Auricularia polysaccharide with function of reducing blood fat and preparation method and application thereof
A technology of fungus polysaccharides and fungus, applied in medical preparations containing active ingredients, functions of food ingredients, polysaccharide/gum-containing food ingredients, etc.
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Embodiment 1
[0027] The preparation of embodiment 1 polysaccharide powder
[0028] (1) Pulverize the fungus fruit body and pass through a 100-mesh sieve to obtain the fungus powder;
[0029] (2) Mix the fungus powder obtained in step (1) with water at a mass ratio of 1:40, and stir evenly;
[0030] (3) adopt hot pressing method, leaching under the condition of 120 ℃, 0.12MPa in airtight container for 80 minutes, obtain extract;
[0031] (4) centrifuge, take the extract of fungus in the upper layer, remove protein by Sevage method, and obtain polysaccharide solution of fungus;
[0032] (5) Precipitate polysaccharide with 95% ethanol at a volume ratio of 1:20, let it stand overnight, centrifuge, take the precipitate and dry it to obtain polysaccharide powder.
Embodiment 2
[0033] Example 2 Preparation of irradiated fungus polysaccharide and investigation of irradiation conditions
[0034] The polysaccharide powder of Example 1 is configured into a polysaccharide solution of 5 g / ml with distilled water; respectively irradiated with Co60-γ rays of 10 kGy, 100 kGy, and 1000 kGy at a dose rate of 7 kGy / min, and the irradiated fungus polysaccharide solution is dried used later.
[0035] Add water to the irradiated fungus polysaccharide powder to prepare a fungus polysaccharide solution with a final concentration of 2mg / ml, stir at 50°C at a speed of 170rpm / min, and measure the time and viscosity for complete dissolution. The effect of irradiation dose on the change of dissolution time is shown in figure 1 .
[0036] The experimental results showed that the dissolution time and viscosity of polysaccharides from fungus could be significantly reduced by irradiation with a dose of 1000kGy. The solubility and viscosity are related to the structural pro...
Embodiment 3
[0037] Embodiment 3 establishment of hyperlipidemia animal model
[0038] After 7 days of adaptive feeding, 50 4-week-old C57 male mice were randomly divided into two groups according to body weight: the first group of 10 mice was the normal group, which was given basal diet; the second group of 40 mice was the high-fat group, which was given high-fat diet Feed (D12451, Beijing Huafukang Biotechnology Co., Ltd.) to create animal models of hyperlipidemia. Mice had free access to food and water. After 12 weeks, blood was collected from the canthus vein of the mice to measure serum total cholesterol, triglyceride, high-density lipoprotein and low-density lipoprotein. The test data was statistically processed by the independent sample t test of SPSS19.0 statistical software.
[0039] The results showed (see Table 1), the serum total cholesterol, triglyceride, and low-density lipoprotein contents of the hyperlipidemia group were significantly higher than those of the normal group...
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