Rapid green synthesis of silver nanoparticles from Chrysanthemum indicum L and its antibacterial and cytotoxic effects: an in vitro study.

The present work reports a simple, cost-effective, and ecofriendly method for the synthesis of silver nanoparticles (AgNPs) using Chrysanthemum indicum and its antibacterial and cytotoxic effects. The formation of AgNPs was confirmed by color change, and it was further characterized by ultraviolet-visible spectroscopy (435 nm). The phytochemical screening of C. indicum revealed the presence of flavonoids, terpenoids, and glycosides, suggesting that these compounds act as reducing and stabilizing agents. The crystalline nature of the synthesized particles was confirmed by X-ray diffraction, as they exhibited face-centered cubic symmetry. The size and morphology of the particles were characterized by transmission electron microscopy, which showed spherical shapes and sizes that ranged between 37.71-71.99 nm. Energy-dispersive X-ray spectroscopy documented the presence of silver. The antimicrobial effect of the synthesized AgNPs revealed a significant effect against the bacteria Klebsiella pneumonia, Escherichia coli, and Pseudomonas aeruginosa. Additionally, cytotoxic assays showed no toxicity of AgNPs toward 3T3 mouse embryo fibroblast cells (25 μg/mL); hence, these particles were safe to use.

Introduction

The advancement in the nanoparticle (NP) system has had an impact in scientific areas. The nature and unique properties of nanomaterials have a wide range of applications in biosensors, tissue engineering, deoxyribonucleic acid (DNA) modification, drug delivery systems, cosmetics, and medical devices.1–5 Silver NPs (AgNPs) are well known biocidal substances that can be incorporated as antimicrobial agents in pharmacology, veterinary medicine, implants, wound dressings, and topical ointments.6–9 AgNPs were also found to exhibit antibacterial and antiplatelet activities.10,11 This biological activity is due to the extremely small size of the NPs (1–100 nm), which enhances their physical, chemical, magnetic, and optical properties.12–14 The synthesis of AgNPs, through physical and chemical methods, are well known;15–19 however, due to their environmental impact, energy consumption, and use of toxic chemicals, the synthesis of AgNPs that uses a green approach is most preferable, as this type of approach is found to be ecofriendly and nontoxic.20,21 This ecofriendly approach might pave the path for researchers across the globe to explore the potential of different herbs in the synthesis of NPs. AgNPs have been reported to be green synthesized from various parts of plants such as the bark of cinnamon,22 neem leaves,23 and various plant leaves.24 Metal NPs have received great attention for their use in developing materials for medical applications.25 In recent times, several groups have reportedly achieved success in the synthesis of Au, Ag, and Pd NPs obtained from the extracts of plant parts (such as leaves);26 biologically active molecules were used for the green synthesis of AgNPs of desired size and morphology using medicinal plants, bacteria, and fungi.27,28 These active molecules act as reducing and capping agents for the synthesis of NPs, which makes these NPs suitable for biomedical applications. Flowers are an area of interest in the synthesis of AgNPs due to their attractive carotenoid pigments. The essential oils from Chrysanthemum indicum flowers showed significant antimicrobial activity;29 it is a well-known herbal tea in the east Asian countries and China. The whole plant is beneficial to humans, but the famous part of the plant is the flower used in chrysanthemum tea.30C. indicum is used in the traditional treatment of several infectious diseases such as pneumonia, colitis, stomatitis, cancer, fever, sores, and it is also used to treat vertigo, pertussis, and hypertensive symptoms.31 The active molecules in C. indicum are glycosides and flavonoids; the plant has the ability to act as antibiotic to many species of bacterial pathogens.30C. indicum is an herb with single, small-head, yellow daisies, which belongs to the family of Sapotaceae. The flowers have been consumed as tea in Chinese medicine to prevent sore throats and fevers. In traditional medicine, the flowers have been used for the treatment of dizziness, ocular inflammation, and skin boils. The flowers possess antimicrobial, anti-inflammatory, and free radical scavenging activity.32,33 Therefore, this work is focused on C. indicum. Only a few works have been carried out using the flowers Lonicera japonica, Nelumbo nucifera, and Carthamus tinctorius.34–36

In this study, the novel, one-step biosynthesis of AgNPs using the flower extract of C. indicum L. at room temperature has been reported. The objective of this study is to synthesize AgNPs using a green synthesis method, and to characterize the NPs using ultraviolet–visible spectroscopy (UV–Vis), X-ray diffraction (XRD), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX), and to evaluate the NPs’ antimicrobial effects against bacteria, as well as their in vitro cytotoxic effects on mouse embryonic fibroblast cells (3T3).

Materials and methods

Media and chemicals

Analytical-grade silver nitrate (AgNO3) was obtained from Sigma-Aldrich (St Louis, MO, USA). All of the media components and analytical reagents were purchased from Hi-Media Laboratories Pvt Ltd (Mumbai, India).

Microorganisms and cell line

Bacillus subtilis (Microbial Type Culture Collection and Gene Bank [MTCC] 121), Staphylococcus aureus (MTCC 96), S. epidermidis (MTCC 435), Escherichia coli (MTCC 433), Klebsiella pneumoniae (MTCC 109), and Pseudomonas aeruginosa (MTCC 1934) were used for this experiment, and they were obtained from the Microbial Type Culture Collection (MTCC), Chandigarh, India, and the mouse embryonic fibroblast cell line (3T3) was obtained from the National Center for Cell Science (Pune, India).

Preparation of flower extract and the synthesis of AgNPs

Fresh, healthy, and disease-free C. indicum flowers were selected and washed repeatedly with Milli-Q deionized water (EMD Millipore, Billerica, MA, USA) to remove surface contaminants. A total of 20 g of flowers were sliced into fine pieces, and 500 mL of Milli-Q deionized water was added and then boiled for 5 minutes before decantation. The crude extract was thus obtained, and it was filtered using Whatman No 1 filter paper (Whatman plc, Kent, UK). Then, 5 mL of flower extract was assorted with 500 mL of a silver nitrate solution (1 mmol). The reaction mixture was kept undisturbed until the colorless solution converted into a reddish-brown color, which indicated the formation of AgNPs. This process was carried out at room temperature. The particles were then purified by centrifugation. To remove excess silver ions, the silver colloids were washed at least three times with deionized water. It was then lyophilized and stored in screw-capped vials under ambient conditions for further characterization and application.

Phytochemical analysis

The aqueous extract obtained from the flower of C. indicum was tested for the presence of the phytochemicals – tannins, saponins, flavonoids, terpenoids, steroids, alkaloids, and glycosides – according to the method described by Trease and Evans.37

Characterization of NPs

UV–Vis spectroscopy

The reduction of silver ions was monitored by measuring the UV–Vis spectrum of the reaction mixture after 2 minutes by using a UV–Vis spectrophotometer (UV100; Cyberlab® Inc, Miami, FL, USA) in the wavelength ranging from 300–650 nm.

X-ray diffraction

The crystalline structures of the synthesized AgNPs were investigated by XRD. Lyophilized and powdered samples were used, and the diffraction patterns were recorded in the scanning mode on an X’pert Pro diffractometer (PANalytical, Almelo, the Netherlands) operated at 40 kV and with a current of 30 mA, with Cu/kα radiation (λ=1.5418 Å) in the range of 20°–80° in 2θ angles. The average particle size of the synthesized silver AgNPs was calculated, using the Debye–Scherrer equation:

Transmission electron microscope and energy dispersive X-ray analysis

TEM and EDX were performed with a JEM 1101 transmission electron microscope (JEOL, Tokyo, Japan) to confirm the size, shape, and elemental composition of the AgNPs. The sample was dispersed in ethanol on a carbon-coated copper TEM grid, and the images were obtained by operating at an accelerating voltage of 120 kV.

Antibacterial activity of synthesized AgNPs

The antibacterial efficacy was assayed by the standard Kirby–Bauer disc diffusion method39 against Gram-positive and Gram-negative pathogenic bacteria. The bacterial suspension (108 colony-forming units/mL) was swabbed on the Mueller Hinton Agar plates using sterile cotton swabs. The sterile disc (Hi-Media Laboratories Pvt Ltd), which was 6 mm in diameter, was impregnated with the following four different components, including an aqueous extract of C. indicum, AgNO3, and synthesized AgNPs at the concentrations of 25 μg/disc. Streptomycin was used as a control. The discs were gently pressed and incubated at 37°C for 24 hours. The zone of inhibition in the diameter of each disc was measured in millimeters using a Hi-Media Laboratories Pvt Ltd. zone scale. The minimum inhibitory concentration (MIC) was determined according to the standard broth microdilution method.40 The experiments were performed in triplicate.

Toxicity study of AgNPs

MTT assay on 3T3 cell lines

The mouse embryonic fibroblast cell line (3T3) was obtained from the National Center for Cell Science (Pune, India). The cells were seeded in a 75 cm2 flask containing Dulbecco’s Modified Eagle’s Medium (DMEM) with 10% fetal bovine serum, 1.5 g/L of sodium bicarbonate, 100 U/mL of penicillin, 100 μg/mL of streptomycin, and 0.25 μg/mL of amphotericin B. The cell line was grown in six-well plates at a density of 5 × 104 cells/mL in DMEM, and it was incubated to 75% confluency after 24 hours in 5% CO2 at 37°C. The cells were then treated with synthesized AgNPs at the concentrations of 25 μg/mL and 50 μg/mL of growth medium. The cells were then washed with phosphate buffered saline solution thrice and stained with 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazoium bromide (MTT) dye.41 The MTT solution (100 μL) was added to each well, followed by incubation at 37°C and 5% CO2 for an additional 4 hours. The insoluble formazan product formed within the living cells was solubilized by adding dimethyl sulfoxide:glycine buffer (125 μL). The intensity of the solutions was measured by a microplate reader (Bio-Rad 680; Bio-Rad Laboratories, Hercules, CA, USA) with relative cell viabilities being determined as a proportion of the control. After this treatment, the cells were added to the plate and incubated for 4 hours in 5% CO2, at 37°C. The viability of the cells was evaluated using a microplate reader (Bio-Rad 680) at 545 nm absorbance. The absorbance is directly proportional to the number of living cells in the culture. The relative cell viability (%) related to the control wells that contained the cell culture medium without NPs as a vehicle was calculated by

where (A) test is the absorbance of the test sample and (A) control is the absorbance of the control sample. Nontreated cells were used as the control, and the samples were imaged using an inverted photomicroscope (Nikon TE2000-E; Nikon Instruments, Melville, NY, USA).

Lactate dehydrogenase (LDH) leakage assay

The cytoplasmic enzyme release (lactate dehydrogenase [LDH]) and cell membrane instability were performed by the method of Borna et al,42 with minor modifications. Various concentrations (25 μg/mL and 50 μg/mL) of the synthesized AgNPs were added to a 1 mL cuvette containing 0.9 mL of a reaction mixture to yield a final concentration of 1 mmol of pyruvate, 0.15 mmol of nicotinamide adenine dinucleotide (NADH) and 10 mmol of disodium hydrogen phosphate. After mixing thoroughly, the absorbance of the solution was measured at 340 nm. LDH activity was expressed as moles of NADH used in a minute per well.

Statistical analysis

All experiments were done in triplicate, and then the values were expressed as the mean ± standard deviation. Statistical significance was evaluated by one-way analysis of variance followed by Student’s t-test (P<0.05), using the Statistical Package for the Social Sciences (SPSS version 11; IBM Corporation, Armonk, NY, USA).

Results and discussion

In the present study, AgNPs were synthesized from the aqueous floral extract of C. indicum which acts as a reducing agent. It was observed that the reduction of silver ions into AgNPs was confirmed by the change of the silver nitrate solution to a reddish-brown color within 2 minutes at room temperature (Figure 1), whereas the control AgNO3 solution (without the leaf extract) showed no change in color. This characteristic difference in color is due to the excitation of the surface plasmon resonance in the metal NPs.43

Figure 1

Schematic illustration of the green synthesis of silver nanoparticles using an aqueous extract of the Chrysanthemum indicum (flower).

The phytochemical analysis of C. indicum revealed the presence of tannins, flavonoids, and glycosides (Table 1). These constituents may be responsible for the formation of AgNPs by reducing AgNO3 and acting as a capping agent to prevent agglomeration and to provide stability to the medium.44 Flavonoids, tannins, proteins, and reducing sugars that are present in plants have been reported to act as bioreductants and capping agents.45

Table 1

Phytochemical screening of the flower extract of Chrysanthemum indicum

Phytochemicals	C. indicum
Tannins	+
Saponins	−
Flavonoids	+
Terpenoids	−
Steroids
Alkaloids	−
Glycosides	+

Notes: + Presence; − absence.

UV–Vis spectroscopic analysis

The UV–Vis spectrum is one of the imperative techniques used to find low-level concentrations of metal NPs in solution. In this study, the absorption spectra were noted at 435 nm (Figure 2), and a broadening of the peak indicated that the particles were polydispersed. A similar report was observed by Loo et al.46

Figure 2

Ultraviolet–visible spectroscopy analysis of synthesized silver nanoparticles, and the peak noted around 435 nm.

XRD

The crystalline nature of the AgNPs that were synthesized using C. indicum was confirmed by XRD pattern analysis (Figure 3). The XRD pattern indicates the five main characteristic peaks at 2θ values of 38°, 44°, 64°, 77° and 81° corresponding to 111, 200, 220, 311 and 222 planes for silver, suggesting that these NPs were crystalline in nature.47 The mean particle diameter of the synthesized AgNPs was calculated from the XRD pattern using Scherrer’s equation:

Figure 3

X-ray diffraction pattern of synthesized silver nanoparticles from the floral extract of Chrysanthemum indicum.

The equation uses the reference peak width at angle θ, where λ is the X-ray wavelength (1.5418 Å), β1/2 is the width of the XRD peak at half-height, and k is a shape factor. From this equation, the average crystalline size of the synthesized AgNPs was found to be 52 nm.

TEM and EDX analysis

The size and morphology of the synthesized AgNPs were studied by TEM (Figure 4). The size of the particles was found to be in the range of 37.71–71.99 nm, and they had a smooth surface and polydispersed particles. Figure 5 shows the clear elemental composition profile of the synthesized AgNPs. The intense signal at 3 keV strongly suggests that Ag was the major element of these NPs, as it has optical absorption in this range due to the surface plasmon resonance.48 The other signals (carbon and oxygen) indicate the presence of plant extract, which corresponds to the biomolecules that were capping over the AgNPs.

Figure 4

Transmission electron microscopy micrograph of the green synthesized silver nanoparticles.

Notes: Scale bars: (A) 200 nm and (B) 500 nm. The arrows indicate the particle size in nm.

Figure 5

Energy-dispersive X-ray spectrum of green synthesized silver nanoparticles.

Antimicrobial activity of AgNPs

The antimicrobial efficacy of the aqueous floral extract of C. indicum and of the AgNPs was examined against three Gram-positive and three Gram-negative bacteria such as B. subtilis (MTCC 121), S. aureus (MTCC 96), S. epidermidis (MTCC 435), E. coli (MTCC 433), K. pneumoniae (MTCC 109), and P. aeruginosa (MTCC 1934). Primary screening revealed that the biologically synthesized AgNPs showed significant activity, as compared to the flower extract. The synthesized AgNPs demonstrated prominent results against K. pneumoniae (19 mm) E. coli (14 mm), and they exhibited moderate activity against P. aeruginosa when compared to streptomycin (Figure 6 and Table 2).

Figure 6

The antimicrobial efficacy of the aqueous extracts of Chrysanthemum indicum, AgNO3, and AgNPs were examined against three selected Gram-positive bacterial strains (D, E, and F) and three selected Gram-negative bacterial strains (A, B, and C).

Notes: The Gram-positive bacterial strains included BS (MTCC 121), SE (MTCC 435), and SA (MTCC 96), and the three Gram-negative bacterial strains included KP (MTCC 109), EC (MTCC 433), and PA (MTCC 1934). The arrows indicate the zone of inhibition.

Abbreviations: PE, plant extract; C, control (streptomycin); KP, Klebsiella pneumoniae; AgNP, silver nanoparticle; EC, Escherichia coli; PA, Pseudomonas aeruginosa; BS, Bacillus subtilis; SE, Staphylococcus epidermidis; SA, Staphylococcus aureus; MTCC, Microbial Type Culture Collection and Gene Bank.

Table 2

Antibacterial activity of AgNPs synthesized by the aqueous flower extract of Chrysanthemum indicum

Indicator bacteria	Inhibitory activity (mm)a
	C. indicum (25 μg/disc)	Silver nitrate (25 μg/disc)	AgNPs (25 μg/disc)	Streptomycin (25 μg/disc)
Gram-positive
Bacillus subtilis (MTCC 121)	–	–	–	13.16±0.28
Staphylococcus aureus (MTCC 96)	–	–	8.33±0.57	08.12±0.57
Staphylococcus epidermidis (MTCC 435)	–	–	–	10.12±0.76
Gram-negative
Escherichia coli (MTCC 433)	–	–	13.00±0.90	10.00±0.90
Klebsiella pneumoniae (MTCC 109)	–	07.00±0.50	19.10±0.50	08.00±0.50
Pseudomonas aeruginosa (MTCC 1934)	–	–	09.60±0.51	14.12±0.76

Notes:

Each value is the mean of three replicates of the diameter (mm) of the inhibition zone in the bacterial layer. Values are the means of three independent experiments. The zone of inhibition was measured after incubating the strains for 17 hours at 37°C in Muller Hinton Agar medium.

Abbreviations: AgNPs, silver nanoparticles; MTCC, Microbial Type Culture Collection and Gene Bank.

The antibacterial potential of the AgNPs in terms of their MIC are shown in Table 3. The AgNPs exhibited a MIC value of 25 μg mL−1 for the Gram-positive bacteria, S. epidermidis, and 6.25 μg mL−1 for the Gram-negative bacteria, K. pneumoniae. The MIC values of the AgNPs were slightly similar to or less than that of the standard broad spectrum antibiotic, streptomycin. This antibacterial activity exhibited by the AgNPs that were synthesized from C. indicum may be due to one or more of these following mechanisms. First, the effect may be due to the ultrafine size and larger surface area of the AgNPs, as their positively charged Ag+ ions bind to the negatively charged bacterial cell wall, deactivating the cellular enzymes, causing disruptions in membrane permeability.49 Second, interactions with the thiol group of L-cysteine protein residues may lead to enzymatic dysfunction.50 Finally, the AgNPs may facilitate the release of reactive oxygen species, which cause damage to proteins and DNA,51 ultimately leading to cell death. This bactericidal effect of the synthesized AgNPs may also be facilitated by the shape of AgNPs. Pal et al52 illustrated that the spherical and hexagonal shapes of AgNPs inhibited the Gram-negative bacterium, E. coli; similarly, our TEM micrographs showed spherical particles. It is noteworthy that the biologically synthesized AgNPs from C. indicum showed significant activity against Gram-negative bacteria when compared to Gram-positive bacteria. This difference was possibly due to the difference in the peptidoglycan layer. Gram-negative bacteria have a thin layer, whereas Gram-positive bacteria have a thick peptidoglycan layer (30–100 nm). As a result, the Gram-positive bacteria are defended from the bactericidal mechanisms, which are released by AgNPs.53,54

Table 3

Minimum inhibitory concentration of AgNPs synthesized by aqueous flower extract of Chrysanthemum indicum

Indicator bacteria	Minimum inhibitory concentration (μg/mL)
	AgNPs	Streptomycin
Gram-positive
Bacillus subtilis (MTCC 121)	>25	25
Staphylococcus aureus (MTCC 96)	>25	12.5
Staphylococcus epidermidis (MTCC 435)	25	>25
Gram-negative
Escherichia coli (MTCC 433)	12.5	12.5
Klebsiella pneumoniae (MTCC 109)	6.25	25
Pseudomonas aeruginosa (MTCC 1934)	37.5	25

Note: Streptomycin was the control antibiotic used for the bacteria.

Abbreviations: AgNPs, silver nanoparticles; MTCC, Microbial Type Culture Collection and Gene Bank.

Cytotoxicity of silver nanoparticles

Recently, researchers have focused on the development of methods to reduce the toxicity of AgNPs. AgNPs are toxic to both microorganisms and human cells, but when exposed to adequate concentrations, different reactions may be observed.55 In this study, the toxicity of AgNPs synthesized from C. indicum were evaluated in vitro against a 3T3 mouse embryo fibroblast cell line at 25 μg/mL and 50 μg/mL concentrations by MTT and LDH assays. In our study, the cells treated with 25 μg/mL of AgNPs did not seem to affect cell viability, which was observed to be 93.33% (Table 4). However, when the cells were treated with increased concentrations of AgNPs (50 μg/mL), they showed decreased cell viability (45.14%). The effect of AgNPs on LDH leakage in 3T3 cells are presented in Table 4. From the results, it is clear that there was no significant increase in LDH at 25 μg/mL (0.12 μmol/NADH) when compared to control, but there is an increase in LDH activity of 0.42 μmol/NADH at a concentration of 50 μg/mL. The toxicity of the synthesized AgNPs depends on their dose. Investigations of the morphological features of treated cells using an inverted microscope revealed that changes in the cell morphology were clearly reflected at 50 μg/mL when compared to the cells treated at concentrations of 25 μg/mL (Figure 7). It can be clearly observed that the cells treated with AgNPs (25 μg/mL) have a well-developed nucleus, devoid of peripheral cellular distribution. Conversely, in the cells treated with a concentration of 50 μg/mL, systematic changes in the morphological features of the cells occurred. Further, with the LDH assay, a rise in LDH enzyme activity was observed at 50 μg/mL when compared to the control cells. LDH is a stable cytoplasmic enzyme that is present in most of the eukaryotic cells, and it is secreted into the culture medium during the damage or rupture of the cell’s cytoplasmic membrane. The elevated levels of LDH enzyme activity are directly proportional to the number of dead or damaged plasma membrane cells.56 In this study, the synthesized AgNPs from the aqueous flower extract of C. indicum were found to exhibit highly antibacterial activity against K. pneumoniae and E. coli at concentrations of 25 μg/mL, and no cytotoxic effects on mouse embryonic fibroblast cells were observed. This result may provide a safe start for the use of AgNPs in pharmaceutical and other medical applications.

Table 4

Cell viability and LDH leakage in control- and AgNP-treated 3T3 cells after 24 hours of exposure

Concentration (μg/mL)	Percentage of viability	LDH activity (μmol/NADH/well/minute)
25	93.33±1.45*	0.12±0.007*
50	45.14±1.38*	0.42±0.003*
Control	97.70±1.49	0.11±0.005

Notes: The values represent the mean ± standard deviation of two independent experiments.

P<0.001 versus control.

Abbreviations: LDH, lactate dehydrogenase; AgNP, silver nanoparticle; NADH, nicotinamide adenine dinucleotide.

Figure 7

Cytotoxicity of synthesized silver nanoparticles on 3T3 mouse embryo fibroblast cells.

Notes: (A) Control (cell + phosphate buffered saline); (B) cell +25 μg/mL of silver nanoparticles; (C) cell +50 μg/mL of silver nanoparticles. The arrows indicate the cell nucleus.

Conclusion

The present study reported on the synthesis of AgNPs by C. indium without using any harmful reducing or capping agents, as confirmed by UV–Vis spectrophotometer, XRD, TEM, and EDX techniques. Spherical, smooth surface, and poly-dispersed particles of sizes ranging from 37.71–71.99 nm with an average size of 52.9±4.6 nm were obtained. The lowest MIC of the AgNPs was exhibited against E. coli and K. pneumoniae (12.5 μg/mL and 6.25 μg/mL, respectively). The synthesized AgNPs act as excellent bactericidal agents, without exhibiting any toxic effects on mouse embryonic fibroblast cells.