Chi lucid ganoderma polysaccharide and prep. and use thereof
A Ganoderma lucidum polysaccharide and polysaccharide technology, applied in the field of anti-tumor drugs, can solve the problems of low molecular weight Ganoderma lucidum polysaccharide anti-tumor research, and achieve the effects of good water solubility, low viscosity, and convenient administration
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Embodiment 1
[0028] Example 1. Red Ganoderma lucidum polysaccharide crude product GLP L preparation of
[0029] Weigh 50 grams of red ganoderma lucidum fruiting body powder, add 1000 mL of distilled water, extract in boiling water bath for 10 hours, and stir intermittently. Centrifuge at 3000rpm to remove the precipitate to obtain the extract. Add 500 mL of distilled water to the residue after centrifugation, extract in a boiling water bath for 6 hours, and remove the residue after centrifugation. Combine the supernatants from the two extractions. The supernatant was concentrated to 500 mL. Add 1 / 5 volume (100mL) of chloroform and 1 / 5 volume (20mL) of n-butanol of the concentrated solution, shake vigorously, let stand and separate layers until there is no precipitation at the interface between chloroform and water, remove the lower organic solvent layer and In the middle layer, retain the water layer to remove protein, repeat 5 times, dialyze the obtained solution against flowing water...
Embodiment 2
[0032] Example 2. Red Ganoderma lucidum polysaccharide crude product GLP L The pilot extraction process
[0033] Weigh 20kg of red ganoderma fruiting body powder, add 400L of deionized water, put it into an extraction tank, and extract under stirring at 100°C for 10h. Add 200L deionized water to the residue after centrifugation, extract at 100°C for 6 hours, and remove the residue after centrifugation. Combine the supernatants from the two extractions. The supernatant was concentrated to 200 L at 100°C. Add 1 / 5 volume of chloroform (40 L) and 1 / 5 chloroform volume of n-butanol (8 L) to the concentrated solution, stir for 30 min, deflate, let stand to separate layers, and siphon to obtain supernatant. The deproteinization operation was repeated 3 times. The deproteinized liquid (volume v 0 ) back to the vacuum tank for vacuuming (60°C, 30min), slowly add 3 / 4 times v 0 volume of industrial ethanol, placed at 4°C for 4h, centrifuged, and retained supernatant (volume v 1 ),...
Embodiment 3
[0034] Example 3. Single polysaccharide GLP L1 and GLP L2 preparation of
[0035] 100mg red ganoderma polysaccharide crude GLP L Fully dissolved in 5mL of distilled water, loaded on a well-balanced boric acid type DE-32 ion exchange column (1.9×20cm), the sample loading flow rate was 0.27mL / min, eluted with 146mL of distilled water and 56mL of 0.05mol / L borax solution respectively, the flow rate 20mL / h, collect the eluate step by step, track and detect the sugar content by anthrone sulfate colorimetry, combine the same components, dialyze the eluate from the first and second parts of the effluent, and freeze-dry to obtain the red ganoderma lucidum of the present invention Single polysaccharide finished product: GLP L1 and GLP L2 .
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