Influence of length on cytotoxicity of multi-walled carbon nanotubes against human acute monocytic leukemia cell line THP-I in vitro and subcutaneous tissue of rats in vivo

被引:253
作者
Sato, Y
Yokoyama, A
Shibata, K
Akimoto, Y
Ogino, S
Nodasaka, Y
Kohgo, T
Tamura, K
Akasaka, T
Uo, M
Motomiya, K
Jeyadevan, B
Ishiguro, M
Hatakeyama, R
Watari, F
Tohji, K
机构
[1] Tohoku Univ, Grad Sch Environm Sci, Aoba Ku, Sendai, Miyagi 9808579, Japan
[2] Hokkaido Univ, Grad Sch Dent Med, Kita Ku, Sapporo, Hokkaido 0608586, Japan
[3] Tohoku Univ, Inst Mat Res, Aoba Ku, Sendai, Miyagi 9808577, Japan
[4] Tohoku Univ, Grad Sch Engn, Aoba Ku, Sendai, Miyagi 9808579, Japan
关键词
D O I
10.1039/b502429c
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Carbon nanotubes (CNTs) are single- or multi-cylindrical graphene structures that possess diameters of a few nanometers, while the length can be up to a few micrometers. These could have unusual toxicological properties, in that they share intermediate morphological characteristics of both fibers and nanoparticles. To date, no detailed study has been carried out to determine the effect of length on CNT cytotoxicity. In this paper, we investigated the activation of the human acute monocytic leukemia cell line THP-1 in vitro and the response in subcutaneous tissue in vivo to CNTs of different lengths. We used 220 nm and 825 nm-long CNT samples for testing, referred to as "220-CNTs" and "825-CNTs", respectively. 220-CNTs and 825-CNTs induced human monocytes in vitro, although the activity was significantly lower than that of microbial lipopeptide and lipopolysaccharide, and no activity appeared following variation in the length of CNTs. On the other hand, the degree of inflammatory response in subcutaneous tissue in rats around the 220-CNTs was slight in comparison with that around the 825-CNTs. These results indicated that the degree of inflammation around 825-CNTs was stronger than that around 220-CNTs since macrophages could envelop 220-CNTs more readily than 825-CNTs. However, no severe inflammatory response such as necrosis, degeneration or neutrophil infiltration in vivo was observed around both CNTs examined throughout the experimental period.
引用
收藏
页码:176 / 182
页数:7
相关论文
共 46 条
[1]  
Balavoine F, 1999, ANGEW CHEM INT EDIT, V38, P1912, DOI 10.1002/(SICI)1521-3773(19990712)38:13/14<1912::AID-ANIE1912>3.0.CO
[2]  
2-2
[3]   Can carbon nanotubes be considered useful tools for biological applications? [J].
Bianco, A ;
Prato, M .
ADVANCED MATERIALS, 2003, 15 (20) :1765-1768
[4]   Cationic carbon nanotubes bind to CpG oligodeoxynucleotides and enhance their immunostimulatory properties [J].
Bianco, A ;
Hoebeke, J ;
Godefroy, S ;
Chaloin, O ;
Pantarotto, D ;
Briand, JP ;
Muller, S ;
Prato, M ;
Partidos, CD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (01) :58-59
[5]   Biomedical applications of functionalised carbon nanotubes [J].
Bianco, A ;
Kostarelos, K ;
Partidos, CD ;
Prato, M .
CHEMICAL COMMUNICATIONS, 2005, (05) :571-577
[6]  
BOKROS JC, 1977, CARBON, V15, P355, DOI 10.1016/0008-6223(77)90324-4
[7]   The potential environmental impact of engineered nanomaterials [J].
Colvin, VL .
NATURE BIOTECHNOLOGY, 2003, 21 (10) :1166-1170
[8]   Fabrication and biocompatibility of carbon nanotube-based 3D networks as scaffolds for cell seeding and growth [J].
Correa-Duarte, MA ;
Wagner, N ;
Rojas-Chapana, J ;
Morsczeck, C ;
Thie, M ;
Giersig, M .
NANO LETTERS, 2004, 4 (11) :2233-2236
[9]   Effect of single wall carbon nanotubes on human HEK293 cells [J].
Cui, DX ;
Tian, FR ;
Ozkan, CS ;
Wang, M ;
Gao, HJ .
TOXICOLOGY LETTERS, 2005, 155 (01) :73-85
[10]   Surface reactivity in the pathogenic response to particulates [J].
Fubini, B .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1997, 105 :1013-1020