Effect of multi-walled carbon nanotube surface modification on bioactivity in the C57BL/6 mouse model

被引:79
作者
Sager, Tina M. [1 ,2 ]
Wolfarth, Michael W. [2 ]
Andrew, Michael [2 ]
Hubbs, Ann [2 ]
Friend, Sherri [2 ]
Chen, Teh-hsun [2 ]
Porter, Dale W. [2 ]
Wu, Nianqiang [3 ]
Yang, Feng [4 ]
Hamilton, Raymond F. [1 ]
Holian, Andrij [1 ]
机构
[1] Univ Montana, Ctr Environm Hlth Sci, Dept Biomed & Pharmaceut Sci, Missoula, MT 59812 USA
[2] NIOSH, Hlth Effects Lab Div, Pathol & Physiol Res Branch, Morgantown, WV 26505 USA
[3] W Virginia Univ, Dept Mech & Aerosp Engn, WVNano Initiat, Morgantown, WV 26506 USA
[4] W Virginia Univ, Dept Ind & Management Syst Engn, Morgantown, WV 26506 USA
关键词
multi-walled carbon nanotube; surface modification; inflammasome activation; fibrosis; pulmonary toxicity; INTRATRACHEAL INSTILLATION; PULMONARY INFLAMMATION; NANOPARTICLES; TOXICITY; LUNG; EXPOSURE; FIBROSIS; MICE; RESPONSES; INJURY;
D O I
10.3109/17435390.2013.779757
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The current study tests the hypothesis that multi-walled carbon nanotubes (MWCNT) with different surface chemistries exhibit different bioactivity profiles in vivo. In addition, the study examined the potential contribution of the NLRP3 inflammasome in MWCNT-induced lung pathology. Unmodified (BMWCNT) and MWCNT that were surface functionalised with -COOH (FMWCNT), were instilled into C57BL/6 mice. The mice were then examined for biomarkers of inflammation and injury, as well as examined histologically for development of pulmonary disease as a function of dose and time. Biomarkers for pulmonary inflammation included cytokines, mediators and the presence of inflammatory cells (IL-1 beta, IL-18, IL-33, cathepsin B and neutrophils) and markers of injury (albumin and lactate dehydrogenase). The results show that surface modification by the addition of the -COOH group to the MWCNT, significantly reduced the bioactivity and pathogenicity. The results of this study also suggest that in vivo pathogenicity of the BMWCNT and FMWCNT correlates with activation of the NLRP3 inflammasome in the lung.
引用
收藏
页码:317 / 327
页数:11
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