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26 November 2022

Synthesis, Characterization, Antibacterial, Antifungal, Antioxidant, and Anticancer Activities of Nickel-Doped Hydroxyapatite Nanoparticles

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Research Department of Physics, Holy Cross College (Autonomous), Nagercoil 629004, Tamil Nadu, India. Affiliated to Manonmaniam Sundaranar University, Tirunelveli 627012, Tamil Nadu, India
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Department of Physics, Manonmaniam Sundaranar University, Tirunelveli 627012, Tamil Nadu, India
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Department of Zoology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia
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College of Medicine, AlMaarefa University, Dariyah 13713, Saudi Arabia
Fermentation2022, 8(12), 677;https://doi.org/10.3390/fermentation8120677
This article belongs to the Special Issue Biofilms from Fermentative Perspective: Structures, Functions and Control
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Abstract

The purpose of this research was to investigate the possible antibacterial, antifungal, antioxidant, and anticancer effects of nickel (Ni2+)-doped hydroxyapatite (HAp) nanoparticles (NPs) synthesized using the sol–gel approach. X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy (Raman), field-emission scanning electron microscopy (FESEM), and elemental analysis were used to characterize the Ni2+-doped HApNPs. X-ray diffraction investigation showed that the nanoscale structure of Ni2+-doped HApNPs was hexagonal, with an average crystallite size of 39.91 nm. Ni2+-doped HApNPs were found to be almost spherical in form and 40–50 nm in size, as determined by FESEM analysis. According to EDAX, the atomic percentages of Ca, O, P, and Ni were 20.93, 65.21, 13.32, and 0.55, respectively. Ni2+-doped HApNPs exhibited substantial antibacterial properties when tested in vitro against several pathogens, including Escherichia coli, Shigella flexneri, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Staphylococcus aureus. Antibacterial activity, at 50 mg tested concentration, demonstrated superior effects on G-ve bacteria than G+ve pathogens. The antifungal activity of Oidium caricae, Aspergillus flavus, and A. niger revealed a zone of inhibition of 23, 11, and 5 mm, respectively. These actions rely on the organism’s cell wall structure, size, and shape. Incorporating Ni2+ into HApNPs allows them to function as powerful antioxidants. Ni2+-doped HApNPs had a good cytotoxic impact against the HeLa cell line, which improved with increasing concentration and was detected at a 68.81 µg/mL dosage. According to the findings of this study, the Ni2+-doped HApNPs are extremely promising biologically active candidates owing to their improved functional features.

1. Introduction

Nanotechnology studies have expanded exponentially during the last three decades. Due to their large surface area concerning their volume, nanoparticles (NPs) have found applications across disciplines [1]. Its primary focus was on three major fields: energy, medicine, and agriculture [2]. The size and shape of nanoparticles might vary because they are synthesized using different methods. It works as intended in the common usages. The necessary size regulation of nanoparticles is achieved by using anionic and cationic surfactants [3]. In physical, chemical, and green synthesis [4,5], controlling nanoparticle size has been accomplished in several ways.
Much attention has been paid to incorporating 3d transition metals like Fe, Mn, and Co into HAP to increase their strength. The formation of the material and its physicochemical characteristics are affected by the doping procedure’s annealing temperature grating. With the metal doping procedure, HAp nanopowder with Fe- and Co-doping exhibited improved antibacterial activity against Shigella dysenteriae, while HAp nanopowder with Mn doping showed more significant antibacterial activity against Staphylococcus aureus. Size, shape, stability, ion-releasing capacity, and the structure of the bacterial cell wall all play a role in the antibacterial activity of metal-doped HAp nanopowder [5].
Several metal nanoparticles are very effective antibacterial agents [6,7]. On the other hand, their prohibitive price prevents widespread commercial use. Therefore, it is important to work on finding alternatives that do not rely on noble metals for their economic viability. The inorganic mineral hydroxyapatite (HAp) is the principal structural component of teeth and bones [8,9], which makes it an attractive candidate in the quest for novel materials. The calcium phosphate in HAp is vitrified and ceramicist [10]. Calcium orthophosphate is a vital calcium potential in all living things. There are more options in dentistry, bone-tissue engineering, dental implant coating, orthopedics, and prosthetics [11,12].
For the most part, researchers have examined calcium-poor apatites, which may include divalent ion replacements. Several biological uses [10,13] are selected for HAp [Ca10(PO4)6OH2], including antibacterial, drug delivery, dental, and orthopedic. When metal ions were present, the activity of Ca-HAp and its nitrate salt returned to normal. Because of its high mechanical strength and resistance to corrosion, Ni2+ is widely used as an orthopedic implant [14]. This element is also essential for all chordate organs. Ni2+ may replace Ca2+ in HAp without compromising the compound’s crystalline structure. Researchers examined how adding Ni2+ to HApNPs preparation changed the final solid solution. Highly crystalline Ni2+-doped HApNPs may be produced by sol–gel synthesis [15] by keeping these critical characteristics under controlled conditions. The present work describes the sol–gel synthesis of Ni2+-doped HApNPs. Characterization of Ni2+-doped HApNPs was performed using XRD, FTIR, Raman, FESEM, and EDAX. In addition, the antimicrobial, antioxidant, and antitumor properties were investigated.

2. Materials and Methods

2.1. Materials

In order to create Ni2+-doped HAp nanoparticles, we mixed together Ni(NO3)2.6H2O, Ca(NO3)2.4H2O, PEG, NH3, and (NH4)2HPO4. All chemicals used in this study were bought from Sigma-Aldrich, USA and were of reagent grade (99.9% purity). From Hi-Media in India, we procured Luria Bertani agar, potato dextrose agar, clotrimazole, and amikacin. Triple-distilled water was utilized in the experiments. The bacterial strains of Shigella flexneri (MTCC 1457), Escherichia coli (MTCC 40), Pseudomonas aeruginosa (MTCC 2642), Klebsiella pneumoniae (MTCC 432), and Staphylococcus aureus (MTCC 1935), as well as the fungal strains of Oidium caricae, Aspergillus flavus, and A. niger, were all obtained from KRIND Institute of Research and Development, Trichy, Tamil Nadu, India.

2.2. Preparation of PEG-Assisted Ni2+doped HAp

Synthesis of PEG-assisted Ni2+-doped HApNPs included employing double-distilled water, ammonia solution, di-ammonium hydrogen phosphate, nickel nitrate, and calcium nitrate. Calcium nitrate, at 0.9 M, and nickel nitrate, at 0.1 M, were each diluted in 50 mL of distilled water and stirred with a magnetic stirrer for 30 min. In 50 mL of sterile water, 0.1 M PEG surfactant was combined with 0.1 M calcium and 0.1 M nickel solutions. A 0.6 M concentration of Di-ammonium hydrogen phosphate was achieved by dissolving the compound in the earlier solution. We slowly added the ammonia solution to the first combination, reaching a pH of 10. After draining in a hot air oven, the product was calcined for 2 h at 500 °C.

2.3. Antimicrobial Activity

Synthesized Ni2+-doped HApNPs at a concentration of 50 g were tested for their antibacterial efficacy against five bacterial and three fungal strains [16]. Luria Bertani medium (pH 7.4) for bacteria and potato dextrose medium (pH 7.4) for fungi were used to incubate the test organisms at 37 °C for 18 to 24 h. Wells were drilled into the exterior of the sterile gel made of agar. Afterward, the triplicate plates were protected against bacteria and fungus. The five most frequent bacteria that cause infections are Staphylococcus flexneri (MTCC 1457), Escherichia coli (MTCC 40), Pseudomonas aeruginosa (MTCC 2642), Klebsiella pneumoniae (MTCC 432), and Staphylococcus aureus (MTCC 1935). Oidium caricae, Aspergillus flavus, and A. niger were used in tests to determine the antifungal activity. Positive control for bacteria and fungi was 30 g of amikacin and 10 g of clotrimazole, while DMSO served as a negative control.

2.4. Antioxidant Activity

Ni2+-doped HApNPs’ antioxidant ability was evaluated using DPPH and radical scavenging, as described by Brand-Williams et al. [17]. Hydrogen donation or free radical scavenging capacity of Ni2+-doped HApNPs formed the basis for their antioxidant action. Scavenging of the products was also quantified with the use of the following equation:
DPPH   scavenging   activity   ( % ) = ( Abs   control − Abs   sample ) ( Abs   control ) × 100

2.5. Anticancer Activity

Ni2+-doped HApNPs were investigated for cytotoxicity against HeLa cells using a MTT assay. The HeLa cells came from the National Centre for Cell Sciences (NCCS) in Pune, India. In a humidified incubator (5% CO2, 37 °C; Galaxy® 170 Eppendorf, Germany), tissues were principally grown in a 25 cm2 tissue culture flask (DMEM in Himedia). The cell viability was examined visually using an inverted phase-contrast microscope.

3. Results and Discussion

3.1. XRD Analysis

Ni2+-doped HApNPs exhibit a crystalline phase in the form of hexagonal HApNPs with well-defined diffraction peaks in the conventional X-ray diffraction (XRD) pattern (JCPDS: 09-0432), as shown in Figure 1. Hexagonal HApNPs doped with Ni2+ have been shown to have a P63/m space group. At 2θ = 26.61°, 27.93°, 28.87°, 31.21°, 32.58°, 34.50°, 40.59°, 47.16°, and 53.15°, diffraction peaks were seen that corresponded to the (002), (102), (210), (211), (300), (202), (221), (312), and (004) planes, respectively. Significantly, the crystal system is unaffected by the PEG surfactant.
Figure 1. XRD analysis of Ni2+-doped HApNPs calcined at 500 °C.
The absence of a secondary phase for a nickel or any other impurity demonstrates that nickel ions have efficiently replaced calcium ions without modifying the crystal structure of HApNPs. The results of this study are in close accord with those of the previous studies [18,19,20,21,22,23]. When Ni2+ ions were replaced for specific Ca2+ sites, however, the dopant was substantially absorbed into the HApNPs lattice, as shown by a slight change in 2θ and distortion in the lattice cell properties. Using the more distinct diffraction peaks at the (102), (211), and (202) planes, we were able to calculate that the crystallite size is around 39.91 nm. Nevertheless, research shows that when Mg is replaced with Ca in stoichiometric HApNPs, the lattice parameters decrease, and the peaks shift toward the lower diffraction angle [24,25]. Adsorption of the remaining Mg prevented additional grain formation onto the surface of the HApNPs, despite the HAp-Mg complex constantly producing random grains [26].

3.2. FTIR Analysis

Figure 2 depicts the FTIR spectrum of Ni2+-doped HApNPs. Frequencies of 558 cm−1 and 608 cm−1 were assigned as the O-P-O bending mode. The 1040–1140 cm−1 range contains bands with a high intensity that have been assigned to the v3 asymmetric stretching mode of O-P-O. The presence of v3 carbonate ions (CO3−2) from the environment during sample preparation has been connected to the weak bands identified at 1460 cm−1. However, the band at 1634 cm−1 is easily explained due to the lattice’s two H2O, H-O-H bending modes. It has been determined that the OH stretching contributes mild intensity to the appearance of two bands in the HApNPs, one wide at 3452 cm−1 and the other sharp at 3575 cm−1. Water in the lattice, rather than absorbed water, is responsible for the persistence of the OH bands even at elevated temperatures. After all, at temperatures over 100 °C, absorbed moisture is evaporated. XRD analyses corroborate these results, suggesting that Ni2+ ions are present in the HAp structure.
Figure 2. FTIR spectrum of Ni2+-doped HApNPs calcined at 500 °C.
Similar FTIR investigations showed that hydroxyl and phosphate functional groups were present in HAp and Mg-HAp, as indicated by the presence of characteristic sharp lines at 1026 cm−1 and 1032 cm−1, respectively, and also showed that the phosphate groups stretched in a certain way [9]. According to an ongoing investigation, FTIR analysis confirms the presence of the PO43− group in HAp, with peaks for HAp ranging from 1749 to 1736 cm−1. In contrast, Mg-HAp formed a covalent bond with the absorbed water molecule [27]. In addition, the small peak at 969 cm−1 indicates symmetric stretching vibrations, which are often linked to a P-O mode [28]. The O-H bond is responsible for weak peaks at 3571 cm−1 for HAp and 3554 cm−1 for Mg-HAp. HAp and Mg-HAp exhibit a sizable stretching band around 1367 cm−1 [29], which may be traced back to the carbonate group. Most of this peak is due to the O-H stretching vibration in HAp.

3.3. Raman Spectrum Analysis

Figure 3 illustrates the Raman spectrum of Ni2+-doped HApNPs. Raman spectra of Ni2+-doped HApNPs revealed vibrational bands related to phosphate group stretching and twisting modes. Most significantly, at 961 cm−1, the symmetric stretching way of PO43− (v1)—one can always recognize this peak as belonging to HApNPs. The low-intensity band at 363, 407, and 480 cm−1 is responsible for the bending behavior of PO43− (v2symmetric). In this investigation, a band at 614 cm−1, estimated at around 591 cm−1, matches the irregular bending style of PO43− (v2). It has been determined that the band saw at 1043 and 1163 cm−1 in the Raman spectra of Ni2+-doped HApNPs is due to mild PO43− (v3) stretching. There is strong agreement between our findings and the previously published values [5].
Figure 3. Raman spectrum of Ni2+-doped HApNPs calcined at 500 °C.

3.4. FESEM Analysis

The morphology of the Ni2+-doped HApNPs was studied by utilizing FESEM. FESEM images of Ni2+-doped HApNPs are shown in Figure 4a,b at different magnifications. The particles have a spherical form and exhibit intense aggregation; their average size is 45 nm, and their length is 40–50 nm. The size-variant spherical and near-spherical shape was observed in Ni2+-doped HApNPs. Agglomerated spherical NPs of about 50 nm in size resulted from an initial pH held constant at 10. The Ni2+-doped HApNPs in the FESEM fit the XRD pattern nicely. This work shows that doping nano-hydroxyapatites with Ni2+ does not significantly alter their crystal structure but substantially reduces their crystallinity [30].
Figure 4. FESEM images of Ni2+-doped HApNPs (a) 40,000×, (b) 80,000×.

3.5. EDAX Analysis

The EDAX spectrum (Figure 5) reveals the stoichiometric occupancy of Ca, O, Ni, and P, proving the synthesis of Ni2+-doped HApNPs and ensuring that the models are in accordance with the HApNPs’ fundamental ingredients and stoichiometry. The existence of P, O, Ca, and Ni may also be confirmed. The EDAX spectrum did not show any secondary phase or contamination signals. This sample elemental analysis confirmed the presence of Ca, O, P, and Ni in Ni2+-doped HApNPs.
Figure 5. EDAX spectrum of Ni2+-doped HApNPs calcined at 500 °C.

3.6. PL Analysis

The PL emission spectra of Ni2+-doped HApNPs synthesized through sol–gel synthesis are shown in Figure 6. The PL emission peaks of Ni2+-doped HApNPs are located between 340 and 600 nm. Emission peaks were measured at 360, 376, 410, 494, 505, 520, 535, 572, 581, and 594 nm for the Ni2+-doped HApNPs. Current research indicates that HAp and MOFE: HAp nanorods (NRs) have similar PL, with a wide visible emission band of about 310 nm. When UV light was applied to HApNPs, holes formed in the material that UV-induced trapholes might exploit, and both band gaps (5.2 and 5.5 eV) were also preserved [10].
Figure 6. PL emission spectrum of Ni2+-doped HApNPs calcined at 500 °C.

3.7. Antimicrobial Activity

3.7.1. Antibacterial Activity

Figure 7 shows the zone of the inhibitory effect of the five most prevalent pathogenic microorganisms. Furthermore, the optimal concentration was 50 g. Ni2+-doped HApNPs were discovered to exhibit a maximum inhibition zone against E. coli of around 22 mm, demonstrating potent antibacterial action. The zone of inhibition shown by P. aeruginosa was rather large, measuring about 19 mm. The growth inhibitory impact of bacteria was modest against S. flexneri and K. pneumoniae. Minimal inhibitory zones were seen for S. aureus (Table 1). The finding demonstrates the high antibacterial activity of the produced Ni2+-doped HApNPs. Similarly, a recent study [31] reported that Ni2+-doped HApNPs showed remarkable antibacterial action against E. coli and S. aureus.
Figure 7. Antibacterial activity of Ni2+-doped HApNPs treated against (a) S. flexneri, (b) E. coli, (c) P. aeruginosa, (d) K. pneumoniae and (e) S. aureus. C-Negative control (DMSO), Std.-Positive control (Amikacin), 7- Ni2+-doped HApNPs.
Table 1. Zone of inhibition of Ni2+-doped HApNPs against bacterial pathogens.
Bacterial inactivation is facilitated by ions in the NPs reacting with SH groups (proteins) [32]. They found a zone of restriction opposed to G-ve (14.9 0.97 mm) and G+ve (9.0 2.56 mm) bacteria, demonstrating that HApNPs’ antimicrobial function can protect microorganisms [33]. Figure 8 depicts the mechanisms that contribute to the antibacterial effects of NPs. Possible mechanisms for the antibacterial effects of metal NPs include the absorption of free metal ions, which interfere with DNA replication, direct damage to cell membranes, reactive oxygen species (ROS), and the creation of ATP [34]. Well-diffusion pattern studies were used to investigate the antibacterial activity of AgNPs. In terms of maximal role containment, Acinetobacter baumannii (31 mm), Staphylococcus aureus (26 mm), and Bacillus subtilis (19 mm) were all successful [35]. The AgNPs were studied for their potential to inhibit DNA replication by interfering with bacterial membrane permeability processes [36].
Figure 8. Illustration of the possible mechanism by which Ni2+-doped HApNPs exert their antibacterial effects.

3.7.2. Antifungal Activity

Synthesized Ni2+-doped HApNPs revealed antifungal activity with an inhibitory zone opposite that of A. flavus, O. caricae, and A. niger (Figure 9; Table 2). However, clotrimazole, a persistent antibiotic, had the greatest activity across all species tested. The antifungal activity also exhibited structure, with the highest activity at 50 g. The maximum inhibitory zone for Ni2+-doped HApNPs was observed at a distance of 23 mm from O. caricae. The zone of inhibition for A. flavus’s growth was modest at 11 mm. A. niger exhibited a minimal inhibitory zone. Ni2+-doped HApNPs were successfully produced, and the results verified their potent antifungal properties. Ag-HApNPs displayed antibacterial activity against O. caricae, A. niger, and A. flavus, with the zone of inhibition values of 27, 23, and 25 mm, respectively, as reported in our earlier studies [23].
Figure 9. Antifungal activity of Ni2+-doped HApNPs treated against (a) O. caricae, (b) A. niger and (c) A. flavus.
Table 2. Antifungal activity of Ni2+-doped HApNPs treated against fungal pathogens.

3.8. Antioxidant Activity

Ni2+-doped HApNPs antioxidant activity was tested using diphenyl phosphate (DPPH), and the results revealed that the free radical scavenging function of the HApNPs increased with increasing concentration (Figure 10). Ni2+-doped HApNPs demonstrated superior scavenging performance. In contrast, standard Rutin only managed 60% efficiency over the whole concentration range (100 to 400 µg/mL). Thus, Ni2+-doped HApNPs are the best option due to their superior antioxidant process. Studies using a similar design have connected the formulation’s 1,1’-diphenyl-2-picrylhydrazyl and hydrogen peroxide scavenging capabilities to stable ascorbic acid, with the increased activity mainly related to the presence of phenols and flavonoids [37,38].
Figure 10. Antioxidant activity of Ni2+doped HApNPs. Different letters above each column indicate significant differences (ANOVA, Tukey’s HSD test, p < 0.05).

3.9. Anticancer Activity

The effect of Ni2+-doped HApNPs on the growth and viability of HeLa cell lines was evaluated using the MTT assay (Figure 11; Table 3). Different concentrations of Ni2+-doped HApNPs were investigated for this test to find an effective dose. When tested against HeLa cell lines, the Ni2+-doped HApNPs sample significantly increased cytotoxicity. Size and cell type have a role in determining the cytotoxicity caused by NPs. At 100 µg/mL, Ni2+-doped HAp had a cell viability of 32.19%, whereas Ni2+-doped HApNPs had viability between 52.12 and 92.5% at 50, 70, and 6.25 µg/mL. Cell death occurred at a rate of 30%, even at a concentration of 100 µg/mL. In contrast to HeLa cell lines, the synthesized Ni2+-doped HApNPs exhibited cytotoxicity as measured by the MTT assay, with an IC50 value of 68.82 µg/mL. Comparatively, silver nanoparticles (AgNPs) were shown to have strong anticancer activity against the breast cancer cell line MCF 7 [35]. CaO NPs exhibited apoptotic characteristics, including cell shrinkage and condensed and fragmented nuclei, in contrast to the cell proliferation structures of A549 cells observed in the previous research article [39].
Figure 11. Anticancer activity of Ni2+doped HApNPs. (a) control, (b) 6.25 µg/mL, (c) 12.5 µg/mL, (d) 25 µg/mL, (e) 50 µg/mL, (f) 100 µg/mL.
Table 3. Anticancer activity of Ni2+-doped HApNPs tested on HeLa cells.

4. Conclusions

The sol–gel method was used to synthesize Ni2+-doped HApNPs. Ni2+-doped HApNPs are shown to be nanocrystalline, as evidenced by their XRD pattern. Typically, a crystallite is about 39.91 nm in size. Functional groups like O-H and O-P-O are confirmed by FTIR and Raman spectroscopy. The EDAX confirmed Ni2+ ion doping in the HAp structure, and the FESEM examination showed the particles to be spherical or nearly spherical in shape. The sample shows significant agglomeration when Ni2+ ions are substituted for other cations. Ni2+-doped HApNPs were shown to be very effective against various bacteria when tested using the disc diffusion technique, including S. flexneri, E. coli, P. aeruginosa, K. pneumoniae, and S. aureus. High levels of antifungal, antioxidant, and anticancer activity are seen in HApNPs doped with Ni2+. As a result, the Ni2+-doped HApNPs have potential in the biomedical sector for implantation in orthopedics and surgical procedures.

Author Contributions

Conceptualization, S.S., M.G. and A.S.L.F.; methodology, S.S. and A.S.L.F.; software, S.S. and A.S.L.F.; validation, S.S., M.G. and A.S.L.F.; formal analysis, S.S.; investigation, S.S. and J.H.; resources, K.G., M.A.W. and S.M.; data curation, K.G., A.M.W. and I.M.; writing—original draft preparation, S.S. and A.S.L.F.; writing—review and editing, M.G., S.M., M.A.W., M.R. and I.M.; visualization, M.R., S.S. and A.S.L.F.; supervision, A.S.L.F.; funding acquisition, S.M. and M.A.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Researchers Supporting Project Number (RSP2022R466) King Saud University, Riyadh, Saudi Arabia.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors express their sincere appreciation to the Researchers Supporting Project Number (RSP2022R466), King Saud University, Riyadh, Saudi Arabia.

Conflicts of Interest

The authors declare no conflict of interest.

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