4.6 Article

Towards understanding mechanisms governing cytotoxicity of metal oxides nanoparticles: Hints from nano-QSAR studies

Journal

NANOTOXICOLOGY
Volume 9, Issue 3, Pages 313-325

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.3109/17435390.2014.930195

Keywords

HaCaT; nano-metal oxides; nano-QSAR; nanoparticles; toxicity

Funding

  1. 711 HPW/RHD [FA8650-10-2-6062]
  2. NSF CREST Interdisciplinary Nanotoxicity Center NSF-CREST [HRD-0833178]
  3. NSF-EPSCoR Award [362492-190200-01\NSFEPS-0903787]
  4. Polish National Science Center [UMO-2011/01/M/NZ7/01445]
  5. Division Of Human Resource Development
  6. Direct For Education and Human Resources [833178] Funding Source: National Science Foundation

Ask authors/readers for more resources

The production of nanomaterials increases every year exponentially and therefore the probability these novel materials that they could cause adverse outcomes for human health and the environment also expands rapidly. We proposed two types of mechanisms of toxic action that are collectively applied in a nano-QSAR model, which provides governance over the toxicity of metal oxide nanoparticles to the human keratinocyte cell line (HaCaT). The combined experimental-theoretical studies allowed the development of an interpretative nano-QSAR model describing the toxicity of 18 nano-metal oxides to the HaCaT cell line, which is a common in vitro model for keratinocyte response during toxic dermal exposure. The comparison of the toxicity of metal oxide nanoparticles to bacteria Escherichia coli (prokaryotic system) and a human keratinocyte cell line (eukaryotic system), resulted in the hypothesis that different modes of toxic action occur between prokaryotic and eukaryotic systems.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available