Functionalized Graphene Derivatives: Antibacterial Properties and Cytotoxicity

被引:38
|
作者
Valentini, Federica [1 ,2 ]
Calcaterra, Andrea [2 ]
Ruggiero, Vincenzo [3 ,4 ]
Pichichero, Elena [4 ]
Martino, Assunta [4 ]
Iosi, Francesca [5 ]
Bertuccini, Lucia [5 ]
Antonaroli, Simonetta [1 ]
Mardente, Stefania [6 ]
Zicari, Alessandra [6 ]
Mari, Emanuela [6 ]
Iovenitti, Giulia [3 ]
Leone, Gemma [3 ]
Botta, Maurizio [3 ]
Talamo, Maurizio [2 ]
机构
[1] Tor Vergata Univ, Dept Chem, Via Ric Sci 1, I-00133 Rome, Italy
[2] Tor Vergata Univ, Inuit Fdn, Via Archiginnasio Snc, I-00133 Rome, Italy
[3] Univ Siena, Dept Biotechnol Chem & Pharm, Via Aldo Moro2, I-53100 Siena, Italy
[4] Tor Vergata Univ, Hygeia Lab Srl, Edificio PP1,Via Ric Sci Snc, I-00133 Rome, Italy
[5] Ist Super Sanita, Core Facil, Viale Regina Elena 299, I-00161 Rome, Italy
[6] Sapienza Univ Roma, Dept Expt Med, Viale Regina Elena, I-00161 Rome, Italy
关键词
ANTIMICROBIAL ACTIVITY; OXIDE; FABRICATION; TRANSPORT; DESIGN;
D O I
10.1155/2019/2752539
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this work, the authors prepared and characterized two different graphene oxides: one chemically synthesized (GO sample) and the other one electrochemically synthesized (GO((LiCl))). Both samples were fully characterized with atomic force microscopy (AFM), Raman and Fourier transform infrared (FTIR) spectroscopies, X-ray photo electron spectroscopy (XPS), thermal analysis (TG/DTA), and Z-potential. The antibacterial properties of both graphene oxides were studied using Gram-negative Escherichia coli ATCC 25922 and Gram-positive Staphylococcus aureus ATCC 25923 by spectrophotometer and viable cell count as indirect and direct methods, respectively. Results demonstrated that the GO((LiCl)) exhibited a significant antibacterial activity compared to GO that showed a bacteriostatic effect on both pathogens. Electron microscopy analysis confirmed the antibacterial effects of both graphene oxides toward the pathogens, especially working at 80 mu g/mL, for 24 h. Additional studies were also performed and both GO samples were not cytotoxic at 2 mu g/mL toward neuroblastoma cells. Moreover, 2 mu g of GO was suitable to carry the minimum effective dose (5.74 ng/mL) of kinase inhibitor S29 (1-(2-chloro-2-(4-chlorophenyl)ethyl)-N-(4-fluorobenzyl)-1H-pyrazolo[3,4-d] pyrimidin-4-amine), providing negligible side effects related to the S29 treatment (this latter being specifically active on the neuroblastoma cell lines (SK-N-BE(2))).
引用
收藏
页数:14
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