Assessing nanotoxicity in cells in vitro

被引:142
作者
Hillegass, Jedd M. [1 ]
Shukla, Arti [1 ]
Lathrop, Sherrill A. [1 ]
MacPherson, Maximilian B. [1 ]
Fukagawa, Naomi K. [2 ]
Mossman, Brooke T. [1 ]
机构
[1] Univ Vermont, Coll Med, Dept Pathol, Burlington, VT 05405 USA
[2] Univ Vermont, Coll Med, Dept Med, Burlington, VT 05405 USA
关键词
TITANIUM-DIOXIDE NANOPARTICLES; CERIUM OXIDE NANOPARTICLES; LOADED PLGA NANOPARTICLES; ULTRAFINE TIO2 PARTICLES; OXIDATIVE STRESS; SILICA NANOPARTICLES; MESOTHELIAL CELLS; GENE-EXPRESSION; CARBON-BLACK; DNA-DAMAGE;
D O I
10.1002/wnan.54
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanomaterials are commonly defined as particles or fibers of less than 1 Am in diameter. For these reasons, they may be respirable in humans and have the potential, based upon their geometry, composition, size, and transport or durability in the body, to cause adverse effects on human health, especially if they are inhaled at high concentrations. Rodent inhalation models to predict the toxicity and pathogenicity of nanomaterials are prohibitive in terms of time and expense. For these reasons, a panel of in vitro assays is described below. These include cell culture assays for cytotoxicity (altered metabolism, decreased growth, lytic or apoptotic cell death), proliferation, genotoxicity, and altered gene expression. The choice of cell type for these assays may be dictated by the procedure or endpoint selected. Most of these assays have been standardized in our laboratory using pathogenic minerals (asbestos and silica) and non-pathogenic particles (fine titanium dioxide or glass beads) as negative controls. The results of these in vitro assays should predict whether testing of selected nanomaterials should be pursued in animal inhalation models that simulate physiologic exposure to inhaled nanomaterials. Conversely, intrathoracic or intrapleural injection of nanomaterials into rodents can be misleading because they bypass normal clearance mechanisms, and non-pathogenic fibers and particles can test positively in these assays. (C) 2009 John Wiley & Sons, Inc. WIREs Nanomed Nanobiotechnol 2010 2 219-231
引用
收藏
页码:219 / 231
页数:13
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