Document Detail

Effect of Polyethylene Glycol Modification of TiO2 Nanoparticles on Cytotoxicity and Gene Expressions in Human Cell Lines.
MedLine Citation:
PMID:  22489177     Owner:  NLM     Status:  In-Data-Review    
Nanoparticles (NPs) are tiny materials used in a wide range of industrial and medical applications. Titanium dioxide (TiO(2)) is a type of nanoparticle that is widely used in paints, pigments, and cosmetics; however, little is known about the impact of TiO(2) on human health and the environment. Therefore, considerable research has focused on characterizing the potential toxicity of nanoparticles such as TiO(2) and on understanding the mechanism of TiO(2) NP-induced nanotoxicity through the evaluation of biomarkers. Uncoated TiO(2) NPs tend to aggregate in aqueous media, and these aggregates decrease cell viability and induce expression of stress-related genes, such as those encoding interleukin-6 (IL-6) and heat shock protein 70B' (HSP70B'), indicating that TiO(2) NPs induce inflammatory and heat shock responses. In order to reduce their toxicity, we conjugated TiO(2) NPs with polyethylene glycol (PEG) to eliminate aggregation. Our findings indicate that modifying TiO(2) NPs with PEG reduces their cytotoxicity and reduces the induction of stress-related genes. Our results also suggest that TiO(2) NP-induced effects on cytotoxicity and gene expression vary depending upon the cell type and surface modification.
Sharmy Saimon Mano; Koki Kanehira; Shuji Sonezaki; Akiyoshi Taniguchi
Related Documents :
22393497 - Genetic connectivity among populations of an endangered snake species from southeastern...
22685277 - Conjugal transfer of polychlorinated biphenyl/biphenyl degradation genes in acidovorax ...
22772967 - Concomitant aberrant methylation of p15 and mgmt genes in acute myeloid leukemia: assoc...
22541597 - Linking genes to diseases with a snpedia-gene wiki mashup.
16945957 - Identification of mirna targets with stable isotope labeling by amino acids in cell cul...
21281787 - Genome-wide expression analysis of middle eastern colorectal cancer reveals foxm1 as a ...
Publication Detail:
Type:  Journal Article     Date:  2012-03-21
Journal Detail:
Title:  International journal of molecular sciences     Volume:  13     ISSN:  1422-0067     ISO Abbreviation:  Int J Mol Sci     Publication Date:  2012  
Date Detail:
Created Date:  2012-04-10     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101092791     Medline TA:  Int J Mol Sci     Country:  Switzerland    
Other Details:
Languages:  eng     Pagination:  3703-17     Citation Subset:  -    
Cell-Materials Interaction Group, Biomaterials Unit, Nano-Bio Field, International Center for Materials Nanoarchitectonics (MANA), National Institute for Materials Science, 1-1, Namiki, Tsukuba, Ibaraki 305-0044, Japan; E-Mail:
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Cellulose biosynthesis inhibitors: comparative effect on bean cell cultures.
Next Document:  Photosensized controlling benzyl methacrylate-based matrix enhanced eu(3+) narrow-band emission for ...