Polymer nanoparticles double-loaded with docetaxel and flavonoid compounds and preparation method of polymer nanoparticle
A technology of docetaxel and nanoparticles, which is applied in the field of anti-tumor drugs, can solve the problems of reducing drug resistance of tumor cells, and the level cannot be satisfied, and achieve the effects of prolonging the action time, less damage, and excellent application prospects
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Embodiment 1
[0052] Example 1 A preparation method of nanoparticles loaded with docetaxel and fisetin
[0053]Weigh 50.0 mg of PEG-PCL (1:1, MW: 10k) and dissolve in 5 ml of ethyl acetate, 5 mg of fisetin and 4 mg of docetaxel in 2 ml of absolute ethanol, and mix the two solutions into a round bottom flask, Form a film layer under the working conditions of a rotary evaporator (45°C, 50rpm, 30min); measure 5ml of PBS solution (0.01M, pH 7.4, 65°C) to dissolve the film, and disperse the nanoparticles uniformly in the aqueous solution by ultrasonic ; and then filtered through a 0.45 μm microporous membrane, and freeze-dried to obtain a solid powder. Its hydrated average particle size diagram is shown in figure 2 As shown in A.
Embodiment 2
[0054] Example 2 A preparation method of nanoparticles loaded with docetaxel and luteolin
[0055] Weigh 200.0mg of PEG-PCL (1:1, MW:20k) and dissolve in 3ml of ethyl acetate, 20.0mg of sweet clover and 16mg of docetaxel are dissolved in 2ml of absolute ethanol, and mix the two solutions into an organic phase for later use; Weigh 50.0mg of poloxamer F127 and dissolve it in 20ml of ultrapure water as the aqueous phase for later use; slowly add the organic phase to the aqueous phase under the emulsification condition (9600rpm / min) of the T25 probe sonicator, and work continuously for 10min . Transfer the emulsified emulsion to a round-bottomed flask, and use a rotary evaporator to filter under reduced pressure (37°C, 60rpm, 15min) to remove the organic solvent to prepare the drug-loaded nanoemulsion, and store it at 4°C. Its hydrated average particle size diagram is shown in figure 2 Shown in B.
Embodiment 3
[0056] Example 3 A preparation method of nanoparticles loaded with docetaxel and fisetin
[0057] Weigh 200.0mg of PEG-PCL (1:2, MW:15k) and dissolve in 3ml of dichloromethane, 14.0mg of fisetin and 10.0mg of docetaxel in 1ml of absolute ethanol, and mix the two solutions into an organic Phase standby; Weigh 50.0mg of polyvinyl alcohol and dissolve it in 20ml ultrapure water as the water phase for standby; Slowly add the organic phase to the water phase under the emulsification condition (9600rpm / min) of the T25 probe ultrasonic emulsion homogeneous disperser, and work continuously 10min. Transfer the emulsified emulsion to a round-bottomed flask, and use a rotary evaporator to filter under reduced pressure (37°C, 60rpm, 15min) to remove the organic solvent to prepare the drug-loaded nanoemulsion, and store it at 4°C. Its hydrated average particle size diagram is shown in image 3 As shown in A.
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