Method for measuring ganoderma polyoses content in ganoderma products by sulfuric acid-phynol method
A technology of Ganoderma lucidum polysaccharide and phenol is applied in the field of determination of Ganoderma lucidum polysaccharides, which can solve the problems such as inability to accurately react active active ingredients of Ganoderma lucidum polysaccharides, inappropriate determination of Ganoderma lucidum products, uneven product quality, etc. Actionable effect
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Embodiment 1
[0029] 1. Remove interfering components: Weigh 5.0083g, 5.0061g, 5.0044g, 5.0054g of Zizhi fungus powder, dissolve in 100ml of 80% ethanol, heat and reflux in a water bath at 60°C for 30min, centrifuge at 4500r / min for 10min, discard the supernatant, Collect the residue. Dissolve in 100ml of 80% ethanol, repeat the above steps twice, to remove interfering components such as monosaccharides, disaccharides and oligosaccharides.
[0030] 2. Extract polysaccharide: Dissolve the above residue with 200ml of distilled water, heat and reflux in a water bath at 95°C for 2 hours, and set the volume to 250ml after cooling (V 1 milliliters), to obtain the extract, mix well, filter, and collect the filtrate to be the sample solution, measure 10ml (V 2 milliliter) sample solution, dilute 10 times, and set the volume to 100ml (V 3 mL), which is the solution to be tested.
[0031] 3. Determination of Ganoderma lucidum polysaccharide content by sulfuric acid-phenol method:
[0032] 3.1. Dr...
Embodiment 2
[0056] 1. Remove interfering components: weigh 5.0061g, 5.0057g, 5.0044g, 5.0035g of Zizhi fungus powder, dissolve in 100ml of 85% ethanol, heat and reflux in a water bath at 61°C for 30min, centrifuge at 3000r / min for 10min, discard the supernatant, Collect the residue. The residue was dissolved in 100ml of 85% ethanol, and the above steps were repeated twice to remove interfering components such as monosaccharides, disaccharides and oligosaccharides.
[0057] 2. Extract polysaccharide: Dissolve the above residue with 200ml of distilled water, heat and reflux in a water bath at 96°C for 1.5h, and set the volume to 250ml after cooling (V 1 milliliters), to obtain the extract, mix well, filter, and collect the filtrate to be the sample solution, measure 10ml (V 2 milliliter) sample solution, dilute 10 times, and set the volume to 100ml (V 3 mL), which is the solution to be tested.
[0058] 3. Determination of Ganoderma lucidum polysaccharide content by sulfuric acid-phenol m...
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