Thalassia hemprichii extract and preparation method and use thereof
A technology of Thalias algae and extracts, applied in the field of preparation of antiviral drugs, can solve problems such as undeveloped economic value, and achieve strong anti-herpes simplex virus HSV-I virus activity, strong inhibition, and good insect antifeedant activity Effect
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Embodiment 1
[0019] Thalassia hemprichii with an air-dried dry weight of 4Kg was used as a raw material, chopped and soaked in about 35 L of ethanol organic solvent at room temperature for 3 times, each time for 5 days, and the extract was concentrated under reduced pressure to obtain a crude extract. The crude extract (70g) was suspended and dissolved in water (1L), extracted three times with chloroform (600mL) and n-butanol (500mL) successively, the aqueous layer was collected and concentrated under reduced pressure, and 23g of the concentrated aqueous layer was subjected to macroporous Resin (D101 macroporous adsorption resin) atmospheric column (atmospheric pressure glass column, diameter 9cm, length 1.8m) chromatography, using water-methanol solvent system as eluent, gradient from volume ratio 100:0 to 0:100 After elution, the fractions eluted with methanol were collected and concentrated under reduced pressure to obtain crude fractions. Rinse the crude components with methanol, colle...
Embodiment 2
[0021] Collect vero cells in the logarithmic growth phase and inoculate them in 96-well culture plates, the number of cells per well is 1.0×10 5 / 100μL, placed in 5%, CO 2 Incubator cultivation. The next day, suck out the growth liquid in the microwells, add 50 μL of the diluted Thaleiella extract solution in Example 1 to each well, immediately add 50 μL of HSV-I virus use solution, and set normal cell control and virus control at the same time, 37 ° C , 5% CO 2 Incubator cultivation. Observe the cytopathic effect (CPE), observe the cell growth every day, and express the cytopathic condition by -, +, ++, +++, ++++. The results show that the compound of the present invention has a maximum nontoxic concentration of 25ug / ml to vero cells, and it inhibits the IC of herpes simplex virus type I lesions. 50 The value is 6.25ug / mL.
Embodiment 3
[0023] HepG2 cells in the logarithmic growth phase were collected and seeded in 96-well culture plates, with the number of cells per well being 1.0×10 5 / 100μL, placed in 5%, CO 2 Incubator cultivation. The next day, the growth liquid in the microwells was aspirated, and 50 μL of the diluted Tailai grass extract solution in Example 1 was added to each well, and 50 μL of the CVB3 virus use solution was immediately added. %CO 2 Incubator cultivation. Observe the cytopathic effect (CPE), observe the cell growth every day, and express the cytopathic condition by -, +, ++, +++, ++++. The results show that the maximum non-toxic concentration of the compound of the present invention to hela cells is 200 μg / mL, and when the concentration is 100 μg / mL, it can inhibit more than half of the pathological changes of the virus.
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