Journal of Nanomaterials

Journal of Nanomaterials / 2020 / Article

Research Article | Open Access

Volume 2020 |Article ID 9754024 |

Urška Gradišar Centa, Petra Kocbek, Anna Belcarz, Srečo D. Škapin, Maja Remškar, "Polymer Blend Containing MoO3 Nanowires with Antibacterial Activity against Staphylococcus epidermidis ATCC 12228", Journal of Nanomaterials, vol. 2020, Article ID 9754024, 11 pages, 2020.

Polymer Blend Containing MoO3 Nanowires with Antibacterial Activity against Staphylococcus epidermidis ATCC 12228

Academic Editor: Angelo Taglietti
Received03 Mar 2020
Revised11 Jun 2020
Accepted17 Jun 2020
Published06 Jul 2020


Antibacterial activity of a polymer nanocomposite containing water-soluble poly(ethylene oxide) (PEO), water insoluble poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP), and MoO3 nanowires or MoO3 microparticles as antibacterial active substances is reported. The UV-vis absorption method was used for the illumination of dissolving of the MoO3 particles of different size and morphology in water. Dissolving of MoO3 nanowires (1 mg ml-1) decreases pH bellow 3.6 in only 3 min and below 3 in 15 min, while dissolving of the PEO/PVDF-HFP/MoO3 nanowires coating (5 mg ml-1) decreases pH bellow 3.6 in 90 min. These coatings completely destroy the Staphylococcus epidermidis ATCC 12228 bacterial strain within 3 h. The proposed applications are antibacterial protective coatings of contact surfaces.

1. Introduction

Infected contact surfaces represent a threat for the health of patients, staff, and visitors in hospitals and for people in crowded areas, such as buses, shopping centers, and schools. Antibacterial agents are of exceptional importance for preventing the spread of infectious diseases [1]. However, their abuse has led to the emergence of antibiotic resistance (e.g., methicillin-resistant bacteria Staphylococcus aureus, vancomycin-resistant Enterococcus species, and Gram-negative microorganisms [2]). As a result, high doses of antibiotics are necessary for treatment, which can cause adverse side effects [1]. Bacteria have developed antibiotic resistance against many common antibiotics, driving a need to develop alternative strategies to treat bacterial diseases. Gram-positive and Gram-negative bacteria differ in the composition of their cell walls. While the cell wall of Gram-negative bacteria contains a peptidoglycan monolayer and lipopolysaccharide layer called the outer membrane, the cell wall of Gram-positive bacteria is composed of several layers of peptidoglycan. If nanomaterials directly interact with bacterial species, then, a membrane stress mechanism occurs [3] in which cell death can result from an elevated level of reactive oxygen species (ROS) following the oxidative stress mechanism.

Various nanomaterials have been investigated as promising antibacterial agents (e.g., titanium dioxide, zinc oxide, copper oxide, silver and gold nanoparticles, molybdenum, and tungsten oxides, among others [1, 2]). These nanostructured inorganic materials must satisfy specific rules regarding morphology, size, surface charge, chemical, and physical properties that exhibit antibacterial properties [2]. The mechanism of cellular uptake of nanoparticles (NPs) and their distribution depends mainly on the physicochemical properties of the particles [4]. Several mechanisms of toxicity against bacteria are proposed, including the attachment of NPs to the bacterial membrane by electrostatic interaction, chemical or physical disruption of the membrane, formation of free radicals (reactive oxygen species-ROS), or induction of frameshift mutations in bacterial strains [1]. As examples, silver ions released from silver NPs affect the surface electric charge of the bacterial membrane and change its penetrability [5]. Similarly, zinc ions released from ZnO NPs damage the bacterial cell membrane and depress the activity of some membranous enzymes [6]. TiO2 [7] and ZnO [8] NPs cause photocatalytic degradation of the bacteria cell wall and cytoplasmic membrane through production of ROS [6]. Iron oxide NPs can penetrate the cell membrane and damage macromolecules, including DNA, lipids, and proteins, leading to bacterial death [8].

Molybdenum as an element does not show any antimicrobial function. It is one of the essential trace elements of primary importance to humans, and it acts as a cofactor for various enzymes (aldehyde, xanthine, and sulphite oxidase) [9]. The molybdenum trioxide (MoO3) was reported as a highly promising antibacterial nanomaterial [2, 10, 11]. The antimicrobial principle of MoO3 in the presence of water is explained by a dissolving process, wherein the acidic reaction with the formation of hydronium (H3O+) and molybdate (MoO42-) ions occurs [10]. The diffusion of H3O+ ions through the bacteria cell wall causes imbalance in the pH equilibrium as well as in the enzyme and transport system of the cell [10]. The acidic low-pH environment caused by dissolving of MoO3 nanoparticles has been reported as a universal antimicrobial agent against susceptible and resistant isolates of bacterial species causing a hospital-acquired infections [12]. Incorporation of MoO3 into polymer coatings enables a controlled solubility and a long-term use of such coatings. Zollfrank et al. [11] found the removal or complete inactivation of pathogenic bacteria S. aureus and P. aeruginosa 3 h after a roll-on test performed with polyurethane tubes filled with MoO3 and acrylic resin. Piçarra et al. have reported on antibacterial activity of MoO3 incorporated into diethylenetriamine (SiDETA against S. aureus in comparison with more efficient silver additive [13]). Shafaei et al. [2] reported the influence of different MoO3 crystalline structures incorporated in various polymer composites on antibacterial activity against S. aureus, E. coli, and P. aeruginosa. The roll-on test showed that all crystalline phases exhibited antimicrobial activity against all three bacteria with elimination in 3 to 9 h. In particular, the orthorhombic phase of MoO3 prepared by calcination at 300°C exhibited the best efficiency. The antibacterial efficiency depending on a particular MoO3 crystallographic phase was explained by a need of direct contact between the metal oxide NPs and E. coli bacteria, with a contact surface area smaller in a case of hexagonal phase. While both orthorhombic and hexagonal phases of MoO3 have antibacterial activity against Gram-positive bacteria (Streptococcus aureus and Bacillus megaterium), antibacterial activity against Gram-negative bacteria E. coli was found only for the orthorhombic phase [3]. On the other hand, Kumar Sen et al. report that hexagonal nanorods exhibited better antibacterial activity than nanoplates and that the antimicrobial activity was decreasing with increasing crystallite size [14]. The antibacterial activity against S. aureus was found dependent also on energy gap of MoO3 nanorods [15]. In all these studies, the solubility of MoO3 is of a critical importance. Solubility of micrometer sized MoO3 in water at neutral pH is 56.0 ± 0.1 mg ml-1 [16].

Here, we present polymer nanocomposites consisting of MoO3 nanowires in the orthorhombic phase incorporated in a mixture of water soluble polymer-poly(ethylene oxide) (PEO) and water insoluble polymer-poly(vinylidene fluoride-co-hexafluoropropylene)-(PVDF-HFP). This particular polymer combination was selected with an aim to create an inhomogeneous structure of the coating with PEO domains surrounded by inert PVDF-HFP host matrix [17]. A high specific surface area of unique MoO3 nanowires enables their fast dissolving. Their incorporation into matrix, which is composed of one slowly dissolving and one inert polymers, represents an interesting combination for quick but lasting antibacterial activity, which was not studied yet. The antimicrobial activity of the selected nanocomposite films was assessed against the Staphylococcus epidermidis ATCC 12228 bacterial strain, which is nowadays the most frequent cause of nosocomial infections and represents the most common source of infections on indwelling medical devices [18]. The morphology and crystal structure of as-grown MoO3 nanowires and of the polymer nanocomposite films are shown together with the kinetics of their dissolution in water, which explains the exceptionally fast elimination of the bacteria. Some results are compared with those obtained on commercial (Sigma-Aldrich) MoO3 and on MoO3 crystals, both of micrometer size with much smaller specific surface areas.

2. Materials and Methods

2.1. Synthesis of MoO3 Particles

Three types of MoO3 particles were used for the comparative studies: nanowires, small microparticles, and larger microparticles. They differ in morphology and specific surface area. The MoO3 nanowires and small microparticles were synthesized from Mo6S2I8 nanowires (Nanotul Ltd.). When these nanowires were oxidized at 285°C for 24 h, the resulting MoO3 product (MoO3@285) maintained a nanowire shape and contained a high degree of porosity [19]. Some of the particles were nanotube-like with faceted and polycrystalline walls. On average, the needle-like particles were around 200 nm in diameter and up to 3 μm in length (Figure 1(a)). The specific surface area was . Oxidation of the Mo6S2I8 nanowires at 600°C for 6 h led to a growth of MoO3 monocrystalline particles (MoO3@600) with a typical size of 2-3 μm, which showed a tendency to form large agglomerates up to 10 μm in size (Figure 1(b)). The specific surface area was . In the comparative study, commercially available MoO3 (Sigma-Aldrich) crystals with an average size of single crystals of 8-10 μm and clearly visible (001) growth terraces were used (Figure 1(c)). The specific surface area of the crystals (Sigma-Aldrich) was .

The XRD spectra of the MoO3@285, MoO3@600, and MoO3 (Sigma-Aldrich) particles presented in Figure 2 show that all three types of particles grew in the orthorhombic crystal structure (JCPD 76-1003). The positions of the peaks all belong to the orthorhombic phase match in all spectra, while widths of the peaks are widened with reduction of the particle size. Variations in the relative intensity of the peaks in the spectrum shown in Figure 2(a) in comparison with the spectra shown in Figures 2(b) and 2(c) are due to the anisotropic shape of the MoO3@285 nanowires.

The polymers, PVDF-HFP (average ) and PEO (average ), both purchased at Sigma-Aldrich, were separately dissolved in dimethylformamide (DMF) () (Acros Organics) at concentrations of 18% and 3%, respectively. The coatings were prepared using different mixing procedures and with different sizes of the MoO3 particles (Table 1). The same mass ratio of 69 : 23 : 8 (PVDF-HFP : PEO : MoO3) was used for all coatings, which were prepared as self-standing thin films. The average film thickness of was determined from optical images.

FilmNanoparticlesMedia 1/temperature (°C)
Step 1
Media 2
Step 2

GMoO3 (Sigma-Aldrich)PEO/RTPVDF-HFP

2.2. Preparation of the MoO3 Polymer Nanocomposites

Parameters of the film preparation are listed in Table 1. The polymer solutions for all nanocomposite films were prepared in the same way; i.e., PVDF-HFP and PEO were separately dissolved in DMF at room temperature (RT) under mixing on the magnetic stirrer (300 rpm) for two hours.

With the aim to understand the influence of MoO3 environment on its solubility, the MoO3 nanoparticles were inserted either firstly to PEO only (Step 1) and then both components were in Step 2 mixed with PVDF-HFP (all films but film D), or added directly to previously mixed PEO/PVDF-HFP (film D). All mixtures were stirred for additional 30 min. Such created nanocomposite dispersions were casted into a glass Petri dish and dried at 80°C for 2 h. The effect of temperature during polymer dissolving was investigated in film B, which was prepared all the way at 80°C. To avoid large MoO3 agglomerates, which sized up to 20 μm in films A and B, the MoO3@285 was dispersed in acetone (, Merck) in 0.5 wt.% and allowed to sediment for 2 min. Dried material from the supernatant called (MoO3@285-N) was used in the films C and D. With the aim to resolve the effect of MoO3 and its crystalline size on antibacterial activity, film E without MoO3 was prepared and film F with added large MoO3@600 particles. For comparison with commercially available MoO3, film G was made using MoO3 purchased at Sigma-Aldrich.

The SEM micrographs (Figure 3) show the topography of films A–D (Table 1) prepared with MoO3@285 particles. Films A and B are continuous and show a typical domain structure; however, this structure is smaller in film B which was prepared at 80°C. Films C and D, which were prepared with material without large agglomerates, have some surface depression appeared due to the rapid evaporation of DMF during film drying. Their appearance is stochastic, but relatively rare. In most cases, agglomerates of MoO3 particles are visible inside the holes or in their vicinity. While film C has a similar domain size as in films A and B and does not contain agglomerates, film D has approx. 10 times larger domains and the presence of MoO3@285 agglomerates, which formed in the mixture of PEO and PVDF-HFP.

2.3. Methods

Powder X-ray diffraction (XRD) of the MoO3 nanomaterials was performed at room temperature (RT) with a D4 Endeavor diffractometer (Bruker AXS) using a quartz monochromator Cu Kα radiation source () and a Sol-X dispersive detector. The range of was chosen from 7° to 95° with a step size of 0.04°. A specific surface area of MoO3 nanotubes and microcrystals was measured by the BET method (Gemini II 2370, Surface Area Analyzer, Micromeritics, USA). The morphology of the nanoparticles and composite films put on an adhesive carbon tape was investigated using a field emission scanning electron microscope (SEM) (Supra 36 VP, Carl Zeiss). The films were sputtered with a 10 nm layer of gold for better conductance. UV-vis spectroscopy was performed using a Perkin Elmer spectrometer Lambda 950 using a quartz cuvette.

The concentration of dissolved MoO3 was determined using UV-vis spectroscopy. For calibration, the value of the absorbance peak at 215 nm in several MoO3-water solutions with known concentrations was measured.

The SevenExcellence Multiparameter (Mettler Toledo) with probe InLab Expert Pro-ISM was used for measuring pH values, and an InLab 731-ISM was used to measure conductivity. The measurements of pH values and conductivity of the solution were sampled in 1-minute time intervals for MoO3@285, MoO3@600, and MoO3 (Sigma-Aldrich) dissolving in water at a concentration of 1 mg/ml at room temperature. Each pH measurement has started with a few measurements of pure water to determine the base pH level, after which point the MoO3 was inserted. Different base levels revealed a degree of pH value variations in pure water. Between individual measurements, the samples in glass beakers were mixed with a magnetic stirrer at 400 rpm.

For dissolving kinetics of the MoO3 particles, the MoO3@285, MoO3@600, and MoO3 (Sigma-Aldrich) crystals were dissolving in water at room temperature in a concentration of 1 mg/ml. The pH values and conductivity of the solutions were measured in 1-minute intervals. Each pH measurement started with measuring of pure water with the aim to determine the base pH level variations. The solutions were mixed with a magnetic stirrer at 400 rpm between individual measurements.

For measurements of dissolving kinetics of the MoO3-based nanocomposite films, they were dissolving in water at room temperature in a concentration of 5 mg/ml. The pH values of the solutions were measured in 5 min intervals and mixed between individual measurements with a magnetic stirrer at 400 rpm.

Antibacterial activity of the PVDF-HFP/PEO polymer films was evaluated according to Japanese Industrial Standard (JIS) Z 2801:2000: antimicrobial products test for antimicrobial activity and efficacy. This standard is designed to evaluate the antimicrobial activity and efficacy on bacteria of antimicrobial product surfaces and is applicable to plastic, metal, and ceramic products. Prior to testing, the polymer films (approx. 7 cm in diameter, 50 μm thick) were UV-sterilized (30 min per each side), which caused curvature of the films. The standardized method was therefore modified to avoid leakage of the inoculate from the curved films by applying the inoculate onto a piece of sterile Whatman paper placed onto the film and not directly onto the tested film. The tested films with inoculum were placed between two pieces of inert polymeric foil and then inserted between two rigid titanium plates to stabilize the films and protect both against water evaporation and contact with titanium. A clean and UV-sterilized polypropylene foil sandwich with an inoculum-soaked piece of Whatman paper inside was used as a control. A reference bacterial strain from the American Type Culture Collection, Staphylococcus epidermidis ATCC 12228, was maintained as stock in sterile Microbanks (Technical Service Consultants Limited, UK) at -20°C. Before the experiment, the bacteria were transplanted onto fresh slant culture medium (Mueller-Hinton Agar) and cultured for 20-24 h at 37°C. Cultured bacteria were transferred into liquid medium (Mueller-Hinton Broth), incubated for 20-24 h at 37°C, centrifuged, and suspended in 500-fold diluted Mueller-Hinton Broth directly before the experiment, at an approximate density of . On the Whatman paper, 40 μl inoculum was applied per 1 cm2 film surface. All samples were incubated with bacterial inoculate for 3 h, 6 h, and 24 h at 37°C. After incubation, the bacteria were eluted from the samples and Whatman papers by shaking in 5 ml 0.9% NaCl for 1 min. The pH of the obtained extract was measured using an HI 8010 pH meter (Hanna Instruments, Romania). The number of eluted viable bacterial cells was quantified using the serial dilution method after 24 h of growth at 37°C on Mueller-Hinton agar plates. The experiments were performed in triplicate, and the mean and standard deviation (SD) values were calculated using Excel 2016.

3. Results

3.1. Dissolving Kinetics of the MoO3 Particles

Figure 4(a) shows the pH curves of dissolving process of first 300 min for all three used MoO3. The MoO3@285 dissolved the quickest. In only 3 min, the pH dropped below 3.5 and in 15 min below 3. This fast dissolving caused a quick increase of conductivity in the solution (Figure 4(b)—curve A). This is consistent with the larger specific surface area of MoO3@285 in comparison with MoO3@600 and MoO3 (Sigma Aldrich), which both dissolved at a slower rate, with the conductivity of these solutions increasing semilinearly in the first 3 h (Figure 4(b)—curves B and C).

The time evolution of the dissolving process is shown via absorption of UV-vis light in Figure 5. The dissolution dynamics of MoO3@285 and MoO3@600 are affected by a specific surface area, oxygen deficiency in MoO3@285, and the presence of individual molybdate species. The surface of MoO3 nanoparticles in contact with water starts to dissolve in the following way [20]:

Simultaneously, the protonation process of the molybdate ions () takes place:

Figure 5 shows the UV-vis spectrum of MoO3@285 solution at different times after addition of the material into the water (5, 10, 30, 90, and 180 min). After 5 min, two peaks were observed with relatively low but comparable intensities. They were centered at 213 nm (peak I) and 231 nm (peak II), indicating that the dissolving had started. The peaks are explained as absorption by the heptamolybdate ions (212 nm), their double protonated form (238 nm), and presence of (207 nm and 228 nm) [21]. In the first 10 min, the peaks and absorption tail at wavelengths larger than 260 nm were increasing. The tail indicates the transitional formation of molybdic acid [22] and its protonated monomers HMoO4- [23, 24]. Later, the tail intensity was decreased, indicating that the solution established a stationary phase where a mixture of monomers and were dominant. After 30 min, the positions of both peaks stabilized at 213.5 nm and 229.5 nm for Peak I and Peak II, respectively. The isosbestic point for MoO3@285, where the total absorption does not change during a chemical reaction, occurs at 245 nm.

Figure 5(b) shows the time evolution of the UV-vis spectrum of the MoO3@600 solution at 5, 10, 30, 90, and 180 min of dissolving. In contrast with MoO3@285, the absorption at wavelengths above 250 nm increased over the time to the end of the experiment indicating that the concentration of monomers was still increasing. The protonation process of the molybdate ions was not observed, and the basic shape of UV spectra did not change with time. The isosbestic point was not present.

3.2. Dissolving Kinetics of the MoO3-Based Nanocomposite Films

The films begin to dissolve very quickly. In 10 min, the pH values dropped below 4 (Figure 6(a)) for all four films containing MoO3@285 nanoparticles (AD: Table 1). In comparison, the first measurements 10 min after film insertion into water showed identical pH values for films A and D (pH~4), a lower value for film C (pH~3.8), and the lowest value for film B (pH~3.7). In 90 min, only film A reached the saturated value of 3.45, while the pH values of the other films were still decreasing. The lowest pH value (3.25) was achieved for film B, which was prepared with PEO dissolved at 80°C, while the highest pH value was 3.5 for film D prepared by the one-step method.

From the similar pH values of films A and D, one can conclude that agglomeration of the primary particles decreased the solubility rate regardless of the local environment and that the order of the mixing of the polymers did not substantially affect the solubility. A higher temperature of the mixing (film B) caused faster dissolution and therefore smaller pH value.

The solubility of the coating without MoO3 (film E) only slightly reduced the pH value (from 9 to 8.5) due to weak PEO dissolving, which was still in progress at the end of the selected time period of 90 min. Dissolution of films F and G, which contained larger MoO3@600 and MoO3 (Aldrich) particles, respectively, decreased the pH value below 5 in 25 min, but the final pH value did not decrease bellow 4.2 (Figure 6(b)).

Concentrations of the dissolved MoO3 by time are shown in Figure 7. The first measurement 5 min after insertion of the films into water showed identical concentrations for films A and B, which have similar surface topography (Figures 3(a) and 3(b)), while concentrations of the dissolved MoO3 from films C and D, which are porous, were higher. The highest concentration was measured for film D, which contained exposed agglomerates of MoO3. After 90 min of dissolving, films A, B, and D, which all contained MoO3 agglomerates, were dissolved to nearly equal amounts (0.15-0.16 mg/ml), while film C, which contained highly dispersed MoO3 nanoparticles, was less dissolved (0.12 mg/ml). A relatively slow dissolution of film C is explained by the slow dissolution of PEO, which covered the MoO3 single nanoparticles more efficiently than their agglomerates, and prevented contact with water.

3.3. Antibacterial Activity of the MoO3/PVDF-HFP/PEO Films

Antibacterial activity of films A, D, and E was tested against the Staphylococcus epidermidis ATCC 12228 (Gram-positive) bacterial strain. Films A and D were selected because of their high solubility and assumption that the local environment of MoO3 particles was different in both films. In film A, which was prepared by mixing MoO3 with PEO and then with PVDF-HFP, MoO3 is more likely to be surrounded by water soluble PEO than in film D. Film E, without MoO3, was used as a reference, while the inoculate incubated with inert polypropylene films was used as a positive control.

Results are shown in Figure 8. The main result is that the antibacterial activity of both films A and D containing MoO3@285 nanoparticles is high. Only 3 h after incubation, no bacteria survived being in contact with the film A and only 0.2% with the film D. A prolonged time of the contact (6 h and 24 h) causes a complete elimination of alive bacteria being in contact with any of film A or D.

During incubation of the tested films with bacterial inoculate, partial dissolution of water-soluble PEO and MoO3 particles was expected to appear and cause the acidic environment. Therefore, pH values in extracts collected from the films, which were incubated for 3, 6, and 24 h with bacterial inoculate, were measured over time. The results are presented in Table 2. Extracts collected from the control and the reference samples exhibited pH values of 5.2-5.3 and 5.2-5.4, respectively. However, for extracts collected from both A and D films, the pH values were much lower: 1.7-1.8 measured 3 h after incubation and 1.54-1.60, 6 h after incubation.

3 h6 h24 h


In contrast, an increase of bacterial CFU (colony forming unit) on reference film E (without MoO3) in comparison with the control film was observed (Figure 8). Three hours after incubation with bacterial inocula, the CFU increased to 243% of the control and in 6 h to 660% of the control. After 24 h, this effect disappeared—only 15% of cells survived in contact with film E in comparison with the control.

4. Discussion

The growth of bacteria and fungi slowed down at pH values between 3.5 and 4 for many types of bacteria (e.g., staphylococci, streptococci, enterococci, Legionella pneumophila, Lactobacillus acidophilus spp., Candida spp., and Aspergillus spp.) [11]. The majority of microorganisms are effectively killed at pH values 3.5–4.0, but many Gram-negative microorganisms are killed at higher pH values up to 5.5 (E. coli, Pseudomonas aeruginosa, Clostridia, and Campylobacter) [11]. The PVDF-HFP/PEO/MoO3 nanocomposite dissolves in water to a sufficient degree such that the dissolved MoO3 locally reduces the pH values below 3.6, consequently providing an effective antimicrobial environment.

The dissolution process of orthorhombic crystalline phase MoO3 particles of different sizes and specific surface areas was studied for their potential application in antimicrobial polymer nanocomposites. The smallest MoO3 nanoparticles synthesized from Mo6S2I8 nanowires dissolved the fastest. Nanoparticles with a specific surface area of approx. 12 m2/g dissolved in water to a concentration of 1 mg/ml, dropping the pH value below 3.5 in 1 min and below 3 in 15 min. The exponential decrease of pH value with time and the related exponential enhancement of conductance provide evidence of a very fast dissolving process. The time dependencies of pH and conductance (Figure 4) were fitted for the first 45 min of the dissolving process with biexponential curves () with two different time constants. For the pH curve, they are , , with and of -908 and -421 mS/cm, while for the conductance curve, they are and , and and are -414 and -627 mS/cm, respectively, The adjusted -square of the pH curve fit is 0.997 and of the conductance fit is 0.9994. Consequently, the UV-vis absorbance of the dissolving MoO3@285 reached a stationary state in 90 min, while the absorbance of the dissolved MoO3@600 increased semilinearly with time and the stationary phase was not reached within 3 h. The UV-vis spectroscopy of the MoO3@285 solution indicated the presence of [HMoO4]-monomers (protonated form of molybdic acid) in the first 10 min and their reduction to monomers, while the protonation reaction in the case of MoO3@600 continued up to the end of the experiment and the isosbestic point was not observed.

The PVDF-HFP/MoO3 nanocomposites were prepared as thin films in various ways with the aim to test how size of the MoO3 particles, the order of mixing polymers, and different preparation temperatures influence composite solubility. Due to the different solubility rates of the MoO3 particles and their aggregates, different final pH values were obtained within the 90 min dissolution testing period in water. All the films containing MoO3@285 nanoparticles decreased the pH value of the water solution below 4 in only 10 min (Figure 4(a)), while larger MoO3@600 and MoO3 (Aldrich) decreased the pH value below 4 in 60 min. The lowest pH value (3.2) was obtained with film B, prepared at 80°C, where the enhanced temperature increased the dispersion of the polymers (Figure 6(a)).

The highest concentration of dissolved MoO3 after 90 min was 0.16 mg/ml. The concentration increased the fastest during dissolution of film D, which was prepared using a one-step procedure which involved mixing MoO3@285 directly into the mixture of PVDF-HFP and PEO. Because both polymers segregate during the drying process, the MoO3 was the most exposed to the water molecules during dissolution.

Two films (A and D) were selected for antibacterial testing because of their high solubility and different local environment of the MoO3@285 particles. The antibacterial activity of both films was found to be quick and efficient. Film A was slightly more effective, because no bacteria survived after 3 h, and only 0.2% on film D. After 6 h, no live bacteria were found on either film. It seems that the strong antibacterial effect can be attributed to the strongly acidic aqueous environment resulting from their dissolution, as suggested elsewhere [10].

In this study, the antibacterial activity of films was evaluated according to the modified standard designed for solid surfaces. Experimental conditions included incubation of tested films with a Whatman paper soaked in bacterial inoculate. Thus, the humidity of the environment of the incubated sample was very limited. Similar conditions usually appear for handles, handrails, or toilet walls—there surfaces are also rich in bacteria but only slightly moistened. On the basis of our results, it is likely that PEO/PVDF-HFP films enriched with MoO3 particles could be used as effective coatings against bacteria deposited on different surfaces in hospitals, buses, schools, and shopping centers. Their application as coatings on handles, handrails, or hospital bed surfaces could limit the risk of infectious microorganism transmission.

Interestingly, for the reference PEO/PVDF-HFP film without MoO3 particles (film E), the initial stimulation of bacterial growth was observed. Most probably, traces of dissolved PEO or other compounds of reference film served as a nutrient and allowed for the division and propagation of bacterial cells during the initial period of incubation. This was not observed in the case of the control (polypropylene foil), because the inoculum itself contains only traces of nutritious substances and supports the metabolism, but not the propagation, of bacteria. This stimulation was then followed by a significant reduction of bacterial viability after 24 h incubation. The reason for this phenomenon may lie in the decreased humidity of the environment (as inoculum was absorbed by the film) and the increase of osmotic strength, causing the inhibition of cell survivability. Moreover, it was previously noted that PEO itself can exhibit antibacterial action because of its ability to prevent the adsorption of plasma proteins, which is the first step of bacterial adhesion and biofilm formation. Based on this property, PEO coatings showed high potential to prevent S. epidermidis adhesion, although stability of the coatings was limited [25]. Therefore, it would be possible that PEO itself contributes to the antibacterial activity of the PEO/PVDF-HFP/MoO3 films, but the stimulation of the bacterial growth being in contact with the film E, which is without MoO3, for 3 h and 6 h, denies this assumption. Therefore, the antibacterial activity of the PEO/PVDF-HFP/MoO3 coatings can be attributed solely to MoO3.

5. Conclusion

We have formulated polymer nanocomposites intended for application as antimicrobial contact surfaces. The nanocomposites are based on a mixture of chemically inert PVDF-HFP polymer, water-soluble PEO polymer, and MoO3 particles of different sizes and morphologies as antibacterial material. Exposed to water (1 mg/ml), the MoO3 nanowires due to their high specific surface area dissolve quickly and decrease pH bellow 3.6 in only 3 min. The MoO3 dissolved from the PVDF-HFP/PEO/MoO3 nanowire composite in water (5 mg/ml) decreases pH bellow 3.6 in 90 min and completely destroys the Staphylococcus epidermidis ATCC 12228 bacterial strain within 3 h.

Data Availability

No data were used to support this study.

Conflicts of Interest

There are no conflicts to declare.


This work was financially supported by the Slovenian Research Agency through contracts P0-5544 and P1-0099. The authors thank Mr. J. Jelenc for the technical assistance in the preparation of the polymer nanocomposites.


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