Lyophyllum decastes polysaccharide extract and preparation method and application thereof
A technology of polysaccharides and extracts from velvet antler mushrooms, which can be used in drug combinations, pharmaceutical formulas, and medical preparations containing active ingredients. Increased yield and simple equipment
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Embodiment 1
[0029] Example 1 High-speed shear extraction of pilose antler polysaccharide
[0030] Take the dried antler mushroom fruiting body, crush it, soak it in 4 times 95% ethanol overnight, filter and collect the filter residue the next day, evaporate the reagents to obtain the degreased antler mushroom powder, and set aside;
[0031] Taking the polysaccharide content of velvet antler mushroom as an index, the influence of three factors of different solid-liquid ratio, rotation speed and extraction time on the polysaccharide content of velvet antler mushroom in high-speed shear extraction was explored, and the results are shown in Table 2;
[0032] Polysaccharide content (%) = total sugar content (%) - reducing sugar content (%)
[0033] Test No.
Ratio of solid to liquid mL / g
Speed r / min
time min
Polysaccharide extraction rate (%)
1
15
9500
1
22.53
2
15
11500
2
22.34
3
15
14500
4
22.23
4
20
...
Embodiment 2
[0037] Example 2 Antler Mushroom Crude Polysaccharides LDS30, LDS60, LDS80—Determination of Reducing Power
[0038] Take the crude polysaccharides LDS30, LDS60, and LDS80 of antler mushroom obtained in Example 1, and make the crude polysaccharides LDS30, LDS60, and LDS80 into aqueous solutions of 0, 0.2, 0.4, 0.6, 0.8, 1.0, and 1.2 mg / mL, respectively, for use;
[0039] Take 0, 0.2, 0.4, 0.6, 0.8, 1.0, 1.2 mg / mL of LDS30 each 1.0 mL in a test tube, add 1.0 mL of 0.2 mol / L phosphate buffer solution with pH = 6.6 and 1.0 mL of 1% ferricyanide Potassium solution, vortex and mix, keep warm at 50°C for 20min, then add 1.0mL of 10% TCA solution, add 1.0mL of 0.1% FeCl after cooling 3 Solution, react for 10min, measure the absorbance value A at 700nm x . Use an equal volume of distilled water instead of LDS30 as a blank control, and measure the absorbance value A 0 , V C As a positive control; LDS60, LDS80 operate as above. The reducing power formula is as follows:
[0040] Reduc...
Embodiment 3
[0043] Example 3 Deer antler mushroom crude polysaccharides LDS30, LDS60, LDS80——Determination of ABTS free radical scavenging ability
[0044] Measure 8.0mL of 7mmol / L ABTS solution and mix with 141μL of 140mmol / L potassium persulfate solution, and then react in the dark at 4°C for 12-16h. Dilute the stock solution with phosphate buffer solution of 10mmol / LpH=7.4 to OD=0.70±0.02 for later use;
[0045] Take 0, 0.2, 0.4, 0.6, 0.8, 1.0, 1.2mg / mL of LDS30 each 1.0mL into a test tube, add 3.0mL ABTS free radical solution, mix well, react in the dark at 30°C for 5min, measure the absorbance at 734nm Value A i ; Use 1.0mL distilled water as a blank control, and measure the absorbance value A under the same conditions 0 ; Replace the ABTS free radical solution with 3.0mL distilled water as the sample control group, measure the absorbance value A j , V C As a positive control; LDS60, LDS80 operate as above. The formula of ABTS free radical scavenging ability is as follows:
[0...
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