We synthesised silica nanoparticles (SiNP) with covalently linked cationic surface modifications and demonstrated their ability to electrostatically bind, condense and protect plasmid DNA. These particles might be utilised as DNA carriers for gene delivery. All nanoparticles were sized between 10 and 100 nm and displayed surface charge potentials from +7 to +31 mV at pH 7.4. They were produced by modification of commercially available (IPAST) or in-house synthesised silica particles with either N-(2-aminoethyl)-3-aminopropyltrimethoxysilane or N-(6-aminohexyl)-3-aminopropyltrimethoxysilane. All particles formed complexes with pCMVbeta plasmid DNA as evidenced by ratio dependent retardation of DNA in the agarose gel and co-sedimentation of soluble DNA with nanoparticles. High salt and alkaline pH did inhibit complex formation. Absorption onto the particles also decreased the hydrodynamic dimensions of plasmid DNA as shown by photon correlation spectroscopy. Complexes formed in water at a w/w ratio of Si26H:DNA (pCMVbeta) of 300 were smallest with a mean hydrodynamic diameter of 83 nm. For effective condensation a w/w ratio of Si26H:DNA of 30 was sufficient. Further, the absorbed DNA was protected from enzymatic degradation by DNase I.

译文

:我们合成了具有共价键连接的阳离子表面修饰的二氧化硅纳米粒子(SiNP),并证明了它们具有静电结合,浓缩和保护质粒DNA的能力。这些颗粒可以用作基因载体的DNA载体。所有纳米颗粒的尺寸在10至100 nm之间,在pH 7.4下显示7至31 mV的表面电荷电位。它们是通过使用N-(2-氨基乙基)-3-氨基丙基三甲氧基硅烷或N-(6-氨基己基)-3-氨基丙基三甲氧基硅烷对市售(IPAST)或内部合成的二氧化硅颗粒进行改性制成的。所有颗粒均与pCMVbeta质粒DNA形成复合物,琼脂糖凝胶中DNA的比例依赖性阻滞作用以及可溶性DNA与纳米颗粒的共同沉淀作用证明了这一点。高盐和碱性pH确实抑制了复合物的形成。如通过光子相关光谱法所示,吸收到颗粒上也降低了质粒DNA的流体力学尺寸。在水中以Si26H:DNA(pCMVbeta)的重量比为300形成的复合物最小,平均流体动力学直径为83 nm。对于有效的缩合,Si26H:DNA的w / w比为30足够。此外,DNase I保护了吸收的DNA免受酶促降解。

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