Research Article | Open Access
Chainika Khatana1, Ashwani Kumar2 , Mashael W. Alruways3, Nazam Khan3, Naveen Thakur4, Dinesh Kumar1 and Amita Kumari5
1Faculty of Applied Sciences and Biotechnology, Shoolini University, Solan – 173 212, Himachal Pradesh, India.
2Patanjali Herbal Research Department, Patanjali Research Institute, Haridwar – 249 405, Uttarakhand, India.
3Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Shaqra University, Shaqra, Saudi Arabia.
4Department of Physics, Career Point University, Hamirpur – 176 045, Himachal Pradesh, India.
5School of Biological and Environmental Sciences, Shoolini University, Solan – 173 212, Himachal Pradesh, India.
J Pure Appl Microbiol. 2021;15(4):1907-1914 | Article Number: 7102 | © The Author(s). 2021
Received: 13/06/2021 | Accepted: 03/09/2021 | Published: 28/09/2021

Microbial infections and antibiotic resistance are some of the prime factors that are ascribed to endanger human health. Several reports have highlighted that drug-resistant pathogens assist in the etiology of various chronic diseases and lead to fatality. The present study deciphered the role of zinc oxide nanoparticles (ZnO NPs) as therapeutics against selected bacterial strains. The plant-based technique was followed to synthesize ZnO NPs. The synthesis was confirmed with different techniques viz. X-ray diffraction, transmission electron microscope (interplanar spacing at 0.126 nm), scanning electron microscope (flower-like structure), and Fourier transform infrared spectroscopy. The antibacterial analysis revealed that ZnO NPs inhibited the growth of all tested strains (Escherichia coli, Staphylococcus aureus, Salmonella typhi, Bacillus subtilis, and Klebsiella pneumoniae) to a greater extent (MIC ranged between 0.013±0.004-0.0625±0 mg/mL) as compared with ZnO compound (Bulk material). In the present study, ZnO NPs were produced in a cost-effective and environmentally sustainable way using a green process and can be used as a remedy for drug-resistant pathogens.


Aloe vera, Zinc oxide nanoparticles, Green synthesis, Characterization, Microbial pathogens


Microbial diseases are one of the major causes of death worldwide.1,2 Scientists are working for the past many decades to develop antibiotics against different pathogenic bacterial strains. However, the misuse of such antibiotics is leading to antibiotic resistance that causes several fatalities every year.3,4 Bacterial strains like Staphylococcus aureus and Mycobacterium tuberculosis have already evaded every possible antibiotic in the clinician’s armamentarium. Treating resistant microbes often requires more expensive or toxic drugs, resulting in further complications.5 Therefore, an innovative and novel approach is necessary to develop new antimicrobial drugs.6,7

Nanotechnology is one of the noble platforms for transforming basic compounds into nanoparticles (NPs) with enhanced properties.7-9 Nanomaterials are used in a wide range of medicinal and diagnostic applications.10 Several NPs have already been reported to be effective antimicrobials, including ZnO, MgO, CuO, Al, TiO2, CdS, and Au.11-18 NPs, in contrast to conventional medications, have a completely distinct mechanism for attacking microbes.19 The size and shape of the NPs are also important factors in their antibacterial action.20,21 As a result, the research focus is now shifting towards nanotechology to prevent microbial infections. Among various methods of synthesis of NPs, green synthesis, which encompasses synthesis using plants, bacteria, fungus, algae, actinomycetes, and other organisms, is environmentally friendly, cost-effective, biocompatible, and safe.22-25 Further, phyto-mediated synthesis is preferred to microbial synthesis, which requires time-consuming and costly downstream processing.26,27 The aim of this research is to synthesize zinc oxide nanoparticles (ZnO NPs) using Aloe vera leaf extract and investigate their antibacterial activity.

Materials and Methods

Aloe vera leaves were harvested in the local area of Solan, Himachal Pradesh, India, and washed with tween 20 followed with distilled water. Briefly, 100 g of the leaves (with gel) were chopped and dried at 40°C in an oven for 2 h followed by boiling in deionized water (100 mL). To remove particulate matter, the extract is subjected to filtration using Whatman paper and stored for 1-2 h at 4°C.

Microbial strains viz. E. coli, Staphylococcus aureus, Salmonella typhi, Bacillus subtilis and Klebsiella pneumoniae were obtained from Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

Green synthesis of ZnO NPs
Briefly, 0.50 g zinc acetate was dissolved in 100 mL water and 8 mL freshly prepared Aloe vera leaves extract was added to the solution with constant stirring for 10 min, and pH was adjusted to 12 with NaOH. The resulting off-white color precipitates were thoroughly washed with water, filtered, and dried in a 60°C oven. The obtained product was grounded into refined grains in a mortar and stored for further use and labeled as ZnO NPs.

Characterization of ZnO NPs
Scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were used to investigate the morphological characteristics of ZnO NPs.28,29

The FEI Nova Nano SEM 450 at 1kV was used to generate SEM micrographs, and TEM images were taken using FP/5022-Tecnai G220S-TWIN (USA) at 200 kV. Agilent Cary-630 FTIR was also used to analyze the characteristic functional groups between 4000 to 400 cm-1 spectrum range. The crystal structure of fabricated ZnO was determined by X-ray diffraction (XRD, PANalytical’s X’Pert Pro), the pattern was obtained with CuKα 1 radiation (45kV/100 mA), scanning was done at a rate of 2°/min in the diffraction angles (2θ), which ranged from 20 to 70°.

Antibacterial activity of ZnO NPs
A modified disc diffusion method was performed to investigate the antibacterial potential of the ZnO compound and ZnO NPs.30 The NPs were suspended in methanol to make a stock solution with a concentration of 10 mg/mL. The resulting solution was then sonicated (15 min) before antibacterial evaluation. On the other hand, isolated colonies (4-5) were transferred into a test tube containing nutrient broth medium (5 mL), followed by 24 hours incubation at 37°C. 0.5 McFarland standard (1-2 × 108 CFU/mL) was used to compare the turbidity of inoculums.

Disc diffusion assay
Briefly, 100 µl inoculums (107-108 CFU/mL) were uniformly spreaded on Mueller Hinton agar (MHA) plates. The discs (6 mm, Whatman filter paper no. 1) were prepared by adding 30 µL of different concentration of NPs. After that, discs with varying concentrations (2, 4, 6 mg/mL) of ZnO compound and ZnO NPs were placed on these MHA plates. Tetracycline was used as a standard drug (30 µg/mL), while methanol was employed as a negative control. Further, the MHA plates were kept at 37°C and inhibition zone diameter (mm) was measured after 24 hours.

Determination of minimum inhibitory concentration (MIC) of ZnO NPs
The MIC was determined using the CLSI M7-A7 broth microdilution method.31 For this, a double-strength Mueller-Hinton broth (MHB), NPs solution (2 X) were prepared, followed by its serial dilutions in the range 2-0.0.0039 mg/mL in a 96 well microtitre plate. Double strength MHB (100 µl) containing varied NPs concentrations was mixed with bacterial inoculum (10 µL) containing 1-2 × 108 CFU/mL. On the other hand, the 10th well (broth + inoculums) was used as a control. In addition, the 11th well was utilized as positive control (antibiotics + inoculums) and the 12th well as negative control (methanol + inoculums). After this, the microtitre plate was kept at 37°C, for 24 hours. The lowest visual growth inhibitory concentration was considered MIC.

Determination of minimum bactericidal concentration (MBC) of ZnO NPs
MBC was determined by spreading suspensions (10 µl) from microtiter plate wells over a nutrient agar plate and incubating at 37°C for 24 h. Agar plates with no colonies were considered as MBC.

Statistical analysis
GraphPad Prism 5.0 was used to examine the results obtained (where applicable) using average, analysis of variance, and standard deviation. A p value < 0.05 was considered to be statistically significant.


Morphology and phase structure composition of ZnO NPs
The SEM images of ZnO revealed uniform distribution of flower-like morphology (Fig. 1a and 1b), which could be correlated with the previously reported literature.32 From TEM images, surface morphology and size were estimated (Fig. 1c), and showed interplanar spacing at 0.126 nm, which were well distributed, and corresponded to standard reported values.33 The SAED image (Fig. 1d) revealed small bright spots representing the poly-nano crystalline nature of the ZnO NPs. Similar findings were observed by Cao et al.34

Fig. 1. Morphological assessment of ZnO NPs (a, b) SEM images, (c) TEM image and (d) SAED pattern.

To decipher the crystal structure, XRD patterns were analyzed and are presented in Fig. 2. The patterns of ZnO NPs which are positioned at 2θ values of 31.5, 34.2, 36.1, 47.4, 56.5, 62.8, 68.8, and 69.0° can be attributed to 100, 002, 101, 102, 110, 103, 112 and 201 planes of ZnO NPs. Similar results have been reported earlier for ZnO NPs by Parthasarathy et al.35 and Alamdari et al.36 The peaks corresponded to the standard card’s values (JCPDS 36-1451).37 Moreover, using the Scherrer equation, the crystalline size of synthesized NPs on average was 15.6 nm (D = Kλ/βcosθ). Constant K was adjusted to be 0.89, diffracting angle is θ, the wavelength (λ) (CuKα =0.15406 nm), and β is the line width at half maximum height of the peak.

Fig. 2. ZnO nanoparticles’ X-ray diffraction spectrum.

Fig. 3. FTIR spectrum of ZnO NPs.

FTIR spectra shown in Fig. 3 show plenteous structural information of prepared NPs. The ZnO stretching modes could be associated with the absorption peak in the 600-700 cm-1 range. Absorption peak between 1100-1600 cm-1 corresponds to the OH, C-OH bending, and C-OH out of plane bending. Further, O-H stretching modes and C-H stretching modes overlap in 2000-3700 cm-1 region. The adsorption band at 1181.98 cm-1 denotes the C=O vibrations of carboxylic acids, alcohols. Similar observations have been reported by Sangeetha et al.38 There was a strong absorption at 528 cm-1, and there were peaks at 3451, 1552, 2170, and 1399 cm-1, which corresponds to the –OH, N-H, C=C, and C-H bond stretching, respectively.

Antibacterial activity of ZnO NPs
In antibacterial activity study, the effect of ZnO NPs is more pronounced as compared with ZnO compound (2-6 mg/mL). Both tested samples exhibited broad-spectrum antibacterial effect towards all selected bacterial strains and the inhibition zone diameter ranged between 10±0 to 28±1.7 mm. The highest inhibition zone diameter i.e. 28±1.7 mm was reported against S. aureus with ZnO NPs at 6 mg/mL, while the lowest (10±0) was observed against Salmonella typhi at 2 mg/mL of ZnO compound (Fig. 4 and 5). On the other hand, standard tetracycline showed inhibition zone diameter ranged between 25±1 to 34±0.52 against all tested microbes, while negative control methanol did not show any activity. Dobrucka and Długaszewska also reported the positive antibacterial effect of green synthesized ZnO NPs against S. aureus, E. coli, and Pseudomonas aeruginosa and showed the highest inhibition zone of 31 mm against S. aureus.39

Fig. 4. Inhibition zone diameter of ZnO Compound (ZnO C) and ZnO NPs at varying concentrations against bacterial pathogens. Different letters were used when mean values were statistically significant (p<0.05). SA- Staphylococcus aureus; KP- Klebsiella pneumoniae; BS- Bacillus subtilis; EC- Escherichia coli; ST- Salmonella typhi.

Fig. 5. Antibacterial potential of ZnO NPs (A) and ZnO compound (B) at varying concentrations (10, 20 and 30 = 2, 4 and 6 mg/mL); Negative control- Methanol; Positive control- Tetracycline.

The MIC as well as MBC values correlate well with the disc diffusion assay. The highest MIC (0.0625±0 mg/mL) and MBC (1±0.29 mg/mL) were observed against Bacillus subtilis. On the other hand, the lowest MIC (0.013±0.01 mg/mL) and MBC (0.10±0.04 mg/mL) were observed against Staphylococcus aureus (Fig. 6). Thakur et al. reported similar activity with green synthesized titanium dioxide NPs.18 Subsequently, only E. coli and Aspergillus niger were found to be susceptible to ZnO NPs made using Aloe vera extract.40 Similarly, ZnO synthesized using Aloe vera exhibited activity against E. coli.33

Fig. 6. ZnO nanoparticles’ MIC and MBC values against microbial pathogens

Several mechanisms have been suggested to explain the antibacterial behavior of NPs, such as the deactivation of cellular enzymes, and DNA via coordination with the donor groups of electrons; and the creation of pits in bacterial cell walls, resulting in increased permeability and, in the end, cell death. Interestingly, hydrogen peroxide development from the ZnO surface is considered to be an effective means of inhibiting bacterial growth.41 On the other hand, one of the plausible reasons for ZnO antibacterial activity is the production of Zn2+ ions, which can disrupt the cell membrane and interfere with cellular content.42


In conclusion, Aloe vera leaves extract mediated synthesis of ZnO NPs is achieved, and this green synthesis is attributed to L-ascorbic acid and bioactive components present in the leaves of Aloe vera. The green approach used for synthesis is environment-friendly. Both ZnO compound and ZnO NPs successfully inhibited the growth of all tested bacterial pathogens including Gram-positive as well as negative cultures. However, the potential of ZnO NPs is found higher as compared with its compound. It was concluded that ZnO NPs could be used as drug-developing candidates after follow-up studies. Further studies are being carried out to assess the impact of various storage conditions on the stability of ZnO NPs.


The authors are grateful to the Indian Institute of Technology, Mandi, India, for providing the necessary facilities for the characterization work.

The authors declare that there is no conflict of interest.

All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.


Not applicable.

All datasets generated or analyzed during this study are included in the manuscript.

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