Preparation method of artemisinin slow-release body
An artemisinin, slow-release technology, applied in the fields of botanical equipment and methods, chemicals for biological control, animal repellents, etc., can solve the problem of high cost, cost reduction, and short effective time of artemisinin for algal inhibition. and other problems to achieve the effect of suppressing outbreaks, prolonging suppression time, and reducing costs
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Embodiment 1
[0008] Weigh 0.2g of artemisinin and dissolve it in 1.5mL of ethyl oleate, add 1mL of co-solvent absolute ethanol, then add 1mL of emulsifier OP-10, make a 50mL solution with distilled water, then add 0.3g of sodium alginate and mix well, Draw the above mixed solution with a syringe and drop it into 100mL glacial acetic acid solution containing 0.75g chitosan and 3g calcium chloride with a glacial acetic acid content of 3%vt to form microspheres, add 1.5mL glutaraldehyde after cooling to room temperature, Suction filtration, washing with petroleum ether and distilled water for 5-8 times; drying for 36h-72h to obtain artemisinin sustained-release body. Use artemisinin slow-release body to carry out acute toxicity experiment to aseptic culture Microcystis aeruginosa, set up three parallel groups, observe once every 24 hours, observe continuously for one week, when the artemisinin slow-release body weighed is 2g, its The 96h inhibition rate of Microcystis aeruginosa reached 75%. ...
Embodiment 2
[0010] Weigh 0.1g of artemisinin and dissolve it in 1mL of ethyl oleate, add 0.5mL of co-solvent absolute ethanol, then add 1mL of emulsifier OP-10, make a 50mL solution with distilled water, then add 0.6g of sodium alginate and mix well, Draw the above mixed solution with a syringe and drop it into 100mL of glacial acetic acid solution containing 0.5g of chitosan and 4g of calcium chloride with a glacial acetic acid content of 3%vt to form microspheres, add 2mL of glutaraldehyde after cooling to room temperature, and pump Filter, rinse with petroleum ether and distilled water for 5-8 times; dry for 36h-72h to obtain artemisinin sustained-release body. Use artemisinin slow-release body to carry out acute toxicity experiment to aseptic culture Microcystis aeruginosa, set up three parallel groups, observe once every 24 hours, observe continuously for one week, when the artemisinin slow-release body weighed is 2g, its The 96h inhibition rate of Microcystis aeruginosa reached 80%....
Embodiment 3
[0012] Weigh 0.3g of artemisinin and dissolve it in 2mL of ethyl oleate, add 1.5mL of co-solvent absolute ethanol, then add 1.5mL of emulsifier OP-10, make a 50mL solution with distilled water, then add 0.9g of sodium alginate and mix well , use a syringe to draw the above mixed solution and drop it into 100mL glacial acetic acid solution containing 0.25g chitosan and 4g calcium chloride with a glacial acetic acid content of 3% vt to form microspheres, add 1.5mL glutaraldehyde after cooling to room temperature , filtered with suction, washed 5-8 times with petroleum ether and distilled water; dried for 36h-72h to obtain artemisinin sustained-release body. Use artemisinin slow-release body to carry out acute toxicity experiment to aseptic culture Microcystis aeruginosa, set up three parallel groups, observe once every 24 hours, observe continuously for one week, when the artemisinin slow-release body weighed is 2g, its The 96h inhibition rate of Microcystis aeruginosa reached 8...
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