Synthesis of Green Copper Nanoparticles Using Medicinal Plant <i>Hagenia abyssinica (Brace) JF. Gmel.</i> Leaf Extract: Antimicrobial Properties

Murthy, H. C. Ananda; Desalegn, Tegene; Kassa, Mebratu; Abebe, Buzuayehu; Assefa, Temesgen

doi:https://doi.org/10.1155/2020/3924081

Journal of Nanomaterials

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Abstract Introduction Materials and Methods Results and Discussion Conclusion Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 3924081 | https://doi.org/10.1155/2020/3924081

Synthesis of Green Copper Nanoparticles Using Medicinal Plant Hagenia abyssinica (Brace) JF. Gmel. Leaf Extract: Antimicrobial Properties

H. C. Ananda Murthy,¹Tegene Desalegn,¹Mebratu Kassa,¹Buzuayehu Abebe,¹and Temesgen Assefa²

Academic Editor: Valeri P. Tolstoy

Received02 Apr 2020

Revised06 May 2020

Accepted13 May 2020

Published01 Jun 2020

Abstract

Indigenous medicinal plant of Ethiopia has been applied for the first time to investigate the synergistic influence of phytoconstituents in green copper nanoparticles (g-Cu NPs) towards the enhancement of antimicrobial properties of NPs. We report the green synthesis of Cu NPs using Hagenia abyssinica (Brace) JF. Gmel. leaf extract. The synthesized g-Cu NPs were characterized by UV-visible, UV-DRS, FT-IR, XRD, SEM, EDXA, TEM, HRTEM, and SAED techniques. The maximum absorbance, , was found to be 403 nm for g-Cu NPs due to surface plasmon resonance. The energy gap, of NPs, was found to be 2.19 eV. FTIR spectra confirmed the presence of polyphenols, tannins, and glycosides in the leaf extract of Hagenia abyssinica. The spectral band at 740 cm^-1 is a characteristic of interaction between Cu and biomolecules of the extract. The XRD analysis revealed that the g-Cu NPs appears to be more crystalline in nature. SEM and TEM micrographs showed a mix of spherical, hexagonal, triangular, cylindrical, and irregularly shaped Cu particles. The average particle size of NPs was found to be 34.76 nm by ImageJ analysis. EDX analysis confirmed the presence of copper in the g-Cu NPs. In addition, the SAED pattern of g-Cu NPs presented concentric circular patterns for 4 major planes of crystalline copper and its oxides. The experimental and calculated -spacing values of one of the crystal planes (111) were found to be 0.2432 nm and 0.2444 nm, respectively. The -spacing values of 0.2444 nm and 0.2040 nm correspond to d₁₁₁Cu₂O and d₁₁₁Cu lattice fringes, respectively. The antibacterial test conducted on E. coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus subtilis showed good zone of inhibitions 12.7, 12.7, 14.7, and 14.2 mm, respectively, proving potentiality of g-Cu NPs as a remedy for infectious diseases caused by tested pathogens.

1. Introduction

Metallic nanoparticles are multifunctional in nature, and they have been extensively used in a variety of sectors of industries and medicine including drug delivery, cancer treatment, wastewater treatment, and DNA analysis, as antibacterial agents and biosensors and in solar power generation and catalysis. The green synthesis of metallic nanoparticles has been proposed as a cost-effective and environmentally friendly alternative to chemical and physical methods. In recent years, copper nanoparticles (Cu NPs) have attracted much attention of researchers due to its applications in industries and medicine. However, other nanoparticles, such as platinum, gold, iron oxide, silicon oxides, and nickel, have not shown bactericidal effects in studies with Escherichia coli [1].

Many plant parts or whole plants have been used for the green synthesis of Cu NPs due to the presence of a large number of bioactive compounds in plants. The extracts of plants have been efficiently applied for this purpose. Synthesis of Cu NPs has been successful with extracts of various parts of plant species that include Punica granatum peel [2], Zingiber officinale stem [3], Citrus medica Linn. (Idilimbu) juice [4], Ziziphus spina-christi (L.) Willd fruit [5], Asparagus adscendens Roxb. root and leaf [6], Eclipta prostrata leaf [7], Ginkgo biloba Linn leaf [8], Plantago asiatica leaf [9], Thymus vulgaris L [10], black tea leaf [11], Terminalia catappa leaf [12], and Azadirachta indica leaf [13].

The study on antibacterial effects of copper nanoparticles using E. coli and Bacillus subtilis revealed the fact that the Cu NPs exhibited superior antibacterial activity compared to the silver nanoparticles. Cu NPs demonstrated good antimicrobial influence on Bacillus spp. and prominent fungicidal influence on Penicillium spp. microorganisms. Cu NPs exhibited greater inhibition on Escherichia coli in comparison with Klebsiella pneumoniae, Pseudomonas aeruginosa, Propionibacterium acnes, and Salmonella typhi. Cu NPs have been synthesized by using extracts of various plants found all over the globe [14]. But no research has been conducted as far as green synthesis of Cu NPs is concerned using extracts of medicinal plants of Ethiopia.

Therefore, the present research work was proposed to explore the synthesis of green Cu NPs (g-Cu NPs) using extracts of medicinal plant of Ethiopia. More than 95% of traditional medical preparations in Ethiopia are of plant origin. A medicinal plant species of Ethiopia identified for the biogenic synthesis of g-Cu NPs in aqueous media is Hagenia abyssinica (Brace) JF. Gmel.

Hagenia abyssinica (Brace) JF. Gmel, a member of the Rosaceae family, is a species of flowering plant native to the high-elevation Afromontane regions of central and eastern Africa from Sudan and Ethiopia. It is known in English as African redwood and East African rosewood and in Amharic language as kosso. Hagenia abyssinica is a slender tree up to 20 m tall, with a short trunk and thick branches. The roots are cooked with meat and the soup drunk for general illness and malaria, while the dried and pounded female inflorescence is used as an anthelmintic (especially for tapeworm). Bark may be pounded and added to cold water and the liquid drunk as a remedy for diarrhea and stomachache. Generally, this is a strong medicine that must not be taken in large quantities; it is sometimes taken as an abortifacient [15].

The aim of this research work was to synthesize g-Cu NPs mediated by Hagenia abyssinica (Brace) JF. Gmel, medicinal plant leaf extract. The integration of bioactive compounds of this medicinal plant with Cu NPs is believed to be extremely beneficial for varieties of ailments. This green synthesis method was devised to eliminate the use of toxic chemicals which play roles of reducing agents and capping agents during chemical synthesis. The biogenically synthesized g-Cu NPs were characterized using UV-visible, UV-DRS, FT-IR, XRD, SEM, EDXA, TEM, HRTEM and SAED techniques. The antimicrobial properties of g-Cu NPs have also been evaluated against gram-positive and gram-negative bacteria. The present research work gives comprehensive report on synthesis and antimicrobial activities of g-Cu NPs which in turn will have significant impact on biomedical applications.

2. Materials and Methods

2.1. Materials and Reagent

All the chemicals (Cu(NO₃)₂·3H₂O, ethanol, Muller agar solution, and dimethyl sulfoxide DMSO) used in the experiments were of analytical grade (purchased from Merck chemical Industrial company) and used without any further purification.

2.2. Collection and Authentication of Plant Materials

Hagenia abyssinica (Brace) JF. Gmel. plant leaves were collected from Ethiopian Institute of Agricultural Research, Wondo Genet, Oromia Regional State, Southern Ethiopia, after conducting the field surveys.

The coordinates of the research center are N 7^°531.5096 E 38°3754.7284 and N 7°535.5128 E 38°3759.0304. The identity of the plant Hagenia abyssinica (Brace) JF. Gmel. (Code EB002) was authenticated by a plant taxonomist at the National Herbarium, Department of Biology, Addis Ababa University Herbarium, Addis Ababa, Ethiopia.

2.3. Preparation of Plant Leaf Extract

The leaves of Hagenia abyssinica were surface cleaned and washed repeatedly with tap water followed by distilled water to remove dust particles and then allowed to dry under shadow for 15 days to remove moisture contents from the leaves. The dried leaves were ground using a grinding machine followed by packing in a brown bottle. The extraction was carried out by taking 20 g of the powdered leaves of Hagenia abyssinica in a 500 ml of conical flask containing 400 ml of deionized water. The flask was later covered with aluminum foil, to prevent the effect of light. After that, the mixture was shaken using a mechanical shaker for 90 minutes and allowed to warm at 50°C for 1 hour on a magnetic stirrer; then it was allowed to cool down to room temperature overnight. The prepared solution was filtered through Whatman No.1 filter paper to get clear solution. The filtrate was stored at 4°C for future experiments.

2.4. Green Synthesis of Cu NPs

A 0.2 M aqueous Cu(NO₃)₂·3H₂O solution was prepared and stored in brown bottles. 100 ml of plant leaf extract was mixed with 400 ml of 0.2 M Cu(NO₃)₂·3H₂O solution (1 : 4) slowly dropwise with constant stirring.

The mixture has been incubated at room temperature for 24 hrs. The color change was checked periodically (after 30 minutes and 60 minutes). The change in color from blue to light brownish visually indicates the formation of Cu NPs, and then, the solution was centrifuged for 15 min at 10000 rpm. The obtained g-Cu NPs (Figure 1) were washed by deionized water and ethanol to remove any impurities. Thereafter, the NPs were allowed to dry and ground so as to be used for further analysis.

2.5. Characterization Techniques

The UV-visible absorbance and reflectance spectra of the samples were recorded in the range of 200–800 nm using Shimadzu’s UV-2600, UV-visible spectrophotometer. UV-visible spectra were measured by transmission, whereas UV-DRS specifically refers to diffuse reflection spectroscopy. The Cu nanoparticle solution was prepared by mixing the freshly prepared plant extract solution with Cu solution after appropriate dilution. An absorbance spectrum was recorded by allowing the instrument to scan wavelengths ranging between 200 and 800 nm, and the absorbance of the nanoparticle solution against blank extract solution was collected. Fourier transform-infrared spectroscopy (FT-IR) spectrum (65 FT-IR PerkinElmer) was recorded using KBr pellets in the range of 400–4000 cm⁻¹ [16]. X-ray diffraction (XRD-Shimadzu X-ray diffractometer) (PXRD-7000) analytical technique was used to reveal the crystalline nature of g-Cu NPs. The scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX-EVO 18 model with low vacuum facility and ALTO 1000 Cryo attachment) and transmission electron microscope with high-resolution (JEOL JEM 2100 HRTEM) were used for understanding morphological and structural features of g-Cu NPs. Gatan Digital Micrograph Software was used to evaluate -spacing values of lattice fringes. Particle size was computed by using ImageJ application.

2.6. Method of Antimicrobial Evaluation

The in vitro antibacterial activity of g-Cu NPs was evaluated using an Agar disc-diffusion method [17] against selected two gram-positive bacteria (Staphylococcus aureus and Bacillus subtilis) and two gram-negative pathogenic bacteria (Escherichia coli and Pseudomonas aeruginosa). Microbial strains were obtained from pastor institute. Prior to an antibacterial activity test, the bacterial strains were cultured in nutrient broth for 24 hours to obtain logarithmic growth phase of the test bacteria. The actively growing bacterial cultures of concentration were inoculated/spread into the Muller Hinton Agar (MHA) [18]. The extract was prepared at 1 mg/ml (dissolved in Dimethyl Sulfoxide). The Whatman filter paper disks were punched at 6 mm diameter and impregnated with the dissolved extract and then placed to the MHA surface. Ampicillin disc was used as a positive control while DMSO was taken as the negative control. The plates were incubated at 37°C for 24 hours. The antimicrobial activity was evaluated in terms of zone of inhibition, measured, and recorded in millimeters using a ruler.

3. Results and Discussion

3.1. Synthesis of g-Cu NPs

The g-Cu NPs were synthesized by using copper nitrate as a precursor and plant leaf extract as a reducing and capping agent. The change in color from blue to light brownish visually indicates the formation of copper NPs. The g-Cu NPs were washed by deionized water and ethanol to remove any unwanted particles. Thereafter, g-Cu NPs were dried and ground (Figure 1) and later subjected to various characterization methods.

The presence of phenolic compounds, tannins, and different glycosides was confirmed during the phytochemical screening of Hagenia abyssinica (Brace) JF. Gmel. leaf extract. The details of the screening are as given in Table 1. It is possibly believed that the bioactive compounds such as phenolic compounds act as a ligand and bind to metal ions and reduce them and cap them to form nanoparticles. These ligands also act as particle size controllers as reported by the earlier researcher [19].

Primary components of Hagenia abyssinica extract are phenolic compounds, tannins, anthraquinone glycosides, and cardiac glycosides [15]. The antioxidant properties of polyphenolic compounds are primarily due to their high inclination towards chelating the metals. Phenolic compounds contain hydroxyl and carboxylic groups which have very high tendency to bind metal ions. Metal ions in solution interact with polyphenolic compound and helps in the nucleation and formation of Cu NPs [20].

3.2. Characterization of g-Cu NPs

The g-Cu NPs were characterized using UV-visible, UV-DRS, FT-IR, XRD, SEM, EDXA, TEM, HRTEM, and SAED techniques.

3.2.1. UV-Visible Spectral Analysis

The UV-visible absorbance spectrum recorded for g-Cu NPs exhibited of 403 as shown in Figure 2(a) [21].

(a)

(b)

(c)

(d)

This absorption band is basically due to surface plasmon resonance of g-Cu NPs. A similar result was reported after the analysis of synthesized Cu NPs using the Ocimum sanctum leaf extract [22]. The surface plasmon absorbance basically depends on the size of NPs, and hence, every researcher reports a different value for NPs synthesized using different plant extracts. Similarly, the UV-visible diffused reflectance spectrum was recorded (Figure 2(b)). The band gap energy of g-Cu NPs was evaluated using Tauc plot as shown in Figure 2(c) by using the data obtained in reflectance spectra utilizing Kubelka-Munk function. The band gap energy, , of g-Cu NPs was found to be 2.19 eV.

3.2.2. XRD Analysis

The XRD diffraction pattern of g-Cu NPs is presented in Figure 2(d). The peaks observed in the pattern at , 44.68°, and 64.37° corresponds to (111), (200), and (220) lattice planes of face centered cubic structure of Cu NPs, and the diffraction data were in good agreement with ICSD file no. 04-0836 [23].

3.2.3. FT-IR Spectral Analysis

The FTIR spectra of g-Cu NPs showed peaks at 3351, 3284, 2920, 2350, 1720, 1625, 1342, 1160, 1058, 740, and 590 cm^-1 (Figure 3). From those indicated peaks, the broad absorption peaks of g-Cu NPs observed at 3351 cm^-1 and 3254 cm^-1 represent the presence of higher concentration of alcohols, with O-H stretches and N-H stretches of amines.

The intense peaks shown at 2929.0 cm^-1 and 2890.6 cm^-1 correspond to asymmetric C–H stretching of the –CH₂ and –CH₃ groups, respectively. The presence of atmospheric CO₂ resulted in a stretching vibration located at a wave number of 2350 cm⁻¹. It is also believed that the amine and carboxylate group present in the leaf extract of Hagenia abyssinica is responsible for the binding of proteins with the surface of Cu and thereby leading to the stabilization of the biosynthesized nanoparticles.

The absorption peaks represented at 1720 cm^-1 and 1625 cm^-1 indicate the presence of C=O and C=C bending modes of vibrations. The peaks represented by 1350 cm^-1 show C-N stretching of amide. The medium peak at 1160 cm^-1 corresponds to C-O stretching of phenolic compounds. The C-O-C stretching appears at 1058 cm^-1. The last peak at 590 corresponds to bending modes of vibrations of the C–H bond. FTIR analysis results confirmed the presence of various phytochemicals of Hagenia abyssinica (Brace) JF. Gmel. leaf extract such as phenolics, tannins, and proteins involved in the synthesis of g-Cu NPs [24]. In addition to this, the FTIR spectrum of Cu NPs shows peaks corresponding to the broad band centered at 740 cm^-1 which represents a characteristic peak believed to be due to the interaction of Cu with biomolecules of extract.

3.2.4. Morphological and Compositional Analysis by SEM-EDAX

The visual displays of size and shape of synthesized g-Cu NPs as depicted by SEM micrographs are shown in Figures 4(a) and 4(b) [25]. The SEM images also demonstrated the nonhomogeneity of the particles in terms of their shape and size. All the possible spherical and irregular shapes such as truncated hexagonal, cylindrical, triangular, and prismatic shapes of Cu NPs with varying particle sizes were found in the micrographs [26]. The average grain size of Cu NPs was found to be in the range of 10–50 nm. It seems particles were found to agglomerate moderately due to a high surface area resulting in the formation of medium-sized particles. The chemical composition of the NPs was studied by EDAX analysis. Figure 4(c) shows the EDAX spectrum obtained for the g-Cu NPs. The peaks corresponding to elemental Cu, C, and O were clearly identified, and no additional peaks were present, which demonstrates the purity of the synthesized NPs, and this was consistent with the XRD studies.

(a)

(b)

(c)

It is also possibly believed that the presence of C and O is basically from the capped bioactive compounds. In addition, it is also expected that very few copper atoms at the surface of the NPs might have been oxidized to yield small amounts of CuO and Cu₂O. The reduction of copper ions to Cu NPs is facilitated by the biomolecules of plant extract containing surface hydroxyl groups.

3.2.5. TEM, HRTEM, and SAED Analysis

To get the further deep insight on the morphology, size, and crystalline nature of the g-Cu NPs, TEM, HRTEM, and SAED analysis was employed. The HRTEM images of as-synthesized g-Cu NPs (Figure 5) shows that the synthesized NPs are mostly spherical but exhibited different shapes. Smaller NPs as small as 10 nm confirm the efficient role of bioactive components of Hagenia abyssinica (Brace) JF. Gmel. plant extract as capping and stabilizing agents. Otherwise, NPs would have been agglomerated to yield larger NPs in an elongated form [5].

(a)

(b)

(c)

(d)

In addition, the variation in size of g-Cu NPs is probably due to the presence of polyphenolic compounds (from Hagenia abyssinica (Brace) JF. Gmel, leaf extract) which have strong attractive forces and holds the particles together.

The TEM micrographs which exhibited very finely grained g-Cu NPs with spherical, cylindrical, prismatic, hexagonal, triangular, and near spherical shapes are presented in Figures 5(a)–5(d).

All these near spherical particles with varying sizes from 14.4 nm to 43.1 nm with an average particle size of 34.76 nm as determined by ImageJ application are as shown in Figures 6(a) and 6(b).

(a)

(b)

(c)

(d)

The SAED pattern of g-Cu NPs (Figure 6(c)) contained six spots each corresponding to specific crystal planes. One of such planes is presented with a -spacing of 0.2444 nm as shown in Figure 6(d).

HRTEM morphologies of g-Cu NPs with magnified lattice fringes, IFFT patterns, and profile of IFFT with a -spacing value for a specified plane (Figure 6(d)) are presented in Figures 7(a)–7(c), respectively. The analysis to arrive at a -spacing value has been carried out by using Gatan Digital Micrograph Software application which resulted in a value of 0.2444 nm for a set of crystal planes at the surface of Cu NPs.

(a)

(b)

(c)

The -spacing values for all the spots depicted in the SAED pattern of g-Cu NPs (Figure 6(c)) are presented in Table 2. Each spot on the SAED pattern corresponds to a specific set of lattice planes. The XRD pattern of g-Cu NPs presented earlier in Figure 2(d) revealed 3 major peaks corresponding to (111), (200), and (220) planes of the fcc structure of pure Cu (ICSD no. 04-0836). The -spacing values of the derived diffraction planes from spot 1 to spot 6: , , , , , and , are in agreement with the -spacing values of CuO (ICSD no. 48-1548, tenorite-C2/c), Cu₂O (ICSD no. 05-0667, cuprite-Pn-3 m), and Cu (ICSD no. 04-0836) structures. The similar result was reported in the recent work [27].

The estimated -spacing value of lattice fringes at the surface of the Cu NPs is 0.2444 nm, which is comparable to the value of the (111) plane of fcc-structured Cu₂O. It can be concluded that few copper atoms at the surface of NPs possibly reacted with air to form their oxides, Cu₂O and CuO.

3.3. Antimicrobial Activity

The g-Cu NPs synthesized by using the leaf extract of Hagenia abyssinica (Brace) JF. Gmel. showed a broad range of antibacterial activities against all tested pathogens: E. coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus subtilis with a zone of inhibition 12.7, 12.7, 14.7, and 14.2 mm, respectively (Table 3). The Cu NPs have proven record of an excellent antimicrobial activity [28]. Accordingly, this result showed that the g-Cu NPs are more active against gram-positive bacteria than gram-negative bacteria which is possibly due to the difference in the structure of cell walls of bacteria. The antimicrobial activity of NPs can be attributed to the presence of bioactive compounds on the surface of NPs as capping and stabilizing agents. In this regard, the activity was pronounceable against S. aureus compared to ampicillin, the standard antibiotic. The highest zone of inhibition (mm) recorded with g-Cu NPs against S. aureus bacteria was 14.7 mm, and the lowest zone of inhibition (mm) recorded against P. aeruginosa bacteria was 12.7 mm. The wide zone of inhibitions (Figure 8) of g-Cu NPs against pathogens confirms their great potential as a remedy for infectious diseases caused by the tested bacterial pathogens.

(a)

(b)

(c)

(d)

Additionally, the standard disc ampicillin showed the comparable zone of inhibition with the g-Cu NPs, which is small, and it can be attributed to the development of resistance by bacteria against ampicillin.

The antimicrobial results obtained using g-Cu NPs were found to be better when compared with an earlier work reported by many researchers (Table 4). The highest zone of inhibition (mm) recorded with g-Cu NPs against bacteria was 14.7 mm which is far above the zone of inhibition exhibited by Cu NPs synthesized by various plant extracts as mentioned in Table 4. The last two plant extracts were proved to exhibit a higher zone of inhibition which can be attributed to the presence of different type of phytoconstituents. Thus, it can be concluded that the synergistic effect of Cu NPs coupled with bioactive compounds such as tannins and glycoside of Hagenia abyssinica (Brace) JF. Gmel. leaf extract was proved to be beneficial against pathogens.

Many mechanisms of antibacterial activity have been reported by the past researchers; accordingly, the action of g-Cu NPs on the bacteria is yet to be explored fully. It is assumed that the g-Cu NPs get adsorbed on to the cell wall of bacteria and interacts with the electronegative elements within the cell membrane. This results in failed metabolism thereby leading to interference and disruption of transcription in bacteria and hence causes antibacterial activity by g-Cu NPs. It is also believed that the synergistic effect of g-Cu NPs with bioactive compounds of extract would have played significant influence to inhibit the activity of pathogenic bacteria as suggested by the recent researcher [29].

It is possibly understood that the helical structure of DNA molecules would have been disrupted by the action of Cu NPs. In addition, electrochemical potential across the cell membrane decreases up on the interaction with the released Cu metal ion by Cu NPs affecting integrity of the membrane.

4. Conclusion

The green copper nanoparticles (g-Cu NPs) were successfully synthesized by using medicinal plant Hagenia abyssinica (Brace) JF. Gmel. leaf extract. The presence of phytoconstituents such as polyphenols of tannins played roles in reducing and capping agents during the formation of g-Cu NPs. The UV-visible absorbance and reflectance spectra showing of 403 nm and of 2.19 eV, respectively, confirmed the formation of g-Cu NPs. FTIR spectra supported the presence of capping agents on the surface of g-Cu NPs. The crystalline nature and composition of g-Cu NPs were confirmed by XRD pattern and EDX spectrum, respectively. The SEM and TEM micrographs provided enough evidence towards the nanomorphology of g-Cu NPs with all possible shapes including spherical, triangular, hexagonal, and cylindrical shapes with an average particle size of 34.76 nm. HRTEM micrographs and SAED patterns confirmed the presence of Cu and surface oxidized Cu₂O NPs. The wide zone of inhibition of g-Cu NPs against pathogens confirms their great potential as a remedy for infectious diseases caused by the tested bacterial pathogens. Finally, it can be concluded that the synergistic effect of bioactive compounds from medicinal plant coupled with Cu NPs has been proved to be beneficial against pathogens.

Data Availability

The [Excel] data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

The concept and experiments were designed, conducted, and manuscript written by H C Ananda Murthy. Characterization of samples was done by Mebratu Kassa and Buzuayehu Abebe. Tegene Desalegn participated in compiling the manuscript. Antimicrobial assay was conducted by Temesgen Assefa. All authors read and approved the final manuscript.

Acknowledgments

The authors gratefully acknowledge Adama Science and Technology University for the financial support and laboratory facility to conduct this research work. This work has been funded by the project (ANSD/04/0453/11-2018) approved by the Research and Technology Transfer Office, sanctioned by Adama Science and Technology University, Ethiopia.

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Copyright © 2020 H. C. Ananda Murthy et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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