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Article

Eco-Friendly Synthesis and Antimicrobial Activity of Silver Nanoparticles Using Dracocephalum moldavica Seed Extract

by
Zahra Haghighi Pak
1,
Hossein Abbaspour
1,*,
Naser Karimi
2,* and
Ali Fattahi
3
1
Department of Biology, Damghan Branch, Islamic Azad University, Damghan 36716-39998, Iran
2
Laboratory of Plant Physiology, Department of Biology, Faculty of Science, Razi University, Kermanshah 67149-67346, Iran
3
Department of Pharmaceutics, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah 67346-67149, Iran
*
Authors to whom correspondence should be addressed.
Appl. Sci. 2016, 6(3), 69; https://doi.org/10.3390/app6030069
Submission received: 13 October 2015 / Revised: 23 January 2016 / Accepted: 28 January 2016 / Published: 2 March 2016
(This article belongs to the Section Nanotechnology and Applied Nanosciences)
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Abstract

:
This paper reports a novel green approach for the synthesis of silver nanoparticles (AgNPs) using aqueous seed extract of Dracocephalum moldavica (L.) under ambient conditions. Processes such as Ultraviolet-visible (UV-vis) spectrometer, field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray analysis (EDX), and transmission electron microscopy (TEM) were carry out to characterize AgNPs. The presence of AgNPs in the prepared solution was approved by a peak to occur at 443 nm. XRD pattern indicated the crystalline structure of the nanoparticles (NPs) while the FTIR spectra confirm the attendance of plant residues adsorbed by these NPs. TEM images revealed a near spherical shape of these NPs, and EDX provided the expected elemental composition. The synthesized AgNPs showed excellent antimicrobial activities against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Serratia marcescens, Staphylococcus epidermidis and Bacillus subtilis.

1. Introduction

The synthesis of nanoparticles (NPs) has become a matter of great interest due to their different beneficial properties and applications in a variety of fields [1,2,3]. Several approaches have been proposed to generate metallic NPs, including electro-chemical, sonochemical, and photochemical processes; however, most of these methods suffer from the utilization of toxic, hazardous chemicals, and difficulty in purification [4,5,6].
Green chemistry synthesis of NPs has recently received wide spread attention among physical and chemical synthesis processes for its emergence as a simple, speedy synthesis, inexpensive, eco-friendly, and size-controlling approach in the synthesis of metal NPs (MNPs) [3]. As a result of its growing popularity, there is an increased need to produce MNPs using biological systems such as bacteria [7], fungi [8], yeast [9], and plant extracts [3,10,11] as reducing and stabilizing agents. The latter synthetic procedure exemplifies a green approach. NPs produced by angiosperms, especially those medicinal in nature, are more stable, display a more speedy synthesis in the case of micro-organisms, reveal greater variation in shape and size and contain important reducing agents in comparison to those produced by other organisms [12,13].
Silver (Ag) has long been known to exhibit a strong antimicrobial, catalysis, and surface-enhanced Raman scattering; therefore, Ag-based compounds have been used extensively in numerous bactericidal applications [3,14]. Since antibiotic resistance to the microorganisms become more common, and a continued preoccupation with health care expenses, researchers have tried to develop new resistance-free, cost-effective antimicrobial reagents [3]. The antimicrobial potential of Ag-based NPs has led to their incorporation in consumer, health-related, and industrial products [3,15]. Moreover, due to its potential application to biological functions such as cancer therapy and imaging, AgNP biosynthesis has recently attracted considerable attention of researchers interested in the field [11,14,15].
Although AgNP synthesis has already been reported in various plant seed extracts such as Medicago sativa [16], Artocarpus heterophyllus [17], Jatropha curcas [18], Strychnos potatorum [19], Foeniculum vulgare [20], Silybum marianum [21], and Syzygium cumini [22], the field continues to receive attention due to the variety and high prospective of plants for producing NPs with different characteristics [11]. Additionally, the plant-based extracts of antioxidant-laden leaves, seeds, fruits, roots, and stems have been considered for use in the synthesis of AgNPs [10,23].
Originating from south Siberia and the Himalayan mountains, dragonhead (Dracocephalum moldavica L.) is a perennial, herbaceous plant belonging to the Lamiaceae family [1,2]. Recent pharmacological studies have confirmed antioxidant, antiseptic, antibacterial, and carminative properties of the plant’s essential oil [1], and the areal parts of D. moldavica are applied in traditional West Azerbaijani (Iranian) medicine for general diuretic, digestive, sedative, and antiemetic uses [2].
Terpenoids are believed to take part in the reduction of Ag ions and the stabilization of following NPs [6]; therefore, we used D. moldavica seed extract as a reducing and stabilizing agent in the synthesis of AgNPs, with the intention of exploring its medicinal properties. As there appears to be no report concerning the synthesis of NPs using D. moldavica seed extract to date, the present study was designed to phytosynthesize AgNPs using D. moldavica seed extract, and to subsequently investigate the antimicrobial activities of synthesized NPs.

2. Materials and Methods

2.1. Collection of Seeds

D. moldavica seeds were purchased from the Pakan Bazr Company in Isfahan, Iran. The seeds were first rinsed with water three times, and then cleansed with Milli-Q water to remove the fine dust particles, and finally air dried for1 week to remove all moisture completely.

2.2. Preparation of Aqueous D. Moldavica Seed Extract, and Synthesis of AgNPs

Twenty grams of D. moldavica seeds were finely stirred with 200 mL of deionized water at 85 °C for 15 min until no foreign material remained. The seed extract was then filtered through filter paper, and the filtrate was then kept at 4 °C for further experimentation regarding use of the extract as a reducing and stabilizing agent. Remaining extract must be used within three days of the filtration process.
The synthesis of AgNPs involved different applications of seed extracts which were dried and then optimized to 1 mL. One milliliter of the extract was added to 100 mL of the previously concocted silver nitrate (AgNO3) solution, shakes and exposed to sunlight irradiation conditions for the reducing Ag+ to Ag0. The solution including AgNPs was centrifuged at 10,000 rpm for 15 min, after which the re-dispersion of the pellet in the Milli-Q water to remove any unbound biological molecules. Purified pellets were then placed onto glass Petri dishes and incubated for 24 h at 60 °C for drying. The color change of AgNO3 solution turned from colorless to brown, indicating the creation of AgNPs. Dried AgNPs were scraped out for the further study [11].

2.3. Characterization of Silver NPs

Nanoparticles are generally characterized by their size, shape, surface area, and dispersity [24,25]. The usual techniques which used to characterizing NPs are as follow: Ultraviolet-visible spectroscopy, FSEM, TEM, FTIR and XRD [11]. For the purposes of this study, synthesized AgNPs were characterized using UV-visible spectroscopy. The biologically reduced brown color solution mixture was recorded as a function of the reaction time on a Shimadzu Lambda UV mini-1240 instrument (from 250 to 800 nm) operating at a resolution of 1 nm [11]. The reaction mixture of seed extracts and AgNPs was subjected to centrifugation at 8000× g for 15 min, and, according to the aforementioned process, the resulting pellet was washed three times with deionized water and filtered. An aliquot of this filtrate was used for FTIR, XRD, FESEM and TEM analysis [26].
Detection of possible biomolecules absorbed on the synthesized AgNPs involved FTIR analysis, which was recorded by its scanning in the range 350–4000 cm−1 at a resolution of 4 cm−1 in potassium bromide pellets [13]. For XRD studies, synthesized AgNPs were coated on an XRD grid, and the spectra were recorded using an Italian APD 2000 X-ray generator operating at a voltage of 40 kV and a current of 30 mA with Cu K−1 radiation. The surface morphology and size distribution of AgNPs were characterized using JEOL JSM 6700F (FE-SEM) and Transmission Electron Microscopy (TEM) measurements from a TECHNA I10-Philphs instrument. The purity and elemental composition of the AgNPs were analyzed using a RONTEC EDX-spectroscopy system model Quan Tax 200, Germany.

2.4. In-Vitro Antimicrobial Activity

Antibacterial activity of AgNPs was assayed against different Gram-positive and Gram-negative pathogenic bacteria such as Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Serratia marcescens, Staphylococcus epidermidis and Bacillus subtilis by using the agar well diffusion technique [27]. In this technique, bacterial cultures were inoculated on nutrient agar containing various contents of constituents. After solidification of the medium, cotton swabs were placed on the surface and holes were punch with the bacterial suspensions. Synthezied AgNPs were included into the wells created in the plates, and the D. moldavica seed extract was used as a control. The samples were incubated for 24 h at a 37 °C temperature. If a zone of inhibition was observed around the well after the incubation period, then a positive result was concluded. Tests were performed in triplicate, and mean values of zone diameter were recorded.
A minimum inhibitory concentration (MIC) test was conducted with the synthesized AgNPs. Various concentrations of seed extract-synthesized AgNPs were prepared with dimethyl sulphoxide (DMSO) in roughly 0.5 mL increments, and subsequently mixed with 50 µL of 24 h-old individual bacterial pathogens. Each mixture was incubated at 37 °C for 48 h, and the visible turbidity was observed in each concentration in order to calculate MIC [28].

3. Results and Discussion

Photochemicals from D. moldavica seed extract can be used as both reducing and capping agents to synthesize AgNPs. Figure 1 shows the D. moldavica seeds extract mixed with Ag+ before and after microwave irradiation, respectively [3]. In this study, the colorless AgNO3 solution turned from yellow to brown or from pale yellow to black brown, indicating the formation of AgNPs, indicating the formation of Ag in the solution and excitation of surface plasmons [16].
The formation of man-sized Ag can be confirmed by employing optical absorption spectroscopy. In the present study, the AgNP mixture was transferred in to a cuvette for UV-visible radiation, and the medium absorbance was recorded. Due to surface plasmon resonance (SPR) phenomena, resonant peak occurs at a variety of wavelengths for various NPs mixture and, according to the theory of resonance maximum wavelength, is absorbed at resonant wavelengths [6,24]. The previous studies suggest that a usual AgNP shows SPR patterns at wavelengths in the range of 400–480 nm. Figure 2 shows that SPR for the prepared mixture occurred at a wavelength of 443 nm, confirming the presence of AgNPs. SPR pattern of metallic nanoparticles depend on the stabilizing molecule, shape and size of particles present in the medium or upon inner particle distance and surrounding media [24,29,30].
Figure 3 presents an absorbance vs. 2θ graph depicting XRD patterns of synthesized AgNPs. Three diffraction peaks as (111), (200), (220), and (311) were observed in the 2 h range of 30–80, indicated expressions of face centered cubic (fcc) structure metallic Ag, respectively. These observations reveal that synthesized AgNPs consist of pure crystalline Ag [3,31,32]. Similar XRD pattern reports were observed in the Eclipta prostrate, Tribulus terrestris, and Prosopis juliflora extracts for synthesized AgNPs [13,30,33,34,35,36,37,38].
FTIR analysis was used to identify and characterize probable biomolecules responsible for the reduction and capping of AgNPs achieved from the D. moldavica seed extract [3]. The biologically synthesized AgNPs and the powdered seeds were mixed with the potassium bromide to make a pellet. Figure 4 shows the FTIR spectra of pre-reaction dried D. moldavica seed extract without AgNO3 (control), and the synthesized post-reaction AgNPs, with AgNO3.
Both FTIR spectra show a shift in peaks: 1401–1396 (due to C–C in-ring stretching of aromatic amines), 1650–1616 (due to –C=C– stretching of alkenes, and N–H bend of primary amines), 2928–2912 (corresponding to C–H stretching of alkanes, and O–H stretching of carboxylic acids), and 3352–3386 cm−1 (due to N–H stretching of amines and amides, O–H stretching of alcohols and phenols). In addition, synthesized AgNPs showed strong band, specifically at a peak of 1067 cm−1, related to aliphatic amines (C–N stretching vibration). In brief, FTIR analysis results showed the presence of alcohols, amides, alkanes, carboxyl, and phenols in synthesized AgNPs. A similar trend is observed in the synthesis of AgNPs using Artocarpus heterophyllus Lam. [39] and Abelmoschus esculentus [33] seed extracts.
The size and morphology of synthesized AgNPs were determined by TEM images, as shown in Figure 5. The morphology of AgNPs is almost spherical, and newly formed NPs exhibited high surface areas, an average size of 31 ± 6 nm in the range of 5–50 nm, and monodispersity in terms of particle size. Figure 6 shows the FESEM images and EDX spectra of AgNPs. FSEM micrographs in Figure 6A reveal that aggregates of AgNPs are not indirect contact, indicating stabilization by capping agents. Of medicinal importance, biocapped molecules help to prevent agglomeration of NPs and also enhance antimicrobial activity.
EDX spectra confirmed that Ag is only the major element present in the NPs under study. The insignificant amounts of observed C and O are attributed to the plant biomass attached to the NPs (Figure 6B). Yallapa et al. reported similar results in previous reports for AgNPs by using A. farnesiana plant extracts [37], and Song and Kim and Raghunadan et al. discovered C and O in MNPs obtained using pine, persimmon, magnolia, ginkgo, platanus, and guava extracts [3,40,41].
The antimicrobial and antibiotics resistance of human pathogens made as problematic issue which needs to discover new natural alternates to overcome this problem [42,43]. The antibacterial activity of synthesized AgNPs was tested against six bacteria: S. aureus, S. epidermidis, B. subtilis as Gram positive bacteria, E. coli, P. aeruginosa, and S. marcescens as Gram negative bacteria. The results are presented in Table 1 as the average values of zone of inhibition radii and MIC. Disc diffusion test results indicate that the maximum zone of inhibition against S. marcescens is 19.5 mm, while E. coli requires 17.6 mm and the remaining four bacteria were only fairly susceptible (Table 1). These results support the findings of Ingle et al. [44], which suggest that AgNPs exhibit significant antimicrobial activity against E. coli and multidrug-resistant bacteria.
Table 1 shows the MIC values of AgNPs for different bacteria. S. marcescens (8 µg/mL) was observed as the most sensitive bacteria, followed by E. coli (11 µg/mL), B. subtilis (22 µg/mL), P. aeruginosa (12 µg/mL) and S. epidermidis (25 µg/mL). S. aureus (25 µg/mL) exhibited the highest MIC value, and, as revealed by the same graphic, an evident MIC value trend is associated with Gram negative and Gram positive bacteria. E. coli as Gram negative bacterium showed a maximum zone of inhibition of 13 mm, due in part to the presence of a peptidoglycan layer in Gram positive bacteria. In the presence of this layer, bacteria form a more inflexible construction, leading to difficulty in penetration by AgNPs. Conversely, Gram negative bacteria encounter a cell wall with a thinner peptidoglycan layer, facilitating AgNP penetration [45,46].
Various possible methods of treat for Ag include interaction with (i) different thiol groups of enzymes or peptides; (ii) chloride ions; or (iii) DNA, among others. Observed manifestations include decrease DNA replication efficiency, membrane structural change, and the formation of granules by silver and sulphur [28,46,47,48,49,50].
MIC values for E. coli and S. aureus recorded in this study are higher than those observed by Vertelov et al. (1 µg/mL for E. coli and 5 µg/mL for S. aureus) [51] and lower than those reported by Chudasama et al. (100 µg/mL for E. coli and 350 µg/mL for S. aureus) [28]. This phenomenon can be explained by strain to strain variation, as is the stabilization of AgNPs. The MIC values which detected in this study are much lower than those recorded by commercially prepared antibacterial products. Improved antibacterial activity of AgNPs is due in part to their uniform shape, small size and partial size distribution. An alternate explanation involves high colloidal stability, through which NPs are easily absorbed into the bacterial wall particle-bacterial interaction is enhanced [28,44,50,52].
These results indicate that biosynthesized AgNPs exhibit greater antibacterial activity in comparison to AgNO3 and chemically synthesized AgNPs. Enhanced antibacterial activity may be attributable to the small size and concentration of the biosynthesized NPs and/or the presence of bioactive compound capping. Small AgNPs may be easily diffused or may penetrate a bacterial cell membrane and inhibit its growth by interfering in the natural metabolism processes. Furthermore, plant-based AgNPs production depends on their metabolism. Metabolites, for instance, phenolics, organic acids, and quinones, as well as ascorbates or catechol (as redox system) play important roles in AgNPs formation [25].
Major chemical constituents of aqueous D. moldavica leaf extracts were identified, and included terpenoids, steroids, flavonoids, alkaloids, lignins, phenols, coumarins, and cyanogenic glucosides. These findings indicate that the slightly increased antimicrobial activity of green synthesized AgNPs may be a result of organic content found in D. moldavica seed extracts. A comparison of antimicrobial activity in D. moldavica seed extracts with green synthesized AgNPs (Table 1) confirmed that secondary metabolites play a significant role in capping Ag ions; therefore, despite the low content of synthesized AgNPs as indicated by EDX, secondary metabolites tend to exhibit activity levels that produce effective antibacterial properties at very low concentrations.

4. Conclusions

Resulting in considerably improved AgNPs production due to its ability to control nanostructures, the suggested plant-mediated synthesis method is an inexpensive approach capable of producing AgNPs at room temperature. Through a process of characterizing nanoparticles, the present study demonstrated that AgNPs are capable of rendering high antibacterial results, and therefore show great potential for the preparation of antibacterial drugs. Results confirmed that the D. moldavica is a higher quality eco-friendly and safe source for AgNPs synthesis than conventional chemical or physical methods, and its utility invites further investigation.

Acknowledgments

This research was supported by Damghan branch of Islamic Azad University, Damghan, Iran.

Author contributions

Z.A. performed the experiments and analyzed the data; N.K. conceived and designed the experiment, wrote the protocol, and wrote the first draft of the manuscript; H.A. designed a part of experiments; A.F. performed and analyzed a part of manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Photograph of colloids; (a) Dracocephalum moldavica (L.) seed extract; (b) silver nitrate solution; (c) silver nanoparticle.
Figure 1. Photograph of colloids; (a) Dracocephalum moldavica (L.) seed extract; (b) silver nitrate solution; (c) silver nanoparticle.
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Figure 2. UV–Visible absorption spectrum of silver nanoparticles (AgNPs) solution observed at ~450 nm as a function of Irradiation time.
Figure 2. UV–Visible absorption spectrum of silver nanoparticles (AgNPs) solution observed at ~450 nm as a function of Irradiation time.
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Figure 3. X-ray diffraction (XRD) patterns of synthesized AgNPs.
Figure 3. X-ray diffraction (XRD) patterns of synthesized AgNPs.
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Figure 4. Fourier transform infrared (FTIR) spectra of Dracocephalum moldavica powder before (a) and after (b) reaction.
Figure 4. Fourier transform infrared (FTIR) spectra of Dracocephalum moldavica powder before (a) and after (b) reaction.
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Figure 5. Transmission electron microscopy (TEM) micrograph of AgNPs synthesized from seed aqueous extract N. arvensis with different magnification.
Figure 5. Transmission electron microscopy (TEM) micrograph of AgNPs synthesized from seed aqueous extract N. arvensis with different magnification.
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Figure 6. (A) FSEM images and (B) EDAX results indicating the synthesis of silver NPs and bioactive components of Dracocephalum moldavica.
Figure 6. (A) FSEM images and (B) EDAX results indicating the synthesis of silver NPs and bioactive components of Dracocephalum moldavica.
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Table
Table 1. Antibacterial activity of biosynthesized silver nanoparticles using D. moldavica seed extract.
Table 1. Antibacterial activity of biosynthesized silver nanoparticles using D. moldavica seed extract.
PathogensD. moldavica Seed ExtractSynthesized Silver NanoparticleAgNO3
Disk Diffusion Assay (mm·dia)MIC (µg·mL−1)Disk Diffusion Assay (mm·dia)MIC (µg·mL−1)Disk Diffusion Assay (mm·dia)MIC (µg·mL−1)
Staphylococcus aureus--8.4 ± 0.7629.6 ± 0.0011.6 ± 0.8816 ± 0.00
Staphylococcus epidermidis--11 ± 1.6625 ± 0.009 ± 0.4325 ± 0.00
Bacillus subtilis--10 ± 0.7722 ± 0.0012 ± 1.3216 ± 0.00
E. coli--17.6 ± 0.6611 ± 0.0015.4 ± 1.139 ± 0.00
Serratia marcescens2 ± 0.00-19.5 ± 1.768 ± 0.0017.5 ± 1.386 ± 0.00
Pseudomonas aeruginosa--13.2 ± 1.8712 ± 0.0013.44 ± 1.1212 ± 0.00
Values ± SD indicates the replicates of three experiments.

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Haghighi Pak, Z.; Abbaspour, H.; Karimi, N.; Fattahi, A. Eco-Friendly Synthesis and Antimicrobial Activity of Silver Nanoparticles Using Dracocephalum moldavica Seed Extract. Appl. Sci. 2016, 6, 69. https://doi.org/10.3390/app6030069

AMA Style

Haghighi Pak Z, Abbaspour H, Karimi N, Fattahi A. Eco-Friendly Synthesis and Antimicrobial Activity of Silver Nanoparticles Using Dracocephalum moldavica Seed Extract. Applied Sciences. 2016; 6(3):69. https://doi.org/10.3390/app6030069

Chicago/Turabian Style

Haghighi Pak, Zahra, Hossein Abbaspour, Naser Karimi, and Ali Fattahi. 2016. "Eco-Friendly Synthesis and Antimicrobial Activity of Silver Nanoparticles Using Dracocephalum moldavica Seed Extract" Applied Sciences 6, no. 3: 69. https://doi.org/10.3390/app6030069

APA Style

Haghighi Pak, Z., Abbaspour, H., Karimi, N., & Fattahi, A. (2016). Eco-Friendly Synthesis and Antimicrobial Activity of Silver Nanoparticles Using Dracocephalum moldavica Seed Extract. Applied Sciences, 6(3), 69. https://doi.org/10.3390/app6030069

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