Antitumor activity of silver nanoparticles in Ehrlich carcinoma-bearing mice

被引:30
作者
Rageh, Monira M. [1 ]
El-Gebaly, Reem H. [1 ]
Afifi, Marwa M. [1 ]
机构
[1] Cairo Univ, Fac Sci, Dept Biophys, Giza, Egypt
关键词
Ehrlich carcinoma; Silver nanoparticles; DNA damage; INDUCED DNA-DAMAGE; OXIDATIVE STRESS; TOXICITY ASSESSMENT; BIOGENIC SILVER; COMET ASSAY; IN-VITRO; CANCER; CELLS; CYTOTOXICITY; RELEASE;
D O I
10.1007/s00210-018-1558-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Silver nanoparticles (AgNPs) have a wide range of industrial and biomedical applications. The aim of the present study was to determine the cytotoxic and genotoxic effects of AgNPs on Ehrlich carcinoma-bearing mice. AgNPs were characterized by ultraviolet-visible absorption spectroscopy, dynamic light scattering, and transmission electron microscopy (TEM). Furthermore, the cytotoxicity and genotoxicity of AgNPs were evaluated using a series of assays: superoxide dismutase (SOD) enzyme activity, malondialdehyde (MDA) levels, DNA damage (comet assay), and histopathological examination of tissues and tumor size in Ehrlich carcinoma-bearing mice. Treatment of Ehrlich carcinoma-bearing mice with various concentrations of AgNPs (6, 24, and 48mg/kg) injected intra peritoneal (IP) and intra tumor (IT) revealed that AgNPs significantly elevated the levels (0.5- to 5-fold) of MDA and reduced the activity (32-64%) of SOD. Furthermore, AgNPs caused a 2- to 3-fold increase in comet parameters such as percent tail DNA. Additionally, AgNPs inhibit the promotion of Ehrlich carcinoma by masses of necrotic and fragmented tumor cells. Consequently, the volume of tumor reduced by about 31-95% compared to control one. The results indicate that AgNPs possess cytotoxic and genotoxic effects against Ehrlich tumor and confirm the antitumor properties of AgNPs.
引用
收藏
页码:1421 / 1430
页数:10
相关论文
共 60 条
[1]   In vivo DNA damaging and apoptotic potential of silver nanoparticles in Swiss albino mice [J].
Al Gurabi, Mohammed A. ;
Ali, Daoud ;
Alkahtani, Saad ;
Alarifi, Saud .
ONCOTARGETS AND THERAPY, 2015, 8 :295-302
[2]  
[Anonymous], PLOS ONE
[3]   Cytotoxicity and ROS production of manufactured silver nanoparticles of different sizes in hepatoma and leukemia cells [J].
Avalos, Alicia ;
Isabel Haza, Ana ;
Mateo, Diego ;
Morales, Paloma .
JOURNAL OF APPLIED TOXICOLOGY, 2014, 34 (04) :413-423
[4]   Assessment of vinyl chloride-induced DNA damage in lymphocytes of plastic industry workers using a single-cell gel electrophoresis technique [J].
Awara, WM ;
El-Nabi, SH ;
El-Gohary, M .
TOXICOLOGY, 1998, 128 (01) :9-16
[5]   Silver nanoparticle induced cytotoxicity, oxidative stress, and DNA damage in CHO cells [J].
Awasthi, Kumud Kant ;
Awasthi, Anjali ;
Kumar, Narender ;
Roy, Partha ;
Awasthi, Kamlendra ;
John, P. J. .
JOURNAL OF NANOPARTICLE RESEARCH, 2013, 15 (09)
[6]   The Release of Nanosilver from Consumer Products Used in the Home [J].
Benn, Troy ;
Cavanagh, Bridget ;
Hristovski, Kiril ;
Posner, Jonathan D. ;
Westerhoff, Paul .
JOURNAL OF ENVIRONMENTAL QUALITY, 2010, 39 (06) :1875-1882
[7]   Bone Marrow-Derived Mesenchymal Stromal Cells Promote Survival and Drug Resistance in Tumor Cells [J].
Bergfeld, Scott A. ;
Blavier, Laurence ;
DeClerck, Yves A. .
MOLECULAR CANCER THERAPEUTICS, 2014, 13 (04) :962-975
[8]   Unique Cellular Interaction of Silver Nanoparticles: Size-Dependent Generation of Reactive Oxygen Species [J].
Carlson, C. ;
Hussain, S. M. ;
Schrand, A. M. ;
Braydich-Stolle, L. K. ;
Hess, K. L. ;
Jones, R. L. ;
Schlager, J. J. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (43) :13608-13619
[9]   Nanosilver: A nanoproduct in medical application [J].
Chen, X. ;
Schluesener, H. J. .
TOXICOLOGY LETTERS, 2008, 176 (01) :1-12
[10]   Oxidative DNA damage: mechanisms, mutation, and disease [J].
Cooke, MS ;
Evans, MD ;
Dizdaroglu, M ;
Lunec, J .
FASEB JOURNAL, 2003, 17 (10) :1195-1214