Himematsutake water soluble polysaccharide and its preparing process and use
A water-soluble polysaccharide and preparation technology, which is applied in the direction of food preparation, application, organic active ingredients, etc., can solve the problems of low alcohol precipitation efficiency, unstable quality, unsatisfactory pharmacological activity and clinical curative effect, etc.
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Embodiment 1
[0154] Example 1 Alcohol Extraction Process Optimization for Removing Small Molecular Components
[0155] 1. Orthogonal experimental optimization of extraction process:
[0156] (1) Orthogonal experimental design:
[0157] A: Ethanol concentration
[0158] A 1 0%; A 2 15%; A 3 30%; A 4 45%; A 5 60%; A 6 75%; A 7 85%; A 8 95%.
[0159] B: sample (kg) / solvent volume (liter)
[0160] B 1 1:6; B 2 1:8
[0161] C: extraction time (h)
[0162] C 1 1.5;C 2 3.0
[0163] D: number of extractions
[0164] D. 1 2;D 2 3.
[0165] Design L based on the above factors and levels 16 (8×2 8 ) is shown in Table 6.
[0166] 1 2 3 4 5 6 7 8 9
[0167] (2) Judgment indicators and measurement results:
[0168] The evaluation and judgment indexes of this orthogonal experiment are the content of trehalose in the extract and the total amount of trehalose, glucose and mannitol. The contents were determined by HPLC-ELSD method. The experimental result...
Embodiment 2
[0175] Example 2. Preparation process and optimization of water-soluble polysaccharide after alcohol extraction and impurity removal of Agaricus blazei
[0176] 1. Establishment of index component content method
[0177] The classic polysaccharide determination method is to measure the total sugar content first, and then subtract the reducing sugar. Since Agaricus has been extracted with 75% ethanol, the small molecular reducing sugar has been extracted completely, so the polysaccharide content is directly determined by the phenol sulfuric acid method.
[0178] (1) Standard curve and linear range
[0179] Accurately weigh 20.0 mg of trehalose in a 500 ml volumetric flask, add water to the mark, and mix well.
[0180] Draw standard solution 0.4ml, 0.6ml, 0.8ml, 1.0ml, 1.2ml, 1.4ml, 1.6ml and 1.8ml respectively, make up to 2.0ml with water, then add 1.0ml of 6% phenol and 5.0ml of concentrated sulfuric acid, Stand still for 10 minutes, shake well, measure the optical density a...
Embodiment 3
[0248] Embodiment 3. The water extraction ultrafiltration process of Agaricus blazei water-soluble polysaccharide
[0249] Agaricus blazei fruiting body coarse powder 1.0Kg, extract with 10 times the amount (weight ratio) of water, extract 2 hours each time, extract continuously 2 times, and combine the extracts. Add 5% ZTC1+1 natural clarifier to the extract, stir well, let stand to cool, and filter by centrifugal filtration to obtain a clarified extract. Pump the extract into an ultrafilter, and perform ultrafiltration with an ultrafiltration membrane with a molecular weight cut-off of 4,000. After several cycles, collect the unpassed part on the membrane and concentrate it to a thick extract (specific gravity ~ 1.10) with a rotary evaporator. , then dried in a vacuum drying oven and pulverized to obtain 68g of Agaricus blazei water-soluble polysaccharide.
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