Method for preparing gene medication carrier by using chitosan modified liposome
A technology of drug delivery carrier and chitosan, applied in the field of gene drug delivery carrier preparation, can solve the problems of low transfection efficiency and low cytotoxicity, and achieve the effects of simple preparation process, good stability and reasonable design
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Embodiment 1
[0013] Example 1 Take 10 to 200 mg of soybean phospholipids and 5 to 100 mg of cholesterol to 7.5 to 150 mL of chloroform, add 2.5 to 50 mL of distilled water, and prepare liposomes by reverse evaporation. Specifically, it is vortexed for 10-30 minutes to make it into milk, and the chloroform is removed by vacuum rotary evaporation on a rotary evaporator to obtain a liposome suspension. The liposome solution is ultrasonically treated with a 100~500W probe, working time is 1~3 seconds, gap time is 2~4 seconds, cycle time is 30~240 times, ultrasonic condition is ice bath, squeezed through membrane, pore size is 0.1~0.22 μm. Take chitosan with a molecular weight of 450kDa and dissolve it in glacial acetic acid with a concentration of 0.1% to 1%. The final concentration of the chitosan solution is 0.2% to 1.0%. The liposome solution is slowly injected into the chitosan solution for 1-10 minutes, and then stirred for 0.5-2 hours to obtain chitosan modified liposomes.
Embodiment 2
[0014] Example 2 Take 10 to 200 mg of lecithin and 5 to 100 mg of cholesterol to 7.5 to 150 mL of chloroform, add 2.5 to 50 mL of distilled water, and prepare liposomes by reverse evaporation. The liposome solution is ultrasonically treated with a 100~500W probe, working time is 1~3 seconds, gap time is 2~4 seconds, cycle time is 30~240 times, ultrasonic condition is ice bath, squeezed through membrane, pore size is 0.1~0.22 μm. Take chitosan with a molecular weight of 900kDa and dissolve it in glacial acetic acid with a concentration of 0.1% to 1%. The final concentration of the chitosan solution is 0.2% to 1.0%. The liposome solution is slowly injected into the chitosan solution for 1-10 minutes, and then stirred for 0.5-2 hours to obtain chitosan modified liposomes.
[0015] Prepared by the thin film dispersion method. Specifically: taking 10 to 200 mg of soybean phospholipids and 5 to 100 mg of cholesterol in 7.5 to 150 mL of chloroform and placing them in a pear-shaped bottle...
Embodiment 4
[0016] Example 4 Take 10 to 200 mg of lecithin and 5 to 100 mg of cholesterol to 7.5 to 150 mL of chloroform, prepare according to the above-mentioned film dispersion method, and add 2.5 to 50 mL of distilled water for ultrasonic hydration. The liposome solution is ultrasonically treated with a 100~500W probe, working time is 1~3 seconds, gap time is 2~4 seconds, cycle time is 30~240 times, ultrasonic condition is ice bath, squeezed through membrane, pore size is 0.1~0.22 μm. Take chitosan with a molecular weight of 900kDa and dissolve it in glacial acetic acid with a concentration of 0.1% to 1%. The final concentration of the chitosan solution is 0.2% to 1.0%. The liposome solution is slowly injected into the chitosan solution for 1-10 minutes, and then stirred for 0.5-2 hours to obtain chitosan modified liposomes.
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