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Title:
Assessing Nanoparticle Toxicity
Date:
7/2012
Link to Journal Abstract
Abstract:
Nanoparticle toxicology, an emergent field, works toward establishing the hazard of nanoparticles, and therefore their potential risk, in light of the increased use and likelihood of exposure. Analytical chemists can provide an essential tool kit for the advancement of this field by exploiting expertise in sample complexity and preparation as well as method and technology development. Herein, we discuss experimental considerations for performing in vitro nanoparticle toxicity studies, with a focus on nanoparticle characterization, relevant model cell systems, and toxicity assay choices. Additionally, we present three case studies (of silver, titanium dioxide, and carbon nanotube toxicity) to highlight the important toxicological considerations of these commonly used nanoparticles.
Non-technical Summary:
In this review paper, the authors discuss experimental considerations for performing in vitro nanoparticle toxicity studies, with a focus on nanoparticle characterization, relevant model cell systems, and toxicity assay choices. Additionally, they present three case studies (of silver, titanium dioxide, and carbon nanotube toxicity) to highlight the important toxicological considerations of these commonly used nanoparticles.
Content Emphasis
Review Article
Exposure Or Hazard Target
Mammalian
Exposure Pathway
Other/Unspecified
Method Of Study
Material Analysis and Applications
In Vitro
Paper Type
Hazard
Applications
Particle Type
Multiple
Production Method
Engineered
Risk Exposure Group
General Population
Target Audience
Technical Research
Citation:
Annual Review of Analytical Chemistry, 5:181-205 (July 2012)
Publication:
Annual Review of Analytical Chemistry
Author:
Love SA, Maurer-Jones MA, Thompson JW, Lin YS, Haynes CL
Volume:
5
Pages:
181-205
Last updated on November 14, 2012
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This work is supported in part by the Nanoscale Science and Engineering Initiative of the National Science Foundation
under NSF Award Number EEC-0118007.
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