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Title: In vitro toxicity of silica nanoparticles in human lung cancer cells

Journal Article · · Toxicology and Applied Pharmacology
OSTI ID:20850499
 [1];  [2];  [3];  [1]
  1. Department of Chemistry and Environmental Research Center, University of Missouri-Rolla, Rolla, MO 65409 (United States)
  2. Department of Biological Sciences and Environmental Research Center, University of Missouri-Rolla, Rolla, MO 65409 (United States)
  3. Pacific Northwest National Laboratory, Richland, WA 99352 (United States)

The cytotoxicity of 15-nm and 46-nm silica nanoparticles was investigated by using crystalline silica (Min-U-Sil 5) as a positive control in cultured human bronchoalveolar carcinoma-derived cells. Exposure to 15-nm or 46-nm SiO{sub 2} nanoparticles for 48 h at dosage levels between 10 and 100 {mu}g/ml decreased cell viability in a dose-dependent manner. Both SiO{sub 2} nanoparticles were more cytotoxic than Min-U-Sil 5; however, the cytotoxicities of 15-nm and 46-nm silica nanoparticles were not significantly different. The 15-nm SiO{sub 2} nanoparticles were used to determine time-dependent cytotoxicity and oxidative stress responses. Cell viability decreased significantly as a function of both nanoparticle dosage (10-100 {mu}g/ml) and exposure time (24 h, 48 h, and 72 h). Indicators of oxidative stress and cytotoxicity, including total reactive oxygen species (ROS), glutathione, malondialdehyde, and lactate dehydrogenase, were quantitatively assessed. Exposure to SiO{sub 2} nanoparticles increased ROS levels and reduced glutathione levels. The increased production of malondialdehyde and lactate dehydrogenase release from the cells indicated lipid peroxidation and membrane damage. In summary, exposure to SiO{sub 2} nanoparticles results in a dose-dependent cytotoxicity in cultural human bronchoalveolar carcinoma-derived cells that is closely correlated to increased oxidative stress.

OSTI ID:
20850499
Journal Information:
Toxicology and Applied Pharmacology, Vol. 217, Issue 3; Other Information: DOI: 10.1016/j.taap.2006.10.004; PII: S0041-008X(06)00352-8; Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0041-008X
Country of Publication:
United States
Language:
English

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