A kind of extraction equipment of total flavonoids of fern
An extraction device and a technology for total flavonoids, which are applied in the field of extraction methods for total flavonoids from Pterocarpus and the extraction equipment using the method, can solve the problems of difficult removal of filter paper, poor sealing performance, poor filtering effect, etc., and achieve low extraction cost and increase Reduced activity, significant antioxidant effect
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Embodiment 1
[0055] See Figure 1-5 , A method for extracting total flavonoids from Potentilla anserina, comprising the following steps;
[0056] A method for extracting total flavonoids of Potentilla anserina, comprising the following steps;
[0057] S1. Take an appropriate amount of Potentilla tuber, wash the Potentilla tuber and put it in a drying oven at 30℃ to dry to constant weight, then crush the dried Potentilla tuber into Potentilla tuber powder and put it in a desiccator for use ;
[0058] S2. Weigh a certain amount of Potentilla tuber root powder and transfer it into a round-bottomed flask, then add ethanol solutions of different concentrations to prepare mixed solutions with different material-to-liquid ratios according to experimental needs, and then put the round-bottomed flask in a microwave oven and set a certain The microwave power, microwave temperature and microwave time of the same to obtain the extract;
[0059] S3. Take a part of the extract for treatment, and then use the ...
Embodiment 2
[0085] Based on Example 1 but different is;
[0086] Extraction of total flavonoids from Potentilla anserina
[0087] Wash the tubers of Potentilla anserina and put them in a drying oven at 30°C to dry them to constant weight. After crushing, put them in a desiccator for later use. Accurately weigh 5g of Potentilla tuber powder and transfer it into a round-bottomed flask, add ethanol solutions of different concentrations, extract for different periods of time at a certain microwave power and temperature, filter the extract under reduced pressure to remove the filter residue, transfer to a 100mL volumetric flask and use 60 Dilute% ethanol to the mark, shake well and set aside.
[0088] Single factor superior level analysis
[0089] Study ethanol concentration (0, 25, 50, 75, 100%, v / v), material-to-liquid ratio (1:10, 1:15, 1:20, 1:25, 1:30), microwave radiation time (1 , 2, 3, 4, 5min), microwave radiation temperature (40, 50, 60, 70, 80, 90 °C) on the influence of four factors on t...
Embodiment 3
[0098] Based on Examples 1 and 2 but different are:
[0099] DPPH method to determine antioxidant capacity
[0100] Dissolve the Potentilla angustifolia extract in 100μl of 50% methanol according to different masses, and mix it with 900μl of DPPH radical solution to make the concentrations respectively 3.125, 6.25, 12.5, 25, 50μg / mL, and use the same volume of 50% methanol as a blank Contrast. After being placed in the dark for 30 minutes, the absorbance was measured at 517 nm with a spectrophotometer. Calculate the scavenging capacity of DPPH by the following formula
[0101] Clearance rate (%)=(1-(A drug / A control))×100
[0102] ABTS+ method to determine antioxidant capacity
[0103] 2.0mmol / LABTS was added to 2.45mmol / L potassium persulfate solution for 4h at room temperature and protected from light to generate ABTS+ free radicals. ABTS+ was diluted with 0.1M sodium phosphate buffer (pH7.4), and the absorbance at 734nm was measured. Dissolve the Potentilla anserina extract in 5...
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