Novel drug delivery system by surface modified magnetic nanoparticles

被引:17
作者
Takeda, Shin-ichi
Terazono, Bungo
Mishima, Fumihito
Nakagami, Hironori
Nishijima, Shigehiro
Kaneda, Yasufumi
机构
[1] Osaka Univ, Grad Sch Engn, Div Sustainable Energy & Environm Engn, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Div Gene Therapy Sci, Suita, Osaka 5650871, Japan
关键词
magnetic nanoparticle; plasmid DNA; cell; drug delivery system; magnetic seeding; CELL-SURFACE; HEPARIN THERAPY; GENE DELIVERY; ACTIVATION; PARTICLES; VECTOR; DEATH; BCL-2; LEADS;
D O I
10.1166/jnn.2006.483
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the recent progress of gene and cell therapy, novel drug delivery system (DDS) has been required for efficient delivery of small molecules/drugs and also the safety for clinical usage. We have already developed the unique transfection technique by preparing magnetic vector and using permanent magnet. This technique can improve the transfection efficiency. In this study, we directly associated plasmid DNA with magnetic nanoparticles, which can potentially enhance their transfection efficiency by magnetic force. Magnetic nanoparticle, such as magnetite, its average size of 18.7 nm, can be navigated by magnetic force and is basically consisted with oxidized Fe that is commonly used as the supplement drug for anemia. The magnetite particles coated with protamine sulfate, which gives a cationic surface charge onto the magnetite particle, significantly enhanced the transfection efficiency in vitro cell culture system. The magnetite particles coated with protamine sulfate also easily associated with cell surface, leading to high magnetic seeding percentage. From these results, it was found that the size and surface chemistry of magnetic particles would be tailored to Met specific demands on physical and biological characteristics accordingly. Overall, magnetic nanoparticles with different surface modification enhance the association with plasmid DNA and cell surface as well as HVJ-E, which potentially help to improve the drug delivery system.
引用
收藏
页码:3269 / 3276
页数:8
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