The intrinsic antimicrobial activity of citric acid-coated manganese ferrite nanoparticles is enhanced after conjugation with the antifungal peptide Cm-p5

Introduction

In recent decades, several new infectious diseases have emerged or reemerged. In many cases, they have been the origin for entirely new and life-threatening infectious emergencies.^1,2 The absence of effective antibiotics for the treatment of certain illnesses combined with the appearance of multidrug-resistance in related strains has prompted even greater urgency for innovative approaches in the control of infections.³ Antimicrobial peptides (AMPs) form part of the first line of defense against pathogens of many organisms. Their use as anti-infective tools represents a novel approach for the development of antimicrobial therapies.^4,5 Even though such peptides have been shown to be both broad spectrum (having antimicrobial, anticancer, immunomodulatory, wound healing and angiogenesis properties) and significantly potent in preclinical studies, this success has not been transmitted to clinical practice yet.⁶ The major disadvantages of AMPs have been low stability, cytotoxicity, biodistribution, and high production costs.^4,7

Development of nanoparticles for delivery or conjugation of AMPs could represent an alternative to bypass the abovementioned clinical obstacles.⁸ In fact, the antimicrobial activity of different types of nanoparticles has been demonstrated. Some metals like silver, zinc, and copper exhibit antibacterial properties themselves, increasing the effect of these metals at nanoscale dimensions.⁹ Magnetic nanoparticles (MNPs) could be a suitable carrier for AMPs due to their wide spectrum of activities (anticancer, antimicrobial, drug delivery, diagnosis) and their low toxicity demonstrated in vivo.^10–12 The potential applications of manganese ferrite nanoparticles (MnFe₂O₄-NPs) for bioanalytical applications have been described, and it is perfectly possible to conjugate such nanoparticles to an anti-Sticholysin II monoclonal antibody, while preserving their antigenic recognition.¹³ The isostructural substitution of Fe(II) by Mn(II) in the magnetite structure provides the possibility of an enhanced peroxidase-like activity and a better material ability to participate in redox reactions, because the manganese ion has a large variety of available oxidation states, for example, Mn(III), Mn(IV), Mn(V), Mn(VII).

Furthermore, iron oxide (eg, magnetite and maghemite) is not antibacterial in its bulk form but may exhibit antibacterial properties in the form of nanoparticles.¹⁴ Such behavior is ascribed to the availability of a large fraction of the particle atoms at surface positions with an unsaturated coordination environment, and from this, enhanced reactivity. For example, magnetite nanoparticles coated with quaternary ammonium were bactericidal against Escherichia coli.¹⁵ Additionally, bacitracin-conjugated iron oxide (Fe₃O₄) nanoparticles have shown higher antimicrobial activity against both Gram-positive and Gram-negative organisms, in comparison with the bacitracin peptide.¹⁶ Additionally, ceragenin CSA-13-coated MNPs (MNP-CSA-13) exhibited strong antibacterial activity and the ability to prevent bacterial biofilm formation in different body fluids, with a significant decrease in its hemolytic activity when the molecule was immobilized on the nanoparticle surface.¹⁷ In contrast, it has been reported that iron-containing nanoparticles may influence the ability of bacteria to absorb iron for growth, increase virulence, and inhibit AMP function.¹⁸

Here, we present the intrinsic antifungal activity of the citric acid-coated MnFe₂O₄-NPs and the improvement of their antifungal activity when these nanoparticles were conjugated with a 12 aa peptide named Cm-p5.¹⁹ This peptide is derived from Cm-p1, which is an MS-MS sequence found in a tryptic chromatographic fraction from the whole animal extract (Cenchritis muricatus [Gastropoda: Littorinidae], Linnaeus, 1758), which was positive for antimicrobial activity. We previously demonstrated that such sequence belongs to the original invertebrate, but we do not know if the corresponding peptide naturally acts as an AMP or if it is part of a major protein potentially undergoing cleavage by induction or not.²⁰ From this sequence we obtained, by bioinformatics, the sequence and corresponding synthetized peptide Cm-p5 with an increased antifungal activity. Therefore, we have based our thinking on previous results in which Cm-p5 showed a minimal loss of activity after conjugation with our manganese ferrite nanoparticles, taking into account that the nonimmunogenic small size of the peptide and its hydrophilicity are probably working together in accordance with our purposes.

Materials and methods

Nanoparticles (modified MnFe₂O₄)

Modified MnFe₂O₄-NPs used in this work were supplied by the Institute of Materials Science and Technology, University of Havana, Havana, Cuba. These nanoparticles were part of a batch characterized by X-ray diffraction (XRD), Mössbauer spectroscopy, and Fourier-transform infrared (IR) spectroscopy by Figueroa-Espi et al.¹³ In brief, XRD patterns were recorded in the Bragg–Brentano geometry using K_α1 radiation. Mössbauer spectrum was collected at room temperature (RT) in the transmission geometry using a ⁵⁷Co/Rh radiation source and provided information on the substitution of Fe(II) by Mn(II) in the spinel-type structure of the host magnetite framework.

Characterization of MNPs by transmission electron microscopy

The size of the MNPs was assessed by transmission electron microscopy (TEM). TEM images were obtained using a Jeol Jem 2010 F30 microscope (JEOL USA, Inc., Peabody, MA, USA) operated at 200 kV. Samples for TEM were prepared by letting a drop of the samples dispersed in ethanol evaporate on top of a carbon-coated copper grid of 200 meshes. Micrographs were taken by a Gatan Orius SC200 high-speed digital camera (Gatan, Inc., Pleasanton, CA, USA).

Dynamic light scattering measurements

Dynamic light scattering (DLS) measurements were made on a Zetasizer Nano ZS (Malvern Instruments, Malvern, UK) for particle size determination. The temperature of the sample cell was controlled to 20°C by a thermostating system. A He–Ne laser with λ =633 nm was used to measure data at 173° noninvasive backscattering using PCS8501 glass cuvette with round aperture. The experiments were performed using the nanoparticles in Tris-HCl buffer, pH 8.0. The final concentrations of the nanoparticles were 2 mg/mL.

Peptide synthesis

Cm-p5 was obtained by solid-phase synthesis using 9-fluorenyl-methoxycarbonyl chemistry,²¹ purified by reversed-phase high-performance liquid chromatography to >98% purity using an acetonitrile/H₂O-trifluoroacetic acid gradient. Purity was evaluated by ion-spray mass spectrometry (Micromass, Manchester, UK).

Determination of peptide concentration

Peptide concentrations were estimated by ultraviolet absorption at 205, 215, and 225 nm (Abs205, Abs215, Abs225) using the following equations:²²

C (mg/mL) = (A + B)/2

(1)

A = (Abs215 − Abs225) ×0.144

(2)

B = (Abs205) ×0.31

(3)

Conjugation of Cm-p5 with modified MnFe₂O₄-NPs

MnFe₂O₄-NPs 4 mg were activated by 1-ethyl-3-(dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide solution (0.5 and 0.7 mg/mL), respectively, in phosphate-buffered saline (PBS) for 30 minutes at RT. The activated nanoparticles were incubated with 0.4 mg of peptide resuspended in 1 mL PBS and mixed at RT for 2 hours. The nanoparticles were washed twice in PBS and in 0.1 M Tris, pH 8.0.

Antibacterial bioassays

The antibacterial bioassays were evaluated for Staphylococcus aureus (ATCC29213) and E. coli (ATCC8739) by a colorimetric microreader (BioTek Instruments, Winooski, VT, USA) using 96-well microplates according to Hetru and Bulet’s methodology.²³ Bioassay analyses against bacteria were performed in Luria-Bertani medium (pH 7.0). Previously, a growth curve of the original culture was established to determine the relationship between colony-forming units and optical density. For antimicrobial activity evaluation, 0.1 mL inoculum was cultured in 4 mL Luria-Bertani medium for 3 hours until it reached the mid-exponential phase. An aliquot corresponding to 5×10⁵ colony-forming units/mL was then added to Luria-Bertani medium to produce a final volume of 0.1 mL in the microplate wells. Nanoparticles were added to reach a final concentration of 250 μg/mL. Chloramphenicol at a concentration of 40 μg/mL and distilled water were used as positive and negative controls, respectively. Microplates were incubated at 37°C, and bacterial growth was monitored at 620 nm every hour. The percentage of survival was determined as the ratio of optical density of normal bacterial growth (100%) and the growth under nanoparticle action. All bioassays were performed in triplicate. To avoid potential optical interference during measurements of the growing cultures caused by the light-scattering properties of the nanoparticles, Luria-Bertani medium without microorganisms but containing the same concentration of nanoparticles cultured under the same conditions was used as a blank control.

Antifungal bioassay

Bioassays against yeast were performed using the broth microdilution method according to the Clinical and Laboratory Standards Institute guidelines.²⁴ The bioassays against the clinically isolated strain of Candida albicans (01U) were performed in Roswell Park Memorial Institute (RPMI)-1640 medium (Thermo Fisher Scientific, Waltham, MA, USA). Amphotericin-B (30 μg/mL) and sterile distilled water were used as positive and negative controls, respectively. Microplates were incubated at 30°C and yeast growth was monitored at 620 nm every hour. The percent (%) of survival was determined as the ratio of optical density of normal fungal growth (100%) and the growth under peptide action. All tests were conducted in triplicate. The background (turbidity due to RPMI medium and MNPs suspension) was eliminated by taking blank readings. The citric acid-modified MnFe₂O₄-NPs concentrations for the antifungal bioassay were 100 and 250 μg/mL. The concentration of the citric acid-modified MnFe₂O₄-NPs conjugated with Cm-p5 was 100 μg/mL in comparison with Cm-p5 at 12 μg/mL.

Cytotoxicity assay

Testing with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT, Sigma-Aldrich, St Louis, MO, USA) assay was performed according to Pasupuleti et al.²⁵ RAW 264.7 murine macrophage-like cells (Rio de Janeiro Cell Bank, Rio de Janeiro, Brazil) were plated at a concentration of 1×10⁵ cells per well in supplemented Dulbecco’s Modified Eagle’s Medium (4 mM glutamine, 10% fetal calf serum, and 100 units/mL penicillin/streptomycin) and incubated with different concentrations of nanoparticles (0–750 μg/mL). After overnight incubation, 10 mL of the MTT solution (5 mg/mL in PBS) was added to each well. Plates were incubated for 4 hours in 5% CO₂ at 37°C. The generated blue formazan product was dissolved by the addition of 100 μL of 100% dimethyl sulfoxide (Mallinckrodt Chemical, Paris, KY, USA) per well. The absorbance was monitored at 575 nm in an enzyme-linked immunosorbent assay plate reader (BioTek, Winooski, VT, USA). The citric acid-modified MnFe₂O₄-NPs concentrations for the viability and proliferation assay were 250, 500, and 750 μg/mL.

Interaction of modified MnFe₂O₄-NPs with C. albicans cells visualized by optical microscopy

C. albicans cells were cultivated in the same way as described in the section of ‘Antifungal bioassay’. Nanoparticles (250 μg/mL) were incubated for 1 hour with C. albicans (10⁵ cells/mL) in RPMI-1640 medium at 30°C. Observations were performed with an AxioPhot epifluorescence microscope equipped with an Axiocam MRc camera and complemented with capture software (AxioVision; Carl Zeiss GmbH, Jena, Germany).

Results and discussion

The MnFe₂O₄-NPs used in this study were prepared by microemulsion method.²⁶ These nanoparticles were characterized by XRD, Mössbauer spectroscopy and high-resolution TEM (HR-TEM) as previously described.¹³ XRD powder pattern corresponds to the face-centered cubic unit cell expected for manganese ferrite, which crystallizes with spinel-type structure. Figure 1 shows TEM micrographies, XRD pattern, and IR spectrum of manganese ferrite nanoparticles under study. Also, no evidence of accompanying phases was found. With the purpose of stabilizing the nanoparticles and creating reactive groups suitable for further conjugation procedures, MnFe₂O₄-NPs were modified with citric acid. As a sensing tool for the coating process, IR spectroscopy was used. The recorded IR spectra show several absorption bands characteristic of citrate groups (Figure 1).¹³

Figure 1 This material crystallizes with the face-centered cubic unit cell typical of spinel 3d metal oxides. Notes: Their crystallite size, according to XRD and TEM images, remains below 12 nm (see Figure 1C). The IR spectrum of citric acid-coated nanoparticles is conclusive regarding the anchoring of the organic molecule on the nanoparticles’ surface. (A–C) HR-TEM micrographs at different resolutions from manganese ferrite nanocrystals. (D) XRD pattern. (E) IR spectrum of Mn-ferrite nanoparticles under study. Abbreviations: IR, infrared; MNPs, magnetic nanoparticles; HR-TEM, high resolution transmission electron microscopy; XRD, X-ray diffraction.

In order to study the crystalline nature of the modified MnFe₂O₄-NPs, HR-TEM images were obtained (Figure 1). We observed well-aligned atomic planes, demonstrating the uniformity of the obtained nanocrystals. The HR-TEM images confirm the formation of MnFe₂O₄ nanocrystals of about 5 nm diameter. This result is in agreement with Vestal et al, who used the same synthesis method and reported a nanoparticle diameter below 15 nm.²⁷ In the same sense, comparable diameter sizes of 4 and 5 nm for manganese ferrite nanoparticles prepared by thermal decomposition have been reported.^28,29

The measurements of the diameter of nanoparticles by DLS differ from HR-TEM analysis. The analysis by DLS shows that 93% of the NPs present a diameter range of 24–51 nm. Observed differences between both techniques are related with the fact that MNPs behave in solvents as a dispersion, in contrast to HR-TEM in which nanoparticles are analyzed as a dried sample. Similar results have been obtained by Nunes et al with citrate-coated manganese ferrite nanoparticles.³⁰

The antimicrobial activity of different coated MNPs has been demonstrated.^9,14 To this end, the citric acid-modified MnFe₂O₄-NPs were evaluated for their antimicrobial activity. These nanoparticles showed a significant antifungal activity against C. albicans at different concentrations (Figure 2). The minimal inhibitory concentration (MIC) of the MNPs was reached at 250 μg/mL in the RPMI medium. The antifungal activity of the nanoparticles was not fungicidal (data not shown). On the other hand, nanoparticles were not effective against the Gram-positive S. aureus and the Gram-negative E. coli bacteria (data not shown).

Figure 2 Candida albicans growth curves in RPMI-1640 medium using different concentrations of modified MnFe2O4-NPs in a final volume of 200 μL/well. Notes: Each value represents the mean of three replicates in three different experiments. Bars represent the standard deviation. Abbreviations: MNPs, magnetic nanoparticles; OD, optical density; RPMI, Roswell Park Memorial Institute.

The antifungal activity of nanoparticles had been recently demonstrated for magnetic binary nanocomposites of iron oxide (magnetite and maghemite) and silver nanoparticles.³¹ These nanoparticles showed very significant antibacterial and antifungal activities against ten tested bacterial strains (MIC from 15.6 to 125 μg/mL) and four Candida species (MIC from 1.9 to 31.3 μg/mL). In this case, the inherent antimicrobial activity of silver can be taken into account, but on the other hand, some attempts to inhibit Candida biofilm formation succeeded by coating MNPs with plant essential oils applied to different surfaces as dressings and medical devices.^32–34 Nevertheless, no direct antifungal activity was demonstrated for these nanoparticles. In fact, no antimicrobial activity has been reported for “naked” MNPs. MnFe₂O₄-NPs have semiconductor behavior with a relatively low band gap, in the visible region, and for such reason, this nanoparticle system is unable to oxidize the water molecule producing radicals. In contrast, for instance, TiO₂ and ZnO nanoparticles have a band gap in the ultraviolet region and the light absorption creates holes in the valence region, which are responsible for oxidizing the water and forming radicals, which are highly reactive species. In our work, it is probable that the antimicrobial activity of citric acid-modified MnFe₂O₄-NPs is related to such coating.

Indeed, the antibacterial activity of citric acid solutions has been previously reported.^35–37 For example, the conjugation of citric acid to ciprofloxacin significantly improved the antibacterial activity of the antibiotic.³⁸ However, the nanoparticles described in this paper were not effective against bacteria. It is possible that this effect could be related to the electrostatic repulsion between citrate groups on the surface of nanoparticles and the transmembrane potential of bacteria. In this sense, it has been reported that positively charged MNPs coated with a chitosan polymeric matrix have the ability to bind to the bacteria cell surface, exerting antimicrobial activity.³⁹ Taking into account the electrostatic differences between prokaryotic bacterial and eukaryotic fungal plasma membrane,⁴⁰ the selectivity of citric acid-modified MnFe₂O₄-NPs could be explained in such terms. Indeed, the interaction of citric acid-adsorbed CoFe₂O₄ nanoparticles with artificial lipid membranes (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine) was demonstrated.⁴¹ This result is relevant in this context since phosphatidylcholine is the most abundant phospholipid in yeast membrane. The mechanism of action for most of the cationic AMPs (and also extendable to our manganese ferrite nanoparticles) depends on the interaction with the microbial membrane to promote membrane destabilization, and these agents can function in vivo but are not toxic to host cells. One explanation is that AMPs produced by mammals will not act on eukaryotic cells because of the cholesterol content of eukaryotic membranes. In contrast, microbial cell membranes are free of cholesterol. Because cholesterol is known to cause condensation of phospholipid bilayers, it might prevent these agents from penetrating into the cytoplasmic membrane of eukaryotic cells. Besides cholesterol, the asymmetric distribution of phospholipids in the cytoplasmic membrane of mammalian cells might also contribute to the insensitivity of eukaryotic cells to this attack.⁴² On the other hand, C. albicans plasma membrane presents ergosterol instead of cholesterol and a combination of phosphatidylcholine, phosphatidylinositol, phosphatidylserine, and phosphatidylethanolamine, not present in mammalian cells; this could favor the interaction with the Mn-ferrite nanoparticles and subsequent destabilization.

With the purpose of discarding any toxic activity of modified MnFe₂O₄-NPs against animal cells, a viability test was conducted. A dose-dependent influence on cell damage was found. Nanoparticles were seen to be nontoxic to a macrophage cell line at concentrations that showed antifungal activity (≤250 μg/mL). Otherwise, higher concentrations (≥500 μg/mL) affected the viability of such cells (Figure 3). As for our antifungal peptide Cm-p5, when it is in contact with C. albicans cells at a sub-MIC concentration, instead of causing disturbing the cell membrane, the orientation and concentration of peptide in the membrane stimulate a higher yeast growth than the control with only cells and medium. For this reason, nanoparticles at 250 μg/mL, like AMPs under MIC concentrations, could favor the cell’s uptake of nutrients. This argument needs to be more thoroughly explored.

Figure 3 Viability and proliferation of the RAW 264.7 cells in RPMI-1640 medium at different concentrations of citric acid-modified MnFe2O4-NPs. Notes: Triton X-100 (3%) was used as a positive control for toxicity, and PBS was used as a negative control. Each column represents the mean of three replicates. Bars represent the standard deviation. Abbreviations: MnFe2O4-NPs, manganese ferrite nanoparticles; NPs, nanoparticles; OD, optical density; PBS, phosphate-buffered saline; RPMI, Roswell Park Memorial Institute.

In agreement with our results, manganese ferrite nanoparticles functionalized with citric acid, with a mean particle size of 8 nm, demonstrated dose-dependent cytotoxic effects from a concentration of 50 μg/mL, as seen in the MTT assay using the mouse Balb/3T3 fibroblast cell line.⁴³

Additionally, citric acid-coated iron oxide nanoparticles showed cytotoxicity on SK-MEL-37 human melanoma cell line with an IC₅₀ (half-maximal inhibitory concentration) value of 433 μg Fe/mL.⁴⁴ Indeed, COOH-modified iron oxide nanoparticles have shown some toxicity in human epithelial carcinoma cell lines at a concentration of 10 μg/mL.^45,46 This behavior can be explained by the charge on the surface of iron oxide nanoparticles, which could play an important role in the intracellular uptake.⁴⁷ In this sense, there was no observable uptake of citrate-coated MNPs at concentrations of up to 0.1 mg/mL for murine macrophage cells (RAW 264.7) and Jurkat cell line (clone E6-1). At concentrations until 0.6 mg/mL, a relevant cellular uptake was observed, but the uptake of nanoparticles did not affect the viability and proliferation of the cells. At higher concentrations, cell viability decreased markedly.⁴⁸

Furthermore, after exposing endothelial cells to citric acid-coated iron oxide nanoparticles, dose-dependent effects on human umbilical vein endothelial cells’ viability, cytoskeleton, and function were demonstrated.⁴⁹ On the other hand, cationic polymeric manganese ferrite nanoparticles exhibited higher cytotoxicity in macrophages (RAW 264.7 cells) and lower cellular membrane rigidity than anionic and nonionic polymeric manganese ferrite nanoparticles.⁵⁰ In general, the toxicity of magnetic particles may depend on different factors, including the concentration, composition, size, structure, solubility, and surface chemistry.⁵¹

In order to explore the antifungal effect of citric acid-modified MnFe₂O₄-NPs, microscopy studies of C. albicans cells grown in RPMI medium in the presence of modified nanoparticles were performed. As shown in Figure 4, C. albicans growth inhibition by MNPs may have occurred due to the aggregation of yeast cells. More experiments are necessary to study such an interaction further.

Figure 4 Interaction of modified MnFe2O4-NPs with Candida albicans cells visualized by optical microscopy. Notes: (A) C. albicans cells (105 cells/mL) in RPMI-1640 medium at 30°C. (B) C. albicans cells (105 cells/mL) in RPMI-1640 medium at 30°C with citric acid-modified MnFe2O4-NPs (250 μg/mL). Abbreviations: MnFe2O4-NPs, manganese ferrite nanoparticles; RPMI, Roswell Park Memorial Institute.

In agreement with our results, MNPs coated with aminated silica were able to interact with the surface of the fungus Fusarium oxysporum. In this case, no antifungal action was detected.⁵²

Taking into account the intrinsic antifungal activity found for the citric acid-functionalized manganese ferrites, we explored the antimicrobial activity of these nanoparticles conjugated with the antifungal peptide Cm-p5. The efficiency of the carbodiimide-based conjugation was above 80%. This type of coupling chemistry has been used for immobilizing AMPs by their amino groups.^53,54 Significantly, the antifungal activity of the conjugated nanoparticles was higher than that of their bulk counterparts (Figure 5). In fact, the MIC of Cm-p5 conjugated to MnFe₂O₄-NPs was 100 μg/mL, which was 2.5 times lower than the MIC of nonconjugated nanoparticles (Figure 5A). On the other hand, with 7.5 times less Cm-p5 in the conjugate regarding the soluble peptide, complete C. albicans growth inhibition was achieved (Figure 5B).

Figure 5 Antifungal activity assays. Notes: (A) Candida albicans growth curves in RPMI-1640 medium of modified MnFe2O4-NPs and Cm-p5-conjugated MnFe2O4-NPs. Each value represents the mean of three replicates in three different experiments. Bars represent the standard deviation. (B) C. albicans growth curves in RPMI-1640 medium of the Cm-p5 peptide and Cm-p5-conjugated MnFe2O4-NPs. Each value represents the mean of three replicates in three different experiments. Bars represent the standard deviation. Abbreviations: MNPs, magnetic nanoparticles; MnFe2O4-NPs, manganese ferrite nanoparticles; OD, optical density; RPMI, Roswell Park Memorial Institute.

These results differ from the work of other authors, who reported that the activity of AMPs decreased upon conjugation to different supports.^55–58 Indeed, Borcherding et al reported that iron-containing nanoparticles affect the activity of soluble AMPs, probably influenced by the ability of bacteria to scavenge iron for growth from nanoparticles and the adsorption of peptides onto nanoparticle surfaces.¹⁸ It is obvious that AMPs with different physicochemical properties can be affected differently by immobilization reactions.⁵⁹

In this sense, Cm-p5 is not an amphipathic peptide, and its antifungal activity does not depend on its amino-terminal group.¹⁹ Also, the mechanism of action of this peptide is related to interactions with the fungal cell surface; therefore, it is possible to have a synergistic antifungal action in the conjugate between the peptide and MNPs. In the same way, the immobilization of the AMP nisin to multiwalled carbon nanotubes improved the antibacterial and antibiofilm properties of noncoated carbon nanotubes.⁶⁰ Furthermore, bacitracin-conjugated iron oxide nanoparticles showed higher antibacterial activity than bacitracin alone. Because of this improved activity, conjugated MNPs allow lower dosages and fewer collateral effects of the antibiotic.¹⁶ Finally, Cm-p5-conjugated MnFe₂O₄-NPs showed a similar pattern of toxicity in the cell line RAW 264.7 as found for citric acid-modified MnFe₂O₄-NPs (data not shown), but less of the conjugate was needed to completely inhibit C. albicans growth.

Conclusion

These results contribute to marking the importance of MNPs in biomedicine, specifically in the antimicrobials field. Herein, the intrinsic antifungal activity of citric acid-coated MnFe₂O₄-NPs was demonstrated. In addition, the improvement of their antifungal activity was achieved when these nanoparticles were conjugated with the AMP Cm-p5. Nowadays, strategies are required to reduce the toxicity and enhance the efficacy and biodistribution of AMPs. MNPs could be an excellent alternative due to their broad spectrum of activities (antimicrobial, drug delivery, diagnosis) and their low toxicity.

Acknowledgments

The authors thank FAPDF (Support Research of the Federal District Foundation, Brasilia DF, Brazil), FUNDECT (Support Foundation The Education Development, Science and Technology state of Mato Grosso do Sul, Brazil), and CAPES-MES (Higher Education Personnel Improvement Coordination-Ministry of Higher Education), Brazil; International Foundation of Science, Sweden (F 4614 and F/5199 projects).

Disclosure

The authors report no conflicts of interest in this work.

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