Water extract of houttuynia cordata thunb and preparation method and application of water extract
A technology for water extract and Houttuynia cordata, which is applied in the field of Houttuynia cordata water extract and its preparation, and achieves the effect of simple extraction process
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Embodiment 1
[0022] Example 1 Extraction and detection of Houttuynia cordata water extract and polysaccharide
[0023] (1) Extraction of Houttuynia cordata water extract and polysaccharide
[0024] Firstly, the dried plant of Houttuynia cordata is washed, dried at low temperature to constant weight, and divided into two parts, one part is used for extracting water extract, and the other part is used for extracting Houttuynia cordata polysaccharide. Add deionized water according to the plant mass and liquid volume ratio of 1:10 (g / ml), keep warm in a water bath at 60°C to 90°C for 2-5 hours, centrifuge at 1000g / min for 10min to obtain the supernatant water extract, and precipitate the filter residue by the same method After leaching twice according to the method, the filtrates were combined, the supernatant was centrifuged at 5000g / min for 10min, and filtered through a 0.45μm filter membrane. The supernatant liquid is directly freeze-dried to obtain the freeze-dried powder of the water ext...
Embodiment 2
[0027] Example 2 Detection of Houttuynia cordata water extract and polysaccharide anti-hand, foot and mouth disease virus activity
[0028] (1) Toxicity test of Houttuynia cordata water extract and Houttuynia cordata polysaccharide on cells
[0029] Cultivate Vero cells in a 96-well plate. After the cells grow into a monolayer, reconstitute the lyophilized powder of the water extract and the alcohol-precipitated polysaccharide obtained above with deionized water, and use final concentrations of 1 μg / ml and 3 μg / ml respectively. , 10 μg / ml, 30 μg / ml, 100 μg / ml, 300 μg / ml, and 1000 μg / ml samples were used to treat Vero cells, and three replicate wells were set up. At the same time, a normal control group without drug treatment was set up. At 37°C, 5% CO 2 Cultivate in an incubator to observe the toxicity of the sample to Vero cells. After culturing for 72 hours, the classic MTT method for detecting cell viability is used to measure the toxicity of the sample to Vero cells. Sp...
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