Abstract
The biogenic synthesis of nanoparticles (NPs) using a plant extract is rapid, simple, efficient, cost-effective, and eco-friendly. This study investigated selective pharmacological activities such as anticancer, antioxidant, and DNA cleavage of S. elaeagnifolium-mediated green synthesizing Ag/AgO/Ag2O NPs. To the best of our knowledge, S. elaeagnifolium has been the first time used to synthesize Ag/AgO/Ag2O NPs. The synthesized NPs were explored by using UV–Vis diffuse reflectance spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, and photoluminescence analyses. Anticancer activity of Ag/AgO/Ag2O NPs was tested on lung cancer cell lines (A-549) and showed activity at the IC50 of 67.09 μg/mL. The maximum 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity were 25.78% and 20.86% at 100 µg/L, respectively. Moreover, S. elaeagnifolium-mediated green synthesized Ag/AgO/Ag2O NPs exhibited considerable DNA cleavage activity. These results assured that the synthesized Ag/AgO/Ag2O NPs using S. elaeagnifolium leaves extract may have potential applications in biomedical engineering.
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Introduction
Nowadays, nanotechnology has stupendous and enormous applications in many sectors of applied science and engineering like agriculture, biotechnology, dye degradation, food technology, wastewater treatment, energy, storage, ceramics, cosmetics, medical applications, drug delivery, bio-sensing, fabric, and textile engineering, etc. (Lin 2015; Thanh et al. 2014; Devadas et al. 2021; Gawande et al. 2016). In particular, metal oxide nanoparticles (NPs) have attracted extensive attention.
Many types of NPs, such as Ag2O (Ghotekar et al. 2020), SnO2 (Matussin et al. 2020), CdO (Ghotekar 2019), CuO (Cuong et al. 2021), Fe3O4 (Yew et al. 2020), ZnO (Bandeira et al. 2020), and ZrO2 (Nikam et al. 2019), have been prepared and applied in various promising applications. They could be manufactured by biological, chemical, and physical approaches; nevertheless, biological protocols are the most recommended and sustainable approach since chemical, and physical approaches have numerous downsides (Gawande et al. 2016). Notably, the eco-friendly approach makes use of algae (AlNadhari et al. 2021), bio-waste materials (Santhosh et al. 2021; Dabhane et al. 2021), microorganisms (Ibrahim et al. 2021), and plants (Cuong et al. 2021). Green synthesis using various medicinal plant parts is most rapid, simple, clean, easy, affordable, and environmentally gracious (Soni et al. 2021). The varied plant parts contain a variety of structurally diverse natural biochemicals such as vitamins, alkaloids, anthocyanins, flavonoids, coumarins, phenols, sugars, glycosides, volatile oils, saponins, tannins, which themselves serve as bio-reducing and/or bio-stabilizing agents for NPs production and hence obviating the use of noxious chemicals and solvents (Nasrollahzadeh et al. 2020).
Among diverse NPs, silver-based NPs, such as Ag, AgCl, Ag2O, and Ag2S NPs, are creating spectacular attention in the scientific arena due to their massive range of application in agriculture (Partila 2019), biomedical devices (Singh et al. 2017), catalysis (Bhosale and Bhanage 2015), ceramics (Göl et al. 2020), environmental remediation (Ghotekar et al. 2020, 2021), pharmaceuticals (Durán et al. 2016), photocatalysis (Ghotekar et al. 2020, 2021; Marimuthu et al. 2020), and sensing (Tagad et al. 2013). The selective morphology and size of the silver-based NPs determine their chemical and physical features (Sharma et al. 2021). Heretofore, various approaches, such as the hydrothermal method (Yang and Pan 2012), microwave-assisted method (Al-Shehri et al. 2020; Babu et al. 2018), sol–gel method (Shahjahan et al. 2017), thermal decomposition (Hosseinpour-Mashkani and Ramezani 2014), have been reported for the manufacturing of silver-based NPs. However, these strategies are highlighted by high manufacturing costs and hazardous substances, which have possibly harmful impacts on human health and the environment. The green synthesis approach, based primarily on plant extracts, is an environmentally benign alternative to handling harmful chemicals in the manufacture of NPs. Noxious chemicals are replaced in these regimens by compounds derived from plant extracts that act as reductants and stabilizers (Aygün et al. 2020; Gur et al. 2022). Previously, facile biosynthesis of silver-based NPs using plant extracts such as Acanthospermum hispidum (Ghotekar et al. 2019), Centella Asiatica (Rashmi et al. 2020), Prunus persica (Patra and Baek 2016), and Cochlospermum Gossypium (Ayodhya and Veerabhadram 2016) have been reported as a bio-reducing/bio-stabilizing agent, and their multifunctional applications are widely investigated.
Noticeably, Solanum elaeagnifolium of the family Solanaceae is a deep-rooted perennial plant that is found initially native to the Americas. As summarized in Fig. 1, Solanum elaeagnifolium extract contains several bioactive compounds, namely stigmasterol, kaempferol, C-glycoside, quercetin, mangiferin, rutin, chlorogenic acid, coumaroyl glycoside, dicaffeoyl quinic acid (Badawy et al. 2013; Elabbar et al. 2014; Balah and AbdelRazek 2020). Also, leaves from Solanum elaeagnifolium have repellent and insecticidal characteristics towards various crop pests and possibly be used as an alternative for synthetic insecticides (Hamouda et al. 2015). However, to the best of our knowledge, Solanum elaeagnifolium has been examined for its pharmacological effects, but it has never been employed to synthesize Ag/AgO/Ag2O NPs.
Herein, this contribution reports on Ag/AgO/Ag2O NPs engineered by an entirely green chemistry approach using Solanum elaeagnifolium natural extract as a fuel addition of any chemical additives. The synthesized Ag/AgO/Ag2O NPs were explored by various techniques to characterize the material further. In addition, selective biomedical applications such as anticancer, antioxidant, and DNA cleavage activities were also investigated.
Experimental
Collection of Solanum elaeagnifolium leaves and extracts preparation
The Solanum elaeagnifolium leaves were collected and appropriately washed using double distilled water. First, 5 g of leaves were poured into 100 mL of distilled water and boiled for 15 min at 85–90 ºC. Next, the extract obtained was filtered through ordinary filter paper and Whatman No. 1 filter paper. Finally, the filtered Solanum elaeagnifolium leaves extract (SELE) was stored at 4 °C for the synthesis of Ag/AgO/Ag2O NPs.
Biosynthesis of Ag/AgO/Ag2O NPs
Eco-benign synthesis of Ag/AgO/Ag2O NPs involved adding 1.69 g silver nitrate to 100 mL of SELE, and then the reaction solution was continuously stirred at 1100 rpm for 30 min at room temperature with a magnetic stirrer. Initial confirmation of Ag/AgO/Ag2O NPs synthesis is by a change in color of the reaction mixture from yellow to dark brown. Then, the resulting solution was then centrifuged at room temperature for 10 min at 3000 rpm and carefully washed to eliminate all the unwanted impurities. After removing the unwanted supernatant liquid, the black precipitate of material was placed in a hot air oven at 200 °C. The as-synthesized Ag/AgO/Ag2O NPs were then crushed into a powder using mortar and pestle. The obtained black color powder was stored in an airtight vial for further utilization.
Characterization of Ag/AgO/Ag2O NPs
Various characterization tools were used to examine the chemical, optical, and physical properties of Ag/AgO/Ag2O NPs. The XRD measurement of synthesized Ag/AgO/Ag2O NPs was carried out using a diffractometer system (XPERT-PRO, PANalytical). The UVDRS of Ag/AgO/Ag2O NPs were recorded using Jasco Spectrophotometer V-770. The functional group’s analysis of biosynthesized Ag/AgO/Ag2O NPs was studied using FT-IR-4600 typeA. The morphological features and elemental composition of bio-fabricated Ag/AgO/Ag2O NPs were analyzed by SEM equipped with an EDX detector (VEGA3 TESCAN). Moreover, size and shape were studied using HRTEM (JEM-2100) operating at an accelerating 60–200 kV voltage. The photoluminescence nature of SELE-mediated Ag/AgO/Ag2O NPs was examined using FP-8200 Spectroflurimeter.
Anticancer activity of Ag/AgO/Ag2O NPs
A549 lung cancer cells were procured from ATCC (American Type Culture Collection). Procured stock cells were grown in DMEM/RPMI supplemented with 10% inactivated Fetal Bovine Serum (FBS), penicillin (100 IU/ml), and streptomycin (100 μg/ml) in a humid environment of 5% CO2 at 37 ºC. The cell was dissociated with cell dissociating solution (0.02% EDTA, 0.2% trypsin, and 0.05% glucose in PBS). The vitality of the cells is tested, and the cells are centrifuged. In addition, 50,000 cells/well were seeded in a 96 well plate and incubated at 37 ºC under a 5% CO2 incubator for 24 h. Different concentrations of Ag/AgO/Ag2O NPs (10, 20, 40, 80, 160, and 320 µg/mL) was added and incubated at 37 ºC for 48 h (Gonzalez and Tarloff 2001). The resulting solutions in the wells were removed after incubation, and 100 μl of MTT (5 mg/10 ml of MTT in PBS) was mixed with every well. The cultured plates were incubated at 37 °C for 4 h under a 5% CO2 environment. The supernatant was discarded, and 100 μl of DMSO was mixed into the plates, which were gently agitated to dissolve the formed formazan (Sangeethaa et al. 2021). An ELISA reader measured the viability of cell lines was measured at 570 nm by an ELISA reader. Triplicates of experiments were carried out, and Doxorubicin standard drug was used in the study as a positive control. The cell viability percentage was estimated by using the formula,
In vitro antioxidant activity of Ag/AgO/Ag2O NPs
ABTS and DPPH radical scavenging assays were used to evaluate the in vitro antioxidant properties of the SELE-mediated Ag/AgO/Ag2O NPs. The varying concentrations of the Ag/AgO/Ag2O NPs and the standard solutions used were 20, 40, 60, 80, and 100 µg/mL. The study employed ascorbic acid as a reference antioxidant. The absorbance was measured to the respective blank solutions using spectrophotometry (Rehana et al. 2017; Jain and Agrawal 2008). The following formula was used to compute the % inhibition:
DPPH radical scavenging assay
Serial dilutions (20, 40, 60, 80, and 100 µg/mL) of Ag/AgO/Ag2O NPs were taken, and 50 μl of 0.659 mM 2,2-diphenyl-1-picrylhydrazyl (DPPH) dissolved in methanol was added, making up to one with distilled water. After that, sample tubes were incubated for 20 min at 25 °C (Jain and Agrawal 2008). A Shimadzu UV 1800 spectrophotometer was employed to record the absorbance at 510 nm.
ABTS radical scavenging assay
Serial dilutions (20, 40, 60, 80, and 100 µg/mL) of Ag/AgO/Ag2O NPs were taken, and 0.3 ml of ABTS radical cation [ABTS solution: 2, 20-Azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) 2 mM (0.0548 gm in 50 ml)] was prepared in double-distilled water. Potassium persulfate 70 mM was prepared in double-distilled water. After mixing 200 μl of potassium persulphate with 50 ml of ABTS for 2 h, 1.7 ml of phosphate buffer pH 7.4 was mixed. After that, sample tubes were incubated for 20 min at 25 ºC (Jamila et al. 2021). A Shimadzu UV 1800 spectrophotometer was employed to record the absorbance at 734 nm.
DNA Cleavage activity of Ag/AgO/Ag2O NPs
The DNA cleavage activity of Ag/AgO/Ag2O NPs was studied using agarose gel electrophoresis. The plasmid DNA (pBR322) was employed as the target DNA for the cleavage activity. Different concentrations of Ag/AgO/Ag2O NPs and pBR322 DNA molecules were incubated for 30 and 90 min at 37 ºC. After that, loading dye (0.25% bromphenol blue, 50% glycerol) was mixed into the reaction solution. The resulting mixtures were carried out on an electrophoresis gel using 0.8% agarose gel in TAE buffer (50 mM Tris base, 50 mM acetic acid, 2 mM EDTA, pH: 7.8) at 50 V (Gulbagca et al. 2021a). Monitoring was done under UV light after the electrophoresis experiment.
Results and discussion
Structural and morphological study
The phase analysis, crystal structure, and composition of the SELE mediated AgxO sample was analyzed through the XRD technique, and the result is evinced in Fig. 2a. It may be observed through this figure that three different phases are present in the sample corresponding to Ag (marked by *), AgO (marked by #), and Ag2O (marked by ●). This indicates that the current biosynthesis method led to the formation of Ag/AgO/Ag2O heterostructured NPs. The existence of these phases was identified based on ICDD card no. 04–0783 (Gauri et al. 2016), 84–1108 (Varthini et al. 2018), and 42–0874 for metallic Ag, AgO, and Ag2O, respectively (Ziashahabi et al. 2019; Yang et al. 2016; Waterhouse et al. 2001). This analysis, therefore, reveals that the three different phases are in the deposited form and not in the doped state since the diffraction peaks of all the phases are visible in the XRD spectrum.
Further, the unassigned peaks belong to AgNO3, which was used as the Ag-precursor in this study (Aziz et al. 2017). This means that the operating temperature was insufficient to eradicate the salt precursor. Nevertheless, based on the intensity of the diffraction peaks, it may be noted that the most dominant phase in this sample is that of AgO. The average crystallite size of the sample was ascertained using Scherrer’s equation and found to be 69.4 nm. Based on the XRD result, it is clear that the biosynthesized AgxO sample is composed of Ag/AgO/Ag2O NPs.
It notes that the plant phytochemicals perform two primary functions: (1) bio-reduction of the metal precursor and (2) control over the particle size and shape. Herein, the functionalization of Ag/AgO/Ag2O NPs by these phytochemicals was confirmed from the FTIR studies. Figure 2b represents the FTIR spectrum of the leaf extract of Solanum elaeagnifolium and Ag/AgO/Ag2O NPs. On comparing these FTIR spectra, it may be revealed that the bands at 1648.8 cm−1 and 1037.8 cm−1 of plant extract have wholly lost their intensities after functionalizing the NPs. This means that during the biosynthesis procedure, the functional groups associated with the corresponding phytochemicals were mainly involved in the reducing mechanism of the salt precursor (AgNO3) (Basnet et al. 2018). Contrariwise, the rest of the assigned bands have shifted their positions in the NPs, which may be attributed to their anchoring onto the surface of the NPs. The FTIR bands observed at 1743.9 cm−1 in plant extract and 1762.6 cm−1 in the NPs correspond to the alkaloid functional group (Masterova and Tomko 1978). The band at 1643.8 cm−1 may be ascribed to the C=O stretching vibrations of the amide group majorly because of protein molecules present in the leaf extract (Durak and Depciuch 2020). The highly intense bands at ~ 1381 cm−1 may be attributed to the lipid functional group (Velsankar et al. 2020). The band at 1037.8 cm−1 represents polysaccharides because of O-substituted glucose residue (Basnet et al. 2019). The band at 783.3 cm−1 is due to the C-H out-of-plane bend of phenyl (Basnet et al. 2019). This band has shifted to 825.1 cm−1 in the NPs. Thus, based on the relative intensities of the prominent FTIR bands of plant extract and the as-synthesized Ag/AgO/Ag2O NPs, it may be concluded that protein and glucose metabolites were responsible for functioning as reductants, lipids, and alkaloid functional groups mainly exhibited the capping agent property. This means the latter functional groups have a more vital ability to bind with the Ag ions and prevent their particles from the undesirable agglomeration phenomenon.
A typical SEM analysis was performed to study the morphological characteristic of the as-synthesized Ag/AgO/Ag2O NPs, as shown in Fig. 2c. In contrast, EDX analysis was employed to detect the elemental composition of this sample, and the results are depicted in Fig. 2d. The SEM image (Fig. 2c) revealed a high density of NPs. Although the particles have mostly agglomerated, it is still possible to clearly distinguish the boundaries between the individual particle grains. From this image, the morphology of the particles was observed to be quasi-spherical in shape. The EDX analysis of Ag/AgO/Ag2O NPs (Fig. 2d) represents the existence of only Ag and O in the sample with no impurity peaks, indicating the method of biosynthesis employed in this study leads to the formation of impurity-free Ag/AgO/Ag2O NPs. In addition, the EDX analysis evinced percentage relative elemental composition, such as Ag (17.76%) and O (82.24%), as presented in the inset table of Fig. 2d.
The microstructural analysis and particle size determination of the as-synthesized sample were performed through HRTEM studies, and the results have been shown in Fig. 3. It may be observed from the TEM images in Fig. 3a, b that the particles have formed quasi-spherical microstructure, which is consistent with the morphology obtained through SEM analysis. However, the particles did not exhibit monodispersity, and hence, their average diameter was calculated to be in the range of 15–40 nm. Furthermore, from Fig. 3c, which represents the HRTEM image of Ag/AgO/Ag2O NPs, the appearance of criss-cross patterns is visible, further confirming the existence of different phases in this sample.
The optical absorbance of the as-synthesized sample was analyzed based on the UV–Vis absorbance data, and the corresponding spectra are presented in Fig. 4a. This figure depicts the existence of two major absorbance bands at 295 nm and 455 nm. The band at 295 nm is due to the presence of the AgO component in the sample (Gauri et al. 2016). This means that AgO primarily absorbs in the UV range. The broad absorbance maximum at 455 nm, as shown in Fig. 4b, may be attributed to the absorbance contribution from the Ag and Ag2O (Ghotekar et al. 2020; Shume et al. 2020) components present in the sample. As a result, the surface plasmon resonance (SPR) effect of Ag NPs (Gauri et al. 2016). Generally, SPR for Ag NPs is observed around 440 nm (Basnet et al. 2019). In this case, a shift in the SPR band may be attributed to the strong interfacial coupling of the Ag NPs with the silver oxide components. Figure 4c represents the Tauc plot fitted using the Tauc equation (Dolgonos et al. 2016) for obtaining the bandgap energy of the as-synthesized sample, which was calculated to be 3.3 eV. Figure 4d corresponds to the PL spectra of the as-synthesized sample. A single emission band centered at 576 nm was observed. This photoluminescence peak corresponds to the bandgap of the as-synthesized NPs as well as its exciting state transition (Lin et al. 2009).
A plausible mechanism for eco-friendly synthesis of Ag/AgO/Ag2O NPs
The flavonoids/polyphenolic biomolecules have been shown as reducing agents during the plant extract mediated biosynthesis of NPs (Jain and Mehata 2017). The SELE is also a rich source of polyphenolic compounds and flavonoidic groups (Badawy et al. 2013; Elabbar et al. 2014; Balah and AbdelRazek 2020; Hamouda et al. 2015). These polyphenolic compounds as a whole could serve as a reducing agent for Ag+1 ion reduction. Figure 5 depicts the schematic representation of a plausible mechanism for Ag ion reduction employing the flavonoids of quercetin of SELE solution. An earlier study using DFT analysis found that the O–H bond dissociation energy of –OH groups of the catechol moiety of flavonoids of quercetin of leaf extract solution is lower than those of other –OH groups in flavonoids (Jain and Mehata 2017). The proposed structure for the Ag-complex development showed that Ag+1 could form complexation with quercetin (Aziz et al. 2019) (refer to Fig. 5). When the extract was mixed with the metal salt solution in the first stage, the polyphenolic compounds' –OH groups formed a complex with the Ag+1 and reduced it to Ag. Metallic Ag atoms generated in this way react with oxygen to form the most stable oxides (AgO or Ag2O). The formation of AgO and Ag2O is not selective, and hence, we may obtain their mixture. This shows that the current biosynthesis approach led to the formation of Ag/AgO/Ag2O heterostructured NPs.
Anticancer activity
The anticancer efficacy of SELE mediated Ag/AgO/Ag2O NPs on human lung cancer cell line (A549) was investigated by MTT assay. For the anticancer study of SELE mediated Ag/AgO/Ag2O NPs on human lung cancer cell line, diverse concentrations of 10, 20, 40, 60, 80, and 100 μg mL−1 were employed, as displayed in Fig. 6. The biogenically fabricated A Ag/AgO/Ag2O NPs have shown a significant cytotoxicity impact on a human lung cancer cell line, with an IC50 value of 67.09 μg mL−1, while Doxorubicin shows an IC50 value of 20.66 μg mL−1 (Fig. 7). Furthermore, when the concentration of Ag/AgO/Ag2O NPs was gradually increased to 360 μg mL−1 on a human lung cancer cell line, the percentage of cell viability was reduced to 18.28%. The present study results were well supported by diverse research reports (Table 1) on the anticancer effectiveness of the biogenically synthesized AgNPs using the extracts of Diospyros malabarica, Rosa damascene, Syzygium aromaticum, and Ruellia tuberosa (Bharadwaj et al. 2021; Venkatesan et al. 2014; Venugopal et al. 2017; Seerangaraj et al. 2021).
Antioxidant activity
The scavenging ability of the Ag/AgO/Ag2O NPs was evaluated using ABTS and DPPH scavenging assays. The radical scavenging potential of Ag/AgO/Ag2O NPs was dependent on the concentration, increasing from 20 to 100 g μg mL−1 as the concentration of Ag/AgO/Ag2O NPs (Fig. 8-ABTS and Fig. 9-DPPH). Ag/AgO/Ag2O NPs also showed considerable ABTS radical scavenging performance with a maximal inhibition of 25.78%. The IC50 value of Ag/AgO/Ag2O NPs against ABTS radicals was 85.12 μg mL−1. Ag/AgO/Ag2O NPs evinced a maximum scavenging inhibition of 20.86% against DPPH radicals with an IC50 value of 89.55 μg mL−1. The antioxidant activity of Ag/AgO/Ag2O NPs justifies their usefulness in the pharmaceutical and biomedical sectors. These two antioxidant activities were found to increase in a dose-dependent manner. Dose-dependent DPPH antioxidant efficacy by AgNPs synthesized employing Mangifera indica seed extract is described by Donga et al. (Donga and Chanda 2021), while Vasiliev et al. (Vorobyova et al. 2020) described by AgNPs synthesized using black currant pomace extract. A concentration-dependent increase in ABTS radical scavenging performance is studied by Sathishkumar et al. (Sathishkumar et al. 2019) and Donga et al. (Donga and Chanda 2021).
DNA cleavage activity
The gel electrophoresis was applied to investigate the DNA cleavage activity. Because of its optimal DNA cleavage ability, the biosynthesized Ag/AgO/Ag2O NPs have a good cleavage performance than the control. Ag/AgO/Ag2O NPs acted on plasmid DNA molecules, as shown by electrophoresis. The DNA cleavage activity of as-synthesized Ag/AgO/Ag2O NPs is displayed in Fig. 10. When compared to control DNA, there are changes in the bands of Lanes 2–5, as indicated in Fig. 10. In Lanes 2–4, the plasmid pBR322 was altered from Form I to Form II. Furthermore, the observations revealed that the SELE-mediated Ag/AgO/Ag2O NPs behaved as chemical nucleases by cleaving DNA Form I into Form III at a concentration of 1 μl for 90 min. This study demonstrated that Ag/AgO/Ag2O NPs could be employed as an alternative cancer therapy as a DNA target drug. However, few reports showed that green synthesized NPs were used for DNA cleavage study (Gulbagca et al. 2021b; Mousavi-Khattat et al. 2018).
Conclusion
The green chemistry approach was successfully proposed to produce Ag/AgO/Ag2O NPs composites, and our experiment chose SELE as a natural reducing and/or stabilizing agent. It was revealed that the SELE could be successfully employed for the facile synthesis of Ag/AgO/Ag2O NPs at room temperature. SELE mediated green synthesizing Ag/AgO/Ag2O NPs were explored using UVDRS, XRD, FTIR, SEM, HRTEM, EDX, and PL analysis. In the HRTEM analysis of Ag/AgO/Ag2O NPs, quasi-spherical-shaped particles were obtained. The mean diameter of the Ag/AgO/Ag2O NPs was 69.4 nm. It was observed that synthesized Ag/AgO/Ag2O NPs showed sound anticancer effects against A-549 lung cancer cell lines. However, antioxidant and DNA cleavage results have also been effective for Ag/AgO/Ag2O NPs. The current study has revealed the possibility of executing SELE-mediated Ag/AgO/Ag2O NPs, which might be exploited as an antioxidant, DNA cleavage, and anticancer agent.
Abbreviations
- Ag:
-
Silver
- DFT:
-
Density functional theory
- DMSO:
-
Dimethyl sulphoxide
- DNA:
-
Deoxyribonucleic acid
- EDTA:
-
Ethylenediamine tetraacetic acid
- EDX:
-
Energy-dispersive X-ray spectroscopy
- FTLR:
-
Fourier transform infrared spectroscopy
- HRTEM:
-
High-resolution transmission electron microscopy
- IC50 :
-
Half maximal inhibitory concentration
- MTT:
-
3-(4,5-Dimethylthiazol-2-Yl)-2,5-Diphenyltetrazolium Bromide
- NPs:
-
Nanoparticles
- PL:
-
Photoluminescence
- SAED:
-
Selected area electron diffraction
- SELE:
-
Solanum elaeagnifolium Leaves extract
- SEM:
-
Scanning electron microscopy
- UVDRS:
-
UV–Vis diffuse reflectance spectroscopy
- XRD:
-
X-ray diffraction
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This work was supported by the Distinguished Scientist Fellowship Program (DSFP) at King Saud University, Riyadh, Saudi Arabia.
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Barwant, M., Ugale, Y., Ghotekar, S. et al. Eco-friendly synthesis and characterizations of Ag/AgO/Ag2O nanoparticles using leaf extracts of Solanum elaeagnifolium for antioxidant, anticancer, and DNA cleavage activities. Chem. Pap. 76, 4309–4321 (2022). https://doi.org/10.1007/s11696-022-02178-0
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DOI: https://doi.org/10.1007/s11696-022-02178-0