Eco-friendly synthesis, characterization, in vitro and in vivo anti-inflammatory activity of silver nanoparticle-mediated Selaginella myosurus aqueous extract.

INTRODUCTION: There is emerging interest in medicinal plants in the biomedical field, due to their multitude of chemicals which show anti-inflammatory, antimicrobial, antiviral, or antitumoral potential. Research on medicinal plants has shown that nanotechnology could offer new solutions in the quality control, delivery aspects, or in sustaining herbal biological activities. This work reports on the preparation and characterization of silver nanoparticle-mediated Selaginella myosurus plant extract.
METHODS: Ultraviolet-visible spectroscopy, Fourier transform infrared spectroscopy, powder X-ray diffraction, energy dispersive X-ray spectroscopy, high-resolution scanning electron microscopy, high-resolution transmission electron microscopy, and selected area electron diffraction have been used to characterize the prepared silver nanoparticles. The synthetic stability was studied by varying concentrations and pH of reactants. Egg albumin denaturation and carrageenan-induced rat paw edema model were used to ascertain the anti-inflammation.
RESULTS: Ultraviolet-visible spectroscopy gave plasmon resonance ranging between 420 and 480 nm while Fourier transform infrared spectroscopy proved nano interface functionalized with organics. The powder X-ray diffraction pattern is in agreement with silver and silver chloride nanoparticles of crystallite size 33.7 nm and 44.2 nm for silver and silver chloride, respectively. Energy dispersive X-ray spectroscopy enables elemental characterization of the particles consisting of silver and silver chloride among main elements. Spherical silver grain of 58.81 nm average size has been depicted with high-resolution scanning electron microscopy and high-resolution transmission electron microscopy. Inhibitions of 99% and 60% were obtained in vitro and in vivo, respectively.
CONCLUSION: The albumin denaturation and carrageenan-induced rat hind paw edema model to assess the anti-inflammatory potential of generated nanoparticles suggests that the silver nanoparticles may act as reducing/inhibiting agents on the release of acute inflammatory mediators. Hence, this work clearly demonstrated that silver nanoparticles mediated-Selaginella myosurus could be considered as a potential source for anti-inflammatory drugs.

Introduction

Inflammation is a physical response that protects against injury, infection, and stress through multiple mechanisms. It is well-known that the oxidative stress that occurs in the inflammatory response can facilitate tumor progression, increase the risk of atherosclerosis, cause coronary heart disease, cause lesions of Alzheimer’s disease, and promote insulin resistance and diabetes.1–3 In such diseases, inflammation is a primary cause, and therefore, treatment of the inflammatory condition may be an effective therapeutic approach. Most clinically, important medicines belong to steroidal or nonsteroidal anti-inflammatory chemical. Although these have potent activity, the long-term administration is required for the treatment of chronic diseases.4 Furthermore, these drugs have various and severe adverse effects that have compelled the need for identification of alternative substances that can resolve inflammation in a way that is homeostatic, modulatory, efficient, and well tolerated by the body.5 One such alternative is the use of medicinal plants because their therapeutic value has been well established for various human diseases. It is well documented that therapeutic effects of herbal medicine are due to active components present in their extract.6 However, most of these active components possess insoluble character leading to lower bioavailability, increased systemic clearance,7 and required unnecessarily high systemic administration.8 Applying nanotechnology to herbal drugs may lead to the development of nano herbal products, which will open a new era of herbal discovery because nanosized drug delivery systems have many advantages to offer including solubility, bioavailability, pharmacological activity enhancement, protection from toxicity, sustained delivery, and protection from physical and chemical degradation.9

Nanotechnology deals with the synthesis and fabrication of materials at the nanoscale level (1–100 nm). It is the critical length scale at which certain novel size-related properties develop and the material starts behaving differently than the molecules or bulk material.10 At this scale, materials exhibit some unexpected and unusual new properties that cannot be defined by the classical laws of physics.11 It is these unusual properties that have attracted the immense attention of researchers from almost every science field including biology and medicine.10 Among all available nanoparticles, silver nanoparticles are the most important because in low concentrations they are not toxic to human health12 and exhibited anti-inflammatory,5 antiviral,13 and antibacterial14 activities, thereby being an excellent choice for multiple roles in the medical field. The literature describes various methods to synthesize silver nanoparticles including physical and chemical engineering, but the use of biological systems (plants and microbes) as potential nanofactories is gaining more importance as they are not expensive, not cumbersome, and respectful for the environment.10

Selaginella myosurus is a terrestrial, perennial, and herbaceous plant that grows in shallow soils on rocky outcrops of slopes of small hills in direct sunlight in humid tropical regions.15 Leaves of 0.5–1 cm long resembling scales are spirally arranged on a creeping stem.16 Known as tunda, the plant is used by Douala community for the traditional feast, burial ceremonies, and to invoke ancestral spirits (personal communication). In pharmacopeia, it is utilized to cure postpartum hemorrhage, menstrual disorder, respiratory and urinary tract infections, skin disease, cardiovascular problems, cancer, headache, fever, rheumatism, bone fracture, diabetes, hepatitis, wounds, and to improve fitness and endurance of the body.17–19 Extracts and isolated compounds of some species have shown great pharmacological activities such as antinociceptive,20 anti-inflammatory,21 antimutagenic,22 antispasmodic,23 cytotoxic, immunostimulant, and RNA reverse transcriptase inhibitory agents.24 In our previous study, we demonstrated the anti-inflammatory potential of S. myosurus aqueous extract.25 The present work was undertaken to synthesize, characterize, and evaluate the anti-inflammatory activity in both in vitro and in vivo systems of silver nanoparticle-mediated S. myosurus aqueous extract. Thereby, the potential advantages of phytomedicine and nanomedicine can be combined to result in a more enhanced and synergistic anti-inflammatory effect.

Materials and methods

Plant collection and preparation of the extract

The whole plant of S. myosurus (Figure 1) was collected at Dibombari (N04° 11.585′; E009° 39.958′), Littoral region, Cameroon, in April 2014 and authenticated by Dr Tchiengue Barthelemy at the National Herbarium, Yaounde, in comparison with a voucher specimen previously deposited (no 18192/ SFR/Cam). The entire freshly collected plant was thoroughly washed with running tap water followed by distilled water to remove all surface contaminants and finely cut. Ten grams of the plant was introduced into a conical flask containing 100 mL preheated distilled water (80°C) and stirred for 5 minutes using a hot plate equipped with a magnetic stirrer. After cooling at room temperature, the solution was filtered using Whatman paper no 1 and used as S. myosurus aqueous extract throughout, being used for 1 week due to gradual loss of plant extract viability for prolonged storage. Ten milliliters of the freshly prepared aqueous extract was introduced into a Petri dish and left overnight in the oven at 45°C. After complete drying, the extract was weighted and the amount of plant extract present in the solution was calculated.

Figure 1

Selaginella myosurus plant.

Biological synthesis of silver nanoparticles

Silver nanoparticles were synthesized according to a well-known procedure with slight modifications.26 Ten milliliters of freshly prepared aqueous extract was added to 50 mL silver nitrate aqueous solution (1 mM) for the bioreduction process. The mixture was incubated at room temperature in the dark to minimize the photoactivation of silver nitrate under static conditions until changing color appearance. The color change involved the formation of silver nanoparticles. The mixture was then centrifuged (D-7200; Hettich, Tuttlingen, Germany) at 6,000 rpm for 20 minutes and washed twice with distilled water and once with ethanol 95%. Purified pellets were kept into a Petri dish, dried in the oven at 60°C for 24 hours, and used for characterization and anti-inflammatory studies.

Stability studies of S. myosurus silver nanoparticles

The optimum synthesis and stability of silver nanoparticles were investigated by varying pH gradients 2, 4, 6, 8, 10, and 12, extract quantities 2, 4, 6, 8, and 10 mL corresponding to 1.2, 2.4, 3.6, 4.8, and 6 mg and silver nitrate concentrations (1, 2, 3, 4, and 5 mM) of the previous reaction mixture.27 Two milliliter aliquots of different samples were taken, and absorbance was measured at 5 minutes, 1 hour, 3 hours, 24 hours, 48 hours, 72 hours, and 192 hours after the beginning of the reaction. The pH was adjusted using 0.1 N H2SO4 and 0.1 N NaOH solutions.

Characterization of silver nanoparticles

Ultraviolet (UV)-visible spectroscopic measurement The reduction of silver ions was monitored by measuring UV-visible spectrum of the reaction mixture at 5 minutes, 1 hour, 3 hours, 24 hours, 48 hours, 72 hours, and 192 hours using the UV-visible spectrophotometer (UV-line 9,100 single beam, halogen light source, 1 nm resolution). Distilled water was used as a blank.

Fourier transform infrared (FTIR) spectroscopy

FTIR spectrum was recorded at room temperature through potassium bromide pellet method. Samples were grinded with KBr pellets and kept in infrared path, and the spectrum was measured using a Nicolet IS5 model of Thermo Scientific operating at a resolution of 0.4 cm−1.

Powder X-ray spectroscopy (PXRD)

The PXRD spectroscopy measurements of purified silver nanoparticles were carried out using a Panalytical Empyrean Serie 2 X-ray diffractometer (Cu K-Alpha1 [Å] 1.54060, KAlpha2 [Å] 1.54443, K-Beta [Å] 1.39225) by preparing a thin film on silicon substrate.

High-resolution scanning electron microscopy (HR-SEM) and energy dispersive X-ray spectroscopy (EDS)

The biosynthesized silver nanoparticles were subjected to HR-SEM for morphology determination. A small amount of sample powder was deposited on a carbon-coated carbon grid and coated with carbon using a coating sputter coater (Quorum Q 150 TES) to increase the conductivity of the sample. SEM images were taken using Carl Zeiss Auriga Field Emission Scanning Electron microscope image at 5 keV. EDS spectrum for elemental analyses was collected with an Oxford Instruments X-Max solid-state silicon drift detector operating at 20 keV coupled to a TECNAI G2 HR-SEM.

High resolution-transmission electron microscopy (HR-TEM) and selected area electron diffraction (SAED)

For the HR-TEM, the sample was prepared by placing a drop of the nanoparticle suspension on the carbon-coated copper grid and allowing water evaporation inside the vacuum dryer. HR-TEM observations as well as SAED were carried out using an FEI Tecnai G2 Field Emission Gun – HR-TEM operating at 200 kV.

Evaluation of anti-inflammatory activities

Animals and ethics

Wistar albinos rats of 8 weeks old, weighing 130–150 g, housed in standard polypropylene cage at room temperature (24°C±2°C) and relative humidity under light and dark cycle (from 6 am to 6 pm) were used for this study. They were obtained from the Laboratory of Animal Biology, Faculty of Science, University of Douala. They were fed with standard pellet food and tap water ad libitum during 1 week of acclimatization. All experiments were carried out according to the approved protocol by the Institutional Ethical Committee of the University of Douala (Protocol approval number CEI-UDo/809/02/2017/T).

Inhibition of albumin denaturation assay

A reaction mixture (5 mL) consisting of 0.2 mL of egg albumin (from fresh hen’s egg), 2.8 mL of PBS (pH 6.4), and 2 mL of varying concentrations of silver nanoparticles (25, 50, 100, 200, and 400 µg/mL) was incubated at 37°C in a biochemical oxygen demand incubator for 15 minutes and then heated at 70°C for 5 minutes. A similar volume of distilled water served as control. After cooling, their absorbance was measured at 660 nm by using the vehicle as blank. Acetylsalicylic acid at concentrations of 5, 10, 15, 25, 50, and 100 mg/mL was used as reference drug and treated similarly for determination of absorbance.28,29 The percentage of inhibition of protein denaturation was calculated by using Equation 1: where Vt is the absorbance of the test sample and Vc is the absorbance of control. The drug concentration for 50% inhibition was determined from the dose–response curve by plotting percentage inhibition with respect to control against treatment concentration.

Carrageenan-induced rat paw edema method

The anti-inflammatory activity of silver nanoparticles was evaluated on a carrageenan-induced rat paw edema model as described by Winter et al.30 The experimental animals were randomly divided into five groups (n=6). Group I served as a control receiving inflammatory inducing agent only. Group II served as standard, and groups III, IV, and V served as test. Acute inflammation was induced by a single subplantar injection of 0.1 mL of carrageenan (1% carrageenan suspended in 0.9% NaCl) in the right hind paw of the rats 1 hour following administration (per os) of silver nanoparticles at doses of 100, 200, and 400 µg/kg for test groups, indomethacin (10 mg/ kg) for standard group, or distilled water (10 mL/kg) for control group. Paw size was measured by means of volume displacement technique using water plethysmometer (No 37140; Ugo Basile, Cologne, Italy) immediately before and 30 minutes, 1 hour, 2 hours, 3 hours, 4 hours, and 5 hours after the carrageenan injection. The edema was expressed as the increase in paw volume, and the percentage of inhibition of edema was expressed as the reduction in volume with respect to the control group using Equation 2: where Vt is the average volume for each group and V0 is the average volume obtained for each group before any treatment.31

Statistical analysis

Results are expressed as mean ± SEM. The difference between treated groups and control group was compared using one-way ANOVA followed by Dunnett’s post hoc test. The analyses were carried out using software PRISMA (version 5.01; GraphPad Software, Inc., San Diego, CA, USA). P-values <0.05 were considered significant.

Results

Visual observations of biosynthesized nanoparticles

Silver nanoparticles were biosynthesized using S. myosurus aqueous extract. The formation of silver nanoparticles was preliminarily observed by the change in the silver nitrate solution color to brownish yellow while adding the aqueous extract as depicted in Figure 2. The brownish yellow color is due to the excitation of free electrons in the nanoparticles and occurs in 3 hours at room temperature. After 24 hours, no further color change was observed due to stabilization of the synthesized nanoparticles.

Figure 2

Silver nitrate (A), plant extract (B), and silver nanoparticles (C) solutions.

Effects of condition reaction on the biosynthesis of nanoparticles

Effect of pH

Effects of condition reaction on the biosynthesis of nanoparticles Effect of pH The UV-visible spectra absorption bands of synthesized silver nanoparticles using S. myosurus at different pH are shown in Figure 3. It can be seen that nanoparticles are well synthesized at basic pH with an optimal pH 12. The plasmon absorbance bands increase with increasing pH from 8 to 12 and decrease with decreasing pH from 6 to 2. Furthermore, the yellowish nanoparticles color (pH 6) tends change to brown (pH 12) with increasing pH, whereas no change in color or absorbance has been recorded in the acid middle.

Figure 3

Ultraviolet-visible spectra of the variation of pH.

Influence of extract quantity

Influence of extract quantity Figure 4A and B shows the color appearance and evolution of surface plasmon, respectively, in the synthesis of silver nanoparticles using 2, 4, 6, 8, and 10 mL aqueous extract. Results were recorded 24 hours following incubation time, and it is notable that the production of nanoparticles increases with increasing extract quantity.

Figure 4

(A) Color of silver nanoparticle solution at different extract quantities. (B) Ultraviolet-visible spectra of the variation of extract quantities.

Silver nitrate concentration impact

Different silver nitrate solutions of different concentrations were utilized for the synthesis of nanoparticles. The color change and the surface plasmon absorbance band evolution using 1, 2, 3, 4, and 5 mM silver nitrate solutions are shown in Figure 5A and B, respectively. As is clearly seen, the synthesis of nanoparticles increased with increasing silver nitrate concentration. Visible spectra were recorded 24 hours following incubation time.

Figure 5

(A) Color of silver nanoparticle solution at different silver nitrate concentrations. (B) Ultraviolet-visible spectra of the variation of silver nitrate concentration.

Characterization of biosynthesized nanoparticles

UV-visible spectral studies

UV-visible spectroscopy was used to detect and confirm the presence of nanoparticles in the sample based on their optical absorbance peaks. The absorption spectra of the synthesized silver nanoparticles were recorded against water in order to monitor their formation and their stability. Figure 6 depicts the UV-visible spectra of synthesized silver nanoparticles using 50 mL of AgNO3 10−3 mol/L with 10 mL of plant extract as a function of time. The characteristic peak of silver nanoparticle known as the surface plasmon resonance timely increased and is in the range 420–480 nm.

Figure 6

Ultraviolet-visible spectra analysis of synthesized nanoparticles.

FTIR spectroscopy results

The FTIR spectrum to determine the various functional groups which acted as capping agents is depicted in Figure 7. The vibrational band in the 3,030 cm−1 region is associated with the stretching modes of C−H, N−H, and O−H bonds. Absorption bands at 2,920 and 2,839 cm−1 are due to stretching vibrations of C−H group. The absorptions occurring at 2,300–2,400 cm−1 can be attributed to O=C=O molecules. The band at 1,606 is attributed to the bending vibration modes of the aromatic ring C=C and N−H bond of amines. The absorption band at 1,323 cm−1 is due to the presence of the C−N-like amine groups. The band at 1,483 represents aliphatic C−H vibrations. The weak band at 1,169 is C−O− stretch. The peak centered at 1,015 cm−1 is the indication of C−H in-plane/C−H out-of-plane deformation. The bonds in the area 670–1,000 cm−1 correspond to stretching vibrational band of =C−H. The two bands at 759 cm−1 and 685 cm−1 are due to the out-of-plane bending vibrations of C−H groups.

Figure 7

Fourier transform infrared spectrum for synthesized silver nanoparticles using Selaginella myosurus.

PXRD results

X-ray diffraction was used for the characterization of the crystal structure of the silver nanoparticles. PXRD pattern of the synthesized silver nanoparticles shown in Figure 8 illustrates crystalline peaks at 2θ values of 38°, 44.2°, 64.4°, and 77.4° that can be indexed to the (111, 200, 220), and (311) planes of the face-centered cubic (fcc) structure, respectively (JCPDS file: 65-2871). The PXRD pattern also showed the presence of the cubic phase of silver chloride at 2θ values of 27.8°, 32.2°, 46.2°, 54.8°, 57.4°, 67.4°, 74.4°, and 76.7° corresponding to the (111, 200, 220, 311, 222, 400, 331) and (420) planes, respectively (JCPDS file: 31-1238). The calculated average crystalline particle size was found to be 33.7 and 44.2 nm for silver and silver chloride, respectively, using the Debye–Scherrer; Equation 3: where Dv is the average crystalline size; K is a dimensionless shape factor, with a value close to unity (0.99); λ is the wavelength of Cu Kα; β is the full width at half-maximum of the diffraction peaks, and θ is Bragg’s angle.

Figure 8

X-ray diffraction pattern of the nanoparticles from Selaginella myosurus; ○ represents silver nanocrystallites and ● represents silver chloride nanocrystallites.

HR-SEM and EDS results

Figure 9 shows the HR-SEM image of the synthesized silver nanoparticles. One can distinguish that almost all the nanoparticles are highly crystalline aggregates of spherical shape with varied size. The elemental analysis of the sample was performed using EDS, and the EDS spectrum is shown in Figure 9. The peaks observed at 0.18, 3.0 and 0.12, 2.71 keV correspond to the binding energies of silver and Cl, respectively. A peak situated at the binding energy of 1.75 keV belonging to Si has been observed. No peaks of other impurities have been detected, indicating that the silver nanoparticles sample contain pure silver, with no oxide. Furthermore, the sample contained a high concentration of silver nanoparticles, and the atomic percentage was 65.89%, which is shown in Table 1.

Figure 9

High-resolution scanning electron microscopy image of silver nanoparticles with energy dispersive X-ray spectroscopy profile.

Table 1

Energy dispersive X-ray spectroscopy elemental composition of synthesized nanoparticles

Elements	Atomic %
Si	3.41
Cl	30.6
Ag	65.99
Total	100

HR-TEM and SAED results

HR-TEM image of silver colloidal solution providing information on the morphology and size of the nanoparticles is shown in Figure 10. It exhibits that the particles were predominantly spherical in shape. Following the digitization phase of various images, the nanoparticle size (largest diagonal) distribution using ImageJ software was estimated. Such a diagonal was found to be within the 15–95 nm range. By fitting the histogram data with a Gaussian distribution, the average size was found to peak at 58.81 nm. Onset on Figure 10 shows the SAED pattern of the synthesized silver nanoparticles obtained by directing the electron beam perpendicular to one of the nanoparticles in the aggregate. The patterns of SAED spots were indexed according to reflections of fcc structure of elemental silver and cubic silver chloride, indicating that synthesized silver nanoparticles from S. myosurus aqueous extract are crystalline spherical particles.32

Figure 10

High-resolution transmission electron microscopy image of silver nanoparticles and selected area electron diffraction pattern.

Inhibition effect of AgNPs on egg albumin denaturation

The in vitro bioassay results of antiarthritic effect of silver nanoparticles assessed against denaturation of egg albumin are summarized in Table 2. All tested concentrations significantly (P<0.001) inhibited the denaturation of egg albumin. The maximum inhibition percentage obtained was 99% at a concentration of 0.2 mg/mL. The acetylsalicylic acid used as a standard drug exhibited an inhibition of 65% at a concentration of 5 mg/mL.

Table 2

Effect of Selaginella myosurus silver nanoparticles on rat paw edema induced by carrageenan

Treatment	Dose (mg/kg)	Edema (ΔV in mL)
		30 minutes	1 hour	2 hours	3 hours	4 hours	5 hours
Control	–	0.26±0.06	0.30±0.05	0.32±0.05	0.39±0.05	0.37±0.06	0.34±0.05
Indomethacin	10	0.21±0.06 (17.80)	0.22±0.04 (25.50)	0.18±0.04 (43.80)	0.20±0.04** (49.50)	0.12±0.04*** (68.60)	0.10±0.02*** (71.50)
AgNPs	0.1	0.17±0.03 (35.70)	0.17±0.04 (44.30)	0.19±0.03 (41.30)	0.24±0.03* (39.20)	0.25±0.04 (31.90)	0.24±0.04 (31.40)
AgNPs	0.2	0.17±0.02 (33.30)	0.17±0.01 (42.30)	0.20±0.02 (36.90)	0.22±0.02* (43.30)	0.18±0.03** (51.90)	0.15±0.04** (57.60)
AgNPs	0.4	0.17±0.02 (35.70)	0.14±0.01* (54.40)	0.17±0.01* (45.60)	0.19±0.02** (50.50)	0.16±0.01*** (55.70)	0.14±0.04*** (60.50)

Notes: Values are expressed as means ± SEM in each group (n=5);

P<0.05,

P<0.01,

P<0.001 compared with the control; values in parenthesis represent the percentage of inhibition.

Abbreviation: AgNPs, silver nanoparticles.

Effect of AgNPs on carrageenan-induced paw edema in rats

The effect of silver nanoparticles on carrageenan-induced rat paw edema is shown in Table 3. The injection of carrageenan produced in control animals, a local edema in the following 30 minutes that increased progressively and reaches its peak 3 hours after carrageenan injection. The oral administration of silver nanoparticles resulted in a significant inhibition of paw edema when compared with control group. The maximum inhibition percentages obtained were 44.30% (1 hour), 57.60% (5 hours), and 60.50% (5 hours) for the doses of 0.1, 0.2, and 0.4 mg/kg (body weight), respectively. Indomethacin used as standard drug showed a significant (P<0.001) protective effect against carrageenan-induced paw edema, by 71.50% at 5 hours.

Table 3

Influence of silver nanoparticles and acetylsalicylic acid against protein denaturation

Sample	Concentration (mg/mL)	Optical density	% inhibition	IC50 (mg/mL)
Control	–	2.53±0.03	–	–
AgNPs	0.4	0.13±0.00	94.87	0.00073
AgNPs	0.2	0.02±0.00***	98.97
AgNPs	0.1	0.05±0.00***	97.77
AgNPs	0.05	0.12±0.00***	95.03
AgNPs	0.025	0.21±0.00***	91.72
Acetylsalicylic acid	100	2.22±0.00	12.42	61.16
Acetylsalicylic acid	50	1.97±0.27	21.97
Acetylsalicylic acid	25	1.25±0.08**	50.57
Acetylsalicylic acid	15	1.21±0.05***	52.16
Acetylsalicylic acid	10	1.08±0.10***	57.20
Acetylsalicylic acid	5	0.87±0.06***	65.42

Notes: Values are expressed as means ± SEM in each group (n=3);

P<0.01,

P<0.001 compared with the control.

Abbreviations: AgNPs, silver nanoparticles; IC50, concentration for 50% inhibition.

Discussion

The synthesis of silver nanoparticles by green novel and environmental friendly pathway using the natural extract of S. myosurus extract as an effective anti-inflammatory agent was demonstrated. The UV-visible spectra as a function of time illustrated increasing absorbance bands indicating gradual reduction as well as nucleation and growing size of nanoparticles. The absorption spectra of the synthesized silver nanoparticles were recorded against water in order to monitor the formation and stability of silver nanoparticles. The color change of the mixture solution (plant extract and silver nitrate) was first recorded through visual observation. The color change following incubation is due to the formation of plasmon at the colloid surface, indicating the synthesis of silver nanoparticles.33 The impact of extract quantity and silver nitrate concentration on the synthesis have been studied. Results show that surface plasmon resonance absorbance band increased with increasing quantities of both reactants. This has been observed for olive leaf extract34 or Megaphrynium macrostachyum leaf extract35 and optimizes the reaction in producing more nanoparticles. S. myosurus aqueous extract acts as a reductant as well as capping agent, therefore, mediates the synthesis as well as stabilization of the silver nanoparticles with characteristic plasmon resonance band in the range 420–480 nm.33 The color intensity of the solution changes from light yellow to deep-brown at the end of the reaction because of increasing amount of silver nanoparticles. It has also been observed that plasmon absorbance bands decreased at lower pH and increased at higher pH. To our knowledge, such an evolution is not described in the literature. Generally, plasmon absorbance bands increase with increasing pH from 2 to 12, such as observed for M. macrostachyum leaf extract-mediated silver nanoparticles.35 A major influence of the reaction pH is its ability to change the electrical charges of biomolecules, which might affect their capping and stabilizing abilities and subsequently the growth of the nanoparticles.33 Previous studies have shown that the size and shape of biosynthesized nanoparticles could be manipulated by varying the pH of the reaction mixtures, thereby increasing the rate of the reduction reaction,27,34 such as observed for olive leaf extracts and Pinus eldarica bark extract.34,36 pH affects the amount of nanoparticle production and their stability. It is a critical factor to control the size and morphology of nanoparticles.36

A typical FTIR spectrum of the obtained silver nano-particles to identify the potential biomolecules in the plant extract responsible for the reduction and also the capping reagent responsible for the stability of the bioreduced silver nanoparticles was associated with absorption bands, indicating various stretching modes including C−H, N−H, O−H, C=C, C=N, C=O, and C−O.37–39 From the FTIR analysis, it is evident that the silver nanoparticles are capped with phytochemicals with various functional groups of organic molecules such as flavonoids, saponins, steroids, terpenoids, tannins, or phenols, which give characteristic peaks in the spectrum.37

The typical PXRD pattern of the prepared nanoparticles presented in Figure 5 is compatible with the cubic phase of silver with various diffraction points corresponding to the fcc structure (JCPDS file: 65–2871). The PXRD pattern also showed the presence of the cubic phase of silver chloride (JCPDS file: 31-1238). No other characteristic peaks were found, indicating the high purity of the as-prepared silver and silver chloride nanoparticles. The most intense peaks of silver and silver chloride were chosen to calculate the average crystalline particle size.40 Thus, we selected the (111) and (200) lattice planes of silver and silver chloride, respectively. The intense and narrow diffraction peaks revealed the crystalline nature of the synthesized nanoparticles.41 Pattern identification shows the formation of pure crystals of silver and silver chloride. Similar observations were made using leaf extracts of Corchorus olitorius, Ipomea batatas, or flowers extract of Albizia julibrissin.26,41 Distribution, surface morphological, and nanostructural studies of synthesized silver nanoparticles have been investigated using HR-SEM and HR-TEM coupled with EDS and SAED, respectively. It has been found that the synthesized silver nanoparticles were crystalline aggregated, spherical in shape with varied size. Such variation in size is common when using biological systems for the synthesis.42 The large polycrystalline nature of the particles may be due to the fact that on the nanometer scale, most of the metals are as fcc structures. They tend to nucleate and grow onto twinned and multiply twinned particles with their surfaces bounded by the lowest energy facets. Silver nanoparticles have the tendency to agglomerate due to their high surface tension of ultrafine nanoparticles.42 The fine particle size results in a large surface area that, in turn, enhances the nanoparticle activities. The EDS profile of bioreduced silver ions indicated that the silver nanoparticles contain pure silver without oxide, and SAED pattern clearly confirmed their crystalline nature.

The ability of the synthesized silver nanoparticles to inhibit albumin denaturation has been investigated for potential anti-inflammatory action mechanism. It is well documented that protein denaturation is involved in arthritic reactions and development of tissue damage during inflammation.43–46 Results reveal that synthesized silver nanoparticles were effective in inhibiting thermally induced albumin denaturation at all tested concentrations, indicating their capability of controlling protein denaturation involved in the inflammatory process. Upon translating from in vitro to in vivo systems, Carrageenan-induced rat hind paw edema model was used to assess the anti-inflammatory potential of silver nanoparticles loaded from S. myosurus aqueous extract. It is a widely used experimental model of acute inflammation that exhibits a high degree of reproducibility.47 The characteristic swelling that occurs in the rat paw is due to increased vascular permeability and edema formation.48 Edema induced by carrageenan is a triphasic response that involves the release of different mediators including histamine and serotonin in the first phase (1 hour). The second phase is mediated through the release of kinins (2 hours), and the third phase is attributed to prostaglandins and cyclooxygenase products, which last from 3 to 5 hours.31,49 Oral pretreatment of animals with silver nanoparticles resulted in a significant inhibition (P<0.001) of edema rate during the three phases of inflammation when compared with control group. The maximum inhibition (60.50%) was obtained at the dose of 0.4 mg/kg, 5 hours after injection of the phlogistic agent. This result suggests that nanoparticles consisting of silver and silver chloride may interfere with the release of acute inflammatory mediators or antagonize their action. Furthermore, the persistent anti-inflammatory activity might be due to enhanced permeability and retention effect of silver nanoparticles in the edema region that has been reported by Moldovan et al.50 Indomethacin, an NSAID used as standard exerted a significant (P<0.001) inhibition of paw edema only at the third phase. Thus, the inhibition of edema formation and albumin denaturation activities of silver nanoparticles from S. myosurus aqueous extract clearly establish their anti-inflammatory potential and therefore could be considered as potential source of the anti-inflammatory drug. However, one should try to further figure out other action mechanisms responsible for this activity via other detailed experimentations.

Conclusion

The concept of nanomedicine has risen to be the future of medicine. Advantages of using silver nanoparticles to treat inflammation have many benefits such as low drug dose efficacy. Silver and silver chloride nanoparticle-mediated S. myosurus have been obtained and characterized. Synthetic optimization shows increases in plasmon resonance bands with the solute and extract concentrations as well as pH. The generated particles are found to be crystalline spherical in shape and biofunctionalized with organic molecules. The synthesized silver nanoparticles exhibited significant inhibition of albumin denaturation, indicating a strong anti-inflammatory potential and of edema formation in rats, hence, could be considered as a potential source of the anti-inflammatory drug.