, the retention time of this peak is consistent with the retention time of kaempferin reference substance.
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