An in vitro toxicity evaluation of gold-, PLLA- and PCL-coated silica nanoparticles in neuronal cells for nanoparticle-assisted laser-tissue soldering

被引:32
作者
Koch, Franziska [1 ]
Moeller, Anja-M. [1 ]
Frenz, Martin [2 ]
Pieles, Uwe [3 ]
Kuehni-Boghenbor, Kathrin [1 ]
Mevissen, Meike [1 ]
机构
[1] Univ Bern, Vetsuisse Fac, CH-3012 Bern, Switzerland
[2] Univ Bern, Inst Appl Phys, CH-3012 Bern, Switzerland
[3] Sch Life Sci, CH-4132 Muttenz, Switzerland
基金
瑞士国家科学基金会;
关键词
Nanoparticle; Neuronal cells; Neurotoxicity; Oxidative stress; Gold; Silica; SIZE-DEPENDENT CYTOTOXICITY; BRAIN MICROGLIA; SH-SY5Y CELLS; VIVO; MECHANISMS; DAMAGE; BIOCOMPATIBILITY; NEUROPROTECTION; DIFFERENTIATION; INTERNALIZATION;
D O I
10.1016/j.tiv.2014.04.010
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The uptake of silica (Si) and gold (Au) nanoparticles (NPs) engineered for laser-tissue soldering in the brain was investigated using microglial cells and undifferentiated and differentiated SH-SY5Y cells. It is not known what effects NPs elicit once entering the brain. Cellular uptake, cytotoxicity, apoptosis, and the potential induction of oxidative stress by means of depletion of glutathione levels were determined after NP exposure at concentrations of 10(3) and 10(9) NPs/ml. Au-, silica poly (epsilon-caprolactone) (Si-PCL-) and silica poly-t-lactide (Si-PLLA)-NPs were taken up by all cells investigated. Aggregates and single NPs were found in membrane-surrounded vacuoles and the cytoplasm, but not in the nucleus. Both NP concentrations investigated did not result in cytotoxicity or apoptosis, but reduced glutathione (GSH) levels predominantly at 6 and 24 h, but not after 12 h of NP exposure in the microglial cells. NP exposure-induced GSH depletion was concentration-dependent in both cell lines. Si-PCL-NPs induced the strongest effect of GSH depletion followed by Si-PLLA-NPs and Au-NPs. NP size seems to be an important characteristic for this effect. Overall, Au-NPs are most promising for laser-assisted vascular soldering in the brain. Further studies are necessary to further evaluate possible effects of these NPs in neuronal cells. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:990 / 998
页数:9
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