Application for morindone G and/or morindone O in preparation for medicine for killing fish parasites
A technology of Kuwanone and fish, which is applied in the field of fish parasite drugs, can solve the problems of high residue, environmental pollution, high toxicity, etc., and achieve the effect of simple extraction and preparation process, broad application prospects, and rich sources
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Embodiment 1
[0025] Example 1: The killing effect of mulberry G, mulberry O, and a mixture of mulberry G and mulberry O (1:1) on the infective larvae of Melon
[0026] (1) Preparation of the drug: Weigh 5 mg of the manganone G, the manganone O monomer, and the mixture powder of the manganone G and the manganone O (mass ratio 1:1), use 20 μL of absolute ethanol to promote the dissolution, and add 3.105 mL of distilled water , Formulated into a 1600mg / L medicinal solution, diluted to the required concentration in the experiment by two-fold gradient dilution method. Taking the content (0.1%) of the absolute ethanol in the highest concentration chemical solution used as the standard as the standard, a control solution containing 0.1% absolute ethanol and no compound was prepared.
[0027] (2) Take a 96-well plate, add 100 μL of larva-containing liquid to each well, and then add 100 μL of different concentrations of medicinal liquid to each well. The medicinal liquids refer to mulberry G, mulberry O...
Embodiment 2
[0030] Example 2: The killing effect of mulberry G, mulberry O, and a mixture of mulberry G and mulberry O (1:1) on the adult (trophozoite) of the worm
[0031] (1) The drug preparation is the same as in Example 1.
[0032] (2) Take a 24-well plate, add 200μL of insect fluid containing about 60 mature trophozoites to each well and accurately count the number of adults in each hole, and then add 200μL of different concentrations of medicinal solution (2-fold gradient dilution) to make the final drug The concentration of the drug is 50, 25, 12.5, 6.25, 3.125, 1.78, and 0 mg / L (control), with 5 replicates of each drug concentration. The temperature of the experiment was kept at 23±0.5℃, and the total lethal time of each foraminifera and the number of surviving adults in each hole were observed and recorded under 4x objective lens, and the 4h lethality rate of mulberry G and mulberry O to the adult worms was calculated. And half effective concentration EC 50 (See Table 3).
[0033] Aft...
Embodiment 3
[0037] Example 3: The killing effect of mulberry G, mulberry O, and a mixture of mulberry G and mulberry O (1:1) on the cysts of the worm
[0038] (1) The drug preparation is the same as in Example 1.
[0039] (2) In a 24-well plate, inhale 200μL of the worm fluid containing about 60 mature cucurbita worm adults into each well, and let it stand for 6h. After the cysts are formed, count the number of cysts in each well, and then add 200μL of different The concentration of the drug solution is such that the final drug concentration is 50, 25, 12.5, 6.25, 3.125, 1.78, and 0 mg / L (control), with 5 replicates of each drug concentration. The mortality rate at 4h after encapsulation was added under a 4X microscope was recorded. After 4 hours, place the 24-well plate (undead cysts) in a constant temperature incubator at 23°C for 12 hours, observe the incubation under a 4x microscope, count the number of hatched larvae in each well, and calculate the average number of hatched cysts The nu...
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