Silica nanoparticles modified with aminosilanes as carriers for plasmid DNA

被引:252
作者
Kneuer, C
Sameti, M
Haltner, EG
Schiestel, T
Schirra, H
Schmidt, H
Lehr, CM
机构
[1] Univ Saarland, Dept Biopharmaceut & Pharmaceut Technol, D-66041 Saarbrucken, Germany
[2] Inst New Mat gGmbH, Saarbrucken, Germany
关键词
silica; nanoparticle; DNA carrier; gene delivery;
D O I
10.1016/S0378-5173(99)00435-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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. Ail particles formed complexes with pCMVbeta plasmid DNA as evidenced by ratio dependend retardation of DNA in the agarosegel 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. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:257 / 261
页数:5
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