Drug-loading particle and preparation method thereof
A particle and drug-carrying technology, applied in the field of pesticide chemistry, can solve the problems of large amount of organic solvents, environmental pollution, etc., achieve good biological activity and improve the effect of drug utilization
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[0034] In the present invention, the metal-organic framework material is preferably Fe-MIL-100, and the present invention has no special requirements on the source of the Fe-MIL-100, which can be commercially available or self-made. In the present invention, the preparation method of the Fe-MIL-100 preferably comprises the following steps:
[0035] Iron powder, trimesic acid, hydrofluoric acid, concentrated nitric acid and water are mixed, and a hydrothermal reaction is carried out under airtight conditions to obtain Fe-MIL-100; the temperature of the hydrothermal reaction is preferably 150-180°C, preferably The temperature is preferably 150°C, and the time is 10 to 15 hours, more preferably 12 hours. The present invention has no special requirements on the heating rate of the hydrothermal reaction.
[0036] In the present invention, the mass ratio of the iron powder to trimesic acid is preferably 250-280:600-750, more preferably 277.5:687.5; the mass concentration of the hyd...
Embodiment 1
[0051] 200 μL of hydrofluoric acid with a mass concentration of 35% and 190 μL of concentrated nitric acid with a mass concentration of 65% were added to 20 mL of ultrapure water to form a mixed solution. Then 277.5 mg of iron powder and 687.5 mg of trimesic acid were weighed and placed in the above mixed solution to obtain the reaction raw materials. The reaction raw materials were transferred to a reaction kettle, placed in an oven, and heated to 150° C. for 12 hours. After the reaction, cool to room temperature, collect the solid product by filtration, wash with ultrapure water three times, then wash the product in hot water at 80°C for 5h, and then wash in ethanol at 60°C for another 3h to remove unreacted raw materials. Cool to room temperature after the reaction, centrifuge at 1000rpm for 10min to collect the high-purity product, and finally vacuum-dry at 80°C for 12h to obtain Fe-MIL-100.
[0052] Take 900mg of azoxystrobin original drug (abbreviated as AZOX), dissolve...
Embodiment 2
[0054] The test was carried out according to the method of Example 1, with the difference that the mass ratio of azoxystrobin original drug and Fe-MIL-100 was controlled to 2:1 to obtain drug-loaded particles AZOX@Fe-MIL-100.
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