Synthesis of Biogenic Silver Nanocatalyst and their Antibacterial and Organic Pollutants Reduction Ability.

Plant-mediated nanoparticles are gaining popularity due to biologically active secondary metabolites that aid in green synthesis. This study describes a simple, environmentally friendly, dependable, and cost-effective production of silver nanoparticles utilizing Cucumis sativus and Aloe vera aqueous leaf extracts. The aqueous leaf extracts of Cucumis sativus and Aloe vera, which worked as a reducing and capping agent, were used to biosynthesize silver nanoparticles (AgNPs). The formation of surface plasmon resonance peaks at 403 and 405 nm corresponds to the formation of colloidal Ag nanoparticles. Similarly, the Bragg reflection peaks in X-ray diffraction patterns observed at 2θ values of 38.01°, 43.98°, 64.24°, and 77.12° representing the planes of [111], [200], [220], and [311] correspond to the face-centered cubic crystal structure of silver nanoparticles. Fourier transform infrared spectroscopy confirms that bioactive chemicals are responsible for the capping of biogenic silver nanoparticles. The size, structure, and morphology of AgNPs with diameters ranging from 8 to 15 nm were examined using transmission electron microscopy. Water contamination by azo dyes and nitrophenols is becoming a more significant threat every day. The catalytic breakdown of organic azo dye methyl orange (MO) and the conversion of para-nitrophenol (PNP) into para-aminophenol using sodium borohydride was evaluated using the prepared biogenic nanoparticles. Our nanoparticles showed excellent reduction ability against PNP and MO with rate constants of 1.51 × 10-3 and 6.03 × 10-4s-1, respectively. The antibacterial activity of the nanomaterials was also tested against four bacteria: Staphylococcus aureus, Klebsiella pneumoniae, Enterobacter, and Streptococcus pneumoniae. These biogenic AgNPs displayed effective catalytic and antibacterial characteristics by reducing MO and PNP and decreasing bacterial growth.

Introduction

Nanomaterials research has exploded in popularity in recent years, affecting nearly every science and industry because of the irreplaceable qualities that massive materials lack. Three key characteristics control and influence the behavior of nanomaterials: shape, size, and crystallinity.[1,2] Noble metal nanoparticles, such as Ag or Au, have been discovered to have unique features among diverse biosynthesized metal nanoparticles, including optical,[3] catalytic,[4] and antibacterial properties.[5] The first step in investigating the many properties of these nanoparticles is to synthesize them. Chemical and physical methods of producing nanoparticles have been interchangeable for decades. Therefore, biological processes were also investigated for the same reason: they provide a straightforward, low-cost, and environmentally beneficial option.[1] The use of various fungi,[6] bacteria,[7] and plant[8] extracts to produce silver nanoparticles (AgNPs) is a well-studied topic these days. Further, extracts from common plants have been utilized to generate Ag nanoparticles from silver salts, but they have not been widely employed. Moreover, on the one hand, plant extracts are often used as reducing agents, responsible for the reduction and stability of nanoparticles when they interact with metal ions. On the other hand, Riaz et al. described that plant extracts could be quite effective because they contain significant reducing and capping agents.[9]

Because of electrostatic interactions between silver ions and proteins in plant material extract, the bioreduction of Ag was considered to involve capturing Ag+ ions on the protein surface. Proteins reduce the Ag+ ions, resulting in a change in secondary structure and the formation of silver nuclei. Silver nuclei are formed by further reducing Ag+ ions and their build-up at the nucleus, resulting in the production of AgNPs.[10] The fundamental mechanism driving the plant-mediated synthesis of AgNPs, according to our findings, is a plant-assisted reduction caused by phytochemicals found in Cucumis sativus and Aloe vera fruit peel extract. The primary phytochemicals in Aloe vera include vitamins (A (beta-carotene), C, and E), enzymes (aliiase, amylase, alkaline phosphatase, bradykinase, carboxypeptidase, cellulase, catalase, lipase, and peroxidase), sugars (monosaccharides glucose and fructose) and polysaccharides (polymannose/glucomannans), fatty acids (plant steroids, campesterol, cholesterol, β-sisosterol, and lupeol), and anthraquinones (phenolic compounds).[11] Organic acids, quinones, and flavones, water-soluble phytochemicals, are responsible for rapidly reducing silver ions in the reaction mixture. According to reports, xerophytes include anthraquinone and emodin, which undergo tautomerization and result in the creation of AgNPs.[12] In most situations, the reducing agent from the plant extract also serves as a capping and stabilizing agent, removing the need for external capping and stabilizing chemicals.[13] It has been discovered that the type of plant extract employed as a reducing agent affects the reduction of silver ions.[14]

Water contamination is currently one of the most important environmental issues, owing to the presence of organic color molecules.[15,16] Among the various nitroaromatic chemicals, nitrophenols are the most common contaminant of industrial effluents. Aqueous nitrophenol effluents are common industrial wastes produced during various organic products, including pharmaceuticals, insecticides, herbicides, plasticizers, dyes, and explosives. Nitrophenols are extremely difficult to biodegrade, posing a threat to the environment, and are carcinogenic to humans.[17−19] Therefore, the Environmental Protection Agency of the United States (U.S. EPA) has designated nitrophenol and its derivatives as priority contaminants, proposing that their concentration in natural water bodies be kept to no more than 10 mg/mL. Nitrophenols irritate the eyes and cause necrosis of the skin. It also harms the liver, kidneys, and muscles. One gram of nitrophenols has been reported to be fatal to an adult.[20] Carcinogenic amines are produced in aquatic bodies due to reducing azo and nitro chemicals.[21] Because of its complex aromatic chemical structure and xenobiotic properties, methyl orange (MO) dye is non-biodegradable. MO is an organic sulfur salt azo dye that is widely used in the food, textiles, paper, pulp, and leather industries as an indicator and reagent. MO dye and its metabolites are widely leaking into the aquatic environment, posing a health danger.[22−24] The use of metal nanoparticles for the catalytic degradation of organic dyes and nitroaromatic compounds is an essential method for converting hazardous chemicals into environmentally beneficial chemicals. Because of its outstanding catalytic activity and eco-friendly characteristics, this approach is widely utilized for the remediation of recalcitrant contaminants.[25] On the one hand, for the photodegradation of organic contaminants, semiconductor-based materials such as CeO2, Fe2O3/ZnO, and WO3/Ce2S3 nanotubes have recently been employed.[26,27] Metal oxides, on the other hand, have a disadvantage in that they do not absorb visible light.

This paper describes the biological generation of silver nanoparticles by reducing Ag+ ions with Cucumis sativus peel extract and Aloe vera leaf extract. The catalytic activity of the colloidal particles was tested using established techniques such as MO dye degradation in the presence of NaBH4 as a reducing agent and catalytic hydrogenation of para-nitrophenol (PNP) to para-aminophenol (PAP). Further to employ beneficial constituents, specifically phytochemicals present in both plant extracts, prepared nanoparticles have been used for antimicrobial activity. Antibacterial activities of these nanoparticles were tested against four bacteria: Staphylococcus aureus, Klebsiella pneumoniae, Enterobacter, and Streptococcus pneumoniae.

Experimental Section

Materials

Aloe vera and Cucumis sativus were purchased from a local market to make the peel extract. Merck provided the AgNO3 (Merck KGaA, purity: 99.0%), MO (Merck), NaBH4 (Merck KGaA, purity: 98.0%), and PNP (Sigma-Aldrich, ≥99%) needed for this project. The University of Ottawa Science Shop was used to purchase four bacterial strains.

Preparation of Silver Nanoparticles

Aloe vera and Cucumis sativus were chosen for the biosynthesis of AgNPs because of their cost-effectiveness, availability, and medicinal properties. Biosynthesis was performed in the manner previously described[28] with minor modifications. A grinder was used to smash 50 g of Aloe vera and cucumber peel extracts, which had been cleaned and crushed in 500 mL of distilled water. It was then filtered and centrifuged at 5000 rpm for 5 min, yielding a clear soup containing both extracts.

The silver nitrate solution was made by dissolving 3.38 g of AgNO3 in 1000 mL of distilled water to make a 20 mM AgNO3 stock solution. 100 mL of 20 mM AgNO3 solution was mixed with each extract, drop by drop, until the medium was half diluted to reduce the number of Ag+ ions in the silver nitrate solution. The reacting mixture was agitated at ambient temperature before a noticeable alteration in the color of the solution, as exhibited in Figure . After the reaction was completed, the mixture was centrifuged for 30 min at 10 000 rpm to separate the nanoparticles from the remaining constituents. The nanoparticle precipitate was redispersed in deionized water (10 mL) in the centrifuge tube. This suspension was centrifuged for 15 min at 5000 rpm in ethanol to remove the biomass residue altogether. The pellet of nanoparticles in the centrifuge tube was dried in a vacuum drier, yielding a dry powder of biogenic AgNPs. These dry AgNPs were used for various characterizations discussed further below.

Figure 1

Pictorial presentation of the synthesis of Aloe vera-mediated biogenic AgNPs (photograph courtesy of Muhammad Riaz. Copyright 2022).

Characterization of Silver Nanoparticles

The absorption spectra of the prepared nanoparticles mixture were recorded by a PerkinElmer UV–visible spectrometer at regular intervals by scanning the reacting mixture from 200 to 800 nm. The Rigaku Ultima-III X-ray diffractometer was used to analyze the crystalline nature of dried biogenic Ag nanoparticles. An IR-Prestige (Shimadzu) Fourier transform infrared (FTIR) spectrometer was used to record the FTIR spectra of biogenic Ag nanoparticles. For the transmission electron microscopy (TEM) analysis, high-resolution JEOL-2010 TEM (operating voltage is 200 kV) was used. The zeta potential of AgNPs was recorded using water as a solvent and Zetasizer Nano S90 (Malvern) at room temperature.

Catalytic Reduction Reactions

AgNPs were used to catalyze the reduction of the dyes MO and PNP. A 1 mM aqueous solution was prepared to catalyze PNP in DI water. The reaction vessel was a UV quartz cuvette. After a quartz cuvette was put in, the UV–visible spectra of 3 mL of PNP solution were obtained. Then added 0.5 mL of freshly prepared 0.5 M concentration NaBH4 solution. The solution color changed from bright yellow to dark yellow. In the quartz cuvette containing the solution mixture, 10 mg of Ag catalyst was added. Reduction began when the nanoparticles were added to the cuvette, and spectra were recorded using a UV–visible spectrometer between 200 and 800 nm (PerkinElmer). For MO dye, 0.04 mM concentration was used, following the same experimental procedure.

The catalytic proficiency of the catalysts was determined from UV–visible spectra with the following equationwhere A0 is the initial absorbance (at λmax 404 nm for PNP and 462 nm for MO), and At is the absorbance at different time intervals (t).

Antibacterial Activity Study

The antibacterial activity of AgNPs was analyzed using the well diffusion method against two Gram-positive bacteria, S. aureus and S. pneumoniae, and two Gram-negative bacteria, K. pneumonia and Enterobacter. The culture strains were kept on appropriate media composed of nutrient agar and regular agar powder. By comparing the results, clarithromycin was used as a positive control. After that, the bacteria were grown in an incubator at 37 °C for 24 h. Following the incubation period, the antibacterial activity was determined by monitoring and measuring the inhibition zone around the wells.

Results and Discussion

Synthesis of Nanoparticles

Aqueous solutions of Cucumis sativus (C. sativus) and Aloe vera extract were used to reduce silver nitrate into AgNPs. The color change primarily proved the reduction of silver ions from light green to dark red.[29] The formation of AgNPs began when the addition of plant extracts started with silver nitrate solution, which changed the color of the reaction from light greenish to yellowish after 10 min. Organic biomolecules of Aloe vera and C. sativus extracts are thought to be effective in the reduction as well as capping nanoparticles. After an hour of extract addition (Figure ), implying the origination of colloidal Ag nanoparticles in the mixture. After 8 h of incubation, the color changed to a dark brown as the reaction time increased.

UV–Vis Spectroscopy

A UV–visible spectrometer was employed to scan the mixture at regular intervals to monitor the formation of silver nanoparticles over time. The peak absorbance was found at 403 nm in the case of C. sativus-mediated AgNPs, as presented in Figure a, and at 405 nm in the case of Aloe vera-mediated AgNPs, as depicted in Figure b. The formation of surface plasmon resonance (SPR) peaks of AgNPs corresponds to colloidal Ag nanoparticles.[30]Figure a,b shows UV–visible spectra acquired at different time intervals (1, 2, 8, and 12 h). The peak absorbance rose with reaction time, and the variance is depicted in the figures. The peak absorbance increased linearly to 12 h of incubation, indicating that more colloidal particles were produced in the reacting media. The formation rate saturates after 12 h of incubation, indicating that the reaction is complete. The absorbance value at 12 h was most excellent, indicating that a substantial number of nanoparticles formed over time.

Figure 2

UV–Visible spectra for the continuous growth of AgNPs. (a) C. sativus-mediated AgNPs and (b) Aloe vera-mediated AgNPs. Experiments were performed at room temperature. Measurements were taken at 1, 2, 8, and 12 h intervals.

XRD Analysis

After the centrifugation and drying of the colloidal silver solution, the XRD analysis of C. sativus- and Aloe vera-mediated AgNPs were performed. The XRD pattern of prepared AgNPs is identical to that reported in our previous paper.[31] All the perceived peaks specify metallic silver crystallite. In the XRD pattern of both C. sativus- and Aloe vera-mediated AgNPs, the Bragg reflection peaks were observed at a 2θ value of 38.01°, 43.98°, 64.24°, 77.12°, and 81.4° representing the planes of [111], [200], [220], [311], and [222] (Figure ). The crystalline face-centered cubic structures of AgNPs match these planes.[32,33] All the peaks in the XRD pattern of AgNPs can be indexed as a standard Ag crystal (JCPDS No. 4-0783).[33,34] XRD patterns of C. sativus and Aloe vera revealed no extra peak, confirming the pure crystalline nature of prepared AgNPs.

Figure 3

XRD patterns of (a) C. sativus-mediated AgNPs and (b) Aloe vera-mediated AgNPs.

The Scherrer equation was used to compute the average crystallite size of biogenic AgNPs.Here, λ (1.5418 Å) is the wavelength of X-rays, θ is the Bragg angle, β1/2 is full width at half-maximum (fwhm) at the 2θ scale, and k is a constant equal to unity.

The average crystallite size of C. sativus-mediated AgNPs was 12–20 nm (mean size of ∼15 ± 2.5 nm), ably supported by TEM images. Similarly, the average crystallite size of Aloe vera-mediated AgNPs was 15–24 nm (mean size of ∼19 ± 3.8 nm). The lack of other peaks in the XRD data implies that the biosynthesized Ag nanoparticles are pure and crystalline.

TEM Analysis

The surface morphology and the average size of the prepared biogenic silver NPs were determined using high-resolution transmission electron microscopy (Figures and 5). In the literature, it has been demonstrated that the shape and size of nanoparticles have a considerable impact on their optical and electrical properties. According to TEM histograms, the synthesized silver NPs are spherical and monodispersed, with some having a highly truncated triangular shape. According to TEM images, C. sativus-mediated silver nanoparticles are generally spherical in shape (Figure ). Figure shows the particle size and a histogram of C. sativus-mediated AgNPs, which have an average diameter of 14.29–14.7 nm. Similarly, TEM images (shown in Figure ) indicate that the silver nanoparticles produced by Aloe vera are spherical. Figure depicts the particle size and histogram of biogenic Ag NPs mediated by Aloe vera, with an average diameter of 8.4–11 nm.

Figure 4

TEM images and particle distribution histogram of C. sativus-mediated AgNPs.

Figure 5

TEM images and particle distribution histogram of Aloe vera-mediated AgNPs.

EDS and Zeta Potential

The elemental composition of our synthesized AgNPs was analyzed using an energy-dispersive X-ray spectrum (EDX). Furthermore, the EDX spectroscopy provides both quantitative and qualitative details about the elements that were present in the NPs. The analysis was performed at the University of Ottawa. The elemental analysis of AgNPs was determined by putting the fabricated nanoparticles on carbon-coated thin films. The EDX spectrum of our synthesized AgNPs exhibited strong signals in the silver region for both samples, and an absorption peak was observed at 3 keV (Figures a,b). On the one hand, the peak in this region at 3 keV is due to the SPR of Ag, indicating the successful formation of AgNPs.[35] On the other hand, some other signals, including carbon, oxygen, chlorine, and silicon, were also detected in both synthesized AgNPs. The presence of these elements could have acted as capping agents of plant extract attached to the surface of synthesized AgNPs.[36]

Figure 6

EDX investigation of (a) C. sativus- and (b) Aloe vera-mediated AgNPs. (c) Zeta potential value of C. sativus- and Aloe vera-mediated AgNPs. (d) FTIR spectra of C. sativus- and Aloe vera-mediated AgNPs.

Zeta potential is the scale of electrostatic interaction in nanoparticles and can be used to predict the stability of the dispersion system. The zeta potential of AgNPs was recorded using water as solvent and Zetasizer Nano S90 (Malvern) at room temperature. Zeta potential is one of the important indicators to speculate on the stability of metallic NPs. According to previous studies, nanoparticles having values of zeta potential less than −25 mV or more than +25 mV exhibit a high degree of stability. On the one hand, because of interparticle attractions, dispersions with a low zeta potential value will ultimately coalesce. The zeta potential of nanoparticles, on the other hand, is highly influenced by the pH and electrolyte content of the dispersion.[37] In the absence of an electrolyte, the zeta potential of dispersed AgNPs in deionized water was −10.6 and −7.29 mV, as presented in Figure c. The zeta potential value of our Aloe vera-mediated AgNPs was −10.6 mV, and this comparatively negative zeta potential value is an origin of the exceptional stability of the silver colloids by the electrostatic repulsion. Carboxylate moieties are found in anionic polysaccharides like pectin, which is often found in Aloe vera extract, and are a likely source of negative zeta potential. Because some of the phytochemicals used are also amphiphilic, green-produced AgNPs might have a high degree of stability even if their zeta potentials were not in the above-mentioned range.[38] These negative values of zeta potential can be attributed to the presence of the negatively charged polyphenolic species, which capped the surface of nanoparticles.[39] For both samples, the magnitude of the zeta potential of Aloe vera-mediated Ag nanoparticles was found to be higher than that of S. sativus-mediated AgNPs indicating the level of stability of the AgNPs prepared by Aloe vera extract.

FTIR Spectroscopy

The identification of stabilizing and reducing agents was performed using an FTIR analysis of prepared AgNPs. FTIR spectroscopy is essential for detecting the organic functional groups in plant extracts, which are responsible for metal ion reduction and stability. Figure d shows the dried Ag nanoparticles’ recorded FTIR spectrum (absorbance mode). There are six different peaks in the whole range of the recorded spectrum. The C–H bending of alkanes and the C=O stretching vibration of amides is responsible for the bands at 1260 and 1625 cm–1, respectively.[40,41] The band at 801 cm–1 could represent the stretching of C–N bonds in amines, and the band between 2946 and 3219 cm–1 represents the stretching of O–H bonds in aromatic compounds (such as phenol).[42] At 1240 and 1533 cm–1, the remaining two bands correspond to hydrocarbon C–O and C–H bond stretching and bending, respectively.[43] According to this investigation, the bioactive functional compounds found in C. sativus and Aloe vera, fruit extracts, such as phenols and amines, may reduce Ag ions and stabilize colloidal particles during the interaction.

Catalytic Reduction of Methyl Orange Dye

The textile industry’s discharge of dye sewage into the aquatic environment is the primary source of water contamination. Methyl orange is a toxic wastewater pollutant that can cause environmental impact. MO is commonly used as a laboratory indicator in the textile industry. The presence of the azo group and its low biodegradability make MO a severe environmental hazard.[44,45] As a result, the treatment of MO is a top priority. In the absence of a sufficient catalyst, reducing MO by sodium borohydride is kinetically inefficient but thermodynamically favorable. The peak intensity of MO at 462 nm has been reported to remain constant for longer time in the absence of a catalyst.[46]

For reduction, 3 mL of MO and 0.5 mL of NaBH4 solutions were mixed in a quartz cuvette. An aqueous MO dye shows a significant absorption at 462 nm in the visible region and a smaller peak at 281 nm in the UV region. No changes in peak intensities occurred even after 20 min and were constant without AgNPs addition. After 5 mg of dry AgNPs was introduced, the drop in λmax at 281 and 462 nm began. The UV–visible absorption spectra of the mixture were constantly collected at intervals of 1 min, as shown in Figure a. The peak intensity at 462 nm continuously decreased over time, as shown in Figure a, although the peak intensity at 282 nm marginally drifted to 252 nm with an increase in absorption. The drop in intensity at 462 nm with the progressive disappearance with AgNPs insertion was caused by the commencement of MO degradation. In the presence of a AgNPs catalyst, sodium borohydride reduced a molecule of MO dye at the azo site and thus formed smaller amino compounds. As a result, the −NH2 group molecule produced during the reduction reaction of MO dye was ascribed to the new peak appearance at 252 nm with an increase in intensity.[47] It has been already reported that AgNPs minimize MO dye at the azo linkage in the presence of sodium borohydride and provoke free amino group hydrazine derivative, low molecular compounds,[48,49] as demonstrated in Scheme .

Figure 7

Catalytic reduction ability of Aloe vera-mediated AgNPs against (a) PNP by NaBH4 and (b) MO by NaBH4. (c) Percent reduction. (d) Plot of ln At/Ao vs time.

Scheme 1

Plausible Reduction Mechanism of MO by AgNPs Catalyst in the Presence of Sodium Borohydride

The percent reduction of the reaction was evaluated using Equation from their UV–visible spectra. Figure c displays that our nanoparticles have a good MO reduction, with a 57% reduction in 14 min. As a result, the reduction/degradation of MO by our biogenic AgNPs is relatively high, especially when compared to a recent study that found that ∼80% of MO degradation takes 45 min utilizing Mussaenda erythrophylla-mediated silver nanoparticles.[48] This proposes that our catalyst has an exceptional catalytic reduction ability.

The reduction/degradation of MO dye by sodium borohydride follows the pseudo-first-order reaction and was calculated from the linear plot of ln(At/A0) versus reduction time using Equation .

Thus, the pseudo-first-order (kapp) calculated for MO dye from the slope for AgNPs at the average temperature was 6.03 × 10–4 s–1 (Figure d).

Hydrogenation of PNP

para-Nitrophenol is a hazardous organic pollutant impervious to biodegradation and is, thus, persistent. Researchers are concentrating their efforts on reducing and removing this pollutant from the environment. Note that the sodium borohydride-mediated PNP reduction has been used as a model reaction to investigate the catalytic activity of the catalyst toward nitroaromatic chemicals because this reaction is simple to measure.[50]

Biogenic AgNPs in the presence of NaBH4 could catalytically convert the hazardous PNP to the corresponding PAP. When 0.5 mL of 0.1 M NaBH4 was added to the cuvette containing 2.5 mL of 0.1 mM PNP solution, the light yellow color of PNP turned bright yellow, and the wavelength shifted from 321 to 401 nm under alkaline conditions.[51] The addition of NaBH4 altered the pH of the solution mixture due to the production of para-nitrophenolate ions that emerged at 401 nm. The reaction mixture containing PNP without AgNPs was stable for up to 30 min using a time-dependent UV–visible spectrophotometer, with higher absorbance at 401 nm. PAP was synthesized with the addition of 10 mg of biogenic AgNPs, which worked as a catalyst, converting PNP to PAP. The solution turns colorless when the reaction is complete, indicating that PNP has been entirely reduced to PAP. The new peak for PAP appeared at 301 nm after 13 min. The catalytic reduction of PNP to PAP results in the loss of the 401 nm peak and a new peak at 301 nm.[25,52,53]

It was previously reported that only NaBH4 cannot reduce/hydrogenate PNP.[52] As earlier verified that at the normal condition, the hydrogenation of PNP (E_1/4 _0.76 V) is possible thermodynamically because, in an aqueous medium, borohydride ions (BH4–) (E_1/4 _1.33 V) act as a reductant. But kinetically, in the absence of a specific catalyst, the hydrogenation of the PNP to PAP is unfavorable and incredibly difficult to occur. This is due to the kinetic barrier of borohydride ions (BH4–) and phenolate ions (C6H4NO3–) that repel mutually each other.[54] For a quick electron transfer from an electron donor (NaBH4) to an electron acceptor (PNP) to catalytically reduce PNP, small AgNPs can supply more catalytic sites than large AgNPs.[55] The plausible hydrogenation mechanism of the PNP to PAP by a AgNPs catalyst in the presence of sodium borohydride is demonstrated in Scheme .

Scheme 2

Plausible Hydrogenation Mechanism of PNP to PAP by AgNPs Catalyst in the Presence of Sodium Borohydride

Thus, the hydrogenation process needed active catalysts like AgNPs to catalyze this process. Equation was used to compute the percent reduction of PNP by AgNPs catalyst. The AgNPs catalyst (Figure c) reduces PNP by 98.23% in 13 min. The apparent rate constant (kapp) of the pseudo-first-order reaction, calculated from the plot of ln(At/A0) versus time of reduction in seconds using Equation at normal temperature, was 1.51 × 10–3 s–1.

Antibacterial Activity

The agar well diffusion method was used to assess in vitro antibacterial activity on nutrient agar. This approach relies on antimicrobial component diffusion from the reservoir hole to the surrounding inoculated nutrient agar medium, inhibiting microbe growth as a zone around the hole. In a 1 mL saline solution, new cultures of K. pneumonia, Enterobacter, S. aureus, and S. pneumonia bacteria were mixed with a wire loop. Inoculums of 10–1 were generated by mixing 1 mL of bacterial-containing saline solution with another saline solution. A sterile spreader was used to disperse a 100 μL bacterial solution on the medium surface, and a cork borer was employed to punch holes. The diameter of the holes punched out in the agar medium was 6 mm. By micropipette, 25, 50, 75, and 100 μL of the AgNPs were poured into wells, while 50 μL of clarithromycin served as a control. For the effective diffusion of the test and standard, the plates were maintained in the refrigerator for 2 h at 2–8 °C. They were then cultured for 24 h at 37 °C in a bacterial strain incubator. The widths of the extract-induced inhibitory zones were compared to those produced by clarithromycin (30 mg/mL), a commercial control antibiotic. The inhibition zone was measured in millimeters.

The in vitro antibacterial activity of Aloe vera and Cucumis sativus AgNPs was tested against the bacterial activity. As shown in the paper, the zone of inhibition extended from 10 ± 0.02 to 22 ± 0.02 (Table ). 25, 50, 75, and 100 μL of Aloe vera and Cucumis sativus-mediated AgNPs were employed. The zone of inhibition against K. pneumoniae was 11 ± 0.02 mm at a concentration of 25 μL, 15 mm at a concentration of 50 μL, 18 mm at a concentration of 75 μL, and 21 mm at a concentration of 100 μL (Figure ). Enterobacter, S. aureus, and S. pneumoniae are three types of bacteria. The maximum activity of the conventional antibiotic clarithromycin against S. pneumoniae was 25 mm at a concentration of 50 μL. The AgNPs of Aloe vera and Cucumis sativus had good anti-K. pneumoniae action. The antimicrobial assay result is depicted in Figure . As shown in the data, the diameter of the inhibitory zone for Gram-negative bacteria is more significant than that of Gram-positive bacteria.

Table 1

Zone of Inhibition of Aloe vera and Cucumis sativus-Mediated AgNPs against Bacteria

Sr. No.	organisms (bacteria)	concentration of AgNPs (Av+Cs)				control (Clarithromycin)
		25 μL	50 μL	75 μL	100 μL	50 μL
1	K. pneumoniae	11 ± 0.02	15 ± 0.02	18 ± 0.02	21 ± 0.02	23 ± 0.02
2	Enterobacter	12 ± 0.02	14 ± 0.02	17 ± 0.02	22 ± 0.02	24 ± 0.02
3	S. aureus	10 ± 0.02	14 ± 0.02	19 ± 0.02	21 ± 0.02	24 ± 0.02
4	S. pneumoniae	11 ± 0.02	16 ± 0.02	18 ± 0.02	22 ± 0.02	25 ± 0.02

Figure 8

Zone of inhibition of AgNPs against K. pneumonia (Photograph courtesy of Muhammad Riaz. Copyright 2022).

Figure 9

Zone of inhibition of AgNPs against Enterobacter, S. aureus (Staph), and S. pneumonia (Photograph courtesy of Muhammad Riaz. Copyright 2022).

This could be because their cell walls’ makeup is different.[56] Gram-negative bacteria have a single-layer peptidoglycan cell barrier, but Gram-positive bacteria have a multilayer peptidoglycan cell wall, making it stiffer for penetration.[57] Previous research claims that silver nanoparticles emit Ag+ ions when they come close to bacterial cells, resulting in antibiotic action.[58] Because silver cations have a slight negative charge, they are drawn to the bacterial cell wall. When Ag+ ions are electrostatically attracted to the bacterial cell wall, they migrate toward it and attach to it. As a result, the cell wall composition changes rapidly, influencing the permeability of the cell wall. Cellular transport is further harmed, and cells die.[59]Aloe vera and Cucumis sativus-mediated AgNPs may have antibacterial action against bacteria that are known to be a primary cause of skin infection and could be helpful in treating the exact in vivo disease pathology.

Conclusion

The present study reported a green approach for the synthesis of AgNPs using a C. sativus and Aloe vera aqueous extract. The procedure is rapid, easy, cost-effective, and eco-friendly and did not require any solvents or reagents except water. Green synthesis approaches are becoming increasingly popular as a one-step, cost-effective, and environmentally friendly alternative to traditional chemical and physical syntheses. In the current study, additional strength has been given for the preparation using Aloe vera and C. sativus, as it is one of the important sources for the synthesis of spherical as well as face centered-cubic shaped AgNPs.

UV–visible spectroscopy revealed an SPR band at 405 nm, which confirms the formation of AgNPs. TEM confirmed the spherical shape AgNPs with an average diameter of ∼8.4 ± 2 nm. XRD confirms the crystalline nature and face-centered cubic structure of AgNPs. FT-IR spectra confirmed that biomolecules of Aloe vera and C. sativus were responsible for the reduction and capping of AgNPs. A catalytic investigation of biogenic silver nanoparticles effectively reduces methyl orange dye and para-nitrophenol. As evidenced by catalytic degradation and antibacterial activities, AgNPs were more active than the precursors.