Composition comprising macrocyclic ester compound and siRNA and preparation method thereof
A compound and macrocyclic ester technology, applied in the field of medicine and biology, can solve the problems of strong inflammatory response, difficulty in passing through the cell membrane, and short half-life, so as to reduce adverse reactions, improve pharmacokinetic characteristics, and change biodistribution Effect
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Embodiment 1
[0028] Embodiment 1 synthetic compound T2C1 compound
[0029] Weigh 100mg of 1,4,7,10-tetraazacyclododecane and C12-14-alkyl glycidyl ether 726.8mg to mix, then in 92 o C under agitation for 43 hours to synthesize T2C1.
Embodiment 2
[0031] Preparation formula siRNA (siRNA+T2C1+cholesterol-polyethylene glycol+DPPE1:1:1:1)
[0032] Preparation of preparation: Weigh a certain amount of 100mg T2C1, cationic lipid DOTMA, phospholipid DPPE, cholesterol-polyethylene glycol cholesterol polyethylene glycol, mix and dissolve in chloroform in a glass container, and remove chloroform under vacuum. Then add 300ml of water, vortex and oscillate to dissolve in water, after homogenization treatment, the homogenization condition is 1000 bar, two cycles (ATS homogenizer).
Embodiment 3
[0034] siRNA: T2C1 cholesterol-polyethylene glycol: DPPE is 1:0.3:0.3:0.4.
[0035] Preparation of preparation: Weigh a certain amount of 100mg T2C1, cationic lipid DOTMA, phospholipid DPPE, cholesterol-polyethylene glycol, mix and dissolve in ethanol in a glass container, and remove ethanol under vacuum. Then add 300ml of water, vortex and oscillate to dissolve in water, after homogenization treatment, the homogenization condition is 1000 bar, two cycles (ATS homogenizer).
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