The effects of serum on the toxicity of manufactured nanoparticles

被引:81
作者
Clift, Martin J. D. [1 ,3 ]
Bhattacharjee, Sourav [2 ,3 ]
Brown, David M. [3 ]
Stone, Vicki [3 ]
机构
[1] Univ Bern, Inst Anat, CH-3000 Bern 9, Switzerland
[2] Wageningen Univ, Organ Chem Lab, NL-6703 HB Wageningen, Netherlands
[3] Edinburgh Napier Univ, Ctr Nano Safety, Sch Life Sci, Edinburgh EH10 5DT, Midlothian, Scotland
关键词
Nanoparticles (NPs); Cytotoxicity Oxidative stress; Pro-inflammatory cytokine stimulation; Serum; Macrophages; FETAL CALF SERUM; OXIDATIVE STRESS; PROTEIN CORONA; SURFACE-AREA; ULTRAFINE; PARTICLES; SIZE;
D O I
10.1016/j.toxlet.2010.08.002
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
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 (20 nm and 200 nm) carboxylated, fluorescent, model polystyrene beads (PBs) at concentrations from 12.5 mu g m1(-1) to 10014 m1-1 were used. Both 20 nm and 200 nm PBs, independent of the suspension media, were observed to cause limited, yet significant (p < 0.05) cytotoxicity over 48 h up to 10014 m1-1. 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-a production after 48 h when the 20 nm PBs were suspended in both the presence and absence of serum, compared to the affects observed by the larger, 200 nm 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. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:358 / 365
页数:8
相关论文
共 23 条
[1]   Size-dependent proinflammatory effects of ultrafine polystyrene particles: A role for surface area and oxidative stress in the enhanced activity of ultrafines [J].
Brown, DM ;
Wilson, MR ;
MacNee, W ;
Stone, V ;
Donaldson, K .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2001, 175 (03) :191-199
[2]   Understanding the nanoparticle-protein corona using methods to quantify exchange rates and affinities of proteins for nanoparticles [J].
Cedervall, Tommy ;
Lynch, Iseult ;
Lindman, Stina ;
Berggard, Tord ;
Thulin, Eva ;
Nilsson, Hanna ;
Dawson, Kenneth A. ;
Linse, Sara .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (07) :2050-2055
[3]   The impact of different nanoparticle surface chemistry and size on uptake and toxicity in a murine macrophage cell line [J].
Clift, Martin J. D. ;
Rothen-Rutishauser, Barbara ;
Brown, David M. ;
Duffin, Rodger ;
Donaldson, Ken ;
Proudfoot, Lorna ;
Guy, Keith ;
Stone, Vicki .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2008, 232 (03) :418-427
[4]   An investigation into the potential for different surface-coated quantum dots to cause oxidative stress and affect macrophage cell signalling in vitro [J].
Clift, Martin J. D. ;
Boyles, Matthew S. P. ;
Brown, David M. ;
Stone, Vicki .
NANOTOXICOLOGY, 2010, 4 (02) :139-149
[5]  
CLIFT MJD, LANGMUIR IN PRESS
[6]  
Duffin R., 2002, Ann. Occup. Hyg, V46, P242, DOI [10.1093/annhyg/46.suppl1.242, DOI 10.1093/ANNHYG/46.SUPPL1.242]
[7]   Proinflammogenic effects of low-toxicity and metal nanoparticles in vivo and in vitro: Highlighting the role of particle surface area and surface reactivity [J].
Duffin, Rodger ;
Tran, Lang ;
Brown, David ;
Stone, Vicki ;
Donaldson, Ken .
INHALATION TOXICOLOGY, 2007, 19 (10) :849-856
[8]   PULMONARY RETENTION OF ULTRAFINE AND FINE PARTICLES IN RATS [J].
FERIN, J ;
OBERDORSTER, G ;
PENNEY, DP .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 6 (05) :535-542
[9]   Measurement of reactive species production by nanoparticles prepared in biologically relevant media [J].
Foucaud, L. ;
Wilson, M. R. ;
Brown, D. M. ;
Stone, V. .
TOXICOLOGY LETTERS, 2007, 174 (1-3) :1-9
[10]   Ultrafine particles cross cellular membranes by nonphagocytic mechanisms in lungs and in cultured cells [J].
Geiser, M ;
Rothen-Rutishauser, B ;
Kapp, N ;
Schürch, S ;
Kreyling, W ;
Schulz, H ;
Semmler, M ;
Hof, VI ;
Heyder, J ;
Gehr, P .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2005, 113 (11) :1555-1560