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DECOY NUCLEIC ACID CATIONIC LIPOSOME CARRIER AND PREPARATION METHOD THEREOF

机译:诱饵核酸阳离子脂质体载体及其制备方法

摘要

A preparation method of a Decoy nucleic acid cationic liposome carrier including: (1) mixing dioleoyl phosphoethanolamine and (2,3-dioleoyl-propyl)-trimethylamine in a mass ratio of 4:1 to 1:4, and adding an organic solvent to obtain a mixed solution through dissolution; (2) completely evaporating the organic solvent in the mixed solution obtained in step (1), dissolving the remaining solid fraction by using an HEPES buffer solution, firstly hydrating the solution for 30 to 60 min, and then ultrasonically processing the solution for 30 to 60 min; (3) filtering the mixed system obtained after processing in the step (2) by a membrane of 0.4 to 0.8 μm, then filtering the mixed system by a membrane of 0.03 to 0.2 μm, and preparing uniformly to distributed blank liposome with small grain size; and (4) mixing the blank liposome with protamine and Decoy nucleic acid according to a mass ratio of (50 to 120):(10 to 20):1, and incubating for 12 to 24 h at the temperature of 2° C. to 8° C. to form the complete Decoy nucleic acid cationic liposome carrier.
机译:诱饵核酸阳离子脂质体载体的制备方法,包括:(1)以4:1至1:4的质量比混合二油酰基磷乙醇胺和(2,3-二油酰基-丙基)-三甲胺,并向其中加入有机溶剂。通过溶解获得混合溶液; (2)将步骤(1)中获得的混合溶液中的有机溶剂完全蒸发,通过使用HEPES缓冲溶液溶解剩余的固体部分,首先将溶液水化30至60分钟,然后将溶液超声处理30至60分钟; (3)用0.4至0.8μm的膜过滤在步骤(2)中处理后得到的混合体系,然后用0.03至0.2μm的膜过滤,将其均匀地制备成小粒径分布的空白脂质体; (4)将空白脂质体与鱼精蛋白和诱饵核酸按质量比(50至120):( 10至20):1混合,并在2℃至20℃温育12至24小时。 8℃形成完整的诱饵核酸阳离子脂质体载体。

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