Nanotoxicity of iron oxide nanoparticle internalization in growing neurons

被引:492
作者
Pisanic, Thomas R., II
Blackwell, Jennifer D.
Shubayev, Veronica I.
Finones, Rita R.
Jin, Sungho
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Dept Anesthesiol, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Mech & Aerosp Engn Dept, La Jolla, CA 92093 USA
[4] San Diego Vet Affairs Med Healthcare Syst, La Jolla, CA 92093 USA
关键词
nanoparticle; magnetism; neural cell; cytotoxicity; biocompatibility; NERVE GROWTH-FACTOR; IN-VIVO TRACKING; MODIFIED SUPERPARAMAGNETIC NANOPARTICLES; MAGNETIC NANOPARTICLES; INTRACELLULAR UPTAKE; MAGHEMITE NANOPARTICLES; PHEOCHROMOCYTOMA CELLS; SURFACE MODIFICATION; DRUG-DELIVERY; VITRO;
D O I
10.1016/j.biomaterials.2007.01.043
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Magnetic nanoparticles (MNPs) have shown great promise for use as tools in a wide variety of biomedical applications, some of which require the delivery of large numbers of MNPs onto or into the cells of interest. Here we develop a quantifiable model cell system and show that intracellular delivery of even moderate levels of iron oxide (Fe2O3) nanoparticles may adversely affect cell function. More specifically, we show that exposure to increasing concentrations of anionic MNPs, from 0.15 to 15mm of iron, results in a dose-dependent diminishing viability and capacity of PC12 cells to extend neurites in response to their putative biological cue, i.e. nerve growth factor. The cytotoxicity results of biomaterials in our model system imply that more study into the acute and long-term effects of cellular Fe2O3 internalization is both warranted and necessary. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2572 / 2581
页数:10
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