Preliminary results on the pathogenic effects of intratracheal exposure to one-dimensional nanocarbons

被引:41
作者
Grubek-Jaworska, H
Nejman, P
Czuminska, K
Przybylowski, T
Huczko, A [1 ]
Lange, H
Bystrzejewski, M
Baranowski, P
Chazan, R
机构
[1] Warsaw Univ, Dept Chem, PL-02093 Warsaw, Poland
[2] Med Univ Warsaw, Dept Pneumol, PL-02091 Warsaw, Poland
[3] Agr Univ Warsaw, Fac Vet Med, PL-02787 Warsaw, Poland
关键词
carbon nanotubes; chemical vapor deposition; electron microscopy; bioactivity;
D O I
10.1016/j.carbon.2005.12.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Because of the unique structural, mechanical, and electrical properties, 1-D (one-dimensional) carbon nanotubes and nanofibers have been studied For possible use in many fields from Molecular electronics to biomedical applications for several years. The 1-D carbon nanomaterials are produced presently on large scale. The inhalation of ultrafine nanocarbons can cause inflammatory lung response. The pathogenicity of 1-D carbon nanostructure remains, however, unclear. We examined in vivo the effects of intratracheal instillation of 1-D carbon nanomaterials (NanoLab nanotubes, Pyrograf and Showa Denko nanofibers) vs. control (pure suspension fluid) on lung tissue in guinea pig model. Three months intratracheal exposure to 1-D nanocarbons caused organizing pneumonitis (Bronchiolitis obliterans organizing pneumonia) with focal non-specific desquamative interstitial prieumonia-like ("DIP-like") reaction without fibrosis or with mild peribronchiolar fibrosis in all experimental animals but not in controls. Infiltration of inflammatory cells and increase of IL-8 concentration in BAL-fluid depended on the nanomaterial used. The protein concentration in BAL-fluids in experimental animals did not differ significantly in comparison to the control group, although exudate to alveoli was observed in all the experimental groups histopathologically. Our results indicate that exposure on intratracheally introduced carbon nanotubes/nanofibers may induce measurable pulmonary pathology. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1057 / 1063
页数:7
相关论文
共 22 条
[11]  
OBERDORSTER G, 1994, INT ARCH OCC ENV H S, V73, pS60
[12]  
REICH S, 1999, CARBON NANOTUBES, P3
[13]   Supramolecular self-assembly of lipid derivatives on carbon nanotubes [J].
Richard, C ;
Balavoine, F ;
Schultz, P ;
Ebbesen, TW ;
Mioskowski, C .
SCIENCE, 2003, 300 (5620) :775-778
[14]  
Service RF, 2003, SCIENCE, V300, P243
[15]   Exposure to carbon nanotube material: Assessment of nanotube cytotoxicity using human keratinocyte cells [J].
Shvedova, AA ;
Castranova, V ;
Kisin, ER ;
Schwegler-Berry, D ;
Murray, AR ;
Gandelsman, VZ ;
Maynard, A ;
Baron, P .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 2003, 66 (20) :1909-1926
[16]   Asbestos-induced pulmonary toxicity: Role of DNA damage and apoptosis [J].
Upadhyay, D ;
Kamp, DW .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2003, 228 (06) :650-659
[17]  
URNAU L, 1996, ASSOCIATES CARRY RES, P6
[18]   Peptides with selective affinity for carbon nanotubes [J].
Wang, SQ ;
Humphreys, ES ;
Chung, SY ;
Delduco, DF ;
Lustig, SR ;
Wang, H ;
Parker, KN ;
Rizzo, NW ;
Subramoney, S ;
Chiang, YM ;
Jagota, A .
NATURE MATERIALS, 2003, 2 (03) :196-200
[19]   Comparative pulmonary toxicity assessment of single-wall carbon nanotubes in rats [J].
Warheit, DB ;
Laurence, BR ;
Reed, KL ;
Roach, DH ;
Reynolds, GAM ;
Webb, TR .
TOXICOLOGICAL SCIENCES, 2004, 77 (01) :117-125
[20]   Nanotechnology - Carbon nanotubes with DNA recognition [J].
Williams, KA ;
Veenhuizen, PTM ;
de la Torre, BG ;
Eritja, R ;
Dekker, C .
NATURE, 2002, 420 (6917) :761-761