Nano assembly co-loaded with rapamycin and curcumin, preparation method and application thereof
A nano-assembly and rapamycin technology, applied in nanotechnology, nanotechnology, nanomedicine, etc., to achieve strong cell affinity, reduce total protein content, and improve lung inflammation
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Embodiment 1
[0041] The preparation method of embodiment 1 rapamycin / curcumin-IR806 nano assembly
[0042] Accurately weigh rapamycin and curcumin according to the mass ratio of 2:1, dissolve in DMSO to prepare a solution with a total drug concentration of 6mg / ml as the oil phase; weigh IR806 and dissolve it in deionized water to prepare a water with a concentration of 1mg / ml phase; 1ml of oil phase was added dropwise to 10ml of water phase, and after 60min of magnetic stirring at room temperature in the dark, it was dialyzed with deionized water (dialysis membrane M W : 1000) to remove DMSO by dialyzing for 6 hours, then collect by ultracentrifugation and disperse to prepare drug-loaded IR806 nano-assemblies, and store them at 4°C.
Embodiment 2
[0043] Example 2 The preparation method of rapamycin / curcumin-IR820 nano assembly
[0044]Accurately weigh rapamycin and curcumin according to a mass ratio of 1:1, dissolve them in ethanol to prepare a solution with a total drug concentration of 6mg / ml as the oil phase; weigh IR820 and dissolve it in deionized water to prepare a water solution with a concentration of 1mg / ml phase; 1ml of the oil phase was added dropwise to 6ml of the water phase, and after magnetic stirring for 120min at room temperature in the dark, it was dialyzed with deionized water (dialysis membrane M W : 1000) to remove ethanol by dialysis for 4 hours, and then the resulting system was subjected to ultrafiltration (ultrafiltration membrane molecular weight cut-off 1000) to intercept nanoparticles, and then the drug-loaded IR820 nano-assembly was prepared and stored at 4°C.
Embodiment 3
[0045] Example 3 Preparation method of rapamycin / curcumin-IR783 lipid nano-assembly
[0046] Accurately weigh rapamycin and curcumin according to a mass ratio of 1:3, dissolve them in DMSO / ethanol (V:V=1:1) mixed solvent, prepare a solution with a total drug concentration of 10mg / ml as the oil phase; weigh IR783 was dissolved in deionized water to prepare a water phase with a concentration of 1mg / ml; 1ml of the oil phase was added dropwise to 8ml of the water phase, stirred at room temperature and protected from light for 90min by magnetic force, and then dialyzed with deionized water (dialysis membrane M W : 1000) dialyzed for 8h to remove DMSO and ethanol, then collected by ultracentrifugation and dispersed to prepare drug-loaded IR783 nano-assemblies.
[0047] The phospholipid mixture obtained by mixing 7 mg of dipalmitoylphosphatidylcholine and 3 mg of distearoylphosphatidylethanolamine-polyethylene glycol 2000 was dissolved in 2.5 mL of chloroform, and the system was vacu...
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