Antimicrobial and Photocatalytic Activities of Selenium Nanoparticles Synthesized from Elaeagnus indica Leaf Extract

Abstract

Selenium nanoparticles (Se NPs) have recently received much interest due to their low toxicity, high bioavailability, and wide applications. This study synthesized Se NPs using selenious acid as a starting material and leaf extract from Elaeagnus indica as a reducing agent. Spectroscopic and electron microscopy investigations have demonstrated the production of aggregated amorphous Se NPs with phytochemicals. Furthermore, the reduction of selenious acid into Se NPs by phytochemicals present in the leaf extract of E. indica was confirmed in a prominent band at 269 nm in the UV-visible spectrum. The biosynthesized selenium nanoparticles have a 10–15 nm particle size distribution. The agar well diffusion assay exhibited remarkable dose-dependent, wide-spectrum antimicrobial efficacy of the Se NPs against all the tested microorganisms. Moreover, the lowest minimum inhibitory concentration (10 µg/mL) was noted against Salmonella Typhimurium and Fusarium oxysporum. The prepared Se NPs degraded methylene blue dye by about 89% after 6 h of exposure to sunlight. In conclusion, the synthesis of Se NPs using E. indica leaf extract shows promise as a method for producing Se NPs with significant antimicrobial activity and potential for methylene blue photodegradation. These properties make them potentially valuable in various fields, including water treatment and biomedical applications, in the future.

1. Introduction

Nanotechnology is becoming a tremendously attractive area of study in material science; it entails the manipulation of matter on the nanoscale via the application of innovative physical and chemical processes to produce new materials with unique features. In recent years, this field has seen substantial development [1,2]. Nanoparticles have a variety of distinct advantages, such as a larger surface area to volume ratio and quantum confinement, resulting in enhanced performance in a range of applications. Several of these benefits of nanomaterials have been employed in the management of energy, the control of environmental contamination, and the treatment of health issues because of their novel properties that their bulk materials cannot deliver [3,4]. Nowadays, the rise in antibiotic-resistant bacteria has led researchers to focus on the development of novel nanomaterial-based antimicrobial agents over synthetic antibiotics [5,6].

Similarly, industrialization and urbanization have caused a critical problem of environmental pollution worldwide. Mainly aquatic pollution caused by industrial waste harms both aquatic and terrestrial life, leading to significant economic losses [7]. Furthermore, organic dyes are harmful to the environment and non-biodegradable, leading to deadly diseases such as human cancer. Although various modern technologies, such as adsorption, filtration, reduction, precipitation, electrolysis, flocculation, coagulation, and microbially mediated process, are available to combat water pollution, they come with certain limitations, such as high costs and the use of harmful chemicals [3,7]. Hence, an urgent need to clean up this polluted water has led to the developing of advanced new technologies [8]. Recently, photocatalytic nanomaterials have gained significant attention due to their potential to mitigate contamination in aquatic environments through photocatalytic processes [9]. Hence, developing nanomaterials for various applications has attracted significant interest recently. Many different types of nanomaterials have been developed and used in various aspects [10,11].

Selenium (Se) is a nonmetal that exists in three forms: amorphous Se, crystalline trigonal, and crystalline monoclinic. Selenium is a significant material that can be used to mitigate environmental pollution and act as an antimicrobial agent [12]. Moreover, selenium is a trace element required for living organisms and is crucial in various critical biological processes. Due to its unique chemical, physical, and biological characteristics, selenium has garnered significant interest in photocatalysis, biosensing, antimicrobial applications, diagnostics, and therapy [13]. Nanomaterials can be synthesized using various bottom-up approaches, such as sol-gel, precipitation, hydrothermal, microemulsion, sonochemical, and microwave-assisted processes [14,15,16]. However, most bottom-up techniques have some drawbacks, such as hazardous chemicals, complex methodology, limited product efficiency, and significant energy consumption [4,17]. Similarly, the chemical and physical nanoparticle synthesis techniques have resulted in hazardous effluents or expensive processes [18,19]. Owing to the drawbacks of chemical and physical NPs, synthesis techniques lead to the finding of novel methods which rectify these problems. Moreover, the cellular uptake of inorganic Se NPs is lower than the organic form, limiting their biological applications. Therefore, synthesizing Se NPs using biomolecules can enhance their biocompatibility and stability. One such alternative method is the green synthesis of selenium nanoparticles (Se NPs), which has gained considerable attention due to its numerous advantages [20].

Different plant, fungal, and bacterial species and their extracts have been used as reducing agents in the process of NPs synthesis [21,22]. Biomolecules generally act as reducing agents that convert Se⁴⁺ (selenate) or Se⁶⁺ (selenite) to Se⁰ to produce Se NPs [23]. Therefore, plant extracts have been used as both reducing and stabilizing agents in the green synthesis of Se NPs, which have been extensively investigated for their potential applications in photocatalysis and antimicrobial activity [20,23]. Further, previous studies have indicated that the concentration and reduction potential of the phytochemicals present in the plant extracts directly influence the phytofabrication of Se NPs [15,16,17,18,19,20,21,22,24,25,26,27,28]. In addition, several secondary metabolites from plants are reported to exhibit various biological functions [29]. Therefore, the presence of phytochemicals in nanoparticles can provide additional functional properties to the nanoparticles [30]. Consequently, various plants are being explored to synthesize selenium nanoparticles for various environmental and biomedical applications.

Elaeagnus indica Servett, a member of the Elaeagnaceae family, is found in the Eastern Ghats region of India [31]. E. indica contains various phytochemicals, including polyphenolics, flavonoids, tannins, alkaloids, fixed oils, glycosides, saponins, steroids, and proteins. Furthermore, extracts of E. indica exhibit significant antioxidant larvicidal, antimicrobial, antiproliferative, and anti-inflammatory activities [32,33]. Previous studies have indicated that silver, copper, and zinc-based nanoparticles synthesized using E. indica extracts exhibit significant antimicrobial and light-dependent organic dye degradation potential [7,34]. However, there is limited research on using E. indica extract for nanoparticle production. To our knowledge, no reports on synthesizing selenium nanoparticles using E. indica extract exist. Therefore, this study aims to fill this research gap using a simple and environmentally friendly approach for synthesizing selenium nanoparticles using E. indica leaf extract. Additionally, we investigated the antimicrobial potential and photocatalytic degradation ability of biosynthesized Se NPs nanoparticles against methylene blue dye.

2. Materials and Methods

2.1. Chemicals

Ciprofloxacin, dimethyl sulfoxide (DMSO), fluconazole, p-iodonitrotetrazolium, methylene blue (MB), Müller Hinton broth, Müller Hinton agar, Sabouraud dextrose broth, Sabouraud dextrose agar, and selenous acid were purchased from Himedia Laboratories, Mumbai, India. All the reagents/chemicals used in this study were analytical grade and used as supplied. All the experiments were performed with double-distilled water.

2.2. Plant Source and Extraction

The fresh, young, and healthy leaves of Elaeagnus indica were collected from the Kolli Hills (latitude—11.316098 and longitude—78.349249) in the Namakkal district of Tamil Nadu, India. The taxonomy of the collected plant material (Reference letter No: BSI/SRC/5/23/2014-15/Tech/1942) was confirmed by the Botanical Survey of India (BSI) in Coimbatore, Tamil Nadu, India. The collected plant materials were washed with running tap water followed by double-distilled water to remove any solid dust particles; later, leaves were dried for two weeks at room temperature in dark. Dried leaves were pulverized, sieved using a 100 mesh sifter, and stored in an air-tight bag. These powdered components were used for phytochemical extraction. A 50 g E. indica leaf powder was loaded in a Soxhlet apparatus and double-distilled water was used as extractive solvent. The plant material was extracted until the efflux solvent was colorless. Further, the extract was filtered using Whatman filter paper (No. 1) and kept at 4 °C in a sealed container until it was utilized for the synthesis of nanoparticles.

2.3. Synthesis of Se NPs

The synthesis of selenium nanoparticles was carried out by the method [35] with some modifications. Selenous acid is used as the starting material for synthesizing Se NPs. The prepared E. Indica extract solution (200 mL) was mixed with 50 mM of selenous acid while vigorously being stirred in a conical flask. The mixture was agitated continuously for 24 h at room temperature. Next, the reaction mixture was centrifuged for 20 min at 4000 rpm to remove unreacted reactants. The nano pellets were washed with distilled water, then acetone, and centrifuged. Then, the obtained precipitates were subjected to drying at 110 °C and ground into powder for further analysis.

2.4. Characterization of Synthesized Se NPs

2.4.1. X-ray Diffraction Analysis

The XRD pattern of the synthesized Se NPs was recorded with a step size of 2°/min in a X’Pert Pro X-ray diffractometer (PANalytical, Malvern, UK) with current settings of 30 mA and voltage settings of 40 kV in the 2θ range of 10–80° using CuKα X-ray source (λ = 1. 5406 Å).

2.4.2. Fourier Transform Infrared Spectroscopy (FTIR) Analysis

For FTIR analysis, 100 mg of KBr powder with 2 mg of the prepared specimen was mixed to form thin discs using a pelletizer. The prepared disc sample was examined in the range of 400 to 4000 cm⁻¹ by a Perkin Elmer RX-I (Perkin Elmer, Waltham, MA, USA), FT-IR spectrometer with a resolution of 1 cm⁻¹.

2.4.3. Particle Size Analyzer

The particle size distribution of the synthesized specimen was examined using a particle size analyzer (NANOPHOX, Sympatec GmbH, Clausthal, Germany). A disposable acrylic glass cuvette was used for measurement. Automated cuvette placement and accurate laser intensity control to optimize measuring signal facilitates quick measuring.

2.4.4. Scanning Electron Microscopy (SEM) and EDX

SEM (JSM-6360, JEOL, Japan) at voltage 7.50 kV was used to conduct a morphological examination on a sample obtained by vacuum drying a drop of NPs solution on a graphite grid. The elements present in the prepared specimen were micro-analyzed on the SEM by an energy-dispersive X-ray microanalyzer (EDS, Oxford INCA, Abingdon, Oxfordshire, UK).

2.4.5. Transmission Electron Microscopy (TEM)

TEM (model JEM 2100, JEOL, Tokyo, Japan), was used to analyze the particle size and shape. Acetone was used to disperse the powdered material on a carbon-coated copper grid before it was allowed to dry so that TEM imaging could be performed.

2.5. Antimicrobial Activity

2.5.1. Agar Well Diffusion Assay

The antimicrobial activity of the synthesized Se NPs was evaluated against four clinically isolated bacteria (two Gram-positive bacteria (Bacillus subtilis and Staphylococcus epidermidis) and two Gram-negative bacteria (Salmonella Typhimurium and Klebsiella pneumoniae) as well as two clinically isolated fungal pathogens (Fusarium oxysporum and Aspergillus niger) by agar well diffusion method as previously described [7]. A total of 5 mL of Müller Hinton broth (MHB) was used to grow the mother culture of selected bacterial strains in a shaking condition (for 16 h) at 37 °C to obtain a turbidity of 1.5 × 10⁸ CFU. Similarly, 5 mL of Sabouraud dextrose broth (SDB) was inoculated with fungal cultures and incubated at room temperature for 72 h to obtain an effective fungal mass of 1 × 10⁶ CFU for antifungal activity. Agar well diffusion test was performed using 10 mg of the prepared nanoparticles dispersed in 1 mL of DMSO. A 50 µL suspension of the selected bacterial and fungal cultures was swabbed on the Müller Hinton agar (MHA) and Sabouraud dextrose agar (SDA) plates, respectively, using a sterilized cotton swab. After swabbing, a 5 mm sterile cork borer was used to bore five holes at equal distances on each MHA and SDA medium plate. Then, 50 μL of the prepared Se NPs suspension at various concentrations (25, 50, and 75 μg) was loaded into wells and diffused at room temperature. Fluconazole (1 μg/mL) and ciprofloxacin (1 µg/mL) were used as positive controls for fungi and bacteria, respectively, and an equal amount of DMSO was used as a negative control. The bacterial and fungal plates were incubated at 37 °C for 24 h and 72 h at room temperature, respectively. After the incubation period, the diameter of the growth inhibition zone was measured and recorded.

2.5.2. Minimum Inhibitory Concentration (MIC)

The broth micro-dilution bioassay method was used to measure the MIC values of synthesized Se NPs. This test was carried out according to the method of Srinivasan et al. (2017). Briefly, 100 µL of different concentrations (1, 5, 10, 15, 20, 25, 30, 40, 50, and 75 µg/mL) of Se NPs was mixed with an equal volume of medium (MHB for bacteria and SDB for fungus) into 96 well microplates. A 20 µL microbial culture was introduced to each well, and the microplate was incubated in appropriate growth conditions, as mentioned in Section 2.5.1. After incubation, 40 µL of p-iodonitrotetrazolium (0.2 mg/mL, as a growth indicator) was introduced to each well and again incubated for 1 h. The development of red color indicated the microbial growth in wells. The lowest concentration of the Se NPs in which red color development was not found was recorded as MIC value.

2.6. Photocatalytic Activity

A 10 mg of prepared Se NPs was added to 100 mL (50 mg/L) of aqueous MB solution and magnetically agitated for 30 min to reach equilibrium. Then, it was subjected to sunlight and the photocatalytic activity of Se NPs was recorded between sunrise and sunset. At appropriate time intervals, aliquots of 2–3 mL supernatant were filtered to test the photodegradation of MB dye. The absorption spectra of the supernatant were observed using a UV-Vis spectrophotometer (Hitachi, Japan). The quantity of dye undergoing disintegration was determined from the standard calibration based on the highest absorbance at 660 nm [7,36]. Furthermore, an experiment serving as a control was conducted without sunlight and Se Nps.

3. Results and Discussion

3.1. Characterization of Synthesized Se NPs

X-ray diffraction (XRD) was performed to investigate the crystalline behavior of the synthesized Se Nps. Figure 1a shows the XRD pattern of the prepared Se NPs specimen. It exhibited a broad peak at roughly 2θ = 19–25° without any sharp Bragg reflections, indicating the amorphous nature of Se NPs [24]. Previous studies have shown that plant extracts can produce amorphous Se NPs [25,26], which coincides with the present study’s findings. By contrast, crystalline selenium has a crystal structure with prominent and sharp peaks at 2θ = 24°and 30° [27]. It is necessary to heat the as-prepared Se NPs around 400 °C to attain crystalline form. However, it may eliminate bioactive molecules essential to this green product’s antibacterial function. Hence, we have intentionally used as-prepared Se NPs for further studies. The FTIR spectrum of Se NPs is shown in Figure 1b, which was acquired in the mid-IR range between 400 and 4000 cm⁻¹. The bands identified at 3272 cm⁻¹, 2915 cm⁻¹, 1640 cm⁻¹, 1330 cm⁻¹, and 1059 cm⁻¹ correspond to O–H, C–H, C = O, C = C, and N–H bonds, respectively, which correlated with the functional groups of phytocompounds such as alcohols, alkenes, amines, flavonoids, and carboxylic acids [37,38]. The bands detected at 540 cm⁻¹ related to the stretching vibration of the C–S bond in the organic residue [31]. Based on these results, it is possible to assert that the biomolecules derived from leaf extract were responsible for capping the surface of the Se NPs and that they play a significant role in the synthesis of Se NPs.

The formation of Se NPs from plant extract was confirmed by the results of UV-visible spectroscopy analysis (Figure 2a. In general, 200–800 nm wavelengths of light were used to characterize the formation of metal oxide nanoparticles. The chemically reduced Se NPs were detected in a prominent band at 269 nm, corresponding to the surface plasmon resonance of the Se NPs; this indicated that the synthesis of Se NPs from plant extract was successful. This peak provided conclusive evidence for Se NPs, which was in line with the findings of the previous publications [38,39,40]. One of the most common approaches to determining the size of NPs is called dynamic light scattering (DLS), also known as photon correlation spectroscopy. When the Se NPs suspension is subjected to a light beam, its direction and intensity are changed due to the scattering phenomenon of Se NPs. Figure 2b depicts the particle size distribution of the synthesized Se NPs, demonstrating that the particle size distribution is in the nanoscale range. The average particle size distribution of the biosynthesized Se NPs was found to be 14 nm. The DLS analysis findings coincide with the Se NPs synthesized using Diospyros montana leaf extract [38].

SEM was used to investigate the surface morphology and microscopic structure of produced Se NPs. Figure 3a shows SEM images of Se NPs obtained using an aqueous leaf extract of E. indica as a reducing agent. The SEM picture reveals spherical selenium nanostructures that are highly aggregated and consistently organized throughout the surface area. Agglomerated nanoparticles may be produced by nucleating and developing particles on the nanoscale scale, followed by interactions with the physical environment [41]. However, because of their tiny sizes and tendency to aggregate, the shape and size of individual particles could not be assessed with a high degree of accuracy. The results of EDX analysis revealed that the synthesized Se NPs harbor a significant amount of Se (49.88 wt.%) and O (46.16 wt.%), and a low amount (3.96 wt.%) of carbon (Figure 3b). The occurrences of carbon and oxygen in the EDX spectrum of the Se NPs were due to the presence of phytochemicals. In most cases, phytochemicals were found to be present in the Se NPs, which are synthesized using plant extracts [35,38,39]. These phytochemicals may play an essential role in the biological activities of the Se NPs [38].

Figure 4 shows TEM images of synthesized Se NPs, which show spherical morphology. Nanoparticles were found to be 10–15 nm in size and homogeneous and highly agglomerated, which aligns with the SEM and DLS analysis. Polyphenols, flavonoids, and terpenoids are some of the phytochemicals found in E. indica leaf extract. This extract is a natural and sustainable source of reducing agents that is cost-effective and ecologically friendly. Phytochemicals found in E. indica leaf extract can interact with selenium precursor and control particle growth in three dimensions, leading to a spherical shape. Most publications have revealed that most green synthesis-produced Se nanoparticles are spherical [42], which agree well with the present study. Compared to the results of other published articles [28,43], the size of the Se NPs found in this study is smaller (5–10 nm).

3.2. Antimicrobial Activity

The synthesized Se Nps showed a dose-dependent, broad-spectrum antimicrobial activity (Figure 5). The antimicrobial results revealed that the Se NPs significantly inhibited the growth of both gram-positive and gram-negative bacteria (

Table 1. Antimicrobial activity of green synthesized Se nanoparticles by well diffusion method.

Organisms Name	Diameter of Zone of Inhibition (in mm)
	25 µg †	50 µg	75 µg	PC *	NC #
	Bacteria
Bacillus subtilis	11.67 ± 1.25	14.00 ± 1.63	17.67 ± 0.47	31.67 ± 1.25	0.00 ± 0.00
Staphylococcus epidermidis	09.00 ± 0.82	15.33 ± 0.47	16.33 ± 1.25	31.00 ± 0.82	0.00 ± 0.00
Salmonella Typhimurium	14.33 ± 1.25	17.00 ± 0.82	18.67 ± 0.94	34.67 ± 0.94	0.00 ± 0.00
Klebsiella pneumonia	10.33 ± 1.25	14.67 ± 0.94	15.00 ± 0.82	30.67 ± 0.47	0.00 ± 0.00
	Fungus
Fusarium oxysporum	13.67 ± 0.47	20.00 ± 1.41	21.33 ± 0.47	22.33 ± 1.25	0.00 ± 0.00
Aspergillus niger	07.00 ± 0.82	9.33 ± 0.47	10.00 ± 1.41	17.00 ± 1.63	0.00 ± 0.00

^†—Amount of synthesized Se NPs. *—Positive control (PC) for antibacterial (Ciprofloxain (1µg/µL) and antifungal (fluconazole, 1µg/µL) activity; ^#—Negative control (NC) (DMSO).

). The high concentration (75 µg) of Se NPs exhibited the maximum zone of growth inhibition of 17.67 ± 0.47, 16.33 ± 1.25, 18.67 ± 0.94, 15.00 ± 0.82, 21.33 ± 0.47, and 10.00 ± 1.41 mm against B. subtilis, S. epidermidis, S. Typhimurium, K. pneumoniae, F. oxysporum, and A. niger, respectively (Table 1). It should be noted that even at a low concentration of Se NPs (25 µg), a zone of growth inhibition of 11.67 ± 1.25, 9.00 ± 0.82, 14.33 ± 1.25, 10.33 ± 1.25, 13.67 ± 0.47, and 7.00 ± 0.82 mm were found against B. subtilis, S. epidermidis, S. Typhimurium, K. pneumoniae, F. oxysporum, and A. niger, respectively. However, minimal growth inhibition was observed in the A. niger even at a high concentration (75 µg) of Se NPs tested.

The MIC values of Se NPs against all the tested microorganisms were in the range of 10–25 µg/mL except A. niger (Figure 6). The lowest MIC values (10 µg/mL) was detected in S. Typhimurium and F. oxysporum, which indicated that these microbes are more sensitive to the synthesized Se NPs. The least growth inhibition effect of Se NPs was observed in A. niger due to the high MIC value (75 µg/mL). The MIC values are correlated with the agar diffusion test. The presence of phytochemicals such as flavonoids, terpenoids, alkaloids, and other bioactive compounds in the NPs is a possible reason for the antimicrobial potential of those NPs synthesized from plant extracts [7]. These phytochemicals can inhibit the enzymes responsible for DNA replication and other gene expansion essential for the survival of microbes. Further, these compounds alternate the cell wall and or cell membrane permeability, leading to microbial cell death [7,37,44] It is also possible that selenium nanoparticles have an antibacterial effect owing to the production of reactive oxygen species or the inactivation of enzymes, which might result in the death of microbial cells [37,44].

3.3. Photodegradation Activity

The Se NPs exhibited a significant light-dependent MB dye degradation potential (Figure 7). About 11% of MB dye degradation efficacy was noted in the dark. In contrast, the sunlight exposure increased the MB dye degradation efficiency of Se NPs up to 89% during the 6 h photoperiod. Electrons can move from the valence band to the conduction band of prepared Se NPs when the energy of solar radiation is greater than the bandgap energy. Those photogenerated electrons produced radicals such as superoxide anion radicals and OH radicals in an aqueous medium. These radicals work fast to convert the MB dye into other by-products that are not harmful [45,46]. The following reaction could take place during the process of MB being broken down by selenium nanoparticles in the presence of light.

$$\mathrm{Se}\mathrm{NPs}\stackrel{hv}{\to }({\mathrm{h}}^{+}{)}_{\mathrm{VB}}+(\mathrm{e}{-}^{}{)}_{\mathrm{CB}}$$

H₂O + (h⁺)_VB → H⁺ + ^•OH

O₂ + (e⁻ )_CB → O₂^•−

MB dye + ^•OH + O₂^•− → organic ions CO₂ + H₂O

Figure 8 illustrates the process when the prepared Se NPs are subjected to solar radiation, forming superoxide anion radicals and OH radicals. This is the consequence of the inherent characteristics and phytochemical makeup of Se NPs obtained via plant extract-mediated synthesis. This might cause fluctuations in the electronic structure, resulting in a typical photocatalytic activity [7]. Previous reports by other researchers well support this finding. Hassanien et al. studied the mechanism of the photocatalytic degradation process of Se NPs obtained using M. Oleifera leaves extract and found that it involved the generation of reactive oxygen species and the breaking of the azo bond in the Sunset yellow azo dye molecule [47]. Moreover, Menon et al. showed that the biosynthesized selenium nanoparticles were highly effective in the degradation of the three industrial dyes (Methylene Orange dye, Coomassie Brilliant Blue, Bromophenol Blue) with high degradation efficiencies [48].

The present study is the first report on synthesizing Se NPs using E. indica leaf extract. Chemical synthesis is the most prevalent method used to manufacture Se NPs. However, this method often involves using hazardous chemicals such as sodium borohydride, which, when combined with water, may produce explosive or combustible gases. The production of Se NPs via biosynthesis from plant extracts is less harmful to the environment since it does not result in the formation of any hazardous chemicals [28,49]. Moreover, selenium is vital for human health, with a daily need of 300 µg [50]. Selenium is an essential trace element in most organisms and plays a crucial role in the scavenging of free radicals, the prevention of oxidation, and the retardation of the aging process in living systems [50,51]. The absorption of Se NPs from antibacterial products such as ointments or gels may not be hazardous since selenium plays a function in the body’s homeostasis. Se NPs outperform other products such as silver or gold nanoparticles [28]. The prepared Se NPs in this study act as a potential antimicrobial for a wide range of microorganisms and as a better photocatalyst for the degradation of MB dye.

4. Conclusions

The present study successfully produced Se NPs using selenous acid as the raw material and E. indica leaves extract as a reducing agent. The results of spectral and microscopy studies such as XRD, FTIR, DLS, UV-visible, SEM, TEM, and EDX conclude that the formation of aggregated amorphous Se NPs were associated with the phytochemicals from E. indica extract. The outcome of the DLS analysis indicated that the particle size distribution of the biosynthesized selenium nanoparticles was averaged to be 14 nm. The synthesized Se NPs exhibited a significant antimicrobial potential against all the tested microbes. Similarly, the Se NPs showed remarkable (89%) MB dye degradation potential in sunlight. Therefore, these green synthesized Se NPs may be used as an effective pharmacological agent and photocatalyst for the environmental remediation process in the future.