Carbon nanotubes: A review of their properties in relation to pulmonary toxicology and workplace safety

被引:791
作者
Donaldson, Ken
Aitken, Robert
Tran, Lang
Stone, Vicki
Duffin, Rodger
Forrest, Gavin
Alexander, Andrew
机构
[1] Univ Edinburgh, MRC, Ctr Inflammat Res, ELEGI Colt Lab,Queens Med Res Inst, Edinburgh EH16 4TJ, Midlothian, Scotland
[2] Inst Occupat Med, Edinburgh EH14 4AP, Midlothian, Scotland
[3] Napier Univ, Sch Life Sci, Edinburgh EH10 5DT, Midlothian, Scotland
[4] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
关键词
carbon nanotubes; graphite; inflammation; oxidative stress; nanoparticles; fibre; toxicology; asbestos; lungs; workplace;
D O I
10.1093/toxsci/kfj130
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Carbon nanotubes (CNT) are an important new class of technological materials that have numerous novel and useful properties. The forecast increase in manufacture makes it likely that increasing human exposure will occur, and as a result, CNT are beginning to come under toxicological scrutiny. This review seeks to set out the toxicological paradigms applicable to the toxicity of inhaled CNT, building on the toxicological database on nanoparticles (NP) and fibers. Relevant workplace regulation regarding exposure is also considered in the light of our knowledge of CNT. CNT could have features of both NP and conventional fibers, and so the current paradigm for fiber toxicology, which is based on mineral fibers and synthetic vitreous fibers, is discussed. The NP toxicology paradigm is also discussed in relation to CNT The available peer-reviewed literature suggests that CNT may have unusual toxicity properties. In particular, CNT seem to have a special ability to stimulate mesenchymal cell growth and to cause granuloma formation and fibrogenesis. In several studies, CNT have more adverse effects than the same mass of NP carbon and quartz, the latter a commonly used benchmark of particle toxicity. There is, however, no definitive inhalation study available that would avoid the potential for artifactual effects due to large mats and aggregates forming during instillation exposure procedures. Studies also show that CNT may exhibit some of their effects through oxidative stress and inflammation. CNT represent a group of particles that are growing in production and use, and therefore, research into their toxicology and safe use is warranted. Key Words: carbon nanotubes; graphite; inflammation; oxidative stress; nanoparticles; fibre; toxicology; asbestos; lungs; workplace.
引用
收藏
页码:5 / 22
页数:18
相关论文
共 149 条
[1]   Diesel exhaust (DE)-induced cytokine expression in human bronchial epithelial cells -: A study with a new cell exposure system to freshly generated DE in vitro [J].
Abe, S ;
Takizawa, H ;
Sugawara, I ;
Kudoh, S .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 22 (03) :296-303
[2]  
ACGIH, 1993, THRESH LIM VAL CHEM
[3]  
[Anonymous], [No title captured], DOI DOI 10.1093/ANNHYG/46.SUPPL_1.242
[4]  
Arden Pope C., 1999, AIR POLLUTION HLTH, P673, DOI [10.1016/b978-012352335-8/50106-x, DOI 10.1016/B978-012352335-8/50106-X]
[5]   Dissolution of small diameter single-wall carbon nanotubes in organic solvents? [J].
Bahr, JL ;
Mickelson, ET ;
Bronikowski, MJ ;
Smalley, RE ;
Tour, JM .
CHEMICAL COMMUNICATIONS, 2001, (02) :193-194
[6]   Rational chemical strategies for carbon nanotube functionalization [J].
Banerjee, S ;
Kahn, MGC ;
Wong, SS .
CHEMISTRY-A EUROPEAN JOURNAL, 2003, 9 (09) :1899-1908
[7]   Oxidative stress and lipid mediators induced in alveolar macrophages by ultrafine particles [J].
Beck-Speier, I ;
Dayal, N ;
Karg, E ;
Maier, KL ;
Schumann, G ;
Schulz, H ;
Semmler, M ;
Takenaka, S ;
Stettmaier, K ;
Bors, W ;
Ghio, A ;
Samet, JM ;
Heyder, J .
FREE RADICAL BIOLOGY AND MEDICINE, 2005, 38 (08) :1080-1092
[8]   Testing of fibrous particles: Short-term assays and strategies - Report of an ILSI risk science institute working group [J].
Bernstein, D ;
Castranova, V ;
Donaldson, K ;
Fubini, B ;
Hadley, J ;
Hesterberg, T ;
Kane, A ;
Lai, D ;
McConnell, EE ;
Muhle, H ;
Oberdorster, G ;
Olin, S ;
Warheit, DB .
INHALATION TOXICOLOGY, 2005, 17 (10) :497-537
[9]   Comparison of Calidria chrysotile asbestos to pure tremolite: Inhalation biopersistence and histopathology following short-term exposure [J].
Bernstein, DM ;
Chevalier, J ;
Smith, P .
INHALATION TOXICOLOGY, 2003, 15 (14) :1387-1419
[10]   The biopersistence of Canadian chrysotile asbestos following inhalation [J].
Bernstein, DM ;
Rogers, R ;
Smith, P .
INHALATION TOXICOLOGY, 2003, 15 (13) :1247-1274