Preparation of Progressive Antibacterial LDPE Surface via Active Biomolecule Deposition Approach

The use of polymers in all aspects of daily life is increasing considerably, so there is high demand for polymers with specific properties. Polymers with antibacterial properties are highly needed in the food and medical industries. Low-density polyethylene (LDPE) is widely used in various industries, especially in food packaging, because it has suitable mechanical and safety properties. Nevertheless, the hydrophobicity of its surface makes it vulnerable to microbial attack and culturing. To enhance antimicrobial activity, a progressive surface modification of LDPE using the antimicrobial agent grafting process was applied. LDPE was first exposed to nonthermal radio-frequency (RF) plasma treatment to activate its surface. This led to the creation of reactive species on the LDPE surface, resulting in the ability to graft antibacterial agents, such as ascorbic acid (ASA), commonly known as vitamin C. ASA is a well-known antioxidant that is used as a food preservative, is essential to biological systems, and is found to be reactive against a number of microorganisms and bacteria. The antimicrobial effect of grafted LDPE with ASA was tested against two strong kinds of bacteria, namely, Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli), with positive results. Surface analyses were performed thoroughly using contact angle measurements and peel tests to measure the wettability or surface free energy and adhesion properties after each modification step. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used to analyze the surface morphology or topography changes of LDPE caused by plasma treatment and ASA grafting. Surface chemistry was studied by measuring the functional groups and elements introduced to the surface after plasma treatment and ASA grafting, using Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS). These results showed wettability, adhesion, and roughness changes in the LDPE surface after plasma treatment, as well as after ASA grafting. This is a positive indicator of the ability of ASA to be grafted onto polymeric materials using plasma pretreatment, resulting in enhanced antibacterial activity.


Introduction
Low-density polyethylene (LDPE) is the most common industrial polymer and is mainly used in food packaging because of its useful properties, such as its ease of shaping, handling, and recycling, and its high cost efficiency [1][2][3][4]. Nevertheless, LDPE lacks proficiency in traits such as printability, adhesion, and some other surface properties, as it has an inert surface with a very low surface free energy (wettability). Changing the bulk properties of LDPE by mixing additives is not recommended for food  Figure 1. Scheme of ascorbic acid (ASA) grafting on low-density polyethylene (LDPE) via plasma treatment.

Hydroperoxide Determination
Iodometric titration was performed to determine the concentration of all hydroperoxide species accumulated on the surface of LDPE after plasma treatment. Plasma-treated LDPE samples were placed into a covered Erlenmeyer flask, which was filled with 50 ml of glacial acetic acid. An excess (1.0 g) of sodium iodide was added, and the flask was purged with argon gas for 15 min to eliminate interactions with air. After 15 min, the well-stirred mixture became yellow (oxidation of iodide to iodine by hydroperoxides incorporated on the LDPE surface) and was titrated with a 0.0005 M sodium thiosulfate pentahydrate aqueous solution. The reactions were carried out in an argon atmosphere and protected from light. The hydroperoxide concentration on the LDPE surface was calculated per area considering two treated sides of the LDPE samples. The titration was repeated 3 times to obtain average values and to ensure reliable results.

Surface wettability Measurements
The changes in hydrophilicity induced by plasma treatment of LDPE films were evaluated by static contact angle measurements using the sessile drop method. An OCA35 surface free energy analysis system (DataPhysics, Filderstadt, Germany) equipped with a CCD camera was employed for this purpose. Water, formamide, and ethylene glycol were used as testing liquids to evaluate the total surface free energy and polar and dispersive components using the conventional Owens-Wendt-Rabel-Kaelble method. A droplet of approximately 3 μl of each testing liquid was placed on the air-facing samples. The contact angle was calculated after approximately 3 s to allow thermodynamic equilibrium between the liquid and the sample interface to be reached. The reported value for each testing liquid corresponds to the mean of at least five measurements taken on different parts of the substrate surface.

Graft Yield Analysis
Graft yield measurements were used to prove the grafting of ASA on the LDPE surface. The graft yield of modified LDPE was calculated by gravimetric measurements. The graft yield (GY) was calculated by Equation (1): (1) where W1 and W2 represent the weights of the LDPE samples before and after the modification.

Film Thickness Investigation
Thickness measurements were carried out by an F20-UVX film thickness analyzer (Filmetrics, San Diego, CA, USA) to analyze the thickness of plasma-affected and ASA-modified layers of the

Hydroperoxide Determination
Iodometric titration was performed to determine the concentration of all hydroperoxide species accumulated on the surface of LDPE after plasma treatment. Plasma-treated LDPE samples were placed into a covered Erlenmeyer flask, which was filled with 50 mL of glacial acetic acid. An excess (1.0 g) of sodium iodide was added, and the flask was purged with argon gas for 15 min to eliminate interactions with air. After 15 min, the well-stirred mixture became yellow (oxidation of iodide to iodine by hydroperoxides incorporated on the LDPE surface) and was titrated with a 0.0005 M sodium thiosulfate pentahydrate aqueous solution. The reactions were carried out in an argon atmosphere and protected from light. The hydroperoxide concentration on the LDPE surface was calculated per area considering two treated sides of the LDPE samples. The titration was repeated 3 times to obtain average values and to ensure reliable results.

Surface Wettability Measurements
The changes in hydrophilicity induced by plasma treatment of LDPE films were evaluated by static contact angle measurements using the sessile drop method. An OCA35 surface free energy analysis system (DataPhysics, Filderstadt, Germany) equipped with a CCD camera was employed for this purpose. Water, formamide, and ethylene glycol were used as testing liquids to evaluate the total surface free energy and polar and dispersive components using the conventional Owens-Wendt-Rabel-Kaelble method. A droplet of approximately 3 µL of each testing liquid was placed on the air-facing samples. The contact angle was calculated after approximately 3 s to allow thermodynamic equilibrium between the liquid and the sample interface to be reached. The reported value for each testing liquid corresponds to the mean of at least five measurements taken on different parts of the substrate surface.

Graft Yield Analysis
Graft yield measurements were used to prove the grafting of ASA on the LDPE surface. The graft yield of modified LDPE was calculated by gravimetric measurements. The graft yield (GY) was calculated by Equation (1): where W 1 and W 2 represent the weights of the LDPE samples before and after the modification.

Film Thickness Investigation
Thickness measurements were carried out by an F20-UVX film thickness analyzer (Filmetrics, San Diego, CA, USA) to analyze the thickness of plasma-affected and ASA-modified layers of the LDPE surface. The film thickness value was evaluated based on the differences in reflectance (%) between reference and measured samples in wavelength range of 190-1700 nm. LDPE substrate (4.5 mm thick, with refractive index of 1.5) and LDPE substrate (4.5 mm thick, with refractive index of 1.4, considering polar functional groups) were used as reference samples for the thickness measurements of plasma-treated and ASA-modified LDPE layers. Analysis of plasma-treated and ASA-modified LDPE samples was performed in air atmosphere. The spectrum was analyzed by varying the measured parameters to obtain the best fit between the theoretical and measured data using FILMeasure software, v7.19.0. Readings from five different areas were captured for each sample, and a mean value was evaluated.

Peel Test
A 90 • peel test was performed to measure the adhesion characteristics of LDPE samples in terms of the peel resistance using a Lloyd 1K Lf plus-UTM standard testing machine (Lloyd Instruments, West Sussex, UK). Samples 19 mm in width and 6 cm in length were attached on a polypropylene tape containing poly(2-ethylhexyl acrylate) adhesive (Scotch tape). The test was undertaken with Scotch tape pressed on top of the treated LDPE surface. The unbonded end of the testing tape was peeled off at 90 • at a crosshead speed of 10 mm/min. The test was stopped after 6 min when the tape was complexly detached from the LDPE surface, and 6 separate readings were carried out to obtain average values of the peeling force.

Surface Chemistry Characterization
Fourier transform infrared spectroscopy with attenuated total reflectance (FTIR-ATR) was used to qualitatively investigate the chemical composition changes of plasma-treated LDPE surfaces. An FTIR Spectrometer Frontier (PerkinElmer, Waltham, MA, USA) equipped with a ZnSe crystal was used for these analyses to capture data from a penetration depth of 1.66 µm. Spectra in the wavenumber range of 4000-550 cm −1 were obtained using an average of 8 scans, with a resolution of 4 cm −1 .
The chemical composition changes caused by corona treatment of the LDPE surface were quantified by X-ray photoelectron spectroscopy (XPS). An AXIS XPS system (Kratos Analytical, Manchester, UK) was used for this study. The XPS system contains a spherical mirror analyzer and a delay-line detector for fast screening of the chemical composition, ensuring high spectral resolution and sensitivity. This system allows the analysis of data at a sampling depth of 1-10 nm.

Surface Morphology Analysis
The surface morphology of LDPE samples was analyzed by scanning electron microscopy (SEM). This technique allowed us to obtain information about surface morphology changes after each modification step. For this purpose, a Nova Nano SEM 450 microscope (FEI, Hillsboro, OR, USA) was employed. A thin Au layer a few nanometers thick was sputter-coated on the LDPE samples to obtain high-resolution images with high magnification (20,000×) and to avoid the accumulation of electrons on the measured layer.
Detailed information about the three-dimensional changes in the surface topography of the LDPE samples was obtained using atomic force microscopy (AFM). An MFP-3D AFM device (Asylum Research, Abingdon, Oxford, UK) was employed in these experiments. Scanning was carried out under ambient conditions by a silicon probe (Al reflex-coated Veeco model, OLTESPA, Olympus, Tokyo, Japan) in tapping mode in air (AC mode), allowing images with a surface area of 1 × 1 µm 2 to be obtained. Moreover, the roughness parameter value (Ra) was calculated from AFM images obtained from Z-sensor.

Antibacterial Tests
A modified ISO 22196, an internationally recognized test method was used to evaluate the antibacterial activity of modified plastic materials (and other nonporous surfaces of products) to inhibit the growth of, or kill, test microorganisms [49]. The LDPE samples were first disinfected by UV radiation and then placed in sterile Petri dishes. This was followed by inoculation of the samples (25 × 25 mm 2 ) using 0.1 ml of standardized bacteria suspension of S. aureus (CCM 4516, 1.8 × 10 6 cfu/mL) and E. coli (CCM 4517, 1.4 × 10 7 cfu/mL). The samples were covered by disinfected polypropylene foil (20 × 20 mm 2 ) with 70% ethanol. Incubation of the inoculated samples was performed at 95% of relative humidity at 35 • C for 24 hours. The polypropylene foil was then removed, and LDPE samples were imprinted on plate count agar (3 times on different areas) and incubated at 35 • C for 24 hours. Then, the results were read, and the increase in the number of bacterial colonies was evaluated based on scaling from 0 to 5, where 0 represents the best antimicrobial effect, with no growth of bacteria colonies. An additional incubation at 35 • C for 24 hours was followed by final reading and evaluation of the results. All of these analyses were performed using 3 different LDPE samples to ensure reliable antimicrobial efficiency results.

Hydroperoxide Concentration
Plasma treatment was used as an effective tool for generation of active species in the LDPE surface necessary for the subsequent grafting process by ASA. As the plasma treatment introduces polar functional groups onto the surface by radicalization, different kinds of functional groups can be found (mainly oxygen-containing groups). Through exposure to air during and after plasma, most of the free radicals are converted into peroxides [50]. However, it is difficult to distinguish the amount of peroxide functionalities in either the infrared (IR) spectroscopy or XPS O1s shift spectra; thus, a classic quantification method by iodometric titration according to Wagner and Thelen [51,52] was used to obtain valid concentration values. In Figure 2, LDPE samples were treated with air plasma at different exposure times. By applying iodometric titration, it was found that the hydroperoxide concentration increased as the treatment time increased from 10 s (7.6 × 10 −8 mol/cm 2 ) to 60 s (9.0 × 10 −8 mol/cm 2 ) of exposure to air plasma. An additional increase in treatment time did not lead to another increase in hydroperoxide concentration. This proves that exposing the polymer samples for a longer time does not increase the formation of hydroperoxides; thus, at the optimum time, the surface would be saturated with a certain amount of peroxides [50]. From this observation, an optimum time for achieving the maximum hydroperoxide concentration was evaluated, and LDPE samples were treated with plasma at 60 s prior to the ASA grafting process. inhibit the growth of, or kill, test microorganisms [49]. The LDPE samples were first disinfected by UV radiation and then placed in sterile Petri dishes. This was followed by inoculation of the samples (25 × 25 mm 2 ) using 0.1 ml of standardized bacteria suspension of S. aureus (CCM 4516, 1.8 × 10 6 cfu/ml) and E. coli (CCM 4517, 1.4 × 10 7 cfu/ml). The samples were covered by disinfected polypropylene foil (20 × 20 mm 2 ) with 70% ethanol. Incubation of the inoculated samples was performed at 95% of relative humidity at 35 °C for 24 hours. The polypropylene foil was then removed, and LDPE samples were imprinted on plate count agar (3 times on different areas) and incubated at 35 °C for 24 hours. Then, the results were read, and the increase in the number of bacterial colonies was evaluated based on scaling from 0 to 5, where 0 represents the best antimicrobial effect, with no growth of bacteria colonies. An additional incubation at 35 °C for 24 hours was followed by final reading and evaluation of the results. All of these analyses were performed using 3 different LDPE samples to ensure reliable antimicrobial efficiency results.

Hydroperoxide Concentration
Plasma treatment was used as an effective tool for generation of active species in the LDPE surface necessary for the subsequent grafting process by ASA. As the plasma treatment introduces polar functional groups onto the surface by radicalization, different kinds of functional groups can be found (mainly oxygen-containing groups). Through exposure to air during and after plasma, most of the free radicals are converted into peroxides [50]. However, it is difficult to distinguish the amount of peroxide functionalities in either the infrared (IR) spectroscopy or XPS O1s shift spectra; thus, a classic quantification method by iodometric titration according to Wagner and Thelen [51,52] was used to obtain valid concentration values. In Figure 2, LDPE samples were treated with air plasma at different exposure times. By applying iodometric titration, it was found that the hydroperoxide concentration increased as the treatment time increased from 10 s (7.6 × 10 −8 mol/cm 2 ) to 60 s (9.0 × 10 −8 mol/cm 2 ) of exposure to air plasma. An additional increase in treatment time did not lead to another increase in hydroperoxide concentration. This proves that exposing the polymer samples for a longer time does not increase the formation of hydroperoxides; thus, at the optimum time, the surface would be saturated with a certain amount of peroxides [50]. From this observation, an optimum time for achieving the maximum hydroperoxide concentration was evaluated, and LDPE samples were treated with plasma at 60 s prior to the ASA grafting process.

Surface Wettability Analysis
The changes in the surface wettability of the modified samples were analyzed through contact angle measurements, which are shown in surface. This indicates that the lower the contact angle of a sample is, the higher its wettability is. To evaluate surface free energy and its components, water (surface free tension = 72.1 mN/m, polar component = 52.2 mN/m and dispersive component = 19.9 mN/m) [53], ethylene glycol (surface free tension = 48.0 mN/m, polar component = 19.0 mN/m, and dispersive component = 29.0 mN/m) [54] and formamide (surface free tension = 56.9 mN/m, polar component = 33.4 mN/m, and dispersive component = 23.5 mN/m) [53] were used. Untreated LDPE has hydrophobic properties and is chemically inert; thus, its wettability is low under basic conditions. Its water contact angel was 95.7 • , with a low total surface free energy (29.3 mJ/m 2 ) and insignificant polar component (1.9 mJ/m 2 ). These results refer to the hydrocarbon skeleton -C-H, which has poor reactivity, and thus, no polarity was observed.
The initiation of reactions on the surface by RF plasma improved the polarity by inducing the surface through radicalization. The introduction of new oxygen-containing functional groups helped to increase the total surface free energy to 49.0 mJ/m 2 , and the contact angle of water decreased to almost half, with a value of 50.0 • . The wettability increased as a result of the new polar functional groups on the surface. Plasma treatment affected the LDPE surface only at very small depth (28.2 nm), which was confirmed by film thickness measurements. Grafting of the antibacterial agent enhanced the polarity even further because of its effective side and defined structure attachment. The ASA-grafted LDPE surface using plasma treatment exhibited the lowest value for the contact angle of water (32.3 • ); therefore, the highest value for the total surface free energy (67.0 m J/m 2 ) and its polar component (63 mJ/m 2 ) was achieved. The introduced functional groups on the LDPE surface were able to effectively react and form new bonds with ASA, and the graft yield was 0.4%, indicating a multilayer formation of ASA. This was confirmed also by film thickness measurements, where the film thickness was 10.1 nm. The graft yield and film thickness analyses confirmed a formation of ASA multilayered structures on the LDPE surface. The effect of plasma treatment on the grafting of ASA onto the LDPE surface was shown, in comparison with untreated LDPE subjected to modification by ASA with subsequent thorough washing. In this case, the contact angle and the total surface free energy were similar to those of untreated LDPE.

Adhesion Analysis
Adhesion properties depend on the wettability and surface morphology (roughness) of a material surface. Roughness occurs as a result of physicochemical interactivity or chemical composition on the surface. Adhesion properties can be effectively analyzed by measurements of the peeling resistance. Figure 5 shows the changes in peeling resistance and the changes in adhesion of LDPE after plasma treatment and ASA grafting. Higher resistance induces higher adhesion, which is an outcome of a rougher surface and better wettability. The untreated LDPE surface exhibited relatively poor adhesion, and therefore, the peel resistance reached a value of 40.5 N/m because of the smooth surface and low wettability. The plasma-treated samples showed significant enhancement in the adhesion of the LDPE surface. The peel resistance increased significantly to 83.5 N/m after plasma treatment. This increase in peel resistance was affected mainly by the increase in the wettability and surface roughness caused by the incorporation of polar functional groups and etching reactions, respectively. ASA grafting onto the LDPE surface led to even higher peel resistance (97.3 N/m) because the highest wettability was achieved. ASA was also subjected to LDPE modification with and without application of plasma treatment to study the effect of plasma

Adhesion Analysis
Adhesion properties depend on the wettability and surface morphology (roughness) of a material surface. Roughness occurs as a result of physicochemical interactivity or chemical composition on the surface. Adhesion properties can be effectively analyzed by measurements of the peeling resistance. Figure 5 shows the changes in peeling resistance and the changes in adhesion of LDPE after plasma treatment and ASA grafting. Higher resistance induces higher adhesion, which is an outcome of a rougher surface and better wettability. The untreated LDPE surface exhibited relatively poor adhesion, and therefore, the peel resistance reached a value of 40.5 N/m because of the smooth surface and low wettability. The plasma-treated samples showed significant enhancement in the adhesion of the LDPE surface. The peel resistance increased significantly to 83.5 N/m after plasma treatment. This increase in peel resistance was affected mainly by the increase in the wettability and surface roughness caused by the incorporation of polar functional groups and etching reactions, respectively. ASA grafting onto the LDPE surface led to even higher peel resistance (97.3 N/m) because the highest wettability was achieved. ASA was also subjected to LDPE modification with and without application of plasma treatment to study the effect of plasma

Adhesion Analysis
Adhesion properties depend on the wettability and surface morphology (roughness) of a material surface. Roughness occurs as a result of physicochemical interactivity or chemical composition on the surface. Adhesion properties can be effectively analyzed by measurements of the peeling resistance. Figure 5 shows the changes in peeling resistance and the changes in adhesion of LDPE after plasma treatment and ASA grafting. Higher resistance induces higher adhesion, which is an outcome of a rougher surface and better wettability. The untreated LDPE surface exhibited relatively poor adhesion, and therefore, the peel resistance reached a value of 40.5 N/m because of the smooth surface and low wettability. The plasma-treated samples showed significant enhancement in the adhesion of the LDPE surface. The peel resistance increased significantly to 83.5 N/m after plasma treatment. This increase in peel resistance was affected mainly by the increase in the wettability and surface roughness caused by the incorporation of polar functional groups and etching reactions, respectively. ASA grafting onto the LDPE surface led to even higher peel resistance (97.3 N/m) because the highest wettability was achieved. ASA was also subjected to LDPE modification with and without application of plasma

Chemical Composition Investigation
The chemical composition of the LDPE samples after each modification step was analyzed using Fourier transform infrared (FTIR) spectroscopy. The FTIR spectra of untreated, plasma-treated, and modified LDPE samples are shown in Figure 6. The FTIR spectrum of untreated LDPE is characterized by specific absorbance bands attributed only to nonpolar hydrocarbons in the main chain and branches. These bands represent carbon-carbon and carbon-hydrogen vibrations. Thus, -C-H stretching vibrational bands are observed at 2915 cm −1 and 2847 cm −1 , and bending and scissoring vibrations are observed at 1473 cm −1 and 717 cm −1 , respectively. Plasma treatment of LDPE was responsible for the introduction of new functional groups by radicalizing some carbons on the polyethylene surface. This process allows the interaction between the plasma-activated surface and air elements. Oxygen-containing groups are the main functional groups following these interactions. However, these new functional groups were not clearly detected by FTIR spectroscopy because of the relatively high penetration depth of the IR beam when using a ZnSe crystal (1.66 μm) compared with the thickness of the plasma-affected layer, which was only a few tens of nm. The incorporation of new oxygen-containing groups was clearly confirmed by XPS analyses. ASA is an organic compound with ether, carbonyl, and 4-hydroxyl groups apparent in the oxygen-containing spectral region. New vibrational absorbance bands appeared in the FTIR spectrum of LDPE grafted by ASA, where -OH was represented by a broad absorbance band between 3650 cm −1 and 3150 cm −1 , C=O was observed at 1623 cm −1 , -COOH was observed at 1776 cm −1 , and C-O-C was observed at 1060 cm −1 . This could indicate the presence of ASA on the LDPE surface after the modification process.

Chemical Composition Investigation
The chemical composition of the LDPE samples after each modification step was analyzed using Fourier transform infrared (FTIR) spectroscopy. The FTIR spectra of untreated, plasma-treated, and modified LDPE samples are shown in Figure 6. The FTIR spectrum of untreated LDPE is characterized by specific absorbance bands attributed only to nonpolar hydrocarbons in the main chain and branches. These bands represent carbon-carbon and carbon-hydrogen vibrations. Thus, -C-H stretching vibrational bands are observed at 2915 cm −1 and 2847 cm −1 , and bending and scissoring vibrations are observed at 1473 cm −1 and 717 cm −1 , respectively. Plasma treatment of LDPE was responsible for the introduction of new functional groups by radicalizing some carbons on the polyethylene surface. This process allows the interaction between the plasma-activated surface and air elements. Oxygen-containing groups are the main functional groups following these interactions. However, these new functional groups were not clearly detected by FTIR spectroscopy because of the relatively high penetration depth of the IR beam when using a ZnSe crystal (1.66 µm) compared with the thickness of the plasma-affected layer, which was only a few tens of nm. The incorporation of new oxygen-containing groups was clearly confirmed by XPS analyses. ASA is an organic compound with ether, carbonyl, and 4-hydroxyl groups apparent in the oxygen-containing spectral region. New vibrational absorbance bands appeared in the FTIR spectrum of LDPE grafted by ASA, where -OH was represented by a broad absorbance band between 3650 cm −1 and 3150 cm −1 , C=O was observed at 1623 cm −1 , -COOH was observed at 1776 cm −1 , and C-O-C was observed at 1060 cm −1 . This could indicate the presence of ASA on the LDPE surface after the modification process.
For the quantification of the chemical composition of LDPE samples, the XPS technique was employed. The XPS spectra of LDPE samples after each modification step are shown in Figure 7. The XPS spectrum of untreated LDPE consists mainly of the C1s peak, with 98 at.% at a binding energy of~285 eV. It also contains low-intensity O1s (2.6 at.%) and N1s (0.2 at.%) peaks associated with oxygenand nitrogen-containing functional groups, originating from processing additives or intermediates coming from air interactions with the LDPE surface. Moreover, other peaks were observed in XPS spectra, which are associated with auger electrons, and therefore they were disregarded from total atomic %. Plasma treatment of the LDPE surface was responsible for the incorporation of new functional groups, as indicated by a significant increase in the intensity of the O1s peak at a binding energy of 530 eV, achieving a value of 12.4 at.%. In addition, the intensity of the N1s peak increased in the XPS spectrum of LDPE after plasma treatment because of the incorporation of some nitrogen-containing groups (C-N or C-NH 3 + ). This led to a reduction in the intensity of the C1s peak to 86.5 at.% due to the removal of some carbons during etching, radicalization, and replacement with oxygen-containing groups. ASA grafting on the LDPE surface led to an increase in the at.% of the O1s peak, which was attributed mainly to the oxygen-containing groups in ASA. The ASA-grafted LDPE samples showed an O1s peak with 15.8 at.%, whereas the intensity of the C1s peak decreased to 83.1 at.%. Furthermore, the N1s intensity remained unchanged in comparison with that of the plasma-treated LDPE sample (1.1%), as ASA does not contain any nitrogen functional groups. For the quantification of the chemical composition of LDPE samples, the XPS technique was employed. The XPS spectra of LDPE samples after each modification step are shown in Figure 7. The XPS spectrum of untreated LDPE consists mainly of the C1s peak, with 98 at.% at a binding energy of ~285 eV. It also contains low-intensity O1s (2.6 at.%) and N1s (0.2 at.%) peaks associated with oxygen-and nitrogen-containing functional groups, originating from processing additives or intermediates coming from air interactions with the LDPE surface. Moreover, other peaks were observed in XPS spectra, which are associated with auger electrons, and therefore they were disregarded from total atomic %. Plasma treatment of the LDPE surface was responsible for the incorporation of new functional groups, as indicated by a significant increase in the intensity of the O1s peak at a binding energy of ~530 eV, achieving a value of 12.4 at.%. In addition, the intensity of the N1s peak increased in the XPS spectrum of LDPE after plasma treatment because of the incorporation of some nitrogen-containing groups (C-N or C-NH3 + ). This led to a reduction in the intensity of the C1s peak to 86.5 at.% due to the removal of some carbons during etching, radicalization, and replacement with oxygen-containing groups. ASA grafting on the LDPE surface led to an increase in the at.% of the O1s peak, which was attributed mainly to the oxygen-containing groups in ASA. The ASA-grafted LDPE samples showed an O1s peak with 15.8 at.%, whereas the intensity of the C1s peak decreased to 83.1 at.%. Furthermore, the N1s intensity remained unchanged in comparison with that of the plasma-treated LDPE sample (1.1%), as ASA does not contain any nitrogen functional groups.   Figure 7. X-ray photoelectron spectroscopy (XPS) spectra of LDPE samples.

Surface Morphology Analysis
The changes in the surface morphology and topography of the LDPE samples after each modification step were studied through SEM and AFM, respectively. SEM and AFM images of LDPE samples are shown in Figure 8. The untreated LDPE surface exhibits characteristic texture and morphology originating from the production process. Plasma treatment did not cause any significant changes in the surface morphology obtained by SEM from larger surface areas. On the

Surface Morphology Analysis
The changes in the surface morphology and topography of the LDPE samples after each modification step were studied through SEM and AFM, respectively. SEM and AFM images of LDPE samples are shown in Figure 8. The untreated LDPE surface exhibits characteristic texture and morphology originating from the production process. Plasma treatment did not cause any significant changes in the surface morphology obtained by SEM from larger surface areas. On the other hand, the LDPE samples grafted with ASA experienced clear changes in their surface morphology, showing bulges and valleys in the functionalized regions on the surface as grafting took place.

Antibacterial Analysis
The antimicrobial activities of the LDPE tested against gram-positive S. aureus and gram-negative E. coli using intensive microbial activity assays are summarized in Table 3 and are shown in Figure 9. The untreated LDPE showed no resistance or inhibition to bacterial growth. This was because of its poor inhibition properties resulting from the chemical composition of LDPE. Plasma treatment of LDPE was responsible for the low resistance to bacterial growth on the surface. On the other hand, ASA grafted on the LDPE surface showed a high ability for inhibition of S. aureus. ASA proved to be highly active against S. aureus, similar to its use alone in free form [19,23,38]. ASA could have affected the protein on the bacterial wall, affecting bacterial growth because of its ability to lower the pH and cause instability of bacterial cell membranes [55]. After ASA was grafted onto the LDPE surface, the inhibition activity against S. aureus was successful, with over 80%-90% total inhibition. Interestingly, the inhibition of E. coli growth was not as intense, although a clear reduction in colony growth and reproduction was observed, as shown in Figure 9.  AFM was used to determine the topographical and roughness changes (Ra) in the LDPE surface that occurred after plasma treatment and ASA grafting in the small surface area (1 × 1 µm 2 ). Moreover, this technique was used to obtain line profiles, clearly indicating specific nanopattern dimensions. As reported in Figure 8, the Ra value of the untreated LDPE surface was only 2.5 nm. An application of plasma treatment led to an increase in surface roughness, while Ra increased by almost 80% to 4.4 nm. The increase in roughness can be attributed to the etching process during plasma treatment, which led to nanosurface topography changes. Grafting of ASA onto the LDPE surface resulted in a less rough surface (Ra = 2.8 nm) in the small surface area, but with a specific texture belonging to the created ASA layer.

Antibacterial Analysis
The antimicrobial activities of the LDPE tested against gram-positive S. aureus and gram-negative E. coli using intensive microbial activity assays are summarized in Table 3 and are shown in Figure 9. The untreated LDPE showed no resistance or inhibition to bacterial growth. This was because of its poor inhibition properties resulting from the chemical composition of LDPE. Plasma treatment of LDPE was responsible for the low resistance to bacterial growth on the surface. On the other hand, ASA grafted on the LDPE surface showed a high ability for inhibition of S. aureus. ASA proved to be highly active against S. aureus, similar to its use alone in free form [19,23,38]. ASA could have affected the protein on the bacterial wall, affecting bacterial growth because of its ability to lower the pH and cause instability of bacterial cell membranes [55]. After ASA was grafted onto the LDPE surface, the inhibition activity against S. aureus was successful, with over 80%-90% total inhibition. Interestingly, the inhibition of E. coli growth was not as intense, although a clear reduction in colony growth and reproduction was observed, as shown in Figure 9.

Conclusions
In this study, ascorbic acid (ASA or vitamin C) was grafted onto an LDPE surface via plasma treatment in order to improve the antimicrobial effect. Plasma treatment was effectively used as a radical initiator with subsequent incorporation of ASA, which served as an antimicrobial agent, on the LDPE surface. This modification was confirmed by enhanced wettability and adhesion properties. The presence of ASA on the LDPE surface after the grafting process was confirmed by chemical composition analyses. Chemical composition and surface morphology or topography analyses were used to confirm the presence of ASA on the LDPE surface. The significant antimicrobial effect of such modified LDPE against gram-positive S. aureus was demonstrated, with an inhibition efficiency of over 80%-90%.

Conclusions
In this study, ascorbic acid (ASA or vitamin C) was grafted onto an LDPE surface via plasma treatment in order to improve the antimicrobial effect. Plasma treatment was effectively used as a radical initiator with subsequent incorporation of ASA, which served as an antimicrobial agent, on the LDPE surface. This modification was confirmed by enhanced wettability and adhesion properties. The presence of ASA on the LDPE surface after the grafting process was confirmed by chemical composition analyses. Chemical composition and surface morphology or topography analyses were used to confirm the presence of ASA on the LDPE surface. The significant antimicrobial effect of such modified LDPE against gram-positive S. aureus was demonstrated, with an inhibition efficiency of over 80-90%.