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Journal of Environmental Science and Health, Part A
Toxic/Hazardous Substances and Environmental Engineering
Volume 39, 2004 - Issue 10
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Original Articles

Effects of Nanophase Materials (≤20 nm) on Biological Responses

Pages 2691-2705 | Published online: 24 Jun 2011
 

Abstract

Nanophase materials have enhanced properties (thermal, mechanical, electrical, surface reactivity, etc.) not found in bulk materials. Intuitively, the enhancement of material properties could occur when the materials encounter biological specimens. Previous investigations of biological interactions with nanometer-scale materials have been very limited. With the ability to manipulate atoms and molecules, we now can create predefined nanostructures with unprecedented precision. In parallel with this development, improved understanding of the biological effects of the nanophase materials, whatever those may be, should also deserve attention. In this study, we have applied precision aerosol technology to investigate cellular response to nanoparticles. We used synthetic nanoparticles generated by an electrospray technique to produce nanoparticles in the size range of 8–13 nm with practically monodispersed aerosol particles and approximately the same number concentration. We report here on the potency of nano-metal particles with single or binary chemical components in eliciting interleukin-8 (IL-8) production from epithelial cell lines. For single-component nanoparticles, we found that nano-Cu particles were more potent in IL-8 production than nano-Ni and nano-V particles. However, the kinetics of IL-8 production by these three nanoparticles was different, the nano-Ni being the highest among the three. When sulfuric acid was introduced to form acidified nano-Ni particles, we found that the potency of such binary-component nanoparticles in eliciting IL-8 production was increased markedly, by about six times. However, the acidified binary nano-Na and -Mg nanoparticles did not exhibit the same effects as binary nano-Ni particles did. Since Ni, a transition metal, could induce free radicals on cell surfaces, while Na and Mg could not, the acidity might have enhanced the oxidative stress caused by radicals to the cells, leading to markedly higher IL-8 production. This result indicates the complexity of biological responses to nanoparticles. We believe that the exposure methodology and aerosol technology employed in our research will provide an effective means to systematically investigate cellular responses to nanoparticles, structured or unstructured, in ongoing research projects. Different cell lines, chemicals, and particle morphology can also be investigated using such a methodology.

Acknowledgments

This research was supported in part by Oak Ridge National Laboratory's Laboratory Director's Research and Development Program, the Department of Energy Office of Transportation Technologies, and the Department of Defense Eglin Air Force Base Material Research Branch Munitions Directorate. Boyd Malone is acknowledged for cell culture, maintenance, and bioassay. The review by Chao-Hsin Lin of the Boeing Company in Seattle is appreciated. The author benefited from discussions with Vicki Colvin (Rice Univ.), Gunter Oberdoster (Univ. Rochester), Kevin Geiss (Wright-Patterson AFB), and Walter Kozumbo (AFOSR). The comments of two reviewers encouraged us to keep raising the important issues of biological responses to nanoparticles and nanophase materials. The author also thanks the guest editor, Guodong Yuan, who invited this manuscript. Oak Ridge National Laboratory is managed by UT-Battelle, LLC, for the U.S. Department of Energy under contract DE-AC05–00OR22725.

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