Toxic and genotoxic effects of graphene and multi-walled carbon nanotubes

被引:27
作者
Demir, Esref [1 ]
Marcos, Ricard [2 ,3 ]
机构
[1] Giresun Univ, Dept Genet & Bioengn, Fac Engn, TR-28200 Gure, Giresun, Turkey
[2] Univ Autonoma Barcelona, Fac Biociencies, Dept Genet & Microbiol, Grp Mutagenesi, Cerdanyola Del Valles, Spain
[3] ISCIII, CIBER Epidemiol & Salud Publ, Barcelona, Spain
来源
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES | 2018年 / 81卷 / 14期
关键词
MOUSE LYMPHOMA ASSAY; THYMIDINE KINASE GENE; IN-VITRO GENOTOXICITY; LUNG EPITHELIAL-CELLS; INTERNATIONAL WORKSHOP; MUTATION ASSAY; MANUFACTURED NANOPARTICLES; ENGINEERED NANOMATERIALS; TOXICOLOGICAL ASSESSMENT; TITANIUM-DIOXIDE;
D O I
10.1080/15287394.2018.1477314
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Graphene and multi-walled carbon nanotubes (MWCNT) are widely used in nanomedicine, and other fields, due to their unique physicochemical properties including high tensile strength, ultra-light weight, thermal and chemical stability, and reliable semi-conductive electronic properties. Although extensive amount of data exist describing their adverse effects including potential genotoxicity, few studies using gene mutation detection approaches in mammalian cells are available, which represents an important gap for risk estimations. The aim of the present study was to determine the effects of graphene or MWCNT [as pure, carboxyl (COOH) functionalized, and amide (NH2) functionalized] on cytotoxicity, intracellular levels of reactive oxygen species, apoptosis, gene expression changes, and gene mutation induction in L5178Y/Tk(+/-)3.7.2C mouse lymphoma cell line. Although some adverse effects were observed at concentrations of 350 and 450 mu g/ml, which are excessive and not environmentally relevant levels, no marked effects were detected at concentrations of 250 mu g/ml and lower. This is the first study reporting cytotoxicity, mutagenicity, and gene expression findings in the mouse lymphoma cell line for graphene and different MWCNT forms at high concentrations; however, the biological relevance of these observations needs to be assessed following chronic in vivo exposure.
引用
收藏
页码:645 / 660
页数:16
相关论文
共 75 条
[1]  
Ai Jafar, 2011, Int J Nanomedicine, V6, P1117, DOI 10.2147/IJN.S16603
[2]   Drosophila melanogaster as a suitable in vivo model to determine potential side effects of nanomaterials: A review [J].
Alaraby, Mohamed ;
Annangi, Balasubramanyam ;
Marcos, Ricard ;
Hernandez, Alba .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART B-CRITICAL REVIEWS, 2016, 19 (02) :65-104
[3]  
[Anonymous], 2011, NANOGENOTOX
[4]   Carbon nanotubes, science and technology part (I) structure, synthesis and characterisation [J].
Aqel, Ahmad ;
Abou El-Nour, Kholoud M. M. ;
Ammar, Reda A. A. ;
Al-Warthan, Abdulrahman .
ARABIAN JOURNAL OF CHEMISTRY, 2012, 5 (01) :1-23
[5]   No cytotoxicity or genotoxicity of graphene and graphene oxide in murine lung epithelial FE1 cells in vitro [J].
Bengtson, Stefan ;
Kling, Kirsten ;
Madsen, Anne Mette ;
Noergaard, Asger W. ;
Jacobsen, Nicklas Raun ;
Clausen, Per Axel ;
Alonso, Beatriz ;
Pesquera, Amaia ;
Zurutuza, Amaia ;
Ramos, Raphael ;
Okuno, Hanako ;
Dijon, Jean ;
Wallin, Hakan ;
Vogel, Ulla .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2016, 57 (06) :469-482
[6]   All in the graphene family - A recommended nomenclature for two-dimensional carbon materials [J].
Bianco, Alberto ;
Cheng, Hui-Ming ;
Enoki, Toshiaki ;
Gogotsi, Yury ;
Hurt, Robert H. ;
Koratkar, Nikhil ;
Kyotani, Takashi ;
Monthioux, Marc ;
Park, Chong Rae ;
Tascon, Juan M. D. ;
Zhang, Jin .
CARBON, 2013, 65 :1-6
[7]   Engineered nanomaterial-induced lysosomal membrane permeabilization and anti-cathepsin agents [J].
Bunderson-Schelvan, Melisa ;
Holian, Andrij ;
Hamilton, Raymond F., Jr. .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART B-CRITICAL REVIEWS, 2017, 20 (04) :230-248
[8]   Multi-walled carbon nanotubes induce cytotoxicity and genotoxicity in human lung epithelial cells [J].
Cavallo, Delia ;
Fanizza, Carla ;
Ursini, Cinzia Lucia ;
Casciardi, Stefano ;
Paba, Emilia ;
Ciervo, Aureliano ;
Fresegna, Anna Maria ;
Maiello, Raffaele ;
Marcelloni, Anna Maria ;
Buresti, Giuliana ;
Tombolini, Francesca ;
Bellucci, Stefano ;
Iavicoli, Sergio .
JOURNAL OF APPLIED TOXICOLOGY, 2012, 32 (06) :454-464
[9]   Differential genotoxic and epigenotoxic effects of graphene family nanomaterials (GFNs) in human bronchial epithelial cells [J].
Chatterjee, Nivedita ;
Yang, JiSu ;
Choi, Jinhee .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2016, 798 :1-10
[10]   Mutant frequencies and loss of heterozygosity induced by N-ethyl-N-nitrosourea in the thymidine kinase gene of L5178Y/TK+-3.7.2C mouse lymphoma cells [J].
Chen, T ;
Harrington-Brock, K ;
Moore, MM .
MUTAGENESIS, 2002, 17 (02) :105-109