Genotoxicity evaluation of amorphous silica nanoparticles of different sizes using the micronucleus and the plasmid lacZ gene mutation assay

  • Margriet V. D. Z. Park*
  • , Henny W. Verharen
  • , Edwin Zwart
  • , Lya G. Hernandez
  • , Jan van Benthem
  • , Andreas Elsaesser
  • , Clifford Barnes
  • , George Mckerr
  • , C. Vyvyan Howard
  • , Anna Salvati
  • , Iseult Lynch
  • , Kenneth A. Dawson
  • , Wim H. de Jong
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

78 Citations (Scopus)

Abstract

We investigated the potential of four well-characterized amorphous silica nanoparticles to induce chromosomal aberrations and gene mutations using two in vitro genotoxicity assays. Transmission electron microscopy (TEM) was used to verify the manufacturer's nominal size of 10, 30, 80 and 400 nm which showed actual sizes of 11, 34, 34 and 248 nm, respectively. The 80 (34) nm silica nanoparticles induced chromosomal aberrations in the micronucleus assay using 3T3-L1 mouse fibroblasts and the 30 (34) and 80 (34) nm silica nanoparticles induced gene mutations in mouse embryonic fibroblasts carrying the lacZ reporter gene. TEM imaging demonstrated that the majority of nanoparticles were localized in vacuoles and not in the nucleus of 3T3-L1 cells, indicating that the observed DNA damage was most likely a result of indirect mechanisms. Further studies are needed to reveal these mechanisms and to determine the biological relevance of the effects of these particular silica nanoparticles in vivo.

Original languageEnglish
Pages (from-to)168-181
Number of pages14
JournalNanotoxicology
Volume5
Issue number2
DOIs
Publication statusPublished - Jun-2011
Externally publishedYes

Keywords

  • Genotoxicity
  • nanoparticles
  • silica
  • micronucleus
  • mutagenic effects
  • LUNG EPITHELIAL-CELLS
  • IN-VITRO
  • SILVER NANOPARTICLES
  • OXIDE NANOPARTICLES
  • CONTROLLED-RELEASE
  • OXIDATIVE STRESS
  • DRUG-DELIVERY
  • PARTICLE-SIZE
  • SURFACE-AREA
  • LOW-TOXICITY

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