Antibacterial activity of
Abstract
The biosynthesis of silver nanoparticles (AgNPs) has become more significant in the recent years owing to its applications in catalysis, imaging, drug delivery, nano-device fabrication and in medicine. We propose the synthesis of silver nanoparticles from the plant extract of Syzygium cumini and evaluation of its antibacterial and chemocatalytic potential. Synthesis of AgNPs carried out by using aqueous silver nitrate. The UV–Vis absorption spectrum of the synthesized AgNPs showed a broad absorption peak at 470 nm. TEM analysis shows the morphology of AgNPs as a hexagonal matrix with average particle size is about 50 nm. XRD analysis displays the crystalline structure of AgNPs. The presence of elemental silver was confirmed with EDX analysis. FTIR analysis shows that amide groups present in proteins are dominant reducing agents and play an important role in the bioreduction of Ag+ ions to Ag0. The bioreduced AgNPs demonstrated significant catalytic properties in a reduction reaction of 4-nitrophenol to 4-aminophenol using NaBH4 in an aqueous condition. The biosynthesized AgNPs have potent antibacterial activity against common clinical pathogens. Considering the remarkable antibacterial activity against common pathogenic microorganisms, AgNPs can be used in the pharmaceutical industries.
Keywords
- Syzygium cumini
- Silver nanoparticles
- Antibacterial activity
- Catalytic reduction
1. Introduction
Nanobiotechnology is an economic alternative to chemical and physical methods for the synthesis of nanoparticles [1]. The nanoparticles are extensively used in cosmetics, tires, textiles, food industries and medicines [2]. Recently, nanotechnology has gained significant attention due to its unique and different properties such as catalytic, electrical, optical, magnetic and thermal, which have wide varieties of applications [3].
Numerous approaches are in practice to generate AgNPs such as chemical, electrochemical, photochemical and radiation. The significance of NPs is recognized when researchers found that size can persuade the physico-chemical properties of a substance [4]. In the past few decades, tremendous awareness and extensive research efforts were intended toward the metallic nanoparticles derived from noble metals, such as silver and gold [5]. However, there is still a need to enhance and develop high yield, low cost, non-toxic and environmentally friendly procedures. Therefore, the biological loom for the synthesis of NPs becomes crucial.
Nanotechnology has focused much more attention in recent years in several research fields. Due to their advanced optical properties, metal NPs find applications in the areas of biological, chemical and electronic sciences [5, 6]. The AgNPs have a well-built report on antimicrobial, anti-inflammatory, anti-viral, anti-angiogenesis and anti-platelet activity [7, 8]. Currently, the green synthesis of AgNPs finding medical application in the area of continued significance [9]. The new drug synthesis from AgNPs can fight against cancer and kill pathogens like bacteria, fungi, and viruses [10]. There are diverse natural sources like plants, bacteria, yeast, and fungi used to synthesize Au and AgNPs [11, 12]. The use of leaf extract for nanoparticle synthesis is low-cost and eliminates the need for culture preparations and maintenance of aseptic conditions required for microorganisms [13]. At present, plant-mediated synthesis of nanoparticles is gaining more attention due to its simplicity, rapid rate of synthesis and eco-friendliness [14]. Diverse bio-molecules such as, carbohydrates, proteins and co-enzymes are existing in plant that reduce the metallic salt into nanoparticles [1]. The phytosynthesis of nanoparticles is advantageous over chemical synthesis concerning the adverse effect of harmful chemicals on the environment [15].
The antimicrobial prospective of nanoparticles is pertinent in the massive area of biology and medicine to prevent infections in burns and open wounds [21, 22]. Therefore, this manuscript describes the antibacterial activity of nanoparticles against common human pathogenic bacteria like
Herein, we report the simple, facile, rapid and efficient process for the synthesis of AgNPs using the aqueous leaf extract of
2. Materials and methods
2.1 Preparation of plant extract
2.2 Synthesis of AgNPs
The well-grinded material was mixed with 100 mL of double distilled water and then transferred in 500 mL Erlenmeyer flask followed by continuous stirring on the magnetic stirrer for 10 min. The content was centrifuged at 10,000 rpm for 10 min for the removal of cell debris. 50 mL of aqueous silver nitrate (1 mM) was added to 10 mL of the leaf extract with continuous stirring. A color change from colorless to yellowish-brown, visually confirms the formation of AgNPs [25].
2.3 Characterization
The resulting solution was then diluted by using double distilled water and characterized using UV–Visible spectroscopy, X-ray diffraction, Energy dispersion spectroscopy, FT-IR and Transmission electron microscopy [26].
2.3.1 UV-visible spectroscopy
Silver nanoparticles were characterized by using Systronics UV–Vis spectrophotometer. The bio-reduction absorption spectra were monitored in 300–700 nm range.
2.3.2 X-ray diffraction spectroscopy
The biosynthesized AgNPs using
2.3.3 Transmission electron microscopy and energy dispersive spectroscopy
In order to know the morphology of the biosynthesized AgNPs, transmission electron microscopy (TEM) studies were carried out. The size and shape of the AgNPs were recorded by using the FEI (Netherland) model TECNAI-G2U twin operated at an accelerating voltage of 200 KV. EDS analysis was carried out at the same time by the EDS compatible with TEM.
2.3.4 Fourier transform infrared spectroscopy (FTIR) analysis
After the biosynthesis, AgNPs were centrifuged for 15 min at 10,000 rpm. The obtained pellet was re-dispersed in double distilled water to ensure the removal of any uncoordinated bio-molecules. In order to obtain the better separation of nanoparticles, the process of centrifugation was repeated twice. The purified pellet was then subjected to FTIR analysis (Shimadzu IR). AgNPs were mixed with KBr and subjected to IR source 500–4000 cm−1.
2.4 Catalytic reduction of 4-nitrophenol
The catalytic reaction was studied as mentioned by Ghosh et al. with slight modification. Briefly in standard quartz cuvette 1 mL of 0.1 mM aqueous NaBH4 solution mixed with 1.5 mL of 4-nitrophenol aqueous solution (0.25 mM). 100 μL of an aqueous suspension of AgNPs of
2.5 Antimicrobial activity
The antimicrobial activity of the biosynthesized AgNPs was tested against pathogenic bacteria such as
3. Result and discussion
3.1 Biosynthesis of AgNPs
The reduction of Ag+ to Ag0 NPs was carried out by using aqueous leaf extract of
3.2 Characterization
3.2.1 Transmission electron microscopy analysis
The TEM image of the AgNPs is shown in Figure 2. TEM has been used to describe the size, shape and morphology of the biosynthesized AgNPs. From the figures, it is observed that the morphology of AgNPs is a hexagonal matrix. Figure 2 shows the average particle size measured from the TEM image is 50 nm, which are in good agreement with the particle size calculated from XRD analysis.
3.2.2 X-ray diffraction analysis
The presence of Ag crystal in the sample was confirmed by using an X-ray diffractometer. In XRD pattern, the Braggs reflections were observed at 2θ value 38.00, 44.80, 47.50, 64.60 and 78.00 confirm the presence of AgNPs (Figure 3). A strong diffraction peak located at 38.00 was ascribed to the (111) facets of Ag. The XRD pattern thus clearly indicated that the AgNPs are in crystalline form. No impurities were observed in the XRD pattern.
3.2.3 Energy dispersive spectroscopy analysis
EDS analysis of synthesized particles showed the presence of elemental silver, which correlates with XRD analysis (Figure 4). We identified the signal energy peaks for hexagonal-shaped AgNPs produced by using
3.2.4 Fourier transform infrared spectroscopy (FTIR) analysis
FTIR absorption spectra of AgNPs are shown in (Figure 5). The different possible functional groups at various positions will be determined by using FTIR analysis. The band at 1559 cm−1 indicates the presence of amide group [32] arises due to carbonyl stretch in proteins. It can be stated from FTIR analysis. The band at 1610 cm−1 is attributed to the stretching vibration of (NH) C=O group. That amide groups present in carbohydrates, proteins are dominant reducing agents and play an important role in the bio-reduction of Ag+ ions to Ag0 leads to nanoparticles synthesis.
3.3 Catalytic reduction of 4-nitrophenol
In order to study the efficiency of bio-synthesized AgNPs, the catalytic reduction of 4-nitrophenol was carried out in an aqueous medium by using NaBH4 as a reductant at room temperature [33, 34, 35]. The 4-nitrophenol (0.1 mM) shows an absorption peak at 400 nm in the visible region with NaBH4 (Figure 6). In a control experiment, it can be concluded that the reduction does not occur in the absence of AgNPs, even after the addition of excess NaBH4. After the addition of AgNPs, the gradual decrease in intensity of the absorption peak at 320 nm was observed due to the formation of 4-aminophenol. The complete reduction of p-nitrophenol was also supported by a change in color from yellow to colorless.
3.4 Antibacterial activity
Antibacterial activity of biosynthesized AgNPs was investigated against human pathogens. The biosynthesized AgNPs showed a high inhibitory effect on bacteria, and it may serve as an option for decreasing bacterial infections [36]. The zone of inhibition was found to be as per Table 1.
Sr. No | Name of organism | Diameter of zone of inhibition (mm) |
---|---|---|
1. | 14 | |
2. | 18 | |
3. | 22 | |
4. | 16 | |
5. | 12 |
4. Conclusion
The
Conflict of interest
The authors of this have declared there is no conflict of interest.
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