Application of 4-hydroxylonchocarpin in preparation of medicine for preventing and treating aphids
An aphid and drug technology, applied in the field of pesticides, can solve the problem of no report on aphid killing active substances, and achieve the effects of being environmentally friendly and low in toxicity to humans and animals
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Embodiment 1
[0037] Extraction method of 4-hydroxylonchocarpin
[0038]The water chestnut bark of 10kg is pulverized, extracted 3 times with 10L of 95% technical grade absolute ethanol at room temperature; after filtering with Buchner funnel, the filtrate is combined under reduced pressure and concentrated (the temperature of under reduced pressure concentration is 45-60 ℃, pressure: Under the vacuum environment, the time is generally half an hour, using a rotary evaporator) to obtain the water chestnut bark ethanol extract; after the extract is kneaded with water, extracted with 30L petroleum ether, and further concentrated under reduced pressure to obtain 156g of petroleum ether extract; The ether extract was subjected to silica gel column chromatography (the size of the column was 1 m in length, and the silica gel with a diameter of 20 cm was 200-300 mesh), followed by petroleum ether: ethyl acetate = 100:0, 100:1, 50:1, 30 : 1, 20: 1, 10: 1, 5: 1, 3: 1, 1: 1 elution (one drop for 5 sec...
Embodiment 2
[0041] Toxicity assay against aphids
[0042] Use the drip method. The compound 4-Hydroxylonchocarpin prepared in Example 1 was dissolved in acetone to prepare a solution with a concentration of 50 mg / mL, and then diluted with 0.1% Tween-80 water into 1 mg / mL, 0.5 mg / mL, 0.25 mg / mL, 0.125mg / mL, 0.625mg / mL. Pick healthy, wingless aphids of the same size, and drop the medicinal solution on the pronotum of aphids with a 0.3 μL microdropper. After the treatment, the test worms were placed in a 9 cm petri dish with filter paper, placed on the broad bean leaves wrapped with moist cotton in the dish, sealed the petri dish with plastic wrap, and pierced holes for ventilation. Acetone was used as a negative control, and 1 mg / mL matrine was used as a positive control. Each treatment was replicated 3 times with 20 aphids per replicate. Place the treated petri dish in a light incubator with a relative humidity of 60% to 70%, a temperature of 25±1°C, and a light-dark cycle of 16:8. Th...
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