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血清对纳米颗粒毒性的影响。

The effects of serum on the toxicity of manufactured nanoparticles.

机构信息

Centre for Nano Safety, School of Life Sciences, Edinburgh Napier University, Merchiston Campus, 10 Colinton Road, Edinburgh EH10 5DT, United Kingdom.

出版信息

Toxicol Lett. 2010 Oct 20;198(3):358-65. doi: 10.1016/j.toxlet.2010.08.002. Epub 2010 Aug 10.

Abstract

The aim of the present study was to assess the effects of the presence and absence of serum in NP suspension media in relation to their cytotoxicity, as well as their potential to cause oxidative stress and stimulate pro-inflammatory cytokine release from J774.A1 murine 'macrophage-like' cells. Different sized (20nm and 200nm) carboxylated, fluorescent, model polystyrene beads (PBs) at concentrations from 12.5μgml(-1) to 100μgml(-1) were used. Both 20nm and 200nm PBs, independent of the suspension media, were observed to cause limited, yet significant (p<0.05) cytotoxicity over 48h up to 100μgml(-1). Significant differences (p>0.05) were also found between NP size and serum content of the suspension media used. The smaller sized PBs were found to affect intracellular glutathione (GSH) levels, causing a significant loss (p<0.05) in GSH when suspended in the presence of serum. Subsequent analysis also showed significant (p<0.05) increases in tumour necrosis factor-α production after 48h when the 20nm PBs were suspended in both the presence and absence of serum, compared to the affects observed by the larger, 200nm sized PBs. In conclusion, the results of the present study show that the interaction of NPs with serum can significantly affect their resultant toxicity in vitro.

摘要

本研究旨在评估 NP 悬浮介质中血清的存在与否对其细胞毒性的影响,以及它们引起氧化应激和刺激 J774.A1 鼠“巨噬样”细胞产生促炎细胞因子释放的潜力。使用不同大小(20nm 和 200nm)的羧化荧光模型聚苯乙烯珠(PBs),浓度从 12.5μgml(-1)到 100μgml(-1)。结果发现,20nm 和 200nm 的 PBs,独立于悬浮介质,在 48h 内观察到有限但显著(p<0.05)的细胞毒性,浓度高达 100μgml(-1)。还发现 NP 大小和悬浮介质中血清含量之间存在显著差异(p>0.05)。较小的 PBs 被发现影响细胞内谷胱甘肽(GSH)水平,当在血清存在的情况下悬浮时,GSH 显著丢失(p<0.05)。随后的分析还表明,与较大的 200nm PBs 相比,当 20nm PBs 在血清存在和不存在的情况下悬浮时,肿瘤坏死因子-α的产生在 48h 后显著增加(p<0.05)。总之,本研究的结果表明,NP 与血清的相互作用可显著影响其在体外的毒性。

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