A kind of liposome-polymer drug-loaded nanoparticle and its preparation method and application
A drug-loading nanometer and nanoparticle technology, which is used in liposome delivery, pharmaceutical formulations, active ingredients of heavy metal compounds, etc., can solve the problem of low tumor tissue specific recognition, improve antitumor effect, and enhance tumor targeting. sexual effect
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Embodiment 1
[0072] In this example, liposome-polymer drug-loaded nanoparticles were prepared by the following method, which specifically included the following steps:
[0073] (1) Dissolve 20 mg of amphiphilic cationic polymer PEI-PLGA in 1 mL of dichloromethane, add 200 μL of water to the organic phase, and use an ultrasonic cell disruptor to sonicate at 35% power for 5 minutes to form colostrum;
[0074] (2) Adding 2 mL of 2% polyvinyl alcohol (PVA) aqueous solution to the colostrum obtained in step (1), and adding 200 μL of doxorubicin in dichloromethane (containing 2 mg of doxorubicin) dropwise, Use an ultrasonic cell breaker to ultrasonicate for 5 minutes at 40% power to form double emulsions;
[0075] (3) under stirring, add the double emulsion obtained in step (2) into 10 mL of PVA aqueous solution with a concentration of 0.6%, continue stirring for 3 min, and remove the organic solvent with a rotary evaporator to obtain a nanoparticle suspension;
[0076] (4) Mix and stir the nanop...
Embodiment 2
[0081] In this example, liposome-polymer drug-loaded nanoparticles were prepared by the following method, which specifically included the following steps:
[0082] (1) Dissolve 10 mg of amphiphilic cationic polymer PEI-PLGA in 1 mL of dichloromethane, add 100 μL of water to the organic phase, and use an ultrasonic cell disruptor to sonicate for 3 minutes at 35% power to form colostrum;
[0083] (2) Adding 5 mL of concentration to the colostrum obtained in step (1) is 3% polyvinyl alcohol (PVA) aqueous solution, and add dropwise the dichloromethane solution of 400 μ L of doxorubicin (containing 2 mg of doxorubicin), Using an ultrasonic cell disruptor to sonicate for 8 minutes at 40% power to form double emulsions;
[0084] (3) under stirring, add the double emulsion obtained in step (2) into 8 mL of 1% PVA aqueous solution, continue stirring for 5 min, and remove the organic solvent with a rotary evaporator to obtain a nanoparticle suspension;
[0085] (4) Mix and stir the nan...
Embodiment 3
[0090] In this example, liposome-polymer drug-loaded nanoparticles were prepared by the following method, which specifically included the following steps:
[0091] (1) Dissolve 40 mg of amphiphilic cationic polymer PEI-PLGA in 1 mL of dichloromethane, add 250 μL of water to the organic phase, add 100 μL of an aqueous solution of doxorubicin hydrochloride (containing 2 mg of doxorubicin hydrochloride ), using an ultrasonic cell disruptor to sonicate for 8 minutes at 35% power to form colostrum;
[0092] (2) Add 2 mL of 1% polyvinyl alcohol (PVA) aqueous solution to the colostrum obtained in step (1), and add 200 μL of paclitaxel in dichloromethane (containing 2 mg of paclitaxel) dropwise. Use ultrasound at 40% power for 3 minutes to form double emulsion;
[0093] (3) under stirring, add the double emulsion obtained in step (2) into 15 mL of 0.8% PVA aqueous solution, continue stirring for 10 min, and remove the organic solvent with a rotary evaporator to obtain a nanoparticle ...
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