Application of rosemarinus officinalis extract in preparation of medicine for preventing and controlling ichthyophthirius multifiliis fouquet
A technology of rosemary extract and multi-seed melon worm, which is applied in the application field of rosemary extract in the preparation of medicines for preventing and controlling multi-seed melon worm, achieving the effect of broad application prospects and abundant resources
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Embodiment 1
[0020] Embodiment 1: the killing action of rosemary extract to the infective larvae (predatory body) of small melon worm
[0021] (1) Drug preparation: Accurately weigh 0.1 g of rosemary extract, dissolve it with 1 mL of dimethyl sulfoxide, prepare a 100 g / L drug solution, and then dilute to the concentration required for the test. At the same time, a compound-free control solution containing 0.02% dimethyl sulfoxide was prepared.
[0022] (2) Set up 6 test groups, 1 dimethyl sulfoxide control group and 1 blank control group, set 3 parallels in each group, and complete the experiment in a 96-well plate. Add 160 μL of solution containing predators to each well of the 96-well plate, pipette 6 drops of 10 μL insect solution in each well and count on a slide to estimate the number of predators contained in 100 μL of the well. Add 100 μL of different concentrations of drug solution to each well, so that the final drug concentration is 8, 4, 2, 1, 0.5, 0.25 mg / L in sequence. Set a...
Embodiment 2
[0027] Embodiment 2: the killing action of rosemary extract to the adult (trophoblast) of small melon worm
[0028] (1) Drug preparation is the same as in Example 1.
[0029] (2) Set up 5 test groups, 1 dimethyl sulfoxide control group and 1 blank control group, set 3 parallels for each group, and complete the test in a 12-well plate. Add 1mL of insect liquid containing about 30 mature trophozoites to each well of the 12-well plate and accurately count the number of trophozoites in each well, and then add 1mL of different concentrations of liquid medicine respectively, so that the final drug concentration is 32, 16, 8, 4, 2 mg / L, the groups added with only distilled water and 0.05% dimethyl sulfoxide were set as negative controls. After incubating in a constant temperature incubator at 24°C for 6 hours, the number of surviving worms in each treatment group was recorded and the mortality rate was calculated. The 12-well plate was placed in a constant temperature incubator at ...
Embodiment 3
[0035] Embodiment 3: the extermination effect of rosemary extract to the cyst of the multi-seed melon worm
[0036] (1) Drug preparation is the same as in Example 1.
[0037] (2) Set up 5 test groups, 1 dimethyl sulfoxide control group and 1 blank control group, set 3 parallels for each group, and complete the test in a 12-well plate. Add 1mL of insect liquid containing about 30 mature trophozoites to each well of the 12-well plate and accurately count the number of trophozoites in each well, place the 12-well plate in a 24°C constant temperature incubator and incubate for 4 hours until the trophozoites develop into cysts Finally, accurately count the number of cysts in each well, and then add 1mL of different concentrations of the drug solution, so that the final concentration of the drug is 32, 16, 8, 4, 2 mg / L, and only distilled water and only 0.05% of the drug will be added. The dimethyl sulfoxide group was used as a negative control. Place the 12-well plate in a consta...
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