Currently, the prevalence of antibiotic-resistant bacteria and costs of treatment has become public health concern . Microorganisms (e.g. fungi and bacteria) can easily attach to the surfaces of medical apparatus and colonize on their surfaces. These contaminations are threat to human health and might lead to economic losses . The advances in the field of nanotechnology has created good opportunities to solve these issues. Consequently, synthesis and application of new material to overcome these threats are highly desirable. In recent years, Nano materials have paved the way to create novel antimicrobial agents with exclusive chemical and physical properties [3-5]. Many nanomaterials including silver (Ag) [6, 7], zinc oxide (ZnO) , titanium dioxide (TiO2) , iron oxide (Fe3O4) , copper oxide (CuO) , magnesium oxide (MgO) , nitric oxide (NO) nanoparticles have been shown to have good antibacterial properties. Thus, expansion of such nanoparticles to combat microbial agents can be an important component for the decontamination process in the near future.
Another kind of nanomaterials that has been investigated widely, are carbon-based nanomaterials. Graphene-based nanomaterials (GBNs) as an important member of this family has been investigated in last decade due to its unique properties, such as large surface-to-volume ratio, mechanical flexibility and thermal stability [14-17]. GBNs are a promising candidate in polymeric nanocomposite synthesis [18, 19], catalysis [20-23], solar cells , biosensors , drug delivery and gene delivery [26, 27], imaging [28-30], photothermal therapy [31, 32], tissue engineering [33, 34], and stem cell technology [35, 36].
Moreover, GBNs have established to have antibacterial activities. Graphene oxide (GO) and reduced graphene oxide (rGO) are toxic to both Gram-positive and Gram-negative bacteria [37, 38]. The antifungal and antibacterial applications of GBNs are still relatively novel. In the last decade attention to GBNs has increased exponentially. Numerous reviews on GBNs are available with different perspective [39-42]. In this review, we summarized the latest progresses towards an understanding of the antifungal and antibacterial properties of GBNs. In the first section, we introduced GBNs, and the approaches to their fabrication. The second part briefly looks at their main antifungal and antibacterial mechanism. The last part include several examples of GBNs application as an antifungal and antibacterial nanomaterial.
The GBN family and their fabrication
GBNs can be defined and classified according to their features including morphology and composition, the average of lateral dimension and the number of G layers, which is determined by the atomic carbon/oxygen ratio, material’s size and degree of deformability, thickness, specific surface area, and the bending elasticity of the material properties  . The morphological and compositional based classification is essential when working with GBNs. Depending on the synthetic methods, G can be prepared in various morphologies for example sheets, platelets, ribbons and quantum dots (QDs). According to this family of nanomaterials, there are various nanostructures including graphene (G), graphene oxide (GO), reduced graphene (rGO), ultrafine graphite that are between 5 to 10 sheets and below 100 nm in thickness, as well as graphene ribbons, graphene quantum dots (GQDs), and pristine graphene (pG) [45-48]. G is a single monolayer of sp2-bonded carbon with a single atom thick of 2D-model graphite carbon material, which can be fabricated from graphite by scotch-tape technique, chemical exfoliation , chemical vapor deposition , arc discharge , and decomposition of carbide phases . GO structure consists of single-atom-thick carbon sheets with carboxylate groups on the periphery, where they provide pH dependent negative surface charge and colloidal stability. GO is a single layer that can be produced via reaction of crystalline graphite with a mixture of oxidizing agents and sonication or other dispersion methods, (Fig. 1) shows G and GO .
Also, it consists of epoxy, hydroxyl and carboxylic acid groups on its surface and edges. rGO is a single layer that can be fabricated from GO through under reducing condition, consisting of high-temperature thermal treatment and chemical treatments with hydrazine (N2H4) or other reducing agents . GQDs are small pieces of G with a 2D lateral size less than 100 nm, which have been synthesized by oxidative cleavage , hydrothermal or solvothermal method [56-58], macrowave-assisted / ultrasonic-assisted process , electrochemical oxidation , and carbonization . pG is an apolar and hydrophobic member of GBNs that its dispersibility in aqueous media is improved by oxidizing. Due to unique arrangement of sp2 bonded carbon atoms, each GBNs can exhibit remarkable different physical, morphological and chemical properties (Fig. 2)
GBNS antifungal and antibacterial mechanisms
The antimicrobial mechanisms responsible for G and GO and other GBNs have been investigated widely. The most common proposed mechanisms are oxidative stress induction, protein dysfunction, membrane damage, and transcriptional arrest (Fig. 3) [62-66]. Generating reactive oxygen species (ROS) is the main reason for nanomaterial toxicity [45, 67-69]. Some antioxidant enzymes, such as glutathione peroxidase or superoxide dismutase, are able to diminish and eliminate ROS generation. By disrupting these enzymes balance, proteins, deoxyribonucleic acid (DNA), and lipids can be damaged. In addition, GO and rGO nanosheets have shown Fenton-like catalytic activity [70, 71]. Hence, there is a structural connection between GBNs and their redox activity that supports the ROS generation ability of GBNs as an antimicrobial mechanisms. Microorganism membrane damage is another possible outcome of hydrophobic interaction between GBNs and the membrane phospholipids that correlate with size of GBNs [72-74]. Although the protein dysfunction and transcriptional arrest were not typically proposed to be the primary antibacterial mechanism of GBNs, sometimes they contribute to the antibacterial activities. Investigations showed that G-Fe3O4 leads to E. coli protein aggregation, while, the Fe3O4 causes less protein degradation by itself, the same as tungsten oxide (WO3) nanoparticles by itself [63, 64]. These results show that protein dysfunction can be augmented by G structure in comparison to when they are alone. Due to π-π stacking interactions, GBNs can interact with DNA in several groups. For instance, the presence of GO alongside Cu2+ can affect DNA cleavage by the chelation of Cu2+ ions to oxygen functional groups on the GO nanosheets . Larger GO nanosheets show significant reduction in E. coli viability assay (40 mg/mL, 2 h) in comparison to smaller nanosheets .
The antifungal activity of GBNs
Fungi are able to easily colonize the surfaces of most materials and devices, and they can quickly spread fungal spores. Human health can be threatened by the formation of fungal contamination that might lead to vast economic losses. Consequently, suitable material against fungi are extremely desired. GBNs antifungal activity was studied by synthesizing different types of GBNs, especially G, GO, and rGO.
The antifungal activity of RGO nanosheets
Antifungal activity of rGO against pathogenic fungi can be used to develop GBNs as a broad spectrum antifungal agents. As a breakthrough, the antifungal activity of rGO (0-500 μg/mL) Sawangphruk et al. , studied against three fungal species of A. niger, A. oryzae, and F. oxysporum, and showed the efficacy of rGO against fungi. The half maximal inhibitory concentration (IC50) values of the rGO against F. oxysporum, A. niger and A. oryzae were 50, 100, and 100 μg/mL, respectively. The probable antifungal mechanism, is the interaction of rGO nanosheets with the cell walls of fungi. After that the ROS generation of rGO nanosheets was able to chemically react with the organic functional groups of chitin and other polysaccharides on the cell walls of fungi and induce antifungal activity.
The antifungal activity of GO nanosheets
The main antifungal activity of GO is related to its sharp edges that can cause plasma membrane stress on pathogenic cells. To understand the interaction mechanism of GO, an investigation was performed by Chen et al.,  on bacterial and fungal pathogens, such as P. syringae and X. campestris pv. Undulosa, F. graminearum, and F. oxysporum. The results showed that GO inhibits nearly 90% of the bacteria and repress 80% macroconidia germination along with partial cell swelling and lysing. The proposed mechanism for the toxicity of GO against both the bacterial and the fungal pathogens was a wide range of GO nanosheets aggregation, which resulted in local perturbation of cell membrane, reduced cell membrane potential, and electrolytes leakage. Moreover, due to the high efficiency of GO for photothermal treatment in the near-infrared (NIR (region, it can be an effective photothermal material. The photothermal treatment of GO was investigated by Khan et al., , for antifungal activity to avoid wound healing infection. As a non-invasive and cheap alternative method, this therapy showed remarkable healing property for infected wounds on the dorsal surface of mice (Fig. 4). The antifungal activity of GO on S. cerevisiae and C. utilis was investigated. Results showed that the laser mediated surface activation of GO causes great antifungal efficiency (Fig. 5)
In a study by Zhu et al.,  selected S. cerevisiae as a model and the potential toxicity of GO was evaluated at the concentration ranging from 0 to 600 mg/mL. The results showed a dose dependent cytotoxicity. The antifungal mechanism was attributed to the synergy of reduced mitochondrial transmembrane potential and increased ROS generation. Hence, the expressions of apoptosis-related genes, such as SOD, Yca1, Nma111 and Nuc1 were significantly changed. Xie et al.,  exposed P. chrysosporium, white rot fungus to GO at the concentration of 0-4 mg/mL for 7 day. Their results showed that low concentrations of GO stimulate the cells growth and causes more acidic pH values of the culture media. In addition, the scanning electron microscopy investigations images exhibited that GO induce the disruption of fiber structure of P. chrysosporium, where some very long and thick fibers were formed at 4 mg/mL. In another study, single-walled carbon nanotubes (SWCNTs), multi-walled carbon nanotubes (MWCNTs), GO, rGO, fullerene (C60) and activated carbon (AC) were examined by Wang et al.,  against two important plant pathogenic fungi, F. graminearum and F. poae. The strongest antifungal activity was observed for SWCNTs, followed by MWCNTs, GO, and rGO, where C60 and AC exhibited no noteworthy antifungal activity. The antifungal mechanism included three steps; depositing on the surface of the spores, preventing water uptake and prompting plasmolysis.
The antifungal activity of GO nanocomposites
The synergistic effect of GO and other nanoparticles can be applied to formulate more efficient antimicrobial products [82, 83]. Hence, in recent years scientists have explored Ag nanocomposites more than ever before. To increase antifungal activity ofcarbon nano scrolls (CNSs), Li et al.,  filled it with silver nanoparticles (AgNPs) and compared it with antifungal activity of GO-AgNPs nanocomposite. The CNSs-AgNPs exhibited prolonged activity against C. albicans and C. tropical in comparison with the GO-AgNPs nanocomposites. The results of antifungal activities of GO and its AgNPs nanocomposites showed that there were no inhibition zone for GO; while for GO-AgNPs samples a clear inhibition zones were observed. By increasing incubation time, the inhabitation zone become smaller, and the viable fungal colony increased (Fig. 6). Moreover, the inhibition zone of C. albicans was much smaller than the C. tropical in the same concentration of GO-AgNPs and same incubation time.
In another study by Chen et al.,  they explored antifungal activity of GO-AgNPs nanocomposite against phytopathogen F. graminearum in vitro and in vivo. The GO-AgNPs nanocomposite showed to be three to seven-times more potent than pure AgNPs and GO, respectively. The antifungal mechanism was based on the notable synergistic effect of GO-AgNPs, making physical injury and generating chemical reactive oxygen species. In addition to silver nanocomposites, G-TiO2 nanocomposite was investigated by Karimi et al.,  as a new route to prepare antibacterial and antifungal cotton fabric without toxicity. The result showed that G-TiO2 nanocomposite-coated cotton has an excellent antibacterial and antifungal activity on bacteria (E. coli and S. aureus) and fungi (C. albicans). Indeed, G was added to TiO2 nanoparticles aiming to facilitate effective bacterial decomposition by increasing the contact between nanoparticles and microorganisms. Furthermore, fabrics treated with GO did not show any antimicrobial activity. Graphene oxide-borneol (GOB) composite, is borneol-grafting with great antifungal effect on M. racemosus. In comparison with GO nanosheet, GOB composite displayed no significant antifungal activity. In addition to long-term antifungal effect of GOB composite, the fallen spore does not germinate even after 5 days . The studies are summarized in the Table 1.
The antibacterial activity of GBNs
World Health Organization (WHO) reports showed that in recent years, death of millions of people has been due to the diseases created by bacterial infections . Thus, the treatment of bacterial diseases using antimicrobial drugs are vital. Also, there is an urgent need for novel and effective antimicrobial agents to fight against the bacterial infections [89, 90]. G has been found to be a capable candidate as an antibacterial material due to its bacterial toxicity. Therefore, the toxicity investigation of GBNs in microorganisms as a new class of antibacterial material, is vital for their production in environmental and clinical applications .
The antibacterial activity of RGO and GO nanosheets
For the first time Hu et al.,  investigated antibacterial properties of GBNs by studying the interaction of Gram-negative bacteria, E. coli DH5a with GO. The results showed that GO at a concentration of 85 μg/mL could significantly suppress the growth of E. coli, while having low cytotoxicity for mammalian cells. Transmission electron microscope (TEM) analysis showed that antibacterial properties were attributed to damage cell membrane, which results in leakage of the cytoplasm (Fig. 7). They further found that macroscopic GO papers prepared by vacuum filtration of the GO suspension could effectively restrain the growth of E. coli.
Also, dental caries and periodontal diseases are related to microbes, such as S. mutans, P. gingivalis and F. nucleatum. The antibacterial influence of GO was examined by He et al., . TEM analysis showed GO can disrupt the cell walls, membrane integrity and leakage of the intracellular contents. The antibacterial activity were also observed for a UV irradiated GO by Veerapandian et al.,  that showed higher antibacterial activity for UV irradiated GO due to more cell disruption action than typical GO nanosheets. The antibacterial activity of GO and rGO was evaluated by Gurunathan et al.,  using cell viability, ROS generation and DNA fragmentation assays. The results suggest that GO and rGO possessed a time and concentration dependent antimicrobial activity against E. coli. In comparison with rGO, GO formed more superoxide anions than rGO. Therefore, the bacterial cell death might be due to oxidative stress that consequently leads to DNA fragmentation. The antibacterial activity of pG, GO, and rGO against food-borne bacterial pathogens, such as L. monocytogenes and S. enterica were evaluated by Kurantowicz et al., . This study reported GO to have the highest antibacterial activity due to bacteria adherence at the surface of GO, while with pG and rGO, they adhered to their edges. Also, Wu et al., observed a concentration dependent antibacterial activity for GO against K. pneumonae.
Some reports showed that GO exhibited no significant antimicrobial effect against E. coli or P. aeruginosa bacteria alone; however, Ag nanoparticle-modified GO could effectively inhibit bacterial growth. Interestingly, another research showed that GO presented neither intrinsic antibacterial functions nor cytotoxicity properties to mammalian cells [96, 97]. Several studies evaluate the antibacterial activity of Gram-negative and Gram-positive bacteria and showed that GO inhibited Gram-positive bacteria more effectively than Gram-negative bacteria, while some Gram-negative bacteria, such as E. coli, were resistant to GO . E. coli, gram-negative and S. aureus, gram-positive were selected by Akhavan et al.,  as model bacteria to investigate the bacterial toxicity of GO and rGO nanowalls. Results showed bacteria interaction between the very sharp edges of the nanowalls causes cell membrane damage. In addition, the cell membrane of Gram-positive S. aureus was strictly damaged in comparison to the Gram-negativeE. coli, which was due to sharp edges and better charge-transfer ability of rGO nanowalls and bacteria. Moreover, rGO nanowalls exhibited stronger antibacterial activity than GO nanowalls. The antibacterial mechanism of G was also studied by exploring the interactions between different types of GBNs with the Gram-negative E. coli. Again, GO showed the strongest antibacterial activity under similar concentrations and incubation time among all materials, followed by rGO, graphite, and graphite oxide. Their antibacterial mechanisms were attributed to the synergy of the membrane stress and oxidative stress induced by the interactions between bacteria and materials. However, by increasing the concentration of GBNs, the inhibition activity against the growth of Gram-negative E. coli and Gram-positive B. subtilis was increased . A similar study by Chen et al.,  studied the antibacterial activity of rGO and GO. And, GO showed higher bactericidal effects due to its sharp edges and production of ROS.
Furthermore, disrupting the membrane integrity, ROS generation can be potentially made by antibacterial activity. Krishnamoorthy et al.,  examined antibacterial activity of G nanosheets that can be applied in the development of biomedical devices. They observed that G nanosheets have antibacterial activities against E. coli, S. typhimurium, E. faecalis, and B. subtilis. These results support the idea of G, as a hopeful antibacterial material with low mammalian cell cytotoxicity. Conversely, recent studies have shown that GO might miss any antibacterial properties . These studies are summarized in Table 2.
The antibacterial activity of GBNs nanocomposites
The advancement of nanotechnology provides opportunities to prepare antibacterial G nanocomposits. Antibacterial properties of GBNs include ZnO/GO , TiO2/GO , Ti-GO-Ag , and CuO/rGO nanocomposites  have been explored recently. To date, Ag nanoparticle-modified GO films, not bare GO, have exhibited stronger antibacterial activity. The oxygen-containing functional group of GO adhere to lipopolysaccharides of bacteria through hydrogen bonds formation between the lipopolysaccharides of the bacteria and the oxygen-containing functional groups of GO [106-108]. Hence, GO decreases the intake of nutrition from the media and increases the interaction between Ag nanoparticles and bacteria . Ag can also disrupt the bacterial membrane that prevents the respiration and replication of bacteria, which leads to cell death . The Ag-modified GO nanostructure exerts its antibacterial effect through a “capturing-killing process” that increases the deposition of bacteria, as well as the contact between cells and Ag-modified GO nanoparticles . Due to these controversial findings, further studies should be carried out to determine the detailed mechanisms and controlling factors with respect to the interaction between GBNs and microbes. There are some studies that have shown recent progress in antimicrobial activity of G nanocomposits [111, 112].
Today antibiotic resistance has emerged as a strong health concern worldwide. To eradicate this problem, synthesis and application of new antimicrobial materials are necessary and required. Emerging nanotechnology has provided a suitable platform to resolve the problem of resistance, by the use of antimicrobial nanomaterials, identified as nanomaterials with antibacterial properties to contest infections by antibiotic-resistant bacteria. Several investigations have focused on the antimicrobial mechanism of GBNS, but a deeper and more consistent understanding of the underlying molecular mechanisms is required. Recent studies revealed that GBNs have high efficiency in antifungal and antibacterial activity via damage of cell membranes and other mechanisms. To increase GBNs antimicrobial effect, nanocomposite preparation by the incorporation of inorganic nanostructures has increased their antimicrobial properties. GBNs preferably as a new group of nanomaterials can be used in nanomedicine in the near future.
CONFLICT OF INTEREST
The authors declare that there are no conflicts of interest regarding the publication of this manuscript.
This work was financially supported by Shiraz University of Medical Sciences (SUMS). The authors also gratefully acknowledge the use of facilities of the Center for Nanotechnology in Drug Delivery at SUMS. The authors wish to thank Mr. H. Argasi at the Research Consultation Center (RCC) of Shiraz University of Medical Sciences for his invaluable assistance in editing this manuscript.
5. Ebrahiminezhad A, Taghizadeh S, Berenjian A, Naeini FH, Ghasemi Y. Green Synthesis of Silver Nanoparticles Capped with Natural Carbohydrates Using Ephedra intermedia. Nanoscience &Nanotechnology-Asia. 2017;7(1):104-12.
7. Mallakpour S, Abdolmaleki A, Borandeh S, Sabzalian MR. One pot fabrication of optically active and efficient antibacterial poly(amide-benzimidazole-imide)/Ag bionanocomposite. Journal of Polymer Research. 2015;22(7).
8. Gordon T, Perlstein B, Houbara O, Felner I, Banin E, Margel S. Synthesis and characterization of zinc/iron oxide composite nanoparticles and their antibacterial properties. Colloids and Surfaces A: Physicochemical and Engineering Aspects. 2011;374(1-3):1-8.
9. Srisitthiratkul C, Pongsorrarith V, Intasanta N. The potential use of nanosilver-decorated titanium dioxide nanofibers for toxin decomposition with antimicrobial and self-cleaning properties. Applied Surface Science. 2011;257(21):8850-6.
11. Jadhav MS, Kulkarni S, Raikar P, Barretto DA, Vootla SK, Raikar US. Green biosynthesis of CuO & Ag–CuO nanoparticles from Malus domestica leaf extract and evaluation of antibacterial, antioxidant and DNA cleavage activities. New Journal of Chemistry. 2018;42(1):204-13.
12. Karthik K, Dhanuskodi S, Prabu Kumar S, Gobinath C, Sivaramakrishnan S. Microwave assisted green synthesis of MgO nanorods and their antibacterial and anti-breast cancer activities. Materials Letters. 2017;206:217-20.
13. Martinez LR, Han G, Chacko M, Mihu MR, Jacobson M, Gialanella P, et al. Antimicrobial and Healing Efficacy of Sustained Release Nitric Oxide Nanoparticles Against Staphylococcus Aureus Skin Infection. Journal of Investigative Dermatology. 2009;129(10):2463-9.
18. Abdolmaleki A, Mallakpour S, Borandeh S. Improving interfacial interaction ofl-phenylalanine-functionalized graphene nanofiller and poly(vinyl alcohol) nanocomposites for obtaining significant membrane properties: Morphology, thermal, and mechanical studies. Polymer Composites. 2015;37(6):1924-35.
20. Wu G, Xu P, Guo Z, Chen Y, Lu NL. Graphene Composite Catalysts for Electrochemical Energy Conversion. Multifunctional Nanocomposites for Energy and Environmental Applications, 2018: 203-230.
22. Yin R, Guo W, Du J, Zhou X, Zheng H, Wu Q, et al. Heteroatoms doped graphene for catalytic ozonation of sulfamethoxazole by metal-free catalysis: Performances and mechanisms. Chemical Engineering Journal. 2017;317:632-9.
23. Keshipour S, Kulaei M, Ahour F. Graphene Oxide Nano-Sheets-Supported Co(II)-d-Penicillamine as a Green and Highly Selective Catalyst for Epoxidation of Styrene. Iranian Journal of Science and Technology, Transactions A: Science. 2017;43(1):85-94.
24. Taki M, Rezaei B, Fani N, Borandeh S, Abdolmaleki A, Ensafi AA. Beneficial effects of amino acid-functionalized graphene nanosheets incorporated in the photoanode material of dye-sensitized solar cells: A practical and theoretical study. Applied Surface Science. 2017;403:218-29.
26. Yao X, Niu X, Ma K, Huang P, Grothe J, Kaskel S, et al. Graphene Quantum Dots-Capped Magnetic Mesoporous Silica Nanoparticles as a Multifunctional Platform for Controlled Drug Delivery, Magnetic Hyperthermia, and Photothermal Therapy. Small. 2016;13(2):1602225.
28. Cheng R, Peng Y, Ge C, Bu Y, Liu H, Huang H, et al. A turn-on fluorescent lysine nanoprobe based on the use of the Alizarin Red aluminum(III) complex conjugated to graphene oxide, and its application to cellular imaging of lysine. Microchimica Acta. 2017;184(9):3521-8.
31. Robinson JT, Tabakman SM, Liang Y, Wang H, Sanchez Casalongue H, Vinh D, et al. Ultrasmall Reduced Graphene Oxide with High Near-Infrared Absorbance for Photothermal Therapy. Journal of the American Chemical Society. 2011;133(17):6825-31.
32. Tayyebi A, Akhavan O, Lee B-K, Outokesh M. Supercritical water in top-down formation of tunable-sized graphene quantum dots applicable in effective photothermal treatments of tissues. Carbon. 2018;130:267-72.
33. Nie W, Peng C, Zhou X, Chen L, Wang W, Zhang Y, et al. Three-dimensional porous scaffold by self-assembly of reduced graphene oxide and nano-hydroxyapatite composites for bone tissue engineering. Carbon. 2017;116:325-37.
36. Shah S, Yin PT, Uehara TM, Chueng S-TD, Yang L, Lee K-B. Guiding Stem Cell Differentiation into Oligodendrocytes Using Graphene-Nanofiber Hybrid Scaffolds. Advanced Materials. 2014;26(22):3673-80.
39. Zhang Q, Wu Z, Li N, Pu Y, Wang B, Zhang T, et al. Advanced review of graphene-based nanomaterials in drug delivery systems: Synthesis, modification, toxicity and application. Materials Science and Engineering: C. 2017;77:1363-75.
44. Pinto AM, Gonçalves IC, Magalhães FD. Graphene-based materials biocompatibility: A review. Colloids Surf., B, 2013; 111: 188-202.
53. de Heer WA, Berger C, Ruan M, Sprinkle M, Li X, Hu Y, et al. Large area and structured epitaxial graphene produced by confinement controlled sublimation of silicon carbide. Proceedings of the National Academy of Sciences. 2011;108(41):16900-5.
59. Zhang C, Cui Y, Song L, Liu X, Hu Z. Microwave assisted one-pot synthesis of graphene quantum dots as highly sensitive fluorescent probes for detection of iron ions and pH value. Talanta. 2016;150:54-60.
61. Dong Y, Shao J, Chen C, Li H, Wang R, Chi Y, et al. Blue luminescent graphene quantum dots and graphene oxide prepared by tuning the carbonization degree of citric acid. Carbon. 2012;50(12):4738-43.
63. Akhavan O, Choobtashani M, Ghaderi E. Protein Degradation and RNA Efflux of Viruses Photocatalyzed by Graphene–Tungsten Oxide Composite Under Visible Light Irradiation. The Journal of Physical Chemistry C. 2012;116(17):9653-9.
64. Santhosh C, Kollu P, Doshi S, Sharma M, Bahadur D, Vanchinathan MT, et al. Adsorption, photodegradation and antibacterial study of graphene–Fe3O4 nanocomposite for multipurpose water purification application. RSC Adv. 2014;4(54):28300-8.
65. Hui L, Piao J-G, Auletta J, Hu K, Zhu Y, Meyer T, et al. Availability of the Basal Planes of Graphene Oxide Determines Whether It Is Antibacterial. ACS Applied Materials & Interfaces. 2014;6(15):13183-90.
67. Zhang Y, Ali SF, Dervishi E, Xu Y, Li Z, Casciano D, et al. Cytotoxicity Effects of Graphene and Single-Wall Carbon Nanotubes in Neural Phaeochromocytoma-Derived PC12 Cells. ACS Nano. 2010;4(6):3181-6.
69. Gurunathan S, Woong Han J, Abdal Daye A, Eppakayala V, Kim J-h. Oxidative stress-mediated antibacterial activity of graphene oxide and reduced graphene oxide in Pseudomonas aeruginosa. International Journal of Nanomedicine. 2012:5901.
72. Chen J, Peng H, Wang X, Shao F, Yuan Z, Han H. Graphene oxide exhibits broad-spectrum antimicrobial activity against bacterial phytopathogens and fungal conidia by intertwining and membrane perturbation. Nanoscale. 2014;6(3):1879-89.
78. Shahnawaz Khan M, Abdelhamid HN, Wu H-F. Near infrared (NIR) laser mediated surface activation of graphene oxide nanoflakes for efficient antibacterial, antifungal and wound healing treatment. Colloids and Surfaces B: Biointerfaces. 2015;127:281-91.
82. Gosheger G, Hardes J, Ahrens H, Streitburger A, Buerger H, Erren M, et al. Silver-coated megaendoprostheses in a rabbit model—an analysis of the infection rate and toxicological side effects. Biomaterials, 2004; 25(24): 5547-5556.
85. Chen J, Sun L, Cheng Y, Lu Z, Shao K, Li T, et al. Graphene Oxide-Silver Nanocomposite: Novel Agricultural Antifungal Agent against Fusarium graminearum for Crop Disease Prevention. ACS Applied Materials & Interfaces. 2016;8(36):24057-70.
86. Karimi L, Yazdanshenas ME, Khajavi R, Rashidi A, Mirjalili M. Using graphene/TiO2 nanocomposite as a new route for preparation of electroconductive, self-cleaning, antibacterial and antifungal cotton fabric without toxicity. Cellulose. 2014;21(5):3813-27.
88. Organization WH. The world health report 2002: reducing risks, promoting healthy life: World Health Organization; 2002.
89. Van Boeckel TP, Gandra S, Ashok A, Caudron Q, Grenfell BT, Levin SA, et al. Global antibiotic consumption 2000 to 2010: an analysis of national pharmaceutical sales data. The Lancet Infectious Diseases. 2014;14(8):742-50.
90. Lesprit P, Landelle C, Brun-Buisson C. Clinical impact of unsolicited post-prescription antibiotic review in surgical and medical wards: a randomized controlled trial. Clinical Microbiology and Infection. 2013;19(2):E91-E7.
92. Veerapandian M, Zhang L, Krishnamoorthy K, Yun K. Surface activation of graphene oxide nanosheets by ultraviolet irradiation for highly efficient anti-bacterials. Nanotechnology. 2013;24(39):395706.
93. Gurunathan S, Han JW, Dayem AA, Eppakayala V, Park M-R, Kwon D-N, et al. Antibacterial activity of dithiothreitol reduced graphene oxide. Journal of Industrial and Engineering Chemistry. 2013;19(4):1280-8.
94. Kurantowicz N, Sawosz E, Jaworski S, Kutwin M, Strojny B, Wierzbicki M, et al. Interaction of graphene family materials with Listeria monocytogenes and Salmonella enterica. Nanoscale Research Letters. 2015;10(1).
95. Wu X, Tan S, Xing Y, Pu Q, Wu M, Zhao JX. Graphene oxide as an efficient antimicrobial nanomaterial for eradicating multi-drug resistant bacteria in vitro and in vivo. Colloids and Surfaces B: Biointerfaces. 2017;157:1-9.
96. Das MR, Sarma RK, Saikia R, Kale VS, Shelke MV, Sengupta P. Synthesis of silver nanoparticles in an aqueous suspension of graphene oxide sheets and its antimicrobial activity. Colloids and Surfaces B: Biointerfaces. 2011;83(1):16-22.
98. Díez-Pascual AM, Díez-Vicente AL. Poly(propylene fumarate)/Polyethylene Glycol-Modified Graphene Oxide Nanocomposites for Tissue Engineering. ACS Applied Materials & Interfaces. 2016;8(28):17902-14.
99. Liu S, Zeng TH, Hofmann M, Burcombe E, Wei J, Jiang R, et al. Antibacterial Activity of Graphite, Graphite Oxide, Graphene Oxide, and Reduced Graphene Oxide: Membrane and Oxidative Stress. ACS Nano. 2011;5(9):6971-80.
101. Krishnamoorthy K, Veerapandian M, Zhang L-H, Yun K, Kim SJ. Antibacterial Efficiency of Graphene Nanosheets against Pathogenic Bacteria via Lipid Peroxidation. The Journal of Physical Chemistry C. 2012;116(32):17280-7.
102. Wang Y-W, Cao A, Jiang Y, Zhang X, Liu J-H, Liu Y, et al. Superior Antibacterial Activity of Zinc Oxide/Graphene Oxide Composites Originating from High Zinc Concentration Localized around Bacteria. ACS Applied Materials & Interfaces. 2014;6(4):2791-8.
104. Jin J, Zhang L, Shi M, Zhang Y, Wang Q. Ti-GO-Ag nanocomposite: the effect of content level on the antimicrobial activity and cytotoxicity. International Journal of Nanomedicine. 2017;Volume 12:4209-24.
107. Xu W-P, Zhang L-C, Li J-P, Lu Y, Li H-H, Ma Y-N, et al. Facile synthesis of silver@graphene oxide nanocomposites and their enhanced antibacterial properties. Journal of Materials Chemistry. 2011;21(12):4593.
108. Liu L, Liu J, Wang Y, Yan X, Sun DD. Facile synthesis of monodispersed silver nanoparticles on graphene oxide sheets with enhanced antibacterial activity. New Journal of Chemistry. 2011;35(7):1418.
110. Chook S, Chia C, Zakaria S, Ayob M, Chee K, Huang N, et al. Antibacterial performance of Ag nanoparticles and AgGO nanocomposites prepared via rapid microwave-assisted synthesis method. Nanoscale Research Letters. 2012;7(1):541.
112. Santos CM, Mangadlao J, Ahmed F, Leon A, Advincula RC, Rodrigues DF. Graphene nanocomposite for biomedical applications: fabrication, antimicrobial and cytotoxic investigations. Nanotechnology. 2012;23(39):395101.