Green Fabrication of Silver Nanoparticles by Gum Tragacanth (<i>Astragalus gummifer</i>): A Dual Functional Reductant and Stabilizer

Kora, Aruna Jyothi; Arunachalam, Jayaraman

doi:https://doi.org/10.1155/2012/869765

Journal of Nanomaterials

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Abstract Introduction Materials and Methods Results and Discussion Conclusion Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2012 | Article ID 869765 | https://doi.org/10.1155/2012/869765

Green Fabrication of Silver Nanoparticles by Gum Tragacanth (Astragalus gummifer): A Dual Functional Reductant and Stabilizer

Aruna Jyothi Kora¹and Jayaraman Arunachalam¹

Academic Editor: Edward Andrew Payzant

Received05 Mar 2012

Accepted13 Apr 2012

Published14 Jun 2012

Abstract

A simple and ecofriendly procedure have been devised for the green synthesis of silver nanoparticles using the aqueous extract of gum tragacanth (Astragalus gummifer), a renewable, nontoxic natural phyto-exudate. The water soluble components in the gum act as reductants and stabilizers. The generated nanoparticles were analyzed using UV-visible spectroscopy, transmission electron microscopy, X-ray diffraction, Fourier transform-infrared spectroscopy, and Raman spectroscopy. The role of gum concentration and reaction time on the synthesis of nanoparticles was studied. By regulating the reaction conditions, spherical nanoparticles of nm size were produced. Also, the possible functional groups involved in reduction and capping of nanoparticles has been elucidated. The antibacterial activity of the fabricated nanoparticles was tested on model Gram-negative and Gram-positive bacterial strains with well-diffusion method. These nanoparticles exhibited considerable antibacterial activity on both the Gram classes of bacteria, implying their potential biomedical applications.

1. Introduction

Gum tragacanth is a naturally occurring complex, acidic polysaccharide derived as an exudate from the bark of Astragalus gummifer (Fabaceae family), a native tree of western Asia. Mostly, it is commercially produced in Iran and Turkey. The name tragacanth is originated from the Greek words tragos (goat) and akantha (thorn), indicating the curved shape of the gum [1]. This biopolymer is an arabinogalactan type of natural gum and its structural, physicochemical, compositional, solution, thermal, rheological and emulsifying properties have been well characterized and studied [2–8].This biopolymer is a high-arabinose, protein containing, acidic heteropolysaccharide, which occurs in nature as mixed calcium, magnesium, and sodium salts. It has a molecular weight of ~8.4 × 10⁵ g/mol. This natural polymer consists of a mixture of water-soluble (tragacanthin) and water-swellable (bassorin) polysaccharide fractions [1, 3]. The water soluble tragacanthin constitutes around 30–40% of the gum, and it is a neutral, highly branched, type II arabinogalactan comprising (1→6)- and (1→3)-linked core chain containing galactose and arabinose and side groups of (1→2)-, (1→3)-, and (1→5)-linked arabinose units occurring as monosaccharide or oligosaccharides. The primary structure of tragacanthin is composed of sugars such as, L-fucose, L-arabinose, D-xylose, D-mannose, D-galactose and D-glucose in a molar ratio of 3: 52: 29: 6: 5: 5 [1, 2].

The gum tragacanth with a CAS number 9000-65-1 is considered as ‘‘generally recognized as safe’’ (GRAS) and approved as a food ingredient (21CFR184.1351) by the Food and Drug Administration, USA under the function of emulsifier, stabilizer, and thickener. It is also approved as a food additive within the class of thickeners, stabilizers, emulsifiers, and gelling agents in European Union and has been accorded with E413, a European food safety E number [1]. It is considered as a food grade additive by the Bureau of Indian Standards, India under Indian Standard IS 7238: 1997 [9]. Several studies have established that gum tragacanth is nontoxic, nonmutagenic, nonteratogenic, noncarcinogenic and has a potential application as a food additive [10–13], dressing bandage for burn healing [14], immobilizing agent in viral plaque assay [15], superabsorbent hydrogel [16] and carrier for controlled release of verapamil hydrochloride, a water-soluble drug [17]. It is also employed as an administration vehicle for insecticide [18], antidepressant [19], and antilipemic agents [20]. In addition, investigations carried out with tragacanth fed rats and white leghorn cockerels have established the hypolipidemic activity of this gum [21, 22]. This hydrocolloid is resistant to gastrointestinal enzymes and known to be degraded enzymatically only by the specific microflora of the colon such as Bifidobacterium longum, thereby aiding in bifidus fermentation [23–25]. Thus, it functions as a soluble dietary fiber, accelerates the digesta passage, and acts as a laxative [26].

The attractive features of gum tragacanth prompted us to use this biopolymer for the synthesis and stabilization of silver nanoparticles due to its (i) nontoxic nature and GRAS; (ii) natural availability; (iii) greater resistance to microbial attacks and long shelf-life [1, 10, 12]. The green synthesis of silver nanoparticles relies on the implementation of the basic requirements of green chemistry [27, 28]. In this perspective, we have devised a simple and green synthetic way for the production of silver nanoparticles using a renewable, biodegradable natural plant polymer, gum tragacanth as both the reducing and stabilizing agent. The synthesis was carried out in an aqueous medium by autoclaving to produce sterile silver nanoparticle, free from microbes. The present study focuses on the production, characterization, capping and stabilization of silver nanoparticles. We have also established the antibacterial activity of the fabricated nanoparticles on Gram-positive and Gram-negative bacteria for their potential biomedical applications.

2. Materials and Methods

2.1. Synthesis of Silver Nanoparticles

Silver nitrate (AgNO₃) (E. Merck, Mumbai, India) of analytical reagent grade was used for the synthesis. “Gum tragacanth,” 99% was purchased from Loba Chemie, Mumbai, India. All the solutions were prepared in ultra pure water. A 0.5% (w/v) of homogenous gum stock solution was prepared by adding this powder to a reagent bottle containing ultra pure water and stirring overnight at room temperature. Then, this solution was centrifuged (5500 × g, 10 min) to remove the insoluble materials, and the supernatant was used for all the experiments. The protein concentration in the aqueous extract was quantified by Lowry’s method using a Bangalore Genei protein estimation kit, Cat number 105560 (Bangalore, India). The silver nanoparticles were synthesized by autoclaving the silver nitrate solutions containing various concentrations of gum extract at 121°C and 15 psi for different durations of time. The effect of concentration of gum and reaction time on nanoparticle synthesis was studied.

2.2. Characterization of Synthesized Silver Nanoparticles

In order to study the formation of silver nanoparticles, the UV-visible absorption spectra of the prepared colloidal solutions were recorded using an Elico SL 196 spectrophotometer (Hyderabad, India), from 250 to 800 nm, against autoclaved gum blank. The absorption spectra of gum before and after autoclaving were also recorded against ultra pure water blank. The size and shape of the nanoparticles were obtained with Hitachi H 7500 (Tokyo, Japan); JEOL 3010 and JEOL 2100 (Tokyo, Japan) coupled to Oxford Instruments Energy Dispersive X-ray (EDX) (High Wycombe, UK) transmission electron microscopes, operating at 80 and 200 kV, respectively. The samples were prepared by depositing a drop of colloidal solution on a carbon-coated copper grid and drying at room temperature. The nanoparticles were recovered from the synthesized solutions by centrifugation and made into powders using a FTS Systems, Dura-DryTM MP freeze dryer (NY, USA). The X-ray diffraction analysis was conducted with a Rigaku, Ultima IV diffractometer (Tokyo, Japan) using monochromatic Cu Kα radiation ( Å) running at 40 kV and 30 mA. The intensity data for the lyophilized nanosilver powder was collected over a 2θ range of 35–85° with a scan rate of 1°/min. The IR spectra of the lyophilized samples were recorded using a Bruker Optics, TENSOR 27 FTIR spectrometer (Ettlingen, Germany); over a spectral range of 400–4000 cm⁻¹. The Raman spectrum of the synthesized nanoparticles was recorded at room temperature using the 532 nm line from a SUWTECH, G-SLM diode laser (Shanghai, China). The scattered light was collected and detected using a CCD-based monochromator, covering a spectral range of 150–1700 cm⁻¹. The sample solution was taken in a standard 1 cm × 1 cm cuvette and placed in the path of the laser beam.

2.3. Antibacterial Assay

The well-diffusion method was used to study the antibacterial activity of the synthesized silver nanoparticles. All the glassware, media, and reagents used were sterilized in an autoclave at 121°C for 20 min. Staphylococcus aureus (ATCC 25923); and Escherichia coli (ATCC 25922), E. coli (ATCC 35218) and Pseudomonas aeruginosa (ATCC 27853) were used as model test strains for Gram-positive and Gram-negative bacteria, respectively. Bacterial suspension was prepared by growing a single colony overnight in nutrient broth and by adjusting the turbidity to 0.5 McFarland standard. Mueller Hinton agar [29] plates were inoculated with this bacterial suspension, and 5 μg of silver nanoparticles were added to the center well with a diameter of 6 mm. The nanoparticles used here were prepared with 0.1% gum solution containing 1 mM AgNO₃, autoclaved for 30 min. Negative control plates were maintained with wells loaded with autoclaved gum. Culture plates loaded with discs of antibiotic, erythromycin (15 μg/disc) were included as positive controls. These plates were incubated at 37°C for 24 h in a bacteriological incubator, and the zone of inhibition (ZOI) was measured by subtracting the well/disc diameter from the total inhibition zone diameter. Three independent experiments were carried out with each bacterial strain.

3. Results and Discussion

3.1. UV-visible Spectroscopy (UV-vis)

The formation of silver nanoparticles was recorded by measuring the absorption spectra of synthesized silver nanoparticles against respective autoclaved gum blanks. The role of gum concentration on the synthesis was studied by autoclaving the different concentrations (0.1–0.5%) of gum solutions containing 1 mM of silver nitrate for 30 min (Figure 1). After autoclaving the silver nitrate containing gum solutions, the appearance of yellow colour in the reaction mixtures was observed. This is a clear indication for the formation of silver nanoparticles by the gum. In the UV-vis spectra strong peaks with maxima around 418–429 nm were observed, which correspond to the typical surface plasmon resonance (SPR) of conducting electrons from the surface of silver nanoparticles. With an increase in gum concentration, there is an enhancement in the nanoparticle synthesis. In addition, the SPR band broadened with a red shift from 418 to 429 nm, indicating an increase in particle size. The synthesis was also evaluated by varying the reaction time (20–60 min), and reduction was studied with 0.1% gum at 1 mM AgNO₃ (Figure 2). It was noticed that the intensity of the absorption increased with time with no significant difference in peak position or shift in SPR (418 nm), signifying a continuous reduction of the silver ions. This also shows the large reduction capability of the gum.

3.2. Transmission Electron Microscopy

Figure 3 shows the TEM images of the silver nanoparticles synthesized with 0.1% gum and 1 mM AgNO₃, autoclaved for 30 min. It was noticed that the nanoparticles are spherical in shape and nearly monodispersed in nature. The size of the particles ranged from 11.4–14.7 nm, and the average particle size obtained from the corresponding diameter distribution was about 13.1 ± 1.0 nm (Figure 3(f)). The selected-area electron diffraction (SAED) pattern depicted in Figure 3(e) exhibits concentric rings with intermittent bright dots, indicating that these nanoparticles are highly crystalline in nature. These rings can be attributed to the diffraction from the (111), (200), (220), and (311) planes of face-centered cubic (fcc) silver. The crystallinity of the synthesized nanoparticles was also supported from the observed clear lattice fringes in high-resolution image (Figure 3(d)). When the concentration of gum was increased from 0.1 to 0.5% at 1 mM AgNO₃ and 30 min of autoclaving, the particle size of the formed nanoparticles increased (Table 1). These nanoparticles are spherical; polydisperse with sizes from 6.0–90.9 nm, and the average particle size was about 24.3 ± 17.9 nm. The increase in average particle size and polydispersity with increase in concentration of the gum was also evident from the broadening and red shift in SPR band of UV-vis spectra (Figure 1). While at 0.1% gum and 1 mM AgNO₃ concentration; with an increase in reaction time from 30 to 60 min the size of the spherical particles ranged from 9.3–48.0 nm. The average particle size was about 28.7 ± 12.4 nm (Table 1). Based on these results, it can be concluded that the particle size of the nanoparticles can be controlled by varying the gum concentration and reaction time.

(a)

(b)

(c)

(d)

(e)

(f)

3.3. X-Ray Diffraction

The XRD technique was used to determine and confirm the crystal structure of silver nanoparticles. There were five well-defined characteristic diffraction peaks at 38.3°, 44.5°, 64.7°, 77.6°, and 81.8° respectively, corresponding to (111), (200), (220), (311), and (222) planes of face-centered cubic (fcc) crystal structure of metallic silver (Figure 4). The interplanar spacing () values (2.348, 2.034, 1.439, 1.229, and 1.176 Å) calculated from the XRD spectrum of silver nanoparticles is in agreement with the standard silver values. Thus, the XRD pattern, further corroborating the highly crystalline nature of nanoparticles observed from SAED pattern and high-resolution TEM image (Figure 3). The lattice constant calculated from this pattern was 4.070 Å, a value which is in agreement with the value reported in literature for silver (JCPDS PDF04-0783). Also, the broadening of the diffraction peaks was observed owing to the effect of nano-sized particles. The intensity of the (111) peak was much higher than the other diffractions. It is important to note that the ratio of the intensity between (200) and (111) peaks is lower than the standard value (0.24 versus 0.4) and also the ratio of (220) and (111) peaks is lower than the standard value (0.15 versus 0.25). These results clearly demonstrate that the (111) lattice plane is the preferred orientation for these silver nanoparticles. These findings are in concurrence with the observations reported by other researchers [30].

3.4. Fourier Transform-Infrared Spectroscopy (FTIR)

The FTIR spectra were recorded for lyophilized gum extract and nanoparticles to detect the functional groups of gum involved in the reduction of silver ions (Figure 5). The major absorbance bands present in the spectrum of gum were at 3435, 2926, 2856, 2150, 1740, 1626, 1429, 1379, 1258, 1153, 1076, and 1040 cm⁻¹, respectively. The broad band observed at 3435 cm⁻¹ could be assigned to stretching vibrations of O–H groups in the gum. The bands at 2926 and 2856 cm⁻¹ correspond to asymmetric and symmetric stretching vibrations of methylene groups, respectively. The broad band at 2150 cm⁻¹ arises from various carbonyl species of the gum. The sharp peak at 1740 cm⁻¹ could be assigned to carbonyl stretching vibrations in aldehydes, ketones and carboxylic acids. The stronger band found at 1626 cm⁻¹ could be assigned to characteristic asymmetrical stretch of carboxylate group. The symmetrical stretch of carboxylate group can be attributed to the bands present at 1429 and 1379 cm⁻¹. The peaks at 1258 and 1153; 1076 and 1040 cm⁻¹ were due to the C–O stretching vibrations of polyols, ether and alcoholic groups, respectively. While, the spectrum of lyophilized nanoparticles showed characteristic absorbance bands at 3435, 2922, 2856, 2071, 1726, 1630, 1452, 1375, 1261, 1163, and 1028 cm⁻¹, respectively. In the IR spectrum of nanoparticles, small (1626 to 1630 cm⁻¹ and 1379 to 1375 cm⁻¹) and large (1429 to 1452 cm⁻¹) shifts in the absorbance peaks with decreased band intensity were observed, suggesting the binding of silver ions with carboxylate groups of the gum [31]. It is pertinent to note that the nanoparticles show a large band shift corresponding to various carbonyl groups (2150 to 2071 and 1740 to 1726 cm⁻¹) in the FTIR spectra. In addition, a shift in the polyols (1258 to 1261 cm⁻¹ and 1153 to 1163 cm⁻¹) and alcoholic groups (1040 to 1028 cm⁻¹) was also observed. This confirms that the reduction of the silver ions is coupled to the oxidation of the hydroxyl and carbonyl groups. Based on these band shifts, it can be inferred that both hydroxyl and carbonyl groups of gum are involved in the synthesis of silver nanoparticles [30].

3.5. Raman Spectroscopy

In order to find out the possible functional groups of capping agents associated in the stabilization of silver nanoparticles, Raman spectrum of the nanoparticles was recorded (Figure 6). The spectrum shows a sharp band at 240 cm⁻¹, attributed to the stretching vibrations of Ag–N [32, 33] and Ag–O bonds [34, 35]. This peak indicates the formation of a chemical bond between silver and amino nitrogen [33]; and silver and carboxylate groups [34, 35] of the gum molecules. It confirms that the gum is bound to the silver nanoparticle surface either through amino or carboxylate group or both [30]. The broad ones at 1365 and 1550 cm⁻¹ correspond to symmetric and asymmetric C=O stretching vibrations of carboxylate group, respectively [33]. The enhancement in the intensity of the CO₂ stretching vibrations suggests the direct binding of the COO⁻ group with the silver surface [34]. The peaks at 1041, 1123, 1165 and 1301 cm⁻¹ ; and 803 and 828 cm⁻¹ come from the C–H in plane bending and out of plane wag, respectively [32] from the saccharide structure of gum. The features at 465 and 496; 637 and 1444 cm⁻¹ assigned, respectively, to the stretching vibrations of (C–N–C), (C–S–C) and phenyl ring [35]. Thus, from the preferential enhancement of these Raman bands; it can be concluded that both amino and carboxylate groups of the gum are involved in the capping of the silver nanoparticles. These results are in concurrence with earlier biosynthesis of silver nanoparticles carried out with fungus Trichoderma asperellum [33] and gum kondagogu [30]. It was reported earlier that the carboxylate groups of glycoprotein of gum Acacia were involved in binding/stabilization of silver nanoparticles [31]. It is known that proteins can bind to nanoparticles either through free amino groups or by electrostatic interaction of negatively charged carboxylate groups [36]. The gum tragacanth is known to contain protein, and the protein content was reported to be in the range of 1.0–3.6% [1]. This observation is further substantiated by the measured protein concentration of 0.93% for the gum extract and the UV-vis absorption spectrum of the 0.5% gum extract against water blank, given in the inset of Figure 6. An absorption peak at 280 nm is evident and is attributed to the electronic excitations in tryptophan and tyrosine residues in the proteins [36], which are present in the gum. Thus, one can conclude that once the silver ions are reduced to silver nanoparticles by the gum, proteins present in the gum subsequently encapsulate and stabilize these particles along with saccharide molecules. Based on these observations, these silver nanoparticles can be used as a possible substrate for SERS. As observed in IR spectra (Figure 5), the gum is rich in various functional groups; their capping on silver nanoparticles provides surface reactivity.

3.6. Antibacterial Assay

For checking the antibacterial activity, silver nanoparticles with an average size of 13.1 ± 1.0 nm were used. These nanoparticles were prepared with 0.1% gum extract containing 1 mM AgNO₃, autoclaved for 30 min. After 24 h of incubation at 37°C, growth suppression was observed in plates loaded with 5 μg of silver nanoparticles. The ZOI of around mm was observed for the Gram-positive bacterial strain S. aureus ATCC 25923. In the case of Gram-negative bacterial strains E. coli ATCC 25922, E. coli ATCC 35218, and P. aeruginosa ATCC 27853; the detected ZOI were , , and mm, respectively.Whereas, the negative control plates loaded with autoclaved gum did not produce any ZOI (Figure 7). In the case of positive control plates loaded with erythromycin discs, growth inhibition was noted (Table 2). Based on these results, it can be concluded that the synthesized silver nanoparticles had significant antibacterial action on both Gram classes of bacteria.

4. Conclusion

By autoclaving the metal precursor silver nitrate with aqueous extract of gum tragacanth, we have produced spherical silver nanoparticles of around 13.1 nm. The renewable, nontoxic components of this natural phytoexudate play dual role of reducing and stabilizing agents for the silver ions. The abundance of the gum makes this green method amenable for large-scale production of silver nanoparticles. Based on Raman spectroscopy studies, these silver nanoparticles can be used as a possible substrate for SERS. Compared to conventional antibiotics, the development of silver resistance in microbes is unlikely due to its action on broad spectrum of targets in cell. As these nanoparticles demonstrated significant antibacterial activity on both Gram classes of bacteria; they can have promising biomedical applications where antibiotic resistance is a major problem. In addition, these functionalized nanoparticles are useful for various applications such as targeted biological interactions [37], drug delivery [38], and biological labels [39].

Acknowledgments

The authors thank Dr. S.V. Narasimhan, associate director and Dr. Tulsi Mukherjee, director, Chemistry Group, BARC for their constant support and encouragement for this work. The support rendered for high-resolution TEM measurements by the DST unit on Nanoscience, Sophisticated Analytical Instrument Facility (SAIF) at IIT-Madras, Chennai, is gratefully acknowledged.

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Copyright

Copyright © 2012 Aruna Jyothi Kora and Jayaraman Arunachalam. 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.

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