Composition for preparing products for improving hyperuricemia
A technology of hyperuricemia and composition, which is applied in the field of composition for improving hyperuricemia, can solve problems such as toxic and side effects, human injury, etc., achieve excellent effects, and contribute to the effect of gout
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Embodiment 1
[0032] 1. Materials and methods
[0033] (1) Animal model establishment
[0034] Select male Kunming mice, add 20% by weight of yeast extract powder in the feed, orally orally for 2 weeks continuously, and establish an animal mouse model with hyperuricemia.
[0035] (2) Preparation of experimental supplies
[0036] Saponin: Take 100g of crushed dry sea cucumber powder, add 1L of 60% ethanol solution to heat reflux extraction for 1 hour, repeat the operation 6 times, combine the supernatant obtained from each extraction, concentrate under reduced pressure to remove ethanol to obtain a concentrated solution, and then use saturated Butanol: water (1:1, v / v) extracts the concentrated solution, collects the supernatant, and evaporates to dryness to obtain saponin.
[0037] (3) Experimental process
[0038] Select 24 male Kunming mice, weighing 20±5g, and randomly divide them into 4 groups with 6 mice in each group. The normal group and the hyperuricemia model group were intragas...
Embodiment 2
[0050] 1. Materials and methods
[0051] (1) Animal model establishment
[0052] Select male Kunming mice, add 20% by weight of yeast extract powder in the feed, orally orally for 2 weeks continuously, and establish an animal mouse model with hyperuricemia.
[0053] (2) Preparation of experimental supplies
[0054]Polysaccharide: Remove the sediment from the dried sea cucumber and crush it, weigh 100g, 2L 0.1M sodium acetate buffer solution (pH=6), 2.92g EDTA, 1.21g cysteine and 100mg papain, stir and react in a water bath at 60°C for 24h Afterwards, the reaction mixture was centrifuged (4900 xg, 10 min). Add 2 times the volume of 95% ethanol solution to the supernatant, ie sea cucumber enzymatic hydrolysis solution, place at 4°C for 24 hours, and centrifuge (4900×g, 10 min). Add 100mL distilled water to the precipitate to redissolve, add 5-10mL trichloroacetic acid, place at 4°C for 4h, and centrifuge (4900×g, 10min). The supernatant was taken, dialyzed with a dialysis ...
Embodiment 3
[0067] 1. Materials and methods
[0068] (1) Animal model establishment
[0069] Select male Kunming mice, add 20% yeast extract powder to the feed, orally orally for 2W continuously, and establish an animal mouse model with hyperuricemia.
[0070] (2) Preparation of experimental supplies
[0071] The preparation scheme of sea cucumber saponin and sea cucumber polysaccharide is the same as that of Experimental Example 1 and Experimental Example 2.
[0072] (3) Experimental method
[0073] 30 male Kunming mice, weighing 20±5g, were randomly divided into 5 groups, 6 mice in each group. The normal group and the hyperuricemia model group were given normal saline at a dose of 100 mg / kg every day, and the saponin group was given intragastric administration. The polysaccharide group was given 3% saponin solution, the polysaccharide group was given 30% polysaccharide solution by intragastric administration, and the sea cucumber saponin and sea cucumber polysaccharide compound group...
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