Cationic solid-lipid nanoparticles can efficiently bind and transfect plasmid DNA

被引:137
作者
Olbrich, C
Bakowsky, U
Lehr, CM
Müller, RH
Kneuer, C [1 ]
机构
[1] Univ Saarland, Dept Biopharmaceut & Pharmaceut Technol, D-66041 Saarbrucken, Germany
[2] Free Univ Berlin, Dept Pharmaceut Technol Biopharm & Biotechnol, D-12169 Berlin, Germany
[3] Univ Groningen, Dept Cell Membrane Biol, NL-9700 AD Groningen, Netherlands
关键词
gene therapy; nanoparticles; nonviral DNA vectors; solid-lipid nanoparticles; atomic force microscopy;
D O I
10.1016/S0168-3659(01)00506-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The suitability of cationically modified solid-lipid nanoparticles (SLN) as a novel transfection agent was investigated. SLN were produced by hot homogenisation using either Compritol ATO 888 or paraffin as matrix lipid, a mixture of Tween 80 and Span 85 as tenside and either EQ1 (NN-di-(beta-steaorylethyl)-N,N-dimethylammonium chloride) or cetylpyridinium chloride as charge carrier. The resulting particles were approximately 100 nm in size and showed zeta potentials around +40 mV at pH 7.4. DNA binding was tested by agarose gel electrophoresis. The resulting SLN-DNA complexes were further characterised by AFM and zeta potential measurements. Only the SLN batch SII-13, composed of 4% Compritol, 4% Tween/Span and 1% EQ1, was able to form stable complexes with DNA. Typical complexes were 300 to 800 nm in size. Cytotoxicity and transfection efficiency was tested in vitro on Cos-1 cells. Cationic SLN produced by modification with EQ1 were well tolerated, with LD50 values >3 mg/ml in the LDH release assay and >0.6 mg/ml in the WST-1 assay. Further, SLN-DNA complexes containing between 10 and 200 weight equivalents of SII-13 (matrix lipid) efficiently transfected the galactosidase expression plasmid pCMVbeta in the absence and presence of the endosomolytic agent chloroquine. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:345 / 355
页数:11
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