Iram Bashir, Syeda Shaista Gillani*, and Fouzia Majeed
Department of Chemistry, Lahore Garrison University, Pakistan
* Corresponding Author: [email protected]
The current study aims to employ an ecologically sustainable method, utilizing a plant-based extract derived from Mimusops elengi as both a reducing and capping agent. Synthesis of zinc oxide nanoparticles (ZnO NPs) was done from aqueous leaves and flower extracts of Mimusops elengi. Different spectroscopic techniques were used to characterize these biosynthesized (ZnO NPs) zinc oxide nanoparticles like UV-visible, FTIR, XRD, SEM, and EDX techniques. UV-visible spectroscopy showed the absorption wavelength of ZnO NPs at 353nm (leaves extracts) and 365nm (flowers extracts). FTIR spectra showed the absorption frequency of different functional groups present in plant extract along with ZnO peak at 637cm-1 (leaves extracts) and 643cm-1 (flowers extracts). XRD results revealed the hexagonal structure and crystalline nature of biosynthesized ZnO NPs. The average grain size calculated for ZnO NPs of leaves and flower extracts was 10.37 and 15.52nm, respectively. SEM analysis showed a hexagonal shape. EDX confirmed the formation and purity of ZnO NPs by showing an abundant % of zinc and oxygen atoms. The significant bactericidal efficacy of biosynthesized ZnO NPs was found against pathogens Escherichia coli and Staphylococcus aureus. When compared to ZnO nanoparticles from flower extracts and biosynthesized ZnO nanoparticles from leaf extract exhibited substantial suppression. ZnO-NPs synthesized from leaves and flower extracts of Mimusops elengi can be subjugated for biomedical and ecologically sustainable applications.
Graphical Abstract
Keywords: antibacterial, biomedical, green synthesis, Mimusops elengi, nanoparticles (NPs)
In 1959, at the California Institute of Technology (Caltech), a Nobel Laureate, Richard Feynman presented a notable speech during a conference hosted by the American Physical Society titled: There's Plenty of Space at the bottom [1], in which he explored the groundbreaking concept of nanotechnology and the potential for crafting intricate molecular machines with atomic accuracy. Nanotechnology is the atomic-scale manipulation of matter and has applications in various fields. Nanoparticles (NPs) are microscopic particles made up of both organic and inorganic materials [2]. Due to their tiny size (1-100 nm), high energy at the surface, and larger (S/V) surface area to volume ratio, their catalytic capabilities and interaction with other molecules increased, significantly [3].
In the last decade, comprehensive research concerning metal oxide nanoparticles has been emphasized due to their myriad applications in several technology sectors. Zinc Oxide (ZnO NPs) is one of the materials in nature that show great diversity in the structure, of all known materials and is an interesting inorganic material with several advantages in current laser medical, biomedical, and optoelectronic technology [4–7]. ZnO NPs are categorized as a semiconductor in material science because of their covalent and ionic bonds. Due to a large energy band (3.37 MeV) and broad energy bond (60MeV), ZnO NPs have captivated a lot of consideration because of their high mechanical capabilities and thermal stability at ambient temperature. ZnO NPs are more appealing and effective in current laser medical technology, electronics, and optoelectronic technology because of this significant characteristic [5].
Figure 1. Some Appealing Properties of Zinc Oxide Nanoparticles
Zinc Oxide nanomaterials possess a range of structures, which act as a novel material and have potential uses in a number of nanotechnology sectors. These particles have showed the potential to photo-oxidize and photo-catalyze chemical reactions and biological species, as a result of this ability, they are a key player in cancer therapy [8].
ZnO is one of five chemicals that are classified as "generally regarded as safe". ZnO has been widely utilized in cosmetics, sunscreens, lotions, medication delivery, and bio-imaging due to its bio safe and biocompatible characteristics [3]. ZnO NPs have been explored as an antibacterial and anticancer agent in several other research investigations [7].
Several techniques are reported for the synthesis of nanoparticles, which are classified into three types: Physical (mechanical), chemical, and biological [9]. Green synthesis is a relatively recent phrase that refers to the employment of ecologically sustainable methods for the creation of new products that do not affect the environment. In physical and chemical methods dangerous substances are being absorbed on the surface [10].
As physical and chemical procedures became more expensive day by day, the necessity for biosynthesis of nanoparticles emerged as a new trend. Chemical synthesis processes usually result in dangerous substances being absorbed on the surface, which may have negative consequences in clinical uses [11, 12]. In order to find cost-effective ways to make nanoparticles, scientists turned to microbial enzymes and plant extracts (phytochemicals), which are generally responsible for the reduction of metals into their respective nanoparticles, due to their antioxidant or reducing capabilities. Green synthesis is less expensive, more eco conscious, and simpler for high yield production than chemical or physical synthesis as it does not need the use of high pressure, power, temperature, or dangerous substances.
The current study focused on the leaves and flowers of Mimusops elengi Linn. (M. elengi), which is a fragrant ornamental tree belonging to the Sapotaceae family. Hindus regard Mimusops elengi as a holy plant and a symbol of love and beauty [13]. The bark of Mimusops elengi is used as a cooling agent, a cardiotonic, the blossoms are used to treat asthma, and are smoked [14]. The fruit of Mimusops elengi is edible; it has astringent properties, is excellent for the teeth and produces flatulence, the seed is used to repair loose teeth and to treat headaches [15]. The phytochemicals present in the aqueous extract of Mimusops elengi, functions as an oxidizing, reducing, and stabilizing agent for the biosynthesis of these zinc oxide nanoparticles (ZnO NPs).
Chemicals: Zinc acetate dihydrate [Zn (C2H3O2)2.2H2O] and sodium hydoxide (NaOH) were purchased from Sigma-Aldrich
All of the reagents and solvents used for this research work were of excellent analytical quality and purchased from Sigma-Aldrich. Solvents were refined by distillation before usage. The leaves and flowers of Mimusops elengi were collected from Baagh-e-Jinnah, Lahore, Pakistan.
2.1. Aqueous Extraction of Leaves and Flowers of Mimusops elengi
Freshly collected leaves and flowers of Mimusops elengi were scrupulously washed with water to remove debris on the surface and then rinsed with distilled water. After that, leaves and flowers were shade-dried for a week, weighed (12g), and crushed to a fine powder, separately. Then, the powder of leaves and flowers was mixed and heated with 100 mL distilled water at 20°C for an hour, while swirling constantly with vigorous stirring, separately. The mixtures were filtered twice, first with muslin cloth and once with Whatman No. 1 filter paper, separately. Dark green extracts (leaves) and pale orange extracts (flowers) were obtained and stored at 4 °C for further processing.
2.2. Preparation of Salt Solution
5.48g of zinc acetate dihydrate was dissolved in 100 mL of distilled water to produce 0.25M zinc acetate dihydrate (Zn (C2H3O2)2.2H2O) solution.
2.3. Green Synthesis of Zinc Oxide Nanoparticles
A 100 mL of 0.25M zinc acetate dihydrate (Zn (C2H3O2)2.2H2O) solution was mixed with 50 mL leaves extract and 50 mL flowers extract in a 250 mL flask, separately. The colour of the mixture changed from dark green to brown for the leaves and pale orange to brown for the flower extracts after 1 hour of incubation at 40°C with continual shaking, suggesting that green manufactured zinc oxide nanoparticles had been generated. Then 0.02 M NaOH was added drop by drop to keep the pH of the solution at 12. As a result, bio-reduced salt sank to the flask's bottom. After that, the sample was washed with distilled water before being exposed to ethanol. The washing procedure was repeated three times to ensure that all contaminants were eliminated. The washed ZnO NPs were then oven-dried for 24 hours at 60°C. The powdered ZnO NPs were then kept for future analysis.
2.4. Antibacterial Assay
The antibacterial activity of biosynthesized ZnO nanoparticles was tested using two bacterium strains. The antibacterial activity was measured using the Agar well diffusion method. The antibacterial activity of biologically produced zinc oxide (ZnO) nanoparticles against gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli) bacterial strains was tested. Three wells were made on each agar plate, added 10 µL ZnO NPs, Ciprofloxacin (standard reference), and left it for 24 hours.
3.1. Characterization Techniques
UV- Visible Spectroscopy (Ultra-3000), Fourier transforms infrared (FTIR) spectroscopy, X-ray Diffraction (XRD) (Bruker AXS D8), Scanning Electron Microscopy (SEM) (HITECH-3400-N), and Energy dispersive X-ray (EDX) analysis was used to characterize the synthesized zinc oxide nanoparticles (ZnO NPs).
3.2. UV-Visible
The UV-visible spectra were recorded on an Ultra 3000 UV-Vis spectrophotometer for these green synthesized ZnO NPs. The spectrophotometer was allowed to scan at wavelength ranges from 200-800nm. The λmax at 353 nm (a) and 365 nm (b) [16] depicts the Surface Plasmon Resonance (SPR) phenomena when the ground state non-bonding electrons excited to a higher energy state [17, 18], as a result, a change in colour was noticed from dark green to brown, while the colour of the flower extract changed from pale orange to light brown. The monodispersed character of NPs distribution is confirmed by the strong absorption peaks of ZnO.
Figure 2. UV-Vis Spectra: (a) ZnO NPs for Leaves Extract and (b) ZnO NPs for Flower Extract
3.2.1. Fourier Transforms Infrared (FTIR). Fourier transforms infrared spectroscopy (4000-400 cm-1) was used to categorize functional groups in aqueous extract and zinc oxide nanoparticles (ZnO NPs). (FTIR) spectrum of biosynthesized ZnO NPs was used for the leaf extract, which is given in Figure 3. By using the FTIR technique, the phytochemical composition of biomolecules resulted in the reduction and stability of ZnO NPs. The broad peak at 3085cm-1 links to the OH [19] group of carboxylic acid along with C=O stretching at 1560cm-1 [20]. The peak at 1560cm-1 may also be due to the N-H bending of alkaloids or the N=O group showing asymmetric stretching vibrations. The peak at 2313cm-1 resulted from =C-H stretch of aromatic aldehyde. The sharp peak at 1408cm-1 showed symmetric stretching of the N=O bond or C-N stretch and the peak at 1014cm-1 was because of C-O stretching vibration [21], which represent acidic, alcoholic, phenolic, and aromatic nitro compounds. The fingerprint region of the spectrum contained a peak at 637cm-1 confirming the presence of Zn-O. Previous literature has reported, the range of 400-500 cm-1for the absorption bands [22] or for higher frequencies, however, 608-731 cm-1 [23] were indicated for the distinctive peaks for ZnO vibrations.
Figure 3. FTIR Spectrum of ZnO NPs (leaves Extract)
Figure 4 shows the IR spectrum of zinc oxide nanoparticles for the flower extract. It showed some characteristic peaks, which were observed because phytochemicals exist in extract and are accountable for nanoparticle fabrication and maintenance. The broad peak at 3120cm-1 was because of the phenolic or alcoholic hydroxyl (OH) group. A small peak at 2868cm-1 resulted from –C-H3 stretching frequency. The high-pitched peak at 1609cm-1 was observed due to carbonyl stretch, aromatic C=C stretching, or N-H bending vibrations. Another sharp peak at 1326cm-1 showed the presence of the C-N group as well as the amide band of proteins [24]. The medium-strong peak at 1103cm-1 links to a stretch of the C-O bond. The signal at 643cm-1 was caused by a Zn-O link, indicating that zinc oxide nanoparticles were synthesized [23].
Figure 4. FTIR Spectrum of ZnO NPs (Flowers Extract)
3.2.2. X-ray Diffraction. XRD examination was done to evaluate the crystallographic nature and phase purity of these biosynthesized zinc oxide nanoparticles (see Figure 5). The XRD peaks of ZnO NPs for the leaves extract diffracted at 2θ angle are 31.63o, 34,31o, 37.12o, 47.80o, 57.68o, 63.52o, ,and 68.84o that showed 100, 002, 101, 102, 110, 103, and 112 Miller indexes planes, respectively. The obtained peaks were consistent with those reported in [25]. The hexagonal wurtzite structure of zinc oxide nanoparticles is represented by all sample's diffraction peaks. Planes of hexagonal ZnO nanoparticles significantly matched with standard card values (JCPDS PDF No 36-1451). The size of the crystalline nanoparticles was enumerated by using the Debye−Scherrer formula [25, 26].
Figure 5. XRD Graph of ZnO NPs (Leaves Extracts)
The X-ray diffraction peaks of green synthesized zinc oxide nanoparticles for the flower extract given in Figure 6 at 2θ diffracted angle are 32.93, 34.70, 37.68, 49.25, 57.67, 63.86, and 69.98 exhibiting 100, 002, 101, 102, 110,103,and 201 Miller indexes planes, respectively. The Peak search approach was used to compare the peak pattern with the previously reported patterns (found in the library), confirming that the synthesized product has a hexagonal structure due to its distinctive pattern. The crystalline nature of ZnO NPs was revealed by the strong peaks. The single-phase purity of the ZnO NPs is also shown by the placement and sharpness of the peaks [27]. The obtained peaks were consistent with those reported in [25]. The average size calculated was 15.52 nm (Debye Scherrer equation).
Figure 6. XRD Graph of ZnO NPs (Flowers Extracts)
3.2.3. Scanning Electron Microscopy (SEM). The surface morphology of ZnO NPs from leaves and flower extracts was hexagonal wurtzite (see Figure 7). The average grain size calculated for ZnO NPs of leaves and flower extracts was 10.37 and 15.52nm, respectively. SEM analysis showed a hexagonal shape. Altered forms of ZnO NPs have previously been observed, with sphere-shaped, hexagonal, and flower-like shapes being the most prevalent among them [28, 29].
Figure 7. SEM Images of ZnO NPs Leaves and Flowers Extracts
3.2.4. Energy Dispersive X-ray (EDX). This technique was utilized to recognize different types of elements present in the selected sample. This study revealed that the current sample contains a significant amount of zinc (52.94% in the leaf and50.96% in the flower) and oxygen (40.94% in the leaf and 40.08% in the flower) with a trace amount of C, Pb, K, Cl, and P elements. The trace elements may come from the soil and environment of the plant. The elemental distribution of the ZnO NPs was confirmed by the EDX spectra, which indicated the main peaks between 0.5-8.5 keV [30]. The purity of zinc oxide nanoparticles (ZnO NPs) was revealed [31] with high Zn and oxygen element composition and the synthesis of ZnO NPs was confirmed. The purity of ZnO NPs from the leaf was 93.88% (40.94%+52.94%) and 91.04% (40.08%+50.96%) for the flower ZnO NPs.
Figure 8. EDX Spectrum of ZnO NPs (Leaves Extracts)
Figure 9. EDX Spectrum of ZnO NPs (Flowers Extracts)
Biosynthesized zinc oxide nanoparticles from leaves have antibacterial action against pathogens of importance (see Figure 10). The antibacterial activity of ZnO NPs from the leaves at 100µg/mL concentration was 13mm, leaves extract showed 6mm, while the reference (Ciprofloxacin) was measured at 20mm zone of inhibition against E.coli (Gram-negative) bacteria. Also, S.aureus (Gram-positive) bacteria showed 15mm for ZnO NPs, 5mm for leaves, and 22mm zones of inhibition against the reference.
Inhibition zones of zinc oxide nanoparticles (ZnO NPs) produced from Mimusops elengi flowers were equally impressive (see Figure 12). Against E.coli, the ZOI for floral ZnO NPs was 10mm, 15mm for the reference, and 3mm for the flower extract. Additionally, the ZOI against S. aureus was measured at 16mm for ZnO NPs 20mm for reference, and 8mm for flowers extract. As the size of ZnO NPs from the leaves is less as compared to ZnO NPs from the flowers, it showed a greater antibacterial effect. Nanoparticles' antibacterial activity is a size-dependent on the characteristics, which gradually improves when the particle size is reduced [32].
` |
|
Gram-negative Escherichia coli |
Gram-positive Staphylococcus aureus |
Figure 10. Zone of Inhibitions by ZnO NPs (Leaves Extract)
Table 1. Measured ZOI against E.coli and S.aureus
Clinical pathogenic strains |
ZOI (mm) |
||
Leaves extract |
ZnO NPs (Leaves extracts) |
Reference (Ciprofloxacin) |
|
(a) Escherichia coli |
6mm |
13mm |
20mm |
(b) Staphylococcus aureus |
5mm |
15mm |
22mm |
Figure 11. Bar Graph for the Measured Zone of Inhibition
Gram-negative Escherichia coli |
Gram-positive Staphylococcus aureus |
Figure12. Zone of Inhibition by ZnO NPs (Flowers Extract)
Table 2. Measured Zones of Inhibition of ZnO NPs from Flower
Clinical pathogenic strains |
Zone of Inhibition (ZOI) (mm) |
||
Flowers extract |
ZnO NPs (Flowers extract) |
Reference (Ciprofloxacin) |
|
(a) Escherichia coli |
3mm |
10 mm |
15mm |
(b) Staphylococcus aureus |
8 mm |
16 mm |
20mm |
Figure 13. Bar Graph Representing the ZOI against E.coli and S.aureus
The presence of an inhibitory zone indicates that ZnO nanoparticles' biocidal action involves membrane rupture with a greater rate of surface oxygen species, which results in pathogen loss. ZnO nanoparticles produced from Mimusops elengi leaves and flower extract exhibit antibacterial properties. According to the findings, ZnO nanoparticles were made from Mimusops elengi leaf and flower extract against E.coli and S.aureus. In comparison to ZnO nanoparticles (flowers), biosynthesized ZnO nanoparticles (leaves) exhibited substantial suppression [33].
Conclusively, this study provided a convenient and cost-effective method to synthesize ZnO NPs by using Mimusops elengi as a novel reducing and stabilizing agent. The ZnO NPs were characterized by SEM, UV−Vis, FTIR, XRD, and EDX spectroscopy. UV-visible spectroscopy showed the maxima absorption of ZnO NPs at 353nm (leaves extracts) and 365nm (flowers extracts). FTIR spectra showed the absorption frequency of different functional groups present in plant extract along with ZnO peak at 637cm-1 (leaves extracts) and 643cm-1 (flowers extracts). XRD results revealed the hexagonal structure and crystalline nature of biosynthesized ZnO NPs. The average grain size calculated for ZnO NPs of leaves and flower extracts was 10.37 and 15.52nm, respectively. SEM analysis showed a hexagonal shape. EDX confirmed the formation and purity of ZnO NPs by showing an ample % of zinc and oxygen atoms. ZnO NPs showed significant antibacterial activity against clinical pathogens Escherichia coli and Staphylococcus aureus. ZnO NPs synthesized from flowers showed a higher bactericidal impact on the tested pathogens in comparison to ZnO NPs synthesized, which was synthesized from leaves. Certainly, green -synthesized zinc oxide nanoparticles (ZnO NPs) were ecologically sustainable, and can be employed in various biological applications.