Genotoxicity of silver and titanium dioxide nanoparticles in bone marrow cells of rats in vivo

被引:100
作者
Dobrzynska, Malgorzata M. [1 ]
Gajowik, Aneta [1 ]
Radzikowska, Joanna [1 ]
Lankoff, Anna [2 ,4 ]
Dusinska, Maria [3 ]
Kruszewski, Marcin [2 ,5 ]
机构
[1] Natl Inst Hyg, Natl Inst Publ Hlth, PL-00791 Warsaw, Poland
[2] Inst Nucl Chem & Technol, PL-03195 Warsaw, Poland
[3] Norwegian Inst Air Res, Kjeller, Norway
[4] Jan Kochanowski Univ, Dept Radiobiol & Immunol, Kielce, Poland
[5] Inst Rural Hlth, Lublin, Poland
关键词
Nanoparticles; Micronuclei; Comet assay; DNA damage; Erythrocytes; Leukocytes; ULTRAFINE TIO2 PARTICLES; DNA-DAMAGE RESPONSE; METAL NANOPARTICLES; CARBON NANOTUBES; TOXICITY; MICRONUCLEI; VITRO; CYTOTOXICITY; NANOMATERIALS; AGGLOMERATION;
D O I
10.1016/j.tox.2013.11.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although nanomaterials have the potential to improve human life, their sideline effects on human health seem to be inevitable and still remain unknown. This study aimed to investigate the cytotoxicity and genotoxicity of titanium dioxide (TiO2) and silver (Ag) nanoparticles (NPs) at different doses and particle sizes to bone marrow cells. Both types of nanoparticles were chosen due to their wide applications of them in consumer products. Rats were injected intravenously with a single dose of 5 or 10 mg/kg bw of 20 nm AgNPs or with 5 mg/kg bw 200 nm AgNPs or with 5 mg/kg bw 21 nm TiO(2)NPs. The samples were taken at 24 h, 1 week and 4 weeks following the exposure. Micronucleus test and the Comet assay were used to detect DNA damage. Neither AgNPs nor TiO(2)NPs caused cytotoxicity to bone marrow red and white cells. The polychromatic erythrocytes are the main target of both nanoparticles. A single exposure to AgNPs induced significantly enhanced frequency of micronuclei not only at 24 h after exposure, but also 1 and 4 weeks later, whereas single exposure to TiO(2)NPs showed positive effect at 24 h only. Negative responses were shown in reticulocytes (micronuclei) and in leukocytes (Comet assay) of bone marrow. Results indicated that different bone marrow cells display different susceptibility toward genotoxicity mediated by both investigated nanoparticles. The use of materials containing nanoparticles and the potential health implication of them should be monitored. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:86 / 91
页数:6
相关论文
共 71 条
[1]   DNA damage response to different surface chemistry of silver nanoparticles in mammalian cells [J].
Ahamed, Maqusood ;
Karns, Michael ;
Goodson, Michael ;
Rowe, John ;
Hussain, Saber M. ;
Schlager, John J. ;
Hong, Yiling .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2008, 233 (03) :404-410
[2]  
Akhaltseva L. V., 2011, Gigiena i Sanitariya, P61
[3]   Anti-proliferative activity of silver nanoparticles [J].
AshaRani, P. V. ;
Hande, M. Prakash ;
Valiyaveettil, Suresh .
BMC CELL BIOLOGY, 2009, 10 :65
[4]   Cytotoxicity and Genotoxicity of Silver Nanoparticles in Human Cells [J].
AshaRani, P. V. ;
Mun, Grace Low Kah ;
Hande, Manoor Prakash ;
Valiyaveettil, Suresh .
ACS NANO, 2009, 3 (02) :279-290
[5]   In vitro evaluation of SiC nanoparticles impact on A549 pulmonary cells: Cyto-, genotoxicity and oxidative stress [J].
Barillet, S. ;
Jugan, M. -L. ;
Laye, M. ;
Leconte, Y. ;
Herlin-Boime, N. ;
Reynaud, C. ;
Carriere, M. .
TOXICOLOGY LETTERS, 2010, 198 (03) :324-330
[6]  
Bartlomiejczyk T, 2013, ANN AGR ENV MED, V20, P48
[7]   Formation of nucleoplasmic protein aggregates impairs nuclear function in response to SiO2 nanoparticles [J].
Chen, M ;
von Mikecz, A .
EXPERIMENTAL CELL RESEARCH, 2005, 305 (01) :51-62
[8]   Nanosilver: A nanoproduct in medical application [J].
Chen, X. ;
Schluesener, H. J. .
TOXICOLOGY LETTERS, 2008, 176 (01) :1-12
[9]  
Cheng D., 2004, CHIN MED EQUIP J, V4, P26
[10]  
Cohen Michael S, 2007, Surg Infect (Larchmt), V8, P397, DOI 10.1089/sur.2006.032