A preparation method of a drug-loaded ultrasound contrast agent using macrophages as a carrier
An ultrasound contrast agent and macrophage technology, which can be used in echo/ultrasonic imaging agents, preparations for in vivo experiments, pharmaceutical formulations, etc. Increased cell labeling rate, wide adaptability, and long lifespan
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Embodiment 1
[0043] A preparation method of a drug-loaded ultrasound contrast agent using macrophages as a carrier, comprising the following steps:
[0044]Step a, preparation of cationic microbubbles: distearoyl phosphatidyl choline DSPC, distearoyl phosphatidyl ethanolamine-polyethylene glycol DSPE-PEG2000, and cationic materials are respectively in a molar mass ratio of 0.75-0.85: 0.05-0.15 : 0.05-0.2 is mixed with organic solvent, nitrogen blowing to form film, vacuum removal of organic solvent, ultrasonic hydration, replacement of fluorocarbon, shaken for 30s in a bubbler, and centrifugal washing to obtain cationic microbubbles;
[0045] Step b, preparation of drug-loaded cationic microbubbles: in step a, the hydrophobic drug is put into an organic solvent and mixed with phospholipids uniformly, and the rest of the operations are consistent to obtain drug-loaded cationic microbubbles;
[0046] Step c, preparation of drug-loaded cationic fluorocarbon droplets: put the drug-loaded catio...
Embodiment 2
[0059] A preparation method of a drug-loaded ultrasound contrast agent using macrophages as a carrier, comprising the following steps:
[0060] Step a, preparation of cationic microbubbles: distearoyl phosphatidyl choline DSPC, distearoyl phosphatidyl ethanolamine-polyethylene glycol DSPE-PEG2000, and cationic materials are respectively in a molar mass ratio of 0.75-0.85: 0.05-0.15 : 0.05-0.2 is mixed with organic solvent, nitrogen blowing to form film, vacuum removal of organic solvent, ultrasonic hydration, replacement of fluorocarbon, shaken for 30s in a bubbler, and centrifugal washing to obtain cationic microbubbles;
[0061] Step b, preparation of drug-loaded cationic microbubbles: in step a, the hydrophobic drug is put into an organic solvent and mixed with phospholipids uniformly, and the rest of the operations are consistent to obtain drug-loaded cationic microbubbles;
[0062] Step c, preparation of drug-loaded cationic fluorocarbon droplets: put the drug-loaded cati...
Embodiment 3
[0075] A preparation method of a drug-loaded ultrasound contrast agent using macrophages as a carrier, comprising the following steps:
[0076] Step a, preparation of cationic microbubbles: distearoyl phosphatidyl choline DSPC, distearoyl phosphatidyl ethanolamine-polyethylene glycol DSPE-PEG2000, and cationic materials are respectively in a molar mass ratio of 0.75-0.85: 0.05-0.15 : 0.05-0.2 is mixed with organic solvent, nitrogen blowing to form film, vacuum removal of organic solvent, ultrasonic hydration, replacement of fluorocarbon, shaken for 30s in a bubbler, and centrifugal washing to obtain cationic microbubbles;
[0077] Step b, preparation of drug-loaded cationic microbubbles: in step a, the hydrophobic drug is put into an organic solvent and mixed with phospholipids uniformly, and the rest of the operations are consistent to obtain drug-loaded cationic microbubbles;
[0078] Step c, preparation of drug-loaded cationic fluorocarbon droplets: put the drug-loaded cati...
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