Extraction and determination method of crude polysaccharide in ganoderma spirulina
A determination method and technology of crude polysaccharides, which are applied in the preparation of test samples, material analysis by observing the influence of chemical indicators, and analysis by causing materials to undergo chemical reactions, etc., can solve the problem of lack of reliable detection methods and determination The accuracy of the data is not high, and there are not many problems, so as to achieve the effect of simplifying the steps of extraction and determination, high sensitivity and high accuracy
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Embodiment 1
[0031] Precisely weigh 0.9552g of Ganoderma lucidum spirulina tablet fine powder, add 30g of 80% ethanol solution, oscillate and stir evenly, ultrasonically extract for 40min, centrifuge and discard the solution. Add 30 g of 80% ethanol solution to the precipitation, oscillate and stir evenly, ultrasonically extract for 40 min, and centrifuge to discard the solution. Add the precipitate to 30ml of purified water and extract in a water bath at 100°C for 3 hours, filter, transfer the filtrate to a 100ml volumetric flask, wash the residue 4 times, transfer the washed solution to the volumetric flask to constant volume, shake well, and use it as a sample solution.
[0032] Accurately weigh 0.1080g of glucose standard product dried to constant weight, add distilled water to dissolve and constant volume in a 1000ml volumetric flask to make a 0.108mg / ml control solution, and take the glucose solution 0, 0.2ml, 0.4ml, 0.6ml, 0.8ml, and 1.0ml were respectively placed in 20ml stoppered ...
Embodiment 2
[0038] Precisely weigh 0.5016g of Ganoderma lucidum spirulina tablet fine powder, add 15g of 80% ethanol aqueous solution, oscillate and stir evenly, ultrasonically extract for 20min, centrifuge and discard the solution. Add 15 g of 80% ethanol aqueous solution to the precipitate, oscillate and stir evenly, ultrasonically extract for 20 min, and centrifuge to discard the solution. Add 50ml of purified water to the precipitate and extract in a water bath at 100°C for 1 hour, filter, transfer the filtrate to a 100ml volumetric flask, wash the residue twice, transfer the washing solution to the volumetric flask to constant volume, shake well, and use it as a sample solution. Draw 1ml sample solution in the stoppered test tube of 20ml, prepare with measuring standard solution method, measure absorbance A=0.356 at 490nm place with ultraviolet spectrophotometer, bring sample solution absorbance into equation and promptly obtain the content of crude polysaccharide in sample solution, ...
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