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In vitro toxicity evaluation of silica-coated iron oxide nanoparticles in human SHSY5Y neuronal cells

机译:二氧化硅包覆的氧化铁纳米粒子对人SHSY5Y神经元细胞的体外毒性评估

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摘要

Iron oxide nanoparticles (ION) have been widely used in biomedical applications, for both diagnosis and therapy, due to their unique magnetic properties. They are intensively explored in neuromedicine mostly because of their ability to cross the blood brain barrier. Hence, their potential harmful effects on neuronal cells need to be carefully assessed. The objective of this study was to evaluate the toxicity of silica-coated ION (S-ION) (10–200 μg ml–1) on human neuronal SHSY5Y cells. Alterations in the cell cycle, cell death by apoptosis or necrosis, and membrane integrity were assessed as cytotoxicity parameters. Genotoxicity was determined by a γH2AX assay, a micronucleus (MN) test, and a comet assay. Complementarily, possible effects on DNA damage repair were also analysed by means of a DNA repair competence assay. All analyses were performed in complete and serum-free cell culture media. Iron ion release from the nanoparticles was notable only in complete medium. Despite being effectively internalized by the neuronal cells, S-ION presented in general low cytotoxicity; positive results were only obtained in some assays at the highest concentrations and/or the longest exposure time tested (24 h). Genotoxicity evaluations in serum-free medium were negative for all conditions assayed; in complete medium, dose and time-dependent increase in DNA damage not related to the production of double strand breaks or chromosome loss (according to the results of the γH2AX assay and MN test), was obtained. The presence of serum slightly influenced the behaviour of S-ION; further studies to investigate the formation of a protein corona and its role in nanoparticle toxicity are necessary.
机译:氧化铁纳米粒子(ION)由于其独特的磁性,已广泛用于诊断和治疗的生物医学应用。人们在神经医学领域对其进行了深入的研究,主要是因为它们具有穿越血脑屏障的能力。因此,需要仔细评估它们对神经元细胞的潜在有害作用。这项研究的目的是评估二氧化硅包覆的ION(S-ION)(10–200μgml –1 )对人神经元SHSY5Y细胞的毒性。将细胞周期的变化,由于凋亡或坏死引起的细胞死亡以及膜完整性评估为细胞毒性参数。基因毒性通过γH2AX分析,微核(MN)试验和彗星分析确定。补充地,还通过DNA修复能力测定法分析了对DNA损伤修复的可能影响。所有分析均在完全无血清的细胞培养基中进行。仅在完全培养基中才从纳米颗粒释放铁离子。尽管被神经元细胞有效地内在化,但S-ION的细胞毒性普遍较低。仅在某些测定中以最高浓度和/或最长暴露时间(24小时)获得阳性结果。在所有试验条件下,无血清培养基中的基因毒性评估均为阴性;在完全培养基中,获得的DNA损伤的剂量和时间依赖性增加与双链断裂或染色体丢失的产生无关(根据γH2AX分析和MN测试的结果)。血清的存在会轻微影响S-ION的行为;有必要进行进一步研究以研究蛋白质电晕的形成及其在纳米粒子毒性中的作用。

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