Anti-cancer medicine liposome preparation sensitive to ray
A technology for liposome preparations and anticancer drugs, which can be used in liposome delivery, antitumor drugs, drug combinations, etc. Anti-tumor effect, improvement of compliance, effect of prolonging circulation time
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Embodiment 1
[0025] Containing 144.4mg hydrogenated soybean lecithin (HSPC), 68.1mg cholesterol (cholesterol), 54.8mg polyethylene glycol 2000-distearoylphosphatidylethanolamine (DSPE-PEG2000), 14.7mg dipalmitoylphosphatidylcholine ( DPPC), dissolved in 12ml of organic solvent, and 3ml of 8mg / ml cisplatin sodium chloride solution was prepared in addition, after mixing, it was homogenized at high speed, and the organic solvent was removed under reduced pressure on a rotary evaporator to make it a uniform suspension. For 1 hour, a translucent liposome suspension formed.
[0026] In this example, the sum of the molar percentages of PC and PG in phospholipids is 51%.
[0027] The preparation prepared in this embodiment was used as the experimental group, and the same dose of cisplatin solution was used as the control group. Compared with the control group, under the CO60r ray 6Gy scheme, the survival time of the tumor-bearing mice was extended from 23 days to 37 (medication After 1h radiother...
Embodiment 2
[0038] Add an organic solvent solution containing 57mg of dipalmitoylphosphatidylglycerol (DPPG) into an eggplant-shaped bottle, place it in a water bath at 30°C, and remove the organic solvent by rotary evaporation to form a film, then keep vacuum for 1 hour to remove the solvent completely, and add to the eggplant-shaped bottle. Add 1ml of 10mg / ml 5-Fu HEPES solution into the bottle, vibrate vigorously, place at room temperature for 2h, and oscillate ultrasonically to form a translucent and uniform liposome suspension.
[0039] In this example, the sum of the molar percentages of PC and PG in phospholipids is 100%.
[0040]The preparation prepared in this example was used as the experimental group, and the same dose of 5-Fu solution was used as the control group. Compared with the control group, under the same radiotherapy regimen, the survival time of tumor-bearing mice was prolonged by 10-15 days .
Embodiment 3
[0042] An organic solution containing 12.6 mg dioleoylphosphatidylglycerol (DOPG), 12.8 mg dipalmitoylphosphatidylcholine (DPPC), 4.7 mg polyethylene glycol 2000-distearoylphosphatidylethanolamine (DSPE-PEG2000) Add the solvent solution into the eggplant-shaped bottle, water bath, rotary evaporation to form a film, add 1ml of 40mg / ml cyclophosphamide solution to the eggplant-shaped bottle, shake, place at room temperature for 2h, pass through the high-pressure homogenizer 10 times, and form Translucent suspension of liposomes.
[0043] In this example, the sum of the molar percentages of PC and PG in phospholipids is 95%.
[0044] The preparation prepared in this example was used as the experimental group, and the same dose of cyclophosphamide solution was used as the control group. Compared with the control group, under the same radiotherapy regimen, the survival time of tumor-bearing mice was prolonged by 7-10 days.
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