B. A. Camacho-Flores 1 and O. Martinez-Álvarez 2 and M. C. Arenas-Arrocena 1 and R. Garcia-Contreras 1 and L. Argueta-Figueroa 3 and J. de la Fuente-Hernandez 1 and L. S. Acosta-Torres 1
Academic Editor:Jin-Ho Choy
1, Escuela Nacional de Estudios Superiores, Unidad Leon, Universidad Nacional Autonoma de Mexico, Boulevard UNAM No. 2011, Predio el Saucillo y el Potrero, 36969, GTO, Mexico
2, Universidad Politecnica de Guanajuato, Avenue Universidad Norte s/n, Juan Alonso, 38438 Cortazar, GTO, Mexico
3, Universidad Autonoma del Estado de Mexico, Calle Jesús Carranza, Esquina Paseo Tollocan, 50130 Colonia Universidad, Toluca, MEX, Mexico
Received 23 July 2015; Revised 1 October 2015; Accepted 4 October 2015; 8 December 2015
This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
1. Introduction
In recent years technology has been applied as a key partner in the emergence of the "nanoscience" more focused on the development of new methods to synthesize, study, analyze, and modify particles and nanosized structures, less than 100 nm. It has been shown that the physical properties of the metal nanoparticles are different from the bulk metal, made of the same atoms, which has taken great interest in their promising applications, such as incorporate antibacterial properties as well as their incorporation in pharmaceuticals and textiles and as photocatalysis [1], electrical conductors [2], biochemical sensors [3], and oxidative capacity [4, 5] so as to modify the surface properties of other materials [6] like cosmetic pigments [7].
Nanotechnology has opened a wide opportunity in the area of materials science and the incorporation of other branches as photochemistry and electrochemistry to better understand its properties [8] has been necessary. The easy adjustment of the size of nanomaterials (<100 nm) [9] allows incorporating into a wide range of materials to improve their properties, such as size; therefore distribution and optical electric properties and potential biological applications are modified too [10]. The copper nanoparticles (Cu NPs) have been a strong focus on applications to health-related processes due to its antibacterial properties and antifungal activity in addition to their catalytic, optical, and electrical properties [11]. Cu NPs are often synthesized by dispersing polymers [12] and solvent evaporation [13]; in order to produce smaller nanometer sized particles, some methods have been suggested, for example, the use of ultrasound or organics separation and the use of solvents for extraction-evaporation or diffusion [14]. In recent years, the implementation of affordable friendly systems with the environment for the synthesis of Cu NPs is a challenge due to the complex obtained metal nanoparticles instead of metal oxides [15, 16]. The development of Cu NPs is in constant growing and developing for future technologies [17]. The highlight of this review is related to the synthesis and characterization of Cu NPs techniques and their biological properties and applications in biomedical science.
2. Techniques for the Synthesis of Copper Nanoparticles
The development of materials at nanometric scale has been increasing in different fields. The properties of these nanomaterials are critical for the technological revolution worldwide, which mainly depend on the methods of synthesis for the potential applications such as the bactericidal and antifungal effect [18]. Some nanomaterials include those derived from metal oxides, metal salts, and metal hydroxides, such as copper oxide, zinc oxide, gold, silver, copper, magnetite and maghemite, titanium, and iron [7]. Metal-based nanoparticles represent an alternative for biomedical treatments, mainly in the fabrication of biomedical devices with antimicrobial coatings. A high antimicrobial activity of nanoparticles depends on the particle size that allows greater surface contact and a direct interaction with the membranes of pathogenic microorganisms. NPs are also used as drug delivery and ions agents as well as for diagnostic imaging [19]. Moreover, the increasing improper use of medications such as antibiotics has led the medical field to explore new alternatives of biocides to combat infectious diseases [20, 21].
The NPs are materials with different properties than those in the bulk form; these features made the nanoparticles have various applications in many fields such as electronics (nanowires and nanosensors), MRI (magnetic devices), pharmaceutical (drug-eluting), cosmetic (nanopigments), and catalytic and materials design (nanodevices) [19]. Silver and Cu NPs are the most usually reported with a high antimicrobial activity; it allows their incorporation in a variety of materials including titanium, polymers, and glasses [22, 23].
Generally, the methods for the synthesis of nanoparticles are usually classified into two categories: the physical and chemical techniques [24]. The physical method consists in the reduction of bulk solids to smaller portions in very fine grains through a grinding process, either by using acidic substances or by the application of energy sources. The grinding process is the most representative example of the physical methods, where highly efficient mills are used to separate the particles of nanometric sized. However it has not been a reliable system to obtain metallic nanoparticles because, generally, the obtained particles are larger than 100 nm, which could not be considered as nanometric size. Another disadvantage of this technique is that the applied energy for grinding must be continuous and it can infer energetic changes into solids producing a significant imbalance, which lead to a decrease of values in the energy activation [25]. In fact, probably it is one of the oldest methods but it is not currently used to obtain Cu NPs with regular size and defined morphology.
Physical techniques are unconventional methods (Table 1), such as those that require vacuum or plasma, sometimes obtaining nanoparticles with low quality. Several physical techniques are incorporated during or after a chemical process, for example, the laser ablation requires a colloidal solution, which minimizes the chances of oxidation on the surface of the nanoparticles, and it must be placed in a vacuum chamber in order to remove or extract atoms from a bulk surface through emission of laser beam; this method is not feasible due to the complexity of the equipment and the use of high energy for the laser [26]. The number of pulses applied of the laser beam and the exposition time are important parameters to define the particle size. These parameters are in the range from 6000 to 10000 pulses in periods of 10 and 30 minutes [25]. The decomposition of volatile compounds inside a vacuum chamber or reactor is used for the deposition of atom by atom or molecule by molecule to form layers on a solid surface at subatmospheric pressure [27]. Unlike other physical techniques, in the Pulsed Wire Discharge (PWD), the ions are implanted on solid substrate by pulse electrical current [28, 29].
Table 1: Physical and chemical synthesis methods of Cu NPs.
Physical methods | Chemical methods |
Ablation [85-87] | Colloidal microemulsion [48, 49] |
Physical Vapor Deposition (PVD) [88] | Sonochemical [52, 89-91] |
Wire discharge [83, 92] | Electrochemical [25, 40, 82, 93] |
Grinding [94] | Microwave [43, 95-97] |
Radiolysis [98] | Hydrothermal [46, 82, 99] |
Aerosol [100] |
|
Mechanical attrition [101] |
|
Chemical synthesis is currently the most used and functional method, which involves condensation of atoms or molecular entities from the gaseous phase or from a solution to obtain nanoparticles with specific size and morphology; these properties are adjusted with the synthesis parameters such as temperature, precursor concentration, stabilizer agent, or solvent [30]. This method for the Cu NPs synthesis shows the relation ratio between the precursor, the reducing agent, stabilizing agent, and the solvent (Table 2). Among the chemical methods, the chemical reduction of copper salts is easy and simple to obtain Cu NPs with controlled size and morphology [31-33].
Table 2: Chemical substances for the Cu NPs synthesis.
Copper precursor | Reducing agent | Stabilizer | Medium | Temperature | Morphology and size (nm) and maximum absorption peak (nm) |
Copper nitrate [99] | Ascorbic acid | Chemical grade starch | Distilled and deionized water | Room temp. | Spherical, 5-12 nm |
| |||||
Copper nitrate (II) [42] | Cethyl trimethylammonium in isoprophyl alcohol | Bromide, cetyl trimethyl ammonium (CTAB) | Aqueous | Room temp. | Spherical, 5-10 nm |
| |||||
Hydrated copper chloride (II) [102] | Cethyl trimethylammonium in isoprophyl alcohol | Ascorbic acid | Acid inert atmosphere | Room temp. | semispherical, 5-12 nm |
| |||||
Copper nitrate (III) [18] | Sodium borohydride | Sodium hydroxide | Aqueous | Room temp. | Asymmetric, 9.25 ± 1.79 nm, |
| |||||
Copper pentasulfide (III) [42] | Cethyl trimethylammonium bromide | Ascorbic acid | Deionized water polyethylene glycol | Room temp. | 20 nm |
| |||||
Copper sulfate pentahydrate (III) [103] | Isonicotinic acid hydrazide | Ascorbic acid sodium hydroxide polyvinylpyrrolidone | Distilled water | 60-70°C | 6.95 nm |
| |||||
Copper chloride dihydrate [48] | Aluminum isopropoxide | Ascorbic acid | Ethanol | Room temp. | - |
| |||||
Copper (II) nitrate [74] | L-ascorbic acid | Chitosan | Distilled water | Microwave | 80-100 nm, 550 nm |
| |||||
Copper (II) sulfate [104] | Hydrazine monohydrate | Sodium dodecyl sulfate | Distilled water | Room temperature | 50-70 nm, 550 nm |
| |||||
Copper (II) nitrate [78, 99] | Ascorbic acid | Starch | Double-distilled water | Microwave | 5-12 nm, 579 nm |
| |||||
Copper (II) acetate [83] | Ethylene glycol | Tween 80 (polyoxyethylene-(80)-sorbitan monooleate) | Tween 80 (polyoxyethylene-(80)-sorbitan monooleate) | 190-200°C, 2-3 h | 45 ± 8 nm, 580 nm |
| |||||
Copper (II) nitrate [18] | Sodium borohydride | Tetra-n-octylammonium | Deionized water | Room temperature | 3-9 nm |
| |||||
Copper (II) chloride [105] | Sodium borohydride ascorbic acid | Polyvinyl alcohol | Deionized water | Room temperature | 3.5 nm, 516 nm |
| |||||
Copper (II) chloride [102] | Sodium borohydride | Ascorbic acid | Aqueous solution | Inert atmosphere | 5.3 ± 0.1 nm, 562 nm |
| |||||
Copper (II) acetate Copper (II) nitrate [47] | Ethanol | L-ascorbic acid | Ethanol | Microwave irradiation (140°C) | 7-15 nm, 580-590 nm |
The chemical reaction is sensitive to the aqueous media and air conditions, where the surface of the nanoparticles is highly oxidizing, so that sometimes it is necessary to use inert environmental conditions (nitrogen or argon atmosphere) or surface-active substances to protect the nanoparticles surface, like ligand agent, surfactants, soluble polymers, weak acids, and so forth (Figure 1) [30, 34].
Figure 1: HRTEM of Cu nanoparticles. [figure omitted; refer to PDF] M of CuSO4 [figure omitted; refer to PDF] 5H2 O and [figure omitted; refer to PDF] M of NaBH4 , under nitrogen gas, were vigorous stirred for 2-3 h. Left image shows Cu NPs with sizes from 25 to 4 nm. Right image is a zoomed image of the characteristic size of Cu NPs.
(a) [figure omitted; refer to PDF]
(b) [figure omitted; refer to PDF]
Chemical reduction method and microemulsion route were used for the first time to synthesize gold metal, and they have been used to reduce other less noble metals such as copper by using mainly copper salts (sulfates, nitrates, and chlorides) and reducing agents (sodium borohydride, isopropyl alcohol, ascorbic acid, and hydrazine) and, sometimes, by using stabilizing agents (polyvinyl pyrrolidone and polyethylene glycol) [35, 36]. Green chemical synthesis by using novel Ginkgo biloba Linn. leaves is a successful option to obtain stable spherical Cu NPs about 15-20 nm [37].
Microemulsion reduction method (Figure 2(a)) or colloidal synthesis involves the use of immiscible water-oil, oil-water, and water supercritical carbon dioxide forming surface-active microarrays [38]. Sonochemical reduction is based on ultrasonic waves (Figure 2(b)) with a frequency about 20 kHz to 10 MHz; the reaction is active by a physical phenomenon of acoustic cavitation [39]. The electrochemical synthesis (Figure 2(c)) is based on the application of an electrical current between two electrodes (cathode and anode) separated by an electrolytic solution; the reduction process occurs on the surface of the cathode electrode [40]. Microwaves and hydrothermal treatment are new alternatives to obtain regular particle size and morphology Cu NPs [41, 42]. The microwave technique consists in an electromagnetic energy with frequencies in the range of 300 MHz to 300 GHz [43-45], where the adequate amounts of energy influence directly the configuration of the Cu NPs. Finally, in the hydrothermal treatment, the chemical reaction requires a sealed autoclave, where the solvents are exposed at temperatures above their boiling points [46].
Figure 2: Synthesis of Cu NPs. (a) Microemulsion technique (oil-water/water-oil): the lipid micelles are surrounding the NPs giving the form of hydrophobic heads or hydrophilic tails, and the interaction of both resulted in spherical shape. (b) Sonochemical technique: applying energy as waves, the micelles found in the middle interacting with the surrounded copper resulting in spherical shape NPs. (c) Electrochemical technique: the interaction between opposite electric charges generated increased energy in the middle of the formation of NPs; these energy emissions are usually constants allowing the fact that between one issue and another the final structure is formed.
(a) [figure omitted; refer to PDF]
(b) [figure omitted; refer to PDF]
(c) [figure omitted; refer to PDF]
The synthesis techniques are also often classified into "bottom-up" and "top-down" by the direction of the nanoparticles formation. The "bottom-up" reaction begins from atomic level through forming molecules; however, in the opposite technique described as "top-down," the scale of the resultant nanoparticles is larger, so that a mechanical process or the addition of acids is required to reduce the particle size. Usually, the "top-down" technique requires the use of complex and complicated instrumentation [47].
Regardless of the technique chosen for the synthesis of Cu PN, conditions should be controlled to adjust the particle size (lower than 100 nm) and shape of the nanoparticles (nanofibers, nanotriangles, and nanospheres), because the wide distribution particle size modified their properties [48-50]. Shankar and Rhim found that nanofibers and triangle and spherical nanoparticles can be obtained by using basic or acidic solution, respectively, which presented different absorbing bands, the first in the range of 280-360 nm and the second from 240 to 280 nm [51]. They also found that both shapes of Cu presented inhibition against Gram-negative E. coli and Gram-positive L. monocytogenes , but nanofibers had stronger antibacterial activity than those triangle and spherical nanoparticles. The synthesis of metal NPs currently requires both physical and chemical systems to incorporate the best features and optimum properties to develop new materials. Certain characteristics can be obtained with notable differences between the physical and chemical methods; chemicals are more beneficial if what is sought is to obtain nanoparticles below 50 nm; both methods obtained effectively Cu NPs; however the properties conferred to nanoparticle size should be considered [52, 53]. Khodashenas and Ghorbani compared three methods (chemical, physical, and biological) concluding that the biological route is more ecofriendly, cheaper, and easier to obtain copper nanoparticles than physical and chemical ones [24].
3. Techniques for Characterization of Copper Nanoparticles
The observation of nanometric scale structures is carried out by different tests consisting of photons, electrons, neutrons, atoms, ions, or an atomically sharp tip, which has different frequencies, in the range from gamma to infrared rays or beyond. The resulting information can be processed to produce images or spectra that reveal topographic, geometric, structural, chemical, or physical details. Several techniques are available for the characterization of nanomaterials [32, 54].
Cu NPs have been physically and chemically characterized in order to obtain the great amount of data to establish the physical and biological characteristics (Table 3). The diminutive sizes of Cu NPs are also their main disadvantage because it represents a challenge for the scientific community to achieve adequate physical and chemical characterization [49, 52].
Table 3: Characterization techniques and response for copper nanoparticles.
Characterization technique | Copper NPs |
UV-Visible Spectroscopy [52] | 566-580 nm |
TEM, Transmission Electron Microscopy [6] | 10-20 nm/elongated aggregates, spheres 5-15 nm/rice, nanocrystals |
HRTEM, High Resolution Transmission Electron Microscopy [30, 106, 107] | Atoms periodicity arrangement |
AFM, Atomic Force Microscopy [6] | Topography |
EDS/SEM, Electronic Data System/Scanning Electron Microscopy [106] | 8 KeV |
XRD, X-Ray Diffraction [108-110] | Diameter estimated: 5-16 nm |
Raman Spectroscopy [30, 107] | Raman shift: 430, 739, 1057, 1314, 1433, and 1459 nm (±5 nm) |
The stability or ability to keep its size and shape as function of time is very important to keep the properties and potential applications as a "bioactive" material. Some relevant data such as the purity of phases, the distribution in the space, the chemical composition of its surface, and its crystallinity are analyzed by various methods, most of them from high energy with large resolutions [55, 56]. The importance of the Cu NPs analysis lies in the growing field of applications, making the knowledge of the nature of this new material imperative [57].
Metals such as copper colloids are generally absorbed in the ultraviolet-visible (UV-Vis) range due to excitation of surface plasmon resonance (SPR). Therefore, the UV-Vis spectroscopy is a convenient method to characterize Cu NP [58]. Some of the colloidal metal materials are different under the macroscopic scale and show distinct absorption peaks in the visible region; copper, silver, and gold are metal with prominent absorption peaks. The Transmission Electron Microscopy (TEM) is the most common characterization technique to determine the shape and size of the Cu NPs. Although other methods such as Dynamic Light Scattering (DLS) and X-Ray Scattering at Small Angles (SAXS) are also used to measure particle size [59], only TEM analysis provides the real images of the morphology and shape of the nanostructures. The Scanning Electron Microscope (SEM) is an instrument that allows the observation of the inorganic materials providing morphological information. The main use of high resolution EDS/SEM (~100Å) is the ability to obtain three-dimensional images with large depth fields by a simple sample preparation [60]. The achievements in recent years allow the precise control over the generated structure in the synthesis of Cu NPs depending on the specific application.
4. Biological Behavior: Antimicrobial Effect and Toxicity
Since a decade, the metal and metal oxide nanoparticles such as silver, zinc, gold, or titanium dioxide have been used as antimicrobial agents. Currently, the behavior of nanometals at nanometrics sizes against pathogenic organisms is still being studied [61]. The high antimicrobial activity of the Cu NPs has been shown in multiple studies focusing on the optimal size range of about 1 to 10 nm [62, 63].
The Cu NPs have been promising for medicine and dentistry fields due to their properties, specially their interaction with pathogens, their large active surface area, and their high chemical and biological reactivity [64].
Copper is an essential element for some metabolic processes but at low concentrations because large doses could be serious consequences in the metabolic performance. It can act as electron donor or electron acceptor in some enzymes due to its redox properties increasing its toxicity for bacterium, which is induced by Cu+1 and Cu+2 ions [65-67]. Some bacteria such as Clostridium difficile developed important mechanisms to protect themselves from the toxic effects of copper ions while they are in contact with the surface of the Cu NPs (Figure 3). A possible mechanism of bacterial resistance to copper is the formation of endospores, which allows its rapid diffusion. However, the antibacterial response of the copper is being studied, mainly in human pathogens [68].
Figure 3: Possible Cu NPs action mechanism in a bacterium membrane.
[figure omitted; refer to PDF]
The most analyzed bacteria species in contact with Cu NPs are C. difficile , E. coli , and P. aeruginosa , which were significantly inhibited with a particle size between 22 and 90 nm, finding a decrease in the viability cells of these microorganisms [18, 69, 70]. Gram-positive bacteria (e.g., S. aureus ) are more sensitive to Cu NPs and Gram-negative bacteria (e.g., E. coli ) are associated with ROS (Reactive Oxygen Species) expression by different sizes of Cu NPs. These features could change through free surface energy of the particles directly associated with size and morphology and the pH inner of cells too [71]. The antimicrobial effect is directly related to the nanoparticle size and minimum inhibitory concentration (MIC) (Table 4) and the oxidation degree of the surface [72].
Table 4: Minimum inhibitory concentrations (MIC) related to biological effect.
Metal NPs | MIC | Size (nm) | Microorganism |
Cu [18] | 140 mg/mL 140-240 mg/mL | 6-16 | S. aureus E. coli |
| |||
Cu [99] | 3.2 ± 0.41 mg/mL1.6 ± 0.22 mg/mL3.6 ± 0.43 | 5-12 | S. aureus E. coli Salmonella typhi |
| |||
Cu [111] | 1.875-3.75 mg/mL3.75 mg/mL | 50 | S. aureus C. albicans |
| |||
Cu [112, 113] | 140 μ g/mL |
| S. aureus |
The cell membranes of the microorganisms interact with the medium, so metal NPs especially Cu NPs will have some interactions to release metal ions that interfere with the processes of the DNA replication, cell membranes formation, cell division, and so forth, of certain microorganisms such as bacteria, which results in an antimicrobial effect [46, 73]. The action mechanism of the copper NPs occurs through the interaction of enzymes and -SH groups causing damage in the DNA and therefore oxidative stress generation [74-76].
5. Applications in Medicine
The bacteria resistance to antimicrobial drugs has been increased, and now it is considered one of the most important public health worldwide challenges [77]. Cu NPs offer a new strategy against drug antimicrobial resistance, reducing the cell adverse effects [37, 78]. In the medical field as well as a possible antibiotic penetrate common infections in the circulatory, respiratory, and digestive systems, it has also been expanded to the oral cavity; the oral cavity provides habitat for a wide range of microorganisms including bacteria, yeast, and viruses associated with oral infections. Bacteria are the predominant components of the resident microflora and the diversity of species found in the oral cavity the wide ranges [70]. Currently, it has been reported that the incorporation of Cu NPs to orthodontics adhesives has showed significant bactericidal effects against S. aureus , E. coli , and S. mutans , without altering the shear bond strength, oppositely increased their adhesive properties by the addition as nanofiller [79].
Nanotechnology provides a cost-effective way to applying a surface treatment of metals oxidizing nanoparticles used as an antimicrobial substance. An innovative nanoparticle treatment may convert antimicrobial medical devices. Materials nanostructured have unique physicochemical properties promising for dental applications [80, 81]. Among the interesting properties are narrow size, high surface area, high reactivity, high biological interaction, and functional structures.
6. Future Trends
Cu NPs have excellent physicochemical properties, high electrical conduction and good biocompatibility and high surface activity, and therefore they are promising for magnetic nanodevices and multiple electronic and medical applications as well as their incorporation in materials and medicines [82]. Currently, researchers are looking for new routes to the synthesis of metallic nanoparticles such as copper in order to find new properties [83]. Microemulsion is the most common method for the copper NPs synthesis involving the use of tensioactive substances and organic solvents and a lot of energy and high costs [16, 17]. These are the main reasons that it seeks to develop new methods friendly with the environment [84] by incorporating low toxicity substances such as alginate used as stabilizing agent [38] or chitosan-silver-copper organometallic to form 33 bimetallic particles. The investigations are new trends to developing a system to obtain NPs that offer the least possible harm to the environment and which are inexpensive, but the road is still long and uncertain, although efforts are increasingly higher. As estimated for 2020, the production of nanoparticles focused on nanomaterials will be 20 times higher than that in the last 10 years [38].
Acknowledgments
The authors of the present paper wish to thank to the projects (DGAPA-UNAM) PAPIIT-TA200414, CONACyT, Mexico (CB176450), and CONACyT INF225393. Our special thanks are due to Dr. Raul A. Morales-Luckie, Dr. Oscar F. Olea-Mejia, and Dr. Rogelio J. Scougall-Vilchis for the TEM figures.
Conflict of Interests
The authors report no conflict of interests for the present paper.
[1] S. Y. Du, Z. Y. Li, "Enhanced light absorption of TiO2 in the near-ultraviolet band by Au nanoparticles," Optics Letters , vol. 35, no. 20, pp. 3402-3404, 2010.
[2] V. E. Ferry, J. N. Munday, H. A. Atwater, "Design considerations for plasmonic photovoltaics," Advanced Materials , vol. 22, no. 43, pp. 4794-4808, 2010.
[3] H. J. Parab, H. M. Chen, T. C. Lai, J. H. Huang, P. H. Chen, R. S. Liu, M. Hsiao, C. H. Chen, D. P. Tsai, Y. K. Hwu, "Biosensing, cytotoxicity, and cellular uptake studies of surface-modified gold nanorods," Journal of Physical Chemistry C , vol. 113, no. 18, pp. 7574-7578, 2009.
[4] H. W. P. Carvalho, A. P. L. Batista, P. Hammer, T. C. Ramalho, "Photocatalytic degradation of methylene blue by TiO2 -Cu thin films: theoretical and experimental study," Journal of Hazardous Materials , vol. 184, no. 1-3, pp. 273-280, 2010.
[5] J. Ping, S. Ru, K. Fan, J. Wu, Y. Ying, "Copper oxide nanoparticles and ionic liquid modified carbon electrode for the non-enzymatic electrochemical sensing of hydrogen peroxide," Microchimica Acta , vol. 171, no. 1, pp. 117-123, 2010.
[6] Z. Zhao, J. Sun, G. Zhang, L. Bai, "The study of microstructure, optical and photocatalytic properties of nanoparticles(NPs)-Cu/TiO2 films deposited by magnetron sputtering," Journal of Alloys and Compounds , vol. 652, pp. 307-312, 2015.
[7] M. Moritz, M. Geszke-Moritz, "The newest achievements in synthesis, immobilization and practical applications of antibacterial nanoparticles," Chemical Engineering Journal , vol. 228, pp. 596-613, 2013.
[8] M. Moritz, M. Geszke-Moritz, "The application of nanomaterials in detection and removal of environmental pollutants," Przemysl Chemiczny , vol. 91, no. 12, pp. 2375-2381, 2012.
[9] J. Park, J. Joo, G. K. Soon, Y. Jang, T. Hyeon, "Synthesis of monodisperse spherical nanocrystals," Angewandte Chemie-International Edition , vol. 46, no. 25, pp. 4630-4660, 2007.
[10] J. Dai, X. Yang, M. Hamon, L. Kong, "Particle size controlled synthesis of CdS nanoparticles on a microfluidic chip," Chemical Engineering Journal , vol. 280, pp. 385-390, 2015.
[11] L. Argueta-Figueroa, R. A. Morales-Luckie, R. J. Scougall-Vilchis, O. F. Olea-Mejia, "Synthesis, characterization and antibacterial activity of copper, nickel and bimetallic Cu-Ni nanoparticles for potential use in dental materials," Progress in Natural Science: Materials International , vol. 24, no. 4, pp. 321-328, 2014.
[12] M. C. Altay, E. Y. Malikov, G. M. Eyvazova, M. B. Muradov, O. H. Akperov, R. Puskas, D. Madarasz, Z. Konya, Á. Kukovecz, "Facile synthesis of CuS nanoparticles deposited on polymer nanocomposite foam and their effects on microstructural and optical properties," European Polymer Journal , vol. 68, pp. 47-56, 2015.
[13] S. Karan, D. Basak, B. Mallik, "Copper phthalocyanine nanoparticles and nanoflowers," Chemical Physics Letters , vol. 434, no. 4-6, pp. 265-270, 2007.
[14] H.-Y. Kwon, J.-Y. Lee, S.-W. Choi, Y. Jang, J.-H. Kim, "Preparation of PLGA nanoparticles containing estrogen by emulsification-diffusion method," Colloids and Surfaces A: Physicochemical and Engineering Aspects , vol. 182, no. 1-3, pp. 123-130, 2001.
[15] P. Calvo, C. Remuñan-Lopez, J. L. Vila-Jato, M. J. Alonso, "Novel hydrophilic chitosan-polyethylene oxide nanoparticles as protein carriers," Journal of Applied Polymer Science , vol. 63, no. 1, pp. 125-132, 1997.
[16] S. Chandra, A. Kumar, P. K. Tomar, "Synthesis and characterization of copper nanoparticles by reducing agent," Journal of Saudi Chemical Society , vol. 18, no. 2, pp. 149-153, 2014.
[17] F. Bensebaa Nanoparticle Technologies: From Lab to Market , vol. 19, of Interface Science and Technology, Elsevier, 2013.
[18] J. P. Ruparelia, A. K. Chatterjee, S. P. Duttagupta, S. Mukherji, "Strain specificity in antimicrobial activity of silver and copper nanoparticles," Acta Biomaterialia , vol. 4, no. 3, pp. 707-716, 2008.
[19] A. Schröfel, G. Kratosova, I. Safarik, M. Safarikova, I. Raska, L. M. Shor, "Applications of biosynthesized metallic nanoparticles-a review," Acta Biomaterialia , vol. 10, no. 10, pp. 4023-4042, 2014.
[20] R. P. Allaker, K. Memarzadeh, "Nanoparticles and the control of oral infections," International Journal of Antimicrobial Agents , vol. 43, no. 2, pp. 95-104, 2014.
[21] D. R. Monteiro, L. F. Gorup, S. Silva, M. Negri, E. R. de Camargo, R. Oliveira, D. B. Barbosa, M. Henriques, "Silver colloidal nanoparticles: antifungal effect against adhered cells and biofilms of Candida albicans and Candida glabrata ," Biofouling , vol. 27, no. 7, pp. 711-719, 2011.
[22] B. Pergolese, M. Muniz-Miranda, A. Bigotto, "Surface-enhanced Raman scattering investigation of the adsorption of 2-mercaptobenzoxazole on smooth copper surfaces doped with silver colloidal nanoparticles," Journal of Physical Chemistry B , vol. 110, no. 18, pp. 9241-9245, 2006.
[23] M. H. Shams, S. M. A. Salehi, A. Ghasemi, "Electromagnetic wave absorption characteristics of Mg-Ti substituted Ba-hexaferrite," Materials Letters , vol. 62, no. 10-11, pp. 1731-1733, 2008.
[24] B. Khodashenas, H. R. Ghorbani, "Synthesis of copper nanoparticles: an overview of the various methods," Korean Journal of Chemical Engineering , vol. 31, no. 7, pp. 1105-1109, 2014.
[25] A. Umer, S. Naveed, N. Ramzan, M. S. Rafique, "Selection of a suitable method for the synthesis of Copper Nanoparticles," Nano , vol. 7, no. 5, 2012.
[26] H. J. Im, E. C. Jung, "Colloidal nanoparticles produced from Cu metal in water by laser ablation and their agglomeration," Radiation Physics and Chemistry , vol. 118, pp. 6-10, 2016.
[27] P. Sanderson, J. M. Delgado-Saborit, R. M. Harrison, "A review of chemical and physical characterisation of atmospheric metallic nanoparticles," Atmospheric Environment , vol. 94, pp. 353-365, 2014.
[28] S. Kojima, Y. Ichino, Y. Yoshida, "Improvement of upper critical field in YBa2 Cu3Oy films by substituting 3d metal for CU sites using combinatorial pulsed-laser deposition," Physics Procedia , vol. 58, pp. 58-61, 2014.
[29] Y. A. Kotov, "Electric explosion of wires as a method for preparation of nanopowders," Journal of Nanoparticle Research , vol. 5, no. 5-6, pp. 539-550, 2003.
[30] A. Subhan, T. Ahmed, R. Awal, R. Makioka, H. Nakata, T. T. Pakkanen, M. Suvanto, B. M. Kim, "Synthesis, structure, luminescence and photophysical properties of nano CuO·ZnO·ZnAl2 O4 multi metal oxide," Journal of Luminescence , vol. 146, pp. 123-127, 2014.
[31] X. Song, S. Sun, W. Zhang, Z. Yin, "A method for the synthesis of spherical copper nanoparticles in the organic phase," Journal of Colloid and Interface Science , vol. 273, no. 2, pp. 463-469, 2004.
[32] S. Kapoor, T. Mukherjee, "Photochemical formation of copper nanoparticles in poly(N -vinylpyrrolidone)," Chemical Physics Letters , vol. 370, no. 1-2, pp. 83-87, 2003.
[33] C. M. Liu, L. Guo, H. B. Xu, Z. Y. Wu, J. Weber, "Seed-mediated growth and properties of copper nanoparticles, nanoparticle 1D arrays and nanorods," Microelectronic Engineering , vol. 66, no. 1-4, pp. 107-114, 2003.
[34] S. Charan, N. Singh, P. K. Khanna, K. R. Patil, "Direct synthesis of nanocrystalline silver from the reaction between silver carboxylates and n-trioctylphosphine," Journal of Nanoscience and Nanotechnology , vol. 6, no. 7, pp. 2095-2102, 2006.
[35] I. Lisiecki, F. Billoudet, M. P. Pileni, "Control of the shape and the size of copper metallic particles," Journal of Physical Chemistry , vol. 100, no. 10, pp. 4160-4166, 1996.
[36] N. Zhang, X. Zhu, "Zhang and Zhu reply," Physical Review Letters , vol. 101, no. 9, 2008.
[37] M. Nasrollahzadeh, S. Mohammad Sajadi, "Green synthesis of copper nanoparticles using Ginkgo biloba L. leaf extract and their catalytic activity for the Huisgen [3+2] cycloaddition of azides and alkynes at room temperature," Journal of Colloid and Interface Science , vol. 457, pp. 141-147, 2015.
[38] H. R. Ghorbani, "Chemical synthesis of copper nanoparticles," Oriental Journal of Chemistry , vol. 30, no. 2, pp. 15-18, 2014.
[39] M. H. Mahdieh, B. Fattahi, "Effects of water depth and laser pulse numbers on size properties of colloidal nanoparticles prepared by nanosecond pulsed laser ablation in liquid," Optics & Laser Technology , vol. 75, pp. 188-196, 2015.
[40] M. Raja, J. Shuba, F. B. Ali, S. H. Ryu, "Synthesis of copper nanoparticles by electroreduction process," Materials and Manufacturing Processes , vol. 23, no. 8, pp. 782-785, 2008.
[41] P. V. Quintana-Ramirez, M. C. Arenas-Arrocena, J. Santos-Cruz, M. Vega-Gonzalez, O. Martinez-Alvarez, V. M. Castaño-Meneses, L. S. Acosta-Torres, J. de la Fuente-Hernandez, "Growth evolution and phase transition from chalcocite to digenite in nanocrystalline copper sulfide: morphological, optical and electrical properties," Beilstein Journal of Nanotechnology , vol. 5, no. 1, pp. 1542-1552, 2014.
[42] P. Kanhed, S. Birla, S. Gaikwad, A. Gade, A. B. Seabra, O. Rubilar, N. Duran, M. Rai, "In vitro antifungal efficacy of copper nanoparticles against selected crop pathogenic fungi," Materials Letters , vol. 115, pp. 13-17, 2014.
[43] S. Komarneni, H. Katsuki, "Nanophase materials by a novel microwave-hydrothermal process," Pure and Applied Chemistry , vol. 74, no. 9, pp. 1537-1543, 2002.
[44] V. V. Namboodiri, R. S. Varma, "Microwave-accelerated Suzuki cross-coupling reaction in polyethylene glycol (PEG)," Green Chemistry , vol. 3, no. 3, pp. 146-148, 2001.
[45] M. Blosi, S. Albonetti, M. Dondi, C. Martelli, G. Baldi, "Microwave-assisted polyol synthesis of Cu nanoparticles," Journal of Nanoparticle Research , vol. 13, no. 1, pp. 127-138, 2011.
[46] J. R. Morones, J. L. Elechiguerra, A. Camacho, K. Holt, J. B. Kouri, J. T. Ramirez, M. J. Yacaman, "The bactericidal effect of silver nanoparticles," Nanotechnology , vol. 16, no. 10, pp. 2346-2353, 2005.
[47] A. M. Raspolli Galletti, C. Antonetti, M. Marracci, F. Piccinelli, B. Tellini, "Novel microwave-synthesis of Cu nanoparticles in the absence of any stabilizing agent and their antibacterial and antistatic applications," Applied Surface Science , vol. 280, pp. 610-618, 2013.
[48] T. Hirai, Y. Tsubaki, H. Sato, I. Komasawa, "Mechanism of formation of lead sulfide ultrafine particles in reverse micellar systems," Journal of Chemical Engineering of Japan , vol. 28, no. 4, pp. 468-473, 1995.
[49] A.-M. L. Jackelen, M. Jungbauer, G. N. Glavee, "Nanoscale materials synthesis. 1. Solvent effects on hydridoborate reduction of copper ions," Langmuir , vol. 15, no. 7, pp. 2322-2326, 1999.
[50] C. Capatina, "The study of copper ruby glass (SnO, CuO phase diagram)," Ceramics-Silikaty , vol. 49, no. 4, pp. 283-386, 2005.
[51] S. Shankar, J. W. Rhim, "Effect of copper salts and reducing agents on characteristics and antimicrobial activity of copper nanoparticles," Materials Letters , vol. 132, pp. 307-311, 2014.
[52] H. Khalil, D. Mahajan, M. Rafailovich, M. Gelfer, K. Pandya, "Synthesis of zerovalent nanophase metal particles stabilized with poly(ethylene glycol)," Langmuir , vol. 20, no. 16, pp. 6896-6903, 2004.
[53] Y. G. Guo, J. S. Hu, L. J. Wan, "Nanostructured materials for electrochemical energy conversion and storage devices," Advanced Materials , vol. 20, no. 15, pp. 2878-2887, 2008.
[54] G. Gouadec, P. Colomban, "Raman Spectroscopy of nanomaterials: how spectra relate to disorder, particle size and mechanical properties," Progress in Crystal Growth and Characterization of Materials , vol. 53, no. 1, pp. 1-56, 2007.
[55] G. R. Patzke, Y. Zhou, R. Kontic, F. Conrad, "Oxide nanomaterials: synthetic developments, mechanistic studies, and technological innovations," Angewandte Chemie-International Edition , vol. 50, no. 4, pp. 826-859, 2011.
[56] J. Conde, J. T. Dias, V. Grazú, M. Moros, P. V. Baptista, J. M. de la Fuente, "Revisiting 30 years of biofunctionalization and surface chemistry of inorganic nanoparticles for nanomedicine," Frontiers in Chemistry , vol. 2, article 48, 2014.
[57] X. Fu, S. Qutubuddin, "Polymer-clay nanocomposites: exfoliation of organophilic montmorillonite nanolayers in polystyrene," Polymer , vol. 42, no. 2, pp. 807-813, 2001.
[58] H. R. Dennis, D. L. Hunter, D. Chang, S. Kim, J. L. White, J. W. Cho, D. R. Paul, "Effect of melt processing conditions on the extent of exfoliation in organoclay-based nanocomposites," Polymer , vol. 42, no. 23, pp. 9513-9522, 2001.
[59] I. Sondi, B. Salopek-Sondi, "Silver nanoparticles as antimicrobial agent: a case study on E. coli as a model for Gram-negative bacteria," Journal of Colloid and Interface Science , vol. 275, no. 1, pp. 177-182, 2004.
[60] M. Gaber, Y. S. El-Sayed, K. El-Baradie, R. M. Fahmy, "Cu(II) complexes of monobasic bi- or tridentate (NO, NNO) azo dye ligands: synthesis, characterization, and interaction with Cu-nanoparticles," Journal of Molecular Structure , vol. 1032, pp. 185-194, 2013.
[61] A. Thit, H. Selck, H. F. Bjerregaard, "Toxicity of CuO nanoparticles and Cu ions to tight epithelial cells from xenopus laevis (A6): effects on proliferation, cell cycle progression and cell death," Toxicology in Vitro , vol. 27, no. 5, pp. 1596-1601, 2013.
[62] J. Verran, G. Sandoval, N. S. Allen, M. Edge, J. Stratton, "Variables affecting the antibacterial properties of nano and pigmentary titania particles in suspension," Dyes and Pigments , vol. 73, no. 3, pp. 298-304, 2007.
[63] N. Cioffi, L. Torsi, N. Ditaranto, G. Tantillo, L. Ghibelli, L. Sabbatini, T. Bleve-Zacheo, M. D'Alessio, P. G. Zambonin, E. Traversa, "Copper nanoparticle/polymer composites with antifungal and bacteriostatic properties," Chemistry of Materials , vol. 17, no. 21, pp. 5255-5262, 2005.
[64] R. P. Allaker, G. Ren, "Potential impact of nanotechnology on the control of infectious diseases," Transactions of the Royal Society of Tropical Medicine and Hygiene , vol. 102, no. 1, pp. 1-2, 2008.
[65] K. D. Karlin, "Metalloenzymes, structural motifs, and inorganic models," Science , vol. 261, no. 5122, pp. 701-708, 1993.
[66] G. Grass, C. Rensing, M. Solioz, "Metallic copper as an antimicrobial surface," Applied and Environmental Microbiology , vol. 77, no. 5, pp. 1541-1547, 2011.
[67] L. Macomber, J. A. Imlay, "The iron-sulfur clusters of dehydratases are primary intracellular targets of copper toxicity," Proceedings of the National Academy of Sciences of the United States of America , vol. 106, no. 20, pp. 8344-8349, 2009.
[68] L. J. Wheeldon, T. Worthington, P. A. Lambert, A. C. Hilton, C. J. Lowden, T. S. J. Elliott, "Antimicrobial efficacy of copper surfaces against spores and vegetative cells of Clostridium difficile : the germination theory," Journal of Antimicrobial Chemotherapy , vol. 62, no. 3, pp. 522-525, 2008.
[69] K. Y. Yoon, J. Hoon Byeon, J.-H. Park, J. Hwang, "Susceptibility constants of Escherichia coli and Bacillus subtilis to silver and copper nanoparticles," Science of the Total Environment , vol. 373, no. 2-3, pp. 572-575, 2007.
[70] S. Mehtar, I. Wiid, S. D. Todorov, "The antimicrobial activity of copper and copper alloys against nosocomial pathogens and Mycobacterium tuberculosis isolated from healthcare facilities in the Western Cape: an in-vitro study," The Journal of Hospital Infection , vol. 68, no. 1, pp. 45-51, 2008.
[71] H. L. Karlsson, M. S. Toprak, B. Fadeel Handbook on the Toxicology of Metals , Elsevier, 2015.
[72] G. Steindl, S. Heuberger, B. Springer Antimicrobial Effect of Copper on Multidrug-Resistant Bacteria , vol. 99, Austrian Agency for Health and Food Safety (AGES), Graz, Austria, 2012.
[73] M. Souli, I. Galani, D. Plachouras, T. Panagea, A. Armaganidis, G. Petrikkos, H. Giamarellou, "Antimicrobial activity of copper surfaces against carbapenemase-producing contemporary Gram-negative clinical isolates," Journal of Antimicrobial Chemotherapy , vol. 68, no. 4, pp. 852-857, 2013.
[74] N. M. Zain, A. G. F. Stapley, G. Shama, "Green synthesis of silver and copper nanoparticles using ascorbic acid and chitosan for antimicrobial applications," Carbohydrate Polymers , vol. 112, pp. 195-202, 2014.
[75] C. E. Santo, D. Quaranta, G. Grass, "Antimicrobial metallic copper surfaces kill Staphylococcus haemolyticus via membrane damage," MicrobiologyOpen , vol. 1, no. 1, pp. 46-52, 2012.
[76] G. Ren, D. Hu, E. W. C. Cheng, M. A. Vargas-Reus, P. Reip, R. P. Allaker, "Characterisation of copper oxide nanoparticles for antimicrobial applications," International Journal of Antimicrobial Agents , vol. 33, no. 6, pp. 587-590, 2009.
[77] D. A. Tadesse, S. Zhao, E. Tong, S. Ayers, A. Singh, M. J. Bartholomew, P. F. McDermott, "Antimicrobial drug resistance in Escherichia coli from humans and food animals, United States, 1950-2002," Emerging Infectious Diseases , vol. 18, no. 5, pp. 741-749, 2012.
[78] M. Valodkar, S. Modi, A. Pal, S. Thakore, "Synthesis and anti-bacterial activity of Cu, Ag and Cu-Ag alloy nanoparticles: a green approach," Materials Research Bulletin , vol. 46, no. 3, pp. 384-389, 2011.
[79] L. Argueta-Figueroa, R. J. Scougall-Vilchis, R. A. Morales-Luckie, O. F. Olea-Mejia, "An evaluation of the antibacterial properties and shear bond strength of copper nanoparticles as a nanofiller in orthodontic adhesive," Australian Orthodontic Journal , vol. 31, no. 1, pp. 42-48, 2015.
[80] A. K. Chatterjee, R. K. Sarkar, A. P. Chattopadhyay, P. Aich, R. Chakraborty, T. Basu, "A simple robust method for synthesis of metallic copper nanoparticles of high antibacterial potency against E. coli ," Nanotechnology , vol. 23, no. 8, 2012.
[81] O. V. Salata, "Applications of nanoparticle in biology and medicine," Journal of Nanobiotechnology , vol. 2, no. 3, pp. 1-6, 2004.
[82] M. E. T. Molares, E. M. Höhberger, C. Schaeflein, R. H. Blick, R. Neumann, C. Trautmann, "Electrical characterization of electrochemically grown single copper nanowires," Applied Physics Letters , vol. 82, no. 13, pp. 2139-2141, 2003.
[83] B. K. Park, S. Jeong, D. Kim, J. Moon, S. Lim, J. S. Kim, "Synthesis and size control of monodisperse copper nanoparticles by polyol method," Journal of Colloid and Interface Science , vol. 311, no. 2, pp. 417-424, 2007.
[84] E. E. Said-Galiev, A. I. Gamzazade, T. E. Grigor'ev, A. R. Khokhlov, N. P. Bakuleva, I. G. Lyutova, E. V. Shtykova, K. A. Dembo, V. V. Volkov, "Synthesis of Ag and Cu-chitosan metal-polymer nanocomposites in supercritical carbon dioxide medium and study of their structure and antimicrobial activity," Nanotechnologies in Russia , vol. 6, no. 5, pp. 341-352, 2011.
[85] N. V. Suramwar, S. R. Thakare, N. T. Khaty, "One pot synthesis of copper nanoparticles at room temperature and its catalytic activity," Arabian Journal of Chemistry , 2012.
[86] G. Schmid Nanoparticles: From Theory to Application , 2004.
[87] R. Serna, C. N. Afonso, J. M. Ballesteros, A. Naudon, D. Babonneau, A. K. Petford-Long, "Size, shape anisotropy, and distribution of Cu nanocrystals prepared by pulsed laser deposition," Applied Surface Science , vol. 138-139, no. 1-4, pp. 1-5, 1999.
[88] C. N. R. Rao, A. K. Cheetham, "Science and technology of nanomaterials: current status and future prospects," Journal of Materials Chemistry , vol. 11, no. 12, pp. 2887-2894, 2001.
[89] K. S. Suslick, S.-B. Choe, A. A. Cichowlas, M. W. Grinstaff, "Sonochemical synthesis of amorphous iron," Nature , vol. 353, no. 6343, pp. 414-416, 1991.
[90] K. S. Suslick, T. Hyeon, M. Fang, J. T. Ries, A. A. Cichowlas, "Sonochemical synthesis of nanophase metals, alloys and carbides," Materials Science Forum , vol. 225-227, no. 2, pp. 903-912, 1996.
[91] V. Hornebecq, Y. Mastai, M. Antonietti, S. Polarz, "Redox behavior of nanostructured molybdenum oxide-mesoporous silica hybrid materials," Chemistry of Materials , vol. 15, no. 19, pp. 3586-3593, 2003.
[92] D. Basset, P. Matteazzi, F. Miani, "Designing a high energy ball-mill for synthesis of nanophase materials in large quantities," Materials Science and Engineering: A , vol. 168, no. 2, pp. 149-152, 1993.
[93] S. Jadhav, S. Gaikwad, M. Nimse, A. Rajbhoj, "Copper oxide nanoparticles: synthesis, characterization and their antibacterial activity," Journal of Cluster Science , vol. 22, no. 2, pp. 121-129, 2011.
[94] J. Li, Q. Fang, L. Zhang, Y. Liu, "The effect of rough surface on nanoscale high speed grinding by a molecular dynamics simulation," Computational Materials Science , vol. 98, pp. 252-262, 2015.
[95] R. S. Varma, V. V. Namboodiri, "An expeditious solvent-free route to ionic liquids using microwaves," Chemical Communications , no. 7, pp. 643-644, 2001.
[96] M. Komarneni, A. Sand, J. Goering, U. Burghaus, "Adsorption kinetics of methanol in carbon nanotubes revisited-solvent effects and pitfalls in ultra-high vacuum surface science experiments," Chemical Physics Letters , vol. 473, no. 1-3, pp. 131-134, 2009.
[97] C. S. Xavier, C. A. Paskocimas, F. V. da Motta, V. D. Araújo, M. J. Aragon, J. L. Tirado, P. Lavela, E. Longo, M. R. B. Delmonte, "Microwave-assisted hydrothermal synthesis of magnetite nanoparticles with potential use as anode in lithium ion batteries," Materials Research , vol. 17, no. 4, pp. 1065-1070, 2014.
[98] I. Calinescu, D. Martin, D. Ighigeanu, A. I. Gavrila, A. Trifan, M. Patrascu, C. Munteanu, A. Diacon, E. Manaila, G. Craciun, "Nanoparticles synthesis by electron beam radiolysis," Central European Journal of Chemistry , vol. 12, no. 7, pp. 774-781, 2014.
[99] M. Valodkar, P. S. Rathore, R. N. Jadeja, M. Thounaojam, R. V. Devkar, S. Thakore, "Cytotoxicity evaluation and antimicrobial studies of starch capped water soluble copper nanoparticles," Journal of Hazardous Materials , vol. 201-202, pp. 244-249, 2012.
[100] M. B. De Castro, B. S. Mitchell Synthesis Functionalization and Surface Treatment of Nanoparticles , American Scientific Publishers, 2002.
[101] M. B. De Castro Synthesis Functionalization and Surface Treatment of Nanoparticles , American Scientific Publishers, 2002.
[102] U. Bogdanovic, V. Lazic, V. Vodnik, M. Budimir, Z. Markovic, S. Dimitrijevic, "Copper nanoparticles with high antimicrobial activity," Materials Letters , vol. 128, pp. 75-78, 2014.
[103] M. A. Vargas-Reus, K. Memarzadeh, J. Huang, G. G. Ren, R. P. Allaker, "Antimicrobial activity of nanoparticulate metal oxides against peri-implantitis pathogens," International Journal of Antimicrobial Agents , vol. 40, no. 2, pp. 135-139, 2012.
[104] J. Ramyadevi, K. Jeyasubramanian, A. Marikani, G. Rajakumar, A. A. Rahuman, "Synthesis and antimicrobial activity of copper nanoparticles," Materials Letters , vol. 71, pp. 114-116, 2012.
[105] M. N. K. Chowdhury, M. D. H. Beg, M. R. Khan, M. F. Mina, "Synthesis of copper nanoparticles and their antimicrobial performances in natural fibres," Materials Letters , vol. 98, pp. 26-29, 2013.
[106] H. H. Kart, H. Yildirim, S. Ozdemir Kart, T. Çagin, "Physical properties of Cu nanoparticles: a molecular dynamics study," Materials Chemistry and Physics , vol. 147, no. 1-2, pp. 204-212, 2014.
[107] E. Giorgetti, P. Marsili, P. Canton, M. Muniz-Miranda, S. Caporali, F. Giammanco, "Cu/Ag-based bifunctional nanoparticles obtained by one-pot laser-assisted galvanic replacement," Journal of Nanoparticle Research , vol. 15, no. 1, article 1360, 2013.
[108] S. Krishnan, A. S. M. A. Haseeb, M. R. Johan, "Synthesis and growth kinetics of spindly CuO nanocrystals via pulsed wire explosion in liquid medium," Journal of Nanoparticle Research , vol. 15, article 1410, 2013.
[109] Y. Hatakeyama, T. Morita, S. Takahashi, K. Onishi, K. Nishikawa, "Synthesis of gold nanoparticles in liquid polyethylene glycol by sputter deposition and temperature effects on their size and shape," The Journal of Physical Chemistry C , vol. 115, no. 8, pp. 3279-3285, 2011.
[110] L. P. Ding, Y. Fang, "The study of resonance Raman scattering spectrum on the surface of Cu nanoparticles with ultraviolet excitation and density functional theory," Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy , vol. 67, no. 3-4, pp. 767-771, 2007.
[111] T. Kruk, K. Szczepanowicz, J. Stefanska, R. P. Socha, P. Warszynski, "Synthesis and antimicrobial activity of monodisperse copper nanoparticles," Colloids and Surfaces B: Biointerfaces , vol. 128, pp. 17-22, 2015.
[112] T. D. Pham, B.-K. Lee, "Disinfection of Staphylococcus aureus in indoor aerosols using Cu-TiO2 deposited on glass fiber under visible light irradiation," Journal of Photochemistry and Photobiology A: Chemistry , vol. 307-308, pp. 16-22, 2015.
[113] D. Chudobova, S. Dostalova, B. Ruttkay-Nedecky, R. Guran, M. A. M. Rodrigo, K. Tmejova, S. Krizkova, O. Zitka, V. Adam, R. Kizek, "The effect of metal ions on Staphylococcus aureus revealed by biochemical and mass spectrometric analyses," Microbiological Research , vol. 170, pp. 147-156, 2015.
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Abstract
Nanosized metal particles show specific physical and chemical properties that allow the creation of new composites materials, which are important for multiple applications in biology and medicine such as infections control. Metal nanoparticles, mainly copper, exhibit excellent inhibitory effect on Gram-positive and Gram-negative bacteria; therefore the exploration about the efficient, economical, and friendly environmental technics to synthesize inorganic nanoparticles is imperative. In this work a brief overview of the several methods is made including the comparison of the methods, mainly between sonochemical, microwave, and chemical routes. It allows determining the optimal parameters and technical conditions to synthesize copper nanoparticles with physical and chemical properties suitable for the oral bacterial inhibition.
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