TY - JOUR
T1 - Cytotoxic and genotoxic characterization of titanium dioxide, gadolinium oxide, and poly(lactic-co-glycolic acid) nanoparticles in human fibroblasts
AU - Setyawati, Magdiel Inggrid
AU - Khoo, Pheng Kian Stella
AU - Eng, Bao Hui
AU - Xiong, Sijing
AU - Zhao, Xinxin
AU - Das, Gautom Kumar
AU - Tan, Timothy Thatt Yang
AU - Loo, Joachim Say Chye
AU - Leong, David Tai
AU - Ng, Kee Woei
PY - 2013/3
Y1 - 2013/3
N2 - Engineered nanomaterials have become prevalent in our everyday life. While the popularity of using nanomaterials in consumer products continues to rise, increasing awareness of nanotoxicology has also fuelled efforts to accelerate our understanding of the ill effects that different nanomaterials can bring to biological systems. In this study, we investigated the potential cytotoxicity and genotoxicity of three nanoparticles: titanium dioxide (TiO2), terbium-doped gadolinium oxide (Tb-Gd2O3), and poly(lactic-co-glycolic acid) (PLGA). To evaluate nanoparticle-induced genotoxicity more realistically, a human skin fibroblast cell line (BJ) with less mutated genotype compared with cancer cell line was used. The nano-particles were first characterized by size, morphology, and surface charge. Cytotoxicity effects of the nanoparticles were then evaluated by monitoring the proliferation of treated BJ cells. Genotoxic influence was ascertained by profiling DNA damage via detection of γH2AX expression. Our results suggested that both TiO2 and Tb-Gd2O3 nanoparticles induced cytotoxicity in a dose dependent way on BJ cells. These two nanomaterials also promoted genotoxicity via DNA damage. On the contrary, PLGA nanoparticles did not induce significant cytotoxic or genotoxic effects on BJ cells.
AB - Engineered nanomaterials have become prevalent in our everyday life. While the popularity of using nanomaterials in consumer products continues to rise, increasing awareness of nanotoxicology has also fuelled efforts to accelerate our understanding of the ill effects that different nanomaterials can bring to biological systems. In this study, we investigated the potential cytotoxicity and genotoxicity of three nanoparticles: titanium dioxide (TiO2), terbium-doped gadolinium oxide (Tb-Gd2O3), and poly(lactic-co-glycolic acid) (PLGA). To evaluate nanoparticle-induced genotoxicity more realistically, a human skin fibroblast cell line (BJ) with less mutated genotype compared with cancer cell line was used. The nano-particles were first characterized by size, morphology, and surface charge. Cytotoxicity effects of the nanoparticles were then evaluated by monitoring the proliferation of treated BJ cells. Genotoxic influence was ascertained by profiling DNA damage via detection of γH2AX expression. Our results suggested that both TiO2 and Tb-Gd2O3 nanoparticles induced cytotoxicity in a dose dependent way on BJ cells. These two nanomaterials also promoted genotoxicity via DNA damage. On the contrary, PLGA nanoparticles did not induce significant cytotoxic or genotoxic effects on BJ cells.
KW - Cytotoxicity
KW - Gadolinium oxide
KW - Genotoxicity
KW - Nanotoxicology
KW - Poly(lactic-co-glycolic acid)
KW - Titanium dioxide
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UR - http://www.scopus.com/inward/citedby.url?scp=84876179895&partnerID=8YFLogxK
U2 - 10.1002/jbm.a.34363
DO - 10.1002/jbm.a.34363
M3 - Article
C2 - 22927021
AN - SCOPUS:84876179895
SN - 1549-3296
VL - 101 A
SP - 633
EP - 640
JO - Journal of Biomedical Materials Research - Part A
JF - Journal of Biomedical Materials Research - Part A
IS - 3
ER -