Graphene oxide nanoribbons exhibit significantly greater toxicity than graphene oxide nanoplatelets

被引:55
作者
Chng, Elaine Lay Khim [1 ]
Chua, Chun Kiang [1 ]
Pumera, Martin [1 ]
机构
[1] Nanyang Technol Univ, Sch Phys & Math Sci, Div Chem & Biol Chem, Singapore 637371, Singapore
关键词
CARBON NANOTUBES; REDUCTION; DELIVERY; DRUGS;
D O I
10.1039/c4nr03608e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene oxide (GOs) has emerged in recent years as a versatile nanomaterial, demonstrating tremendous potential for multifunctional biomedical applications. GOs can be prepared by the top-down or bottom-up approach, which leads to a great variability of GOs being produced due to the different procedures and starting carbon sources adopted. This will have an effect on the physiochemical properties of GOs and their resultant toxic behavior. In this study, we examined the cytotoxicity of graphene-oxide nanoribbons (GONRs; similar to 310 x 5000 nm) and graphene-oxide nanoplatelets (GONPs; 100 x 100 nm), prepared from the oxidative treatment of multi-walled carbon nanotubes (MWCNTs; similar to 100 x 5000 nm) and stacked graphene nanofibers (SGNFs; 100 x 5000 nm), respectively. In vitro assessments revealed that the GONRs exhibited a much stronger cytotoxicity over the GONPs, and we correlated that observation with characterization data that showed GONRs to have a greater amount of carbonyl groups as well as greater length. Therefore, we put forward that the stronger toxic behavior of GONRs is a result of the synergistic effect between these two factors, and the type of carbon source used to prepare GOs should be carefully considered in any future bioapplications.
引用
收藏
页码:10792 / 10797
页数:6
相关论文
共 34 条
[1]  
Bae S, 2010, NAT NANOTECHNOL, V5, P574, DOI [10.1038/nnano.2010.132, 10.1038/NNANO.2010.132]
[2]  
Bai JW, 2010, NAT NANOTECHNOL, V5, P655, DOI [10.1038/NNANO.2010.154, 10.1038/nnano.2010.154]
[3]   The reliability and limits of the MTT reduction assay for carbon nanotubes-cell interaction [J].
Belyanskaya, Larisa ;
Manser, Plus ;
Spohn, Philipp ;
Bruinink, Arle ;
Wick, Peter .
CARBON, 2007, 45 (13) :2643-2648
[4]   Are quantum dots ready for in vivo imaging in human subjects? [J].
Cai, Weibo ;
Hsu, Andrew R. ;
Li, Zi-Bo ;
Chen, Xiaoyuan .
NANOSCALE RESEARCH LETTERS, 2007, 2 (06) :265-281
[5]  
Cai WB, 2012, AM J NUCL MED MOLEC, V2, P136
[6]   The Toxicity of Graphene Oxides: Dependence on the Oxidative Methods Used [J].
Chng, Elaine Lay Khim ;
Pumera, Martin .
CHEMISTRY-A EUROPEAN JOURNAL, 2013, 19 (25) :8227-8235
[7]   Graphene Sheet Orientation of Parent Material Exhibits Dramatic Influence on Graphene Properties [J].
Chua, Chun Kiang ;
Sofer, Zdenek ;
Pumera, Martin .
CHEMISTRY-AN ASIAN JOURNAL, 2012, 7 (10) :2367-2372
[8]   Silver-Graphene Nanoribbon Composite Catalyst for the Oxygen Reduction Reaction in Alkaline Electrolyte [J].
Davis, Danae J. ;
Raji, Abdul-Rahman O. ;
Lambert, Timothy N. ;
Vigil, Julian A. ;
Li, Lei ;
Nan, Kewang ;
Tour, James M. .
ELECTROANALYSIS, 2014, 26 (01) :164-170
[9]   The chemistry of graphene oxide [J].
Dreyer, Daniel R. ;
Park, Sungjin ;
Bielawski, Christopher W. ;
Ruoff, Rodney S. .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (01) :228-240
[10]   The big picture on nanomedicine: the state of investigational and approved nanomedicine products [J].
Etheridge, Michael L. ;
Campbell, Stephen A. ;
Erdman, Arthur G. ;
Haynes, Christy L. ;
Wolf, Susan M. ;
McCullough, Jeffrey .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2013, 9 (01) :1-14