Buscar en
Journal of Applied Research and Technology. JART
Toda la web
Inicio Journal of Applied Research and Technology. JART 2-Imino-(3,4-dimethoxybenzyl) ethanesulfonic acid Schiff base anchored silver na...
Journal Information
Vol. 14. Issue 1.
Pages 38-46 (February 2016)
Download PDF
More article options
Vol. 14. Issue 1.
Pages 38-46 (February 2016)
Open Access
2-Imino-(3,4-dimethoxybenzyl) ethanesulfonic acid Schiff base anchored silver nanocomplex mediated by sugarcane juice and their antibacterial activities
Elias Emeka Elemikea,
Corresponding author

Corresponding author.
, Enock Olugbenga Dareb,c, Inyang David Samuela, Jude Chinedu Onwukab
a Department of Chemistry, Federal University of Petroleum Resources Effurun, Nigeria
b Department of Chemistry, Federal University Lafia, Nigeria
c Department of Chemistry, Federal University of Agriculture Abeokuta, Nigeria
Article information
Full Text
Download PDF
Figures (8)
Show moreShow less
Tables (1)
Table 1. Antibacterial results of the synthesized ligand and nanocompounds.

In this present investigation, 2-imino-(3,4-dimethoxybenzyl)ethane sulphonic acid was anchored on a silver nanoparticle mediated by sugarcane sap. The Schiff base was synthesized from 2-aminoethanesulphonic acid and 3,4-dimethoxybenzaldehyde under lemon juice catalyzed conditions while the nanoparticles were obtained by careful stirring of sugarcane sap and 1mM AgNO3 in the ratio of 1:10 respectively at room temperature. The resulting nanocomplex was formed by gentle heating and stirring of the silver nanoparticles solution and the ligand at a temperature of about 80°C for 3h. The ligand, nanoparticles and nanocomplex were characterized using UV–vis spectrophotometer, scanning electron microscope, FT-IR and XRD machines. From the UV–vis results, surface plasmon bands (SPBs) were observed at 475nm for the nanoparticle within 1h of the reaction and 450nm for the nanocomplex. The ligand exhibited absorption bands at 310nm, 280nm and 230nm which are due to π-electron transitions within the chromophores. The strikingly broad nature of the SPBs especially in the nanoparticles revealed that the particles are kinetically favored, nucleate easily and are polydispersed and the blue shift observed in the nanocomplex suggested further reduction in the particle size therefore giving us a clue on how to tailor the products by tuning the raw materials. From the scanning electron micrographs, the morphologies and growth mechanisms revealed oriented attachment for the nanoparticles onwards digestive ripening for the nanocomplex. All the synthesized materials proved to be potential antibacterial agents as they showed great inhibition to the growth of some bacterial strains with the activity enhanced in the nanocomplex.

Surface plasmon bands
Schiff base
Full Text

Green nanotechnology is expanding its frontier in the world of science and technology and has been termed “the miracle of science” by some researchers as it continues to provide solutions and alternatives to technological, environmental, energy and health challenges (Mata, Palmer, Tejeda-Montes, & Stupp, 2012). Nanostructures are the matter of interest for all applications of Nanotechnology wherein shape and size of the nanoparticles (NPs) determine their characteristic properties. Due to the growing demand for various nanoparticles, it is necessary to develop synthetic routes that are cost-effective and environment-friendly. The majority of the existing procedures used for nanoparticle synthesis rely upon physical and chemical methods which could introduce toxic and hazardous materials into the system (Ai, Biazar, & Jafarpour, 2011; Mukherjee, Roy, & Mandal, 2008) Moreover, the specific requirement for size and shape of nanoparticles cannot be met with the physico-chemical methods. Thus, biological methods involving microorganisms or plant extracts have shown to be more effective but in this recent research, there is a drift from the already known biological substrates to a new option which is plant sap. The integration of the principles of green chemistry to nanotechnology as regards to size manipulation of the nanoparticles is an unprecedented technique (Maryam, Niloofar, Ahmad, Fatemeh, & Sassan, 2012).

Nanocomplexes of Schiff bases on the other hand are among the least areas of research in nanoscience that may hold great pharmaceutical applications. In our present world where new disease causing organisms such as Avian influenza, HIV/AIDS, Middle East respiratory syndrome (MERS), Ebola virus, etc., are discovered on daily basis, some being so tiny, posing difficulties in their disease treatment. It is reasonable to tackle these nano cum micro disease causing organisms with effective complex tools at nanoscale.

Kaushik in 2012, utilized grape juice to synthesis silver nanoparticles using different concentrations of the silver nitrate in the dark and at room temperature (Kaushik, 2013). In his work, the SPB was noticed at 450nm and the particle size of the nanoparticles was 18–20nm. According to his reports, the nanoparticles exhibited high antimicrobial activities.

This present research focuses on using specific bio-molecules present in plant sap (sugarcane juice) as substrate to synthesize nanoparticles while anchoring it with Schiff base ligand to form a silver nanocomplex. The limitation of green silver nanoparticles and its antimicrobial activities vis-a-vis the strategies to improve the production of green antimicrobial drugs have also been discussed but not much information are available on nanocomplexes with Schiff base ligand. The development of nano-metal complexes by biological method is yet to be explored by researchers and on that note; it becomes a paramount objective in this study.

Moreover, in present times, clothing, respirators, household water filters, contraceptives, antibacterial sprays, cosmetics, detergent, dietary supplements, cell phones, laptop keyboards, and children's toys are among the products being marketed that purportedly exploit the antimicrobial properties of silver nanomaterials (Mohammad, Niloofar, & Marjan, 2013). Apart from capitalizing on the antimicrobial potentials of the nano-form of silver, the focus upon the green methods of synthesis is of primary interest so as to counter the physiological and environmental peril associated with the use of chemicals for the fabrication and use of silver nanomaterials (Geoprincy, Vidhya Srii, Poonguzhali, Gandhi, & Renganathan, 2013). Synthesis of green silver nanoparticles using plant extracts is a very simple and cost-effective way that satisfies the demand of the research community and simultaneously eliminates the possibility of environmental hazards; the plant sap seems to offer better opportunities though the results of this research will guide us appropriately. Our major aim therefore is to biologically synthesis silver nanoparticles using sugarcane juice while anchoring it with a Schiff base ligand.

The silver nanoparticles is synthesized using sugarcane sap while the ligand is a reaction between 3,4-dimethoxybenzaldehyde and 2-aminoethanesulfonic acid employing lemon juice as a green-catalytic approach.

2Materials and methods2.1Synthesis of silver nanoparticles using sugarcane (Saccharum officinarum) juice

Fresh sugarcanes (Sa. officinarum) were collected from Okoripere village in Delta State, washed, peeled and chopped into smaller parts. It was further blended and filtered using Whatman filter paper and the filtrate used for the nanoparticle synthesis.

1000ml of 1mM AgNO3 was mixed with 100ml of surgarcane juice and stirred with a mechanical shaker at room temperature for 5h.

The colorless sample was noticed to turn into light wine-red and the color intensified with time as shown in Figure 1. At different times; 0h, 1h, 2h, and 5h while stirring the solution at room temperature, they were sampled and analyzed using UV–vis spectrophotometer (Elemike et al., 2014; Sepideh, Seyedeh, Seyed, & Soheila, 2012). It was observed that the surface plasmon band appeared at 475nm after 1h of reaction, showing the formation of silver nanoparticles and the spectra shown in Figure 2b.

Figure 1.

Color change of the silver nanoparticles at different times.

Figure 2.

UV–vis spectra of (a) Schiff base ligand, (b) silver nanoparticles and (c) silver nanocomplex.

2.2Preparation of 2-imino-(3,4-dimethoxybenzyl)ethanesulfonic acid Schiff base

In a 50ml Erlenmeyer flask, 0.01mole (1.710g) 3,4-dimethoxybenzaldehyde and 0.01mole (1.255g) 2-aminoethanesulfonic acid was reacted in a 30ml of deionised water/15ml ethanol media mixture. Three drops of lemon juice was added as catalyst. The reacting mixture was stirred while heating at about 70°C for 3h (Ugwu & Okoro, 2014). Light brown solution was observed, filtered and was left to stand for 2 days and crystals formed thereafter. The presence of the lemon juice catalyzed the reaction as without it, the solution could not crystallize for some days under observation (Scheme 1).

Scheme 1.

Proposed structure of the Schiff base ligand.

2.3Preparation of nano-silver complex mediated by the Schiff base

Synthesis of the silver nanocomplex was done by anchoring the ligand as prepared above on the synthesized silver nanoparticles (Sujarania, Sironmani, & Ramu, 2012).

The ligand in a 30:15ml water–ethanol ratio respectively was mixed with 10ml of the aqueous silver nanoparticles solution prepared using sugarcane juice and little quantity of lemon juice added as catalyst. The entire solution was gently stirred for an hour at room temperature. Afterwards, it was left to stand for 2 days and the resultant light brown crystals were dried and characterized.

2.4Instrumental characterization

The absorption spectrum of the materials was measured on a T-60 UV–vis spectrophotometer and the spectra shown in Figure 2a–c. The phase identity and crystalline size of the nanoparticles and nanocomplex were characterized by X-ray diffractometer and the representative plot shown in Figure 4. Morphological features were studied by using Hitachi-7000 scanning electron microscope (SEM), and the functional groups and possible bioreductants determined by the 8500S Fourier transform infra-red spectrophotometer.

Figure 3.

FTIR spectra of (a) Schiff base ligand, (b) sugarcane mediated silver nanoparticles and (c) silver nanocomplex.

Figure 4.

Representative XRD plot of the Ag nanocomplex.

2.5Antibacterial analysis

The synthesized ligand, nanoparticles and nanocomplex were screened against some clinical bacteria isolates obtained from Standard Diagnostics Laboratory Effurun using Agar well dilution method. Bacterial cultures were prepared and different concentrations of the test samples and the control drug (Ciprofloxacin) were equally prepared up to a minimum concentration of 20μg/ml using standard methods (Nelson et al., 2007; Prabakaran, Subha, Thennarasu, & Merinal, 2012). The growth of the microorganisms was monitored and the results are shown in Table 1 and Figure 5.

Table 1.

Antibacterial results of the synthesized ligand and nanocompounds.

Isolates  40μg/ml20μg/ml
  Control  Ligand  Silver nanoparticles  Nanocomplex  Control  Ligand  Silver nanoparticles  Nanocomplex 
Staphylococcus aureus  - -  - -  - -  - -  - - 
Staphylococcus aubeus  - -  - -  - -  - -  - - 
Escherichia coli  - -  - -  - -  - -  - - 
Figure 5.

Scanning electron micrographs of silver nanoparticles (a, b) and nanocomplex (c, d) in different magnifications.

3Results and discussion

The substrate or biomolecules used for synthesis of nanoparticles play very important role in the surface reactions, size and morphology of nanoparticles. As is well known, biomolecules can carry on slow kinetics to self-reduce metal precursors and develop stable coating layers to avoid particle aggregation (Renquan, Dapeng, Daxiang, Zhongyang, & Lin, 2012).

3.1Uv–vis spectra analysis

From Figure 1, it is seen that the color started changing gradually to wine-red and this was confirmed by surface plasmon bands displayed by the nanoparticles within 1h of the reaction at a wavelength of about 475nm. This wavelength persisted even at the subsequent periods of sampling showing that the substrate (sugarcane juice) acts as both reducing and stabilizing agent as shown in Figure 2b.

The major component of sugarcane juice that has caused the bio-reduction of Ag+ to Ag0 is glucose and other components such as proteins, minerals etc. which are in minor quantities. Sucrose is the major component of cane juice but may not have affected the reduction since it is not a reducing agent. In fact, the same molecular mechanisms that give antioxidant properties to these molecules must have promoted the reduction of Ag+ ions to Ag atoms. The exact mechanism of the extracellular biosynthesis of metal nanoparticle is not well understood. However, two possible mechanisms have been hypothesized. These are; hydrogen abstraction, due to the OH groups in the sucrose molecules and redox reaction of nicotinamide adenine dinucleotide (NADH) coenzyme which works as an electron shuttle to neutralize Ag+ ion (Labrenz et al., 2000; Roh et al., 2001; Swarnalatha, Christina, Shruti, & Payas, 2012). For the formation of silver nanoparticles, the sample changed its visual appearance within 1h after addition of the extract, indicating that a reduction reaction took place. Initially, the reacting mixture was slightly brownish liquid; as the reaction proceeded, the solution became deep wine-red showing the strong absorption of visible light due to excitation of the nanoparticle surface plasmons (Amendola, Bakr, & Stellacd, 2010; Ericka et al., 2012; Hartland, 2011; Kwon, Lee, Wark, & Lee, 2012; Ray, 2010). Figure 2b shows that the SPBs was formed within 1h and stabilized even after the 5thhour of sampling. The sugarcane extract did not give bands within the range of 400–500nm which is a clear evidence that it is not nanoparticles. The surface plasmon absorption in the nanoparticles is due to the collective oscillation of the free conduction band electrons which is excited by the incident electromagnetic radiation. This type of resonance is seen when the wavelength of the incident light far exceeds the particle diameter (Naika et al., 2015).

The nature of the broad band shows that the nanoparticles are polydisperse and have greater distribution of particle size (Hale, Maddox, Shapter, & Voelcker, 2005). Moreover, the constant nature of the bands in the subsequent reaction times proves the stable nature of the nanoparticles formed thereby reassuring the substrate as a good bio-reducing and stabilizing agent.

In the case of the Schiff base ligand, absorption bands were observed at 310nm, 280nm and 230nm which could be attributed to the chromophores in the ligand.

In Figure 2c, the spectra of the nanocomplex showed a broad peak with a maximum absorption at 450nm. The blue shift in the surface plasmon bands as compared to Figure 2b is an indication of smaller colloids equally supported by the broader peak which also indicates a greater distribution of the particle size.

3.2FTIR spectra

Figure 3a–c shows the FTIR spectra of 2-imino-(3,4-dimethoxybenzyl) ethanesulfonic acid Schiff base, silver nanoparticles and nanocomplex. The absence of spikes above 3300cm−1 in Figure 3a show that the primary amine has formed an imine in the ligand and cannot be absorbed within that frequency range (Wade, 2006). The weak absorption around 3442cm−1 could be attributed to some water molecules. The strong absorption peaks at 2939 and 2841cm−1 for the ligand and 2357cm−1 for the nanocomplex indicates the CH stretching vibrations. The imine (CN) functional group absorbed strongly at 1679cm−1 for the ligand and at 1678cm−1 for the nanocomplex. The presence of the benzene ring conjugated to imine group in both the ligand and nanocomplex were noticed at 1589 and 1590cm−1 respectively (Okoli, Adewuyi, Zhang, Diagboya, & Guo, 2014). The striking feature of SO3H group was shown by the absorptions at 1259cm−1 and 1256cm−1 for the ligand and nanocomplex respectively. The CO stretching vibrations which is characteristic of ether groups were observed at 1018, 1135cm−1 for the ligand and 1025, 1133cm−1 for the nanocomplex. The strong absorption at 360cm−1 in the nanocomplex which is absent in the Schiff base ligand is a strong indication of presence of silver metal. Figure 3b which shows the spectra of the silver nanoparticles has weak absorptions at 3386cm−1 which indicates OH molecules. The other absorptions at 1650cm−1 and 1041cm−1 are attributed to CO bonds probably due to glucose molecules while the band at 386cm−1 represents the silver metal (Morrison & Boyd, 2002).

3.3Powder X-ray diffraction analysis

The XRD diffraction pattern of dry nanosilver powder in Figure 4 shows a crystalline nanocomplex of about 15nm with the peaks suggesting high purity of the compound. The other observed peak and noise were probably related to the effect of nanosized particles and the presence of various crystalline biological macromolecules in the sugarcane sap. The obtained results illustrate that silver ions had indeed been reduced to Ag by the sap and ligand under reaction conditions (Forough & Farhadi, 2010; Rajesh, Raja, Rathi, & Sahayaraj, 2012). The nanoparticles showed higher particle sizes of about 25–30nm.

3.4Scanning electron microscopy (SEM) analysis

The SEM showed interesting morphologies both for the sugarcane nanoparticles and the nanocomplex as shown in Figure 5a–d. Figure 5a showed an intermediate morphology between cube and cone that may have potential applications as molecular grippers in nanomedicine.

Based on the micrographs and supporting UV–vis spectra, the early stages of growth of the nanoparticles could be seen to follow the oriented attachment (OA) since the nanocrystallites grow on the already existing nanocubes followed by surface crystallization and a phase transformation to an intermediate cube–cone nanostructures as shown in Figure 5a.

The OA mechanism has attracted preponderant interests due to its fundamental role in designing and exploring materials with size and morphology controllability (Zhang, Huang, & Lin, 2010). Peculiar structures and morphologies displayed by the nanosystems are due to reduction in surface energy and coherent crystallographic orientation which provides a route for the incorporation of defects like stacking faults, twins and misorientation.

The anchoring of ligand on the nanocubes and cones seems to affect the crystal growth kinetics of the system thereby giving rise to the small spherical nanoparticles exhibited by the nanocomplex as shown in Figure 5c and d. The introduction of the organic ligand which has unstable surface adsorption property could be destroyed or desorbed in the hydrothermal medium. Evidently, the appearance of the small spherical particles in the nanocomplex indicates that the mass transportation was incessant. There was further crystallization which extended inwards at the expense of the ligand nutrients creating large interior space and surface area (Greer, 2014). This could equally be supported by the UV–vis spectra shown in Figure 2a and c where there was a blue shift from 475nm in the nanoparticles to 450nm in the nanocomplex. It would be expected that the Ostwald ripening should have set in since the ligand molecules may not be able to penetrate into the core region of the nanosystems but based on the evidence from the results, digestive ripening which is the inverse of Ostwald ripening could be suggested as the growth mechanisms (Greer, 2014). The process of formation is controlled by the surface energy of the particle within solution where the larger particles redissolve and the smaller ones grow (Nguyen, Maclean, & Mahiddine, 2014). Moreso, the diffusion of the ligands along the surface of the nanosystems could have changed the shape of the particle. This situation occurs under specific conditions where the energy of the ligands within the solution is probably low, forming a gap between the shell and the core particle (Yanjun et al., 2012).

3.5Growth kinetics; oriented attachment onwards digestive ripening

The type of kinetics displayed by the sugarcane nanoparticles based on the spectral and micrograph evidence is a typical oriented attachment. Moreover, this experimental result is in consonance with the theoretical as well as other experimental studies which suggest that growth of nanoparticles can be greatly influenced by surface reactions thereby proceeding from a diffusion controlled mechanism onwards to oriented attachment (Dare et al., 2015). It could be suggested that the surface adsorption of the capping organic molecules (such as sucrose) present in the sugarcane sap, which was not involved in bioreduction could have been purely responsible for the exclusive OA growth as shown in Scheme 2. According to Penn, OA mechanism is due to the degree of electrostatic interactions such as the Vander waal forces which consequently determines the kinetic rate constant (Penn & Banfield, 2004). While Ribeiro, Lee, Longo, and Leite, 2005, considers the diffusion and coagulation of the colloids thereby suggesting that the viscosity of the medium played a significant role in the OA mechanism, which is governed by an inverse proportional relationship with respect to the rate constant. In the above-mentioned models, only primary particles are assumed to combine to give secondary particles and the reaction stops; but experimentally, the OA mechanism has proven that growth behavior can go beyond collision and reaction of molecules. The nanocrystals may be capped with easily destroyed and desorbed organic ligands with the coalescence of some multilevel particle being neglected. This mechanism can be likened to the classical Smoluchowski equation which is a limiting case of aggregation that involves monomer–monomer and monomer–multimer reactions neglecting the multimer–multimer reactions.

Scheme 2.

Schematic diagram of possible reaction pathway and growth mechanism of the nanoparticles and nanocomplex.


The incorporation of organic ligands into the nanoparticle medium seems to arrest the OA growth process and introduces the digestive ripening. The polydisperse nanocrystal lattices emanating from the initial sugarcane mediated system was modified upon refluxing with ligand molecules leading to digestive ripening and nucleating the colloid at the phase boundary (Yijun, Deepa, Christopher, & Kenneth, 2013). Unlike the well-known Ostwald ripening in which large particles grow at the expense of small particles, this process narrows the distribution by sharing material among different sizes of particles until a thermodynamically stable size segregation can further select the specific particle size (Lin, Sorensen, & Klabunde, 2000). Many works have been reported on the stabilization of nanoparticles suggesting that control may be due to thermodynamics other than the kinetics of nucleation and crystal growth (Chikan & Kelley, 2002). In this work, the nanoparticle size resulted from a combination of the ligand–silver binding energy and the surface free energy of the particles to reach the minimum energy of the whole system. The ligand–silver binding energy favors smaller particles with larger surface areas, while the surface free energy favors larger particles with smaller surface curvature. Therefore, these two effects oppose each other and led to a minimum energy with a thermodynamically favored size for each silver–ligand colloid system.

From the results, we could draw a conclusion that iminosulphonic acid does play a significant role as a capping ligand in stabilizing the nanocomplex and giving smaller particle sizes.

3.6Antibacterial evaluation of the ligand, Ag NPs and the nanocomplex

The ligand, silver nanoparticles and the nanocomplex were screened against Escherichia coli, Staphylococcus auerus and S. aubeus bacterial strains and the results are presented in Table 1. Using Agar well dilution method, the ligand, Ag Nps and nanocomplex showed significant antibacterial activity on all the three bacterial strains. Nano-silver inside bacterial cells disrupts the biochemical processes by binding with DNA molecules which leads to disordering of the helical structure by cross-linking within and between the nucleic acid strands (Kim, Cho, Ryu, & Choi, 2000). Indirect effects through changes in the surrounding charge environment also have an impact on the effectiveness of nanoparticulate metals against microorganisms (Stohs & Bagchi, 1995). Moreover, the silver released from the nanoparticles get attached to the negatively charged bacterial cell wall, rupturing it thereby leading to protein denaturation and finally causes cell death (Sondi & Sondi, 2004). It is evident from Table 1 and Figure 6, that the growth of the three bacterial strains was severely inhibited by the nanocomplex than the ligands and nanoparticles.

Figure 6.

Aqeous solution of the synthesized ligand, nanoparticles and nanocomplex with the microbes.


From the research work, we have synthesized a Schiff base derived from 3,4-dimethoxybenzaldehyde and 2-aminoethanesulfonic acid and its silver nanocomplex. The formation of the nanocomplex, the ligand and the silver nanoparticles were analyzed using UV–vis spectrophotometer, FTIR, XRD and SEM. The ligand introduced digestive ripening on the nanoparticles framework thereby establishing stable spherical structures with high surface area and mechanical strength. The ligand with typical imine sulphonic acid group act as useful capping and stabilizing agent for silver nanoparticles while the refluxing close to the boiling point of water effected good digestive ripening. The antibacterial activities results shows that the nanocomplex has enhanced antibacterial properties on E. coli, S. aureus and S. aubeus than its parents Schiff base and nanoparticles. The greater efficacy of the nanocomplex is positively modified upon coordination of the ligand with the nano-silver metal. The established structure in this research therefore acts as self sacrificial templates to fabricate other structural nanosystems with enhanced functionalities. There is scarce information on the synthesis of silver nanocomplex. The results of this study have furnished us with some information but we need more analysis and further research to establish the unfolding success believed to be associated with this emerging bionanoparticulate inorganic system.

Conflict of interest

The authors have no conflicts of interest to declare. All authors participated in this research and have endorsed the publication of this work.


The authors wish to thank the Vice chancellor, Federal University of Petroleum Resources Effurun, Prof Akii Ibhadode for the excellent drive toward research. Mr Bawa Hamza and other technologists in the department of chemistry FUPRE are also greatly acknowledged in this work for their immense contribution toward the antibacterial analysis.

[Ai et al., 2011]
J. Ai, E. Biazar, M. Jafarpour.
Nanotoxicology and nanoparticle safety in biomedical designs.
International Journal of Nanomedicine, 6 (2011), pp. 1117-1127
[Amendola et al., 2010]
V. Amendola, O.M. Bakr, F. Stellacd.
A study of the surface plasmon resonance of silver nanoparticles by the discrete dipole approximation method: Effect of shape, size, structure, and assemble.
Plasmonics, 5 (2010), pp. 85-97
[Chikan and Kelley, 2002]
V. Chikan, D.F. Kelley.
Size dependent spectroscopy of MoS2 nanoclusters.
Journal of Physical Chemistry B, 106 (2002), pp. 3794-3804
[Dare et al., 2015]
E.O. Dare, C.O. Oseghale, A.H. Labulo, E.T. Adesuji, E.E. Elemike, J.C. Onwuka, et al.
Green synthesis and growth kinetics of nanosilver under bio-diversified plant extracts influence.
Journal of Nanostructure in Chemistry, 5 (2015), pp. 85-94
[Elemike et al., 2014]
E.E. Elemike, C.O. Oseghale, A. Chuku, A.H. Labulo, M.C. Owoseni, R. Mfon, et al.
Evaluation of antibacterial activities of silver nanoparticles green-synthesized using pineapple leaf.
[Ericka et al., 2012]
R. Ericka, I. Ramon, N. Rosa, H. Ronaldo, T. Judith, I. Claudia, et al.
Synthesis of silver nanoparticles using reducing agents obtained from natural sources (Rumex hymenosepalus extracts).
Springer Open Journal, 3 (2012), pp. 1-5
[Forough and Farhadi, 2010]
M. Forough, K. Farhadi.
Biological and green synthesis of silver nanoparticles.
Turkish Journal of Engineering and Environmental Sciences, 34 (2010), pp. 281-287
[Geoprincy et al., 2013]
G. Geoprincy, B.N. Vidhya Srii, U. Poonguzhali, N.N. Gandhi, S. Renganathan.
A review on green synthesis of silver nanoparticles.
Asian Journal of Pharmaceutical and Clinical Research, 6 (2013), pp. 8-12
[Greer, 2014]
H.F. Greer.
Non classical crystal growth of inorganic and organic materials.
Material Science and Technology, 30 (2014), pp. 611-625
[Hale et al., 2005]
P.S. Hale, L.M. Maddox, J.G. Shapter, N.H. Voelcker.
Growth kinetics and modeling of ZnO nanoparticles.
Journal of Chemical Education, 82 (2005), pp. 775-778
[Hartland, 2011]
G.V. Hartland.
Optical studies of dynamics in noble metal nanostructures.
Chemical Reviews, 111 (2011), pp. 3858-3887
[Kaushik, 2013]
R. Kaushik.
Green synthesis of silver nanoparticles by using grape fruit extract: Characterization of the particles & study of antibacterial activity.
Research Journal of Pharmaceutical, Biological and Chemical Sciences, 4 (2013), pp. 1271-1276
[Kim et al., 2000]
J.H. Kim, H. Cho, S. Ryu, M. Choi.
Effects of metal ions on the activity of protein tyrosine phosphatase VHR: Highly potent and reversible oxidative inactivation by Cu2+ ion.
Archives of Biochemistry and Biophysics, 382 (2000), pp. 72-80
[Kwon et al., 2012]
M.J. Kwon, J. Lee, A.W. Wark, H.J. Lee.
Nanoparticle-enhanced surface plasmon resonance detection of proteins at molar concentrations: Comparing different nanoparticle shape and sizes.
Analytical Chemistry, 84 (2012), pp. 1702-1707
[Labrenz et al., 2000]
M. Labrenz, G.K. Druschel, E.T. Thomsen, B. Gilbert, S.A. Welch, K.M. Kemner.
Formation of sphalerite (ZnS) deposits in natural biofilms of sulfate-reducing bacteria.
Science Journal, 1 (2000), pp. 744-747
[Lin et al., 2000]
X.M. Lin, C.M. Sorensen, K.J. Klabunde.
Digestive ripening, nanophase segregation and superlattice formation in gold nanocrystal colloids.
Journal of Nanoparticle Research, 2 (2000), pp. 157-164
[Maryam et al., 2012]
M. Maryam, R. Niloofar, R.S. Ahmad, N. Fatemeh, R. Sassan.
Extracellular production of silver nanoparticles by using three common species of dermatophytes: Trichophyton rubrum, Trichophyton mentagrophytes and Microsporum canis.
Iranian Biomedical Journal, 16 (2012), pp. 52-58
[Mata et al., 2012]
A. Mata, L. Palmer, E. Tejeda-Montes, S. Stupp.
Design of biomolecules for nanoengineered biomaterials for regenerative medicine.
Methods in Molecular Biology, 811 (2012), pp. 39-49
[Mohammad et al., 2013]
M. Mohammad, Y. Niloofar, M. Marjan.
Antibacterial properties of nanosilver finish cellulose fabric.
Journal of Nanostructure in Chemistry, 3 (2013), pp. 43
[Morrison and Boyd, 2002]
R.T. Morrison, R.N. Boyd.
Organic chemistry.
6th ed., Prentice and Hall India, (2002), pp. 590-592
[Mukherjee et al., 2008]
P. Mukherjee, M. Roy, B.P. Mandal.
Green synthesis of highly stabilized nanocrystalline silver particles by a non-pathogenic and agriculturally important fungus T. asperellum.
Nanotechnology, 19 (2008), pp. 075103-075110
[Naika et al., 2015]
H.R. Naika, K. Lingaraju, K. Manjunath, K. Danith, G. Nagaraju, D. Suresh, et al.
Green synthesis of CuO nanoparticles using Gloriosa superba L. extract and their antibacterial activity.
Journal of Talibah University of Science, 9 (2015), pp. 7-12
[Nelson et al., 2007]
D. Nelson, D. Priscyla, Marcato, I.H.D. Gabriel, L.A. Oswaldo, E. Elisa.
Antibacterial effect of silver nanoparticles produced by fungal process on textile fabrics and their effluent treatment.
Journal of Biomedical Nanotechnology, 3 (2007), pp. 203-208
[Nguyen et al., 2014]
T.K.T. Nguyen, N. Maclean, S. Mahiddine.
Mechanisms of nucleation and growth of nanoparticles in solution.
Chemical Reviews, 114 (2014), pp. 7610-7630
[Okoli et al., 2014]
P.C. Okoli, G.O. Adewuyi, Q. Zhang, P.N. Diagboya, Q. Guo.
Mechanism of diakyl phthalates removal from aqeous solution using γ-cyclodextrin and starchbased polyurethane polymer adsorbents.
Carbohydrates Polymers, 114 (2014), pp. 440-449
[Penn and Banfield, 2004]
R.L. Penn, J.F. Banfield.
Kinetics of orientated aggregation.
Journal of Physical Chemistry B, 108 (2004), pp. 12707-12712
[Prabakaran et al., 2012]
M. Prabakaran, K. Subha, V. Thennarasu, S. Merinal.
Biosynthesis of silver nanoparticles using Sphaerulina albispiculata and evaluation of antibacterial activity.
European Journal of Experimental Biology, 2 (2012), pp. 297-303
[Rajesh et al., 2012]
R. Rajesh, D.P. Raja, J.M. Rathi, K. Sahayaraj.
Biosynthesis of silver nanoparticles using Ulva fasciata (Delile) ethyl acetate extract and its activity against Xanthomonas campestris pv. Malvacearum.
Journal of Biopesticides, 5 (2012), pp. 119-128
[Ray, 2010]
P.C. Ray.
Size and shape dependent second order nonlinear optical properties of nanomaterials and their application in biological and chemical sensing.
Chemical Reviews, 110 (2010), pp. 5332-5365
[Renquan et al., 2012]
L. Renquan, Y. Dapeng, C. Daxiang, W. Zhongyang, G. Lin.
Egg white mediated green synthesis of silver nanoparticles with excellent biocompatibility and enhanced radiation effects on cancer cells.
International Journal of Nanomedicine, 7 (2012), pp. 2101-2107
[Ribeiro et al., 2005]
C. Ribeiro, E.J.H. Lee, E. Longo, E.R. Leite.
A kinetic model to describe the nanocrystal growth by the oriented attachment mechanism.
ChemPhysChem, 6 (2005), pp. 690-695
[Roh et al., 2001]
Y. Roh, J. Bai, R.J. Lauf, A.D. Mcmillan, T.J. Phelps, C.J. Rawn.
Microbial synthesis of metal-substituted magnetites.
Solid State Communications, 11 (2001), pp. 529-534
[Sepideh et al., 2012]
H. Sepideh, M.G. Seyedeh, A.S. Seyed, S. Soheila.
Comparative study of silver nanoparticles produced by green methods.
Iranian Journal of Biotechnology, 10 (2012), pp. 191-197
[Sondi and Sondi, 2004]
I. Sondi, B.S. 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, 275 (2004), pp. 177-182
[Stohs and Bagchi, 1995]
J. Stohs, D. Bagchi.
Oxidative mechanisms in the toxicity of metal ions.
Free Radical Biology and Medicine, 18 (1995), pp. 321-336
[Sujarania et al., 2012]
S. Sujarania, T.A. Sironmani, A. Ramu.
Synthesis, characterization and toxicity studies of Schiff bases [2-(2,2-diphenylethylimino)methyl)phenols] anchored silver nanoparticles.
Digest Journal of Nanomaterials and Biostructures, 7 (2012), pp. 1843-1857
[Swarnalatha et al., 2012]
L. Swarnalatha, R. Christina, R. Shruti, B. Payas.
Evaluation of in-vitro antidiabetic activity of Sphaeranthus amaranthoides silver nanoparticles.
International Journal of Nanomaterials and Biostructures, 2 (2012), pp. 25-29
[Ugwu and Okoro, 2014]
D.I. Ugwu, U.C. Okoro.
Synthesis, characterization and antifungal activities of [4-methylphenylsulphonamido]-N-(pyridin-2-yl)acetamide derivatives.
Medicinal Chemistry, 4 (2014), pp. 330-333
[Wade, 2006]
L.G. Wade.
Organic chemistry.
6th ed., Prentice and Hall, (2006), pp. 523-532
[Yanjun et al., 2012]
F. Yanjun, X. Zhenbo, Y. Fengjiao, S. Jian, W. Yewu, Z. Wuzong.
Formation mechanism of hollow microspheres consisting of ZnO nanosheets.
CrystEngComm, 14 (2012), pp. 8615-8619
[Yijun et al., 2013]
S. Yijun, J. Deepa, S. Christopher, J.K. Kenneth.
Alkyl and aromatic amines as digestive ripening/size focusing agents for gold nanoparticles.
Nanomaterials, 3 (2013), pp. 370-392
[Zhang et al., 2010]
J. Zhang, F. Huang, Z. Lin.
Progress of nanocrystalline growth kinetics based on oriented attachment.
Nanoscale, 2 (2010), pp. 18-34

Peer Review under the responsibility of Universidad Nacional Autónoma de México.

Article options