Synthesis, dispersion, and cytocompatibility of graphene oxide and reduced graphene oxide

被引：363
|
作者：
Wojtoniszak, Malgorzata [1 ]
Chen, Xuecheng [1 ]
Kalenczuk, Ryszard J. [1 ]
Wajda, Anna [2 ]
Lapczuk, Joanna [2 ]
Kurzawski, Mateusz [2 ]
Drozdzik, Marek [2 ]
Chu, Pual K. [3 ]
Borowiak-Palen, Ewa [1 ]
机构：
[1] Westpomeranian Univ Technol Szczecin, Dept Environm & Chem Engn, Pulaskiego 10, PL-70322 Szczecin, Poland
[2] Pomeranian Med Univ, Dept Pharmacokinet & Therapeut Drug Monitoring, PL-70111 Szczecin, Poland
[3] City Univ Hong Kong, Dept Phys & Mat Sci, Kowloon, Hong Kong, Peoples R China
来源：
COLLOIDS AND SURFACES B-BIOINTERFACES | 2012年 / 89卷
关键词：
Graphene oxide; Graphene; In vitro toxicology; CARBON NANOTUBES; RAMAN-SPECTROSCOPY; CYTOTOXICITY; GRAPHITE;
D O I：
10.1016/j.colsurfb.2011.08.026
中图分类号：
Q6 [生物物理学];
学科分类号：
071011 ;
摘要：
The synthesis, characterization, and toxicity of graphene oxide and reduced graphene oxide are reported. Prior to the cytocompatibility tests the stability of the suspensions in a wide range of concentrations (3.125-100 mu g/mL) of three different dispersants is studied. Polyethylene glycol (PEG), polyethylene glycol-polypropylene glycol-polyethylene glycol (Pluronic P123), and sodium deoxycholate (DOC) are investigated as the dispersants. The toxicity depends on the type of dispersant and concentration of the nanomaterials in the suspensions. Detailed analysis suggests that graphene oxide functionalized with PEG in the concentration range between 3125 mu g/mL and 25 mu g/mL exhibits the best biocompatibility with mice fibroblast cells (line L929). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码：79 / 85
页数：7
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