Extraction method for total flavone of potentilla anserine L. and extraction equipment utilizing extraction method
An extraction method and a technology for total flavonoids are applied in the field of extraction methods for total flavonoids from Pterocarpus and the field of extraction equipment applying the method, which can solve the problems of difficult removal of filter paper, poor sealing performance, poor filtering effect, etc., and achieve low extraction cost and increase in extraction cost. Reduced activity, significant antioxidant effect
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Embodiment 1
[0055] see Figure 1-5 , a method for extracting total flavonoids from Bracken, comprising the following steps;
[0056] A method for extracting total flavonoids from Bracken, comprising the following steps;
[0057] S1. Take an appropriate amount of junima tubers, wash the junima tubers and put them in a drying oven at 30°C to dry to constant weight, then crush the dried junima tubers into juna tuber powder, and put them in a desiccator for later use ;
[0058] S2. Weigh a certain amount of fern root powder and move it into a round bottom flask, then add different concentrations of ethanol solutions, and prepare mixed solutions with different material-liquid ratios according to the needs of the experiment, then put the round bottom flask into the microwave oven, set a certain The microwave power, the microwave temperature and the microwave time are obtained to obtain the extract;
[0059] S3, take a part of the extract for processing, and then use the extract to measure it...
Embodiment 2
[0085] Based on Example 1 but with some differences;
[0086] Extraction of Total Flavonoids from Bracken
[0087] After cleaning the fern tuber, put it into a drying oven at 30°C and dry to constant weight, and put it into a desiccator after crushing for subsequent use. Accurately weigh 5g of Juema root tuber powder and transfer it into a round bottom flask, add ethanol solutions of different concentrations, extract at a certain microwave power and temperature for different times, filter the extract under reduced pressure to remove the filter residue, transfer to a 100mL volumetric flask and use 60 % ethanol to the mark, shake well and set aside.
[0088] One-way optimal level analysis
[0089] Study ethanol concentration (0, 25, 50, 75, 100%, v / v), solid-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) four factors on the extraction of flavonoids from the root of Bracken. ...
Embodiment 3
[0098] Based on Example 1 and 2 but different:
[0099] Determination of antioxidant capacity by DPPH method
[0100] Dissolve the fern extract in 100 μl of 50% methanol according to different masses, and mix it with 900 μl of DPPH free radical solution, so that the concentrations are 3.125, 6.25, 12.5, 25, and 50 μg / mL, and use the same volume of 50% methanol as a blank control. After standing in the dark for 30min, the absorbance was measured at 517nm by a spectrophotometer. The scavenging capacity of DPPH was calculated by the following formula
[0101] Clearance rate (%)=(1-(A drug / A control))×100
[0102] Determination of antioxidant capacity by ABTS+ method
[0103] 2.0mmol / LABTS was added to 2.45mmol / L potassium persulfate solution and treated for 4 hours at room temperature in the dark to generate ABTS+ free radicals. Dilute ABTS+ with 0.1M sodium phosphate buffer (pH7.4), and measure the absorbance at 734nm. Dissolve the fern extract in 50 μl 50% methanol accord...
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