Pulmonary applications and toxicity of engineered nanoparticles

被引:202
作者
Card, Jeffrey W. [1 ]
Zeldin, Darryl C. [2 ]
Bonner, James C. [3 ]
Nestmann, Earle R. [1 ]
机构
[1] Cantox Hlth Sci Int, Mississauga, ON L5N 2X7, Canada
[2] NIEHS, Div Intramural Res, NIH, Res Triangle Pk, NC 27709 USA
[3] N Carolina State Univ, Dept Environm & Mol Toxicol, Raleigh, NC 27695 USA
基金
美国国家卫生研究院;
关键词
nanotechnology; nanomaterials; respiratory system; lung;
D O I
10.1152/ajplung.00041.2008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Because of their unique physicochemical properties, engineered nanoparticles have the potential to significantly impact respiratory research and medicine by means of improving imaging capability and drug delivery, among other applications. These same properties, however, present potential safety concerns, and there is accumulating evidence to suggest that nanoparticles may exert adverse effects on pulmonary structure and function. The respiratory system is susceptible to injury resulting from inhalation of gases, aerosols, and particles, and also from systemic delivery of drugs, chemicals, and other compounds to the lungs via direct cardiac output to the pulmonary arteries. As such, it is a prime target for the possible toxic effects of engineered nanoparticles. The purpose of this article is to provide an overview of the potential usefulness of nanoparticles and nanotechnology in respiratory research and medicine and to highlight important issues and recent data pertaining to nanoparticle-related pulmonary toxicity.
引用
收藏
页码:L400 / L411
页数:12
相关论文
共 164 条
[91]   Assessing exposure to airborne nanomaterials: Current abilities and future requirements [J].
Maynard, Andrew D. ;
Aitken, Robert J. .
NANOTOXICOLOGY, 2007, 1 (01) :26-41
[92]   Alteration of deposition pattern and pulmonary response as a result of improved dispersion of aspirated single-walled carbon nanotubes in a mouse model [J].
Mercer, R. R. ;
Scabilloni, J. ;
Wang, L. ;
Kisin, E. ;
Murray, A. R. ;
Schwegler-Berry, D. ;
Shvedova, A. A. ;
Castranova, V. .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2008, 294 (01) :L87-L97
[93]   Do inhaled carbon nanoparticles translocate directly into the circulation in humans? [J].
Mills, NL ;
Amin, N ;
Robinson, SD ;
Anand, A ;
Davies, J ;
Patel, D ;
de la Fuente, JM ;
Cassee, FR ;
Boon, NA ;
MacNee, W ;
Millar, AM ;
Donaldson, K ;
Newby, DE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 173 (04) :426-431
[94]  
Mitchell LA, 2007, TOXICOL SCI, V100, P203, DOI 10.1093/toxsci/kfm196
[95]   Deposition, retention, and translocation of ultrafine particles from the central airways and lung periphery [J].
Moller, Winfried ;
Felten, Kathrin ;
Sommerer, Knut ;
Scheuch, Gerhard ;
Meyer, Gabriele ;
Meyer, Peter ;
Haussinger, Karl ;
Kreyling, Wolfgang G. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2008, 177 (04) :426-432
[96]   The pro-inflammatory effects of low-toxicity low-solubility particles, nanoparticles and fine particles, on epithelial cells in vitro: the role of surface area [J].
Monteiller, Claire ;
Tran, Lang ;
MacNee, William ;
Faux, Steve ;
Jones, Alan ;
Miller, Brian ;
Donaldson, Ken .
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 2007, 64 (09) :609-615
[97]   Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature [J].
Christian Mühlfeld ;
Marianne Geiser ;
Nadine Kapp ;
Peter Gehr ;
Barbara Rothen-Rutishauser .
Particle and Fibre Toxicology, 4 (1)
[98]   Respiratory toxicity of multi-wall carbon nanotubes [J].
Muller, J ;
Huaux, F ;
Moreau, N ;
Misson, P ;
Heilier, JF ;
Delos, M ;
Arras, M ;
Fonseca, A ;
Nagy, JB ;
Lison, D .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 207 (03) :221-231
[99]  
Murr L E, 2005, Int J Environ Res Public Health, V2, P31, DOI 10.3390/ijerph2005010031
[100]   Toxic potential of materials at the nanolevel [J].
Nel, A ;
Xia, T ;
Mädler, L ;
Li, N .
SCIENCE, 2006, 311 (5761) :622-627