Green Synthesized Polymeric Iodophors with Thyme as Antimicrobial Agents

Antimicrobial resistance (AMR) is a growing concern for the future of mankind. Common antibiotics fail in the treatment of microbial infections at an alarming rate. Morbidity and mortality rates increase, especially among immune-compromised populations. Medicinal plants and their essential oils, as well as iodine could be potential solutions against resistant pathogens. These natural antimicrobials abate microbial proliferation, especially in synergistic combinations. We performed a simple, one-pot synthesis to prepare our formulation with polyvinylpyrrolidone (PVP)-complexed iodine (I2), Thymus Vulgaris L. (Thyme), and Aloe Barbadensis Miller (AV). SEM/EDS, UV-vis, Raman, FTIR, and XRD analyses verified the purity, composition, and morphology of AV-PVP-Thyme-I2. We investigated the inhibitory action of the bio-formulation AV-PVP-Thyme-I2 against 10 selected reference pathogens on impregnated sterile discs, surgical sutures, cotton gauze bandages, surgical face masks, and KN95 masks. The antimicrobial properties of AV-PVP-Thyme-I2 were studied by disc diffusion methods and compared with those of the antibiotics gentamycin and nystatin. The results confirm AV-PVP-Thyme-I2 as a strong antifungal and antibacterial agent against the majority of the tested microorganisms with excellent results on cotton bandages and face masks. After storing AV-PVP-Thyme-I2 for 18 months, the inhibitory action was augmented compared to the fresh formulation. Consequently, we suggest AV-PVP-Thyme-I2 as an antimicrobial agent against wound infections and a spray-on contact killing agent.

This study is based on our previous investigations related to "smart" triiodides and AV biohybrids [34][35][36].Our new plant-based formulation AV-PVP-Thyme-I 2 consists of Thyme maceration extract in synergy with AV gel, PVP, and iodine in accordance with our previous studies [34][35][36].The bio-formulation AV-PVP-Thyme-I 2 was studied using the analytical methods such as SEM/EDS, Raman spectroscopy, UV-vis, FTIR, and X-ray diffraction (XRD), which confirmed its purity and morphology.Our aim is to offer facile, non-toxic, sustainable, low-cost antimicrobial agents prepared by readily available basic ingredients (Thyme, AV, and PVP-I 2 ) through one-pot synthesis.Such formulations can be potential solutions against AMR and could improve quality of life in times of crisis with supply shortages related to disinfectants, PPE, or antimicrobial agents.
Antimicrobial properties of the title bio-formulation AV-PVP-Thyme-I 2 were verified using disc diffusion methods against 10 of our reference strains in comparison to gentamycin and nystatin.The studied microorganisms consisted of the fungus C. albicans WDCM 00054 Vitroids; the Gram-positive bacteria S. pneumonia ATCC 49619, S. aureus ATCC 25923, S. pyogenes ATCC 19615, E. faecalis ATCC 29212, and B. subtilis WDCM0003; as well as the Gram-negative E. coli WDCM 00013 Vitroids, P. mirabilis ATCC 29906, P. aeruginosa WDCM 00026 Vitroids, and K. pneumonia WDCM00097 Vitroids.Storing AV-PVP-Thyme-I 2 for 18 months in the fridge in darkness ameliorated the antimicrobial properties against the same reference strains.We also investigated the inhibitory action of the biohybrid AV-PVP-Thyme-I 2 by impregnating surgical PGA sutures, cotton bandages, and disposable surgical facemasks and KN95 facemasks.
C. albicans WDCM 00054 Vitroids was highly susceptible to AV-PVP-Thyme-I 2 , followed by Gram-positive and Gram-negative pathogens.The KN95 mask, the surgical face mask layers, and the cotton bandages showed the highest zones of inhibition (ZOI) against the microorganisms in descending order.The title formulation shows enhanced antimicrobial properties even after 18 months of storage.These results suggest the use of the bio-hybrid as an antifungal and antibacterial agent on KN95, surgical face masks, and cotton bandages to mitigate infections.They can be potentially utilized as spray-on contact killing agents on those materials, oral cavities, wounds, and inanimate surfaces in public or hospital settings.Future investigations are needed to verify the suggested applications of our bio-formulation AV-PVP-Thyme-I 2 in the form of cell culture and cytotoxicity studies, as well as in vivo experiments.

Elemental Composition and Morphological Examination of AV-PVP-Thyme-I 2
Scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopic (EDS) analyses were performed to analyze the morphology and composition of AV-PVP-Thyme-I 2 , respectively (Figure 1).AV-PVP-Thyme-I2 shows an interesting morphology consisting of amorphous round-shaped entities with a smooth surface and semi-crystalline, flaked structures covered with white cube-like or almost spherical spots or lines (Figure 1a and Supplementary File S1).The EDS reveals carbon (40%), oxygen (39%), and iodine (4%) (Figure 1b).Aluminum with 13% is a result of the sample preparation for the SEM, while AV-PVP-Thyme-I 2 shows an interesting morphology consisting of amorphous roundshaped entities with a smooth surface and semi-crystalline, flaked structures covered with white cube-like or almost spherical spots or lines (Figure 1a and Supplementary File S1).The EDS reveals carbon (40%), oxygen (39%), and iodine (4%) (Figure 1b).Aluminum with 13% is a result of the sample preparation for the SEM, while chlorine (1.7%), potassium (1.6%), sodium (0.4%), and iron (0.3%) are from the thyme extract and the AV gel [90].Au appears as well in the EDS because of the gold coating.
The formulation AV-PVP-Thyme-I 2 (11 µg/mL) was impregnated on sterile surgical face masks, bandages, and braided polyglycolic acid (PGA) sutures to investigate the inhibitory action against a selection of 10 microorganisms.Figure 2  AV-PVP-Thyme-I2 shows an interesting morphology consisting of amorphous round-shaped entities with a smooth surface and semi-crystalline, flaked structures covered with white cube-like or almost spherical spots or lines (Figure 1a and Supplementary File S1).The EDS reveals carbon (40%), oxygen (39%), and iodine (4%) (Figure 1b).Aluminum with 13% is a result of the sample preparation for the SEM, while chlorine (1.7%), potassium (1.6%), sodium (0.4%), and iron (0.3%) are from the thyme extract and the AV gel [90].Au appears as well in the EDS because of the gold coating.
The formulation AV-PVP-Thyme-I2 (11 µg/mL) was impregnated on sterile surgical face masks, bandages, and braided polyglycolic acid (PGA) sutures to investigate the inhibitory action against a selection of 10 microorganisms.Figure 2 represents the SEM and EDS of dip-coated surgical PGA sutures.Figure 2b and c shows the SEM of the braided surgical PGA suture coated with AV-PVP-Thyme-I 2 .These can be compared to our previous investigation showing the same, uncoated, plain PGA suture (Figure 2a) [34].The coated suture has clear patches of semi-crystalline nature distributed all over.These patches are covering the braids of the suture homogenously.The EDS reveals again carbon (53%), oxygen (40%), iodine (2%), and chlorine (0.2%) (Figure 2d and Supplementary File S2).Cupper with 4% originates from the suture itself.The homogenously coated PGA sutures have a potential to be used in surgical operations to prevent surgical-site infections.Figure 3 depicts the SEM analysis of impregnated surgical facemasks (Supplementary File S3).
The medical face masks consisted of two layers.The white inner layer, which is directed towards the face, and the blue outer layer.The morphology of the two layers under the microscope differs from each other completely.The white layer shows a dense structure of entangled thin fibers (Figure 3a), while the blue outer layer shows a net-like structure with robustly ordered fibers next to each other (Figure 3c). Figure 3b,d shows semi-crystalline depositions of small, cube-like or spherical moieties on the surface of the face mask tissues.Figure 3c,d reveals a thin layer of coating on the tissue surface, while Figure 3b shows hives of title bio-material on the originally white, thin, entangled fibers.
The thin, homogenous layer on the blue face mask tissues indicates successful adsorption.As a conclusion, the formulation AV-PVP-Thyme-I 2 is homogenously distributed on the face mask tissues and does not compromise breathability or air movement (Figure 3a,b).Therefore, our impregnated face mask tissues could be used to mitigate viral load and inflammatory processes in the upper respiratory tract.However, further studies are needed to confirm the antiviral activity of our formulation, which will be part of our future investigations.
SEM and EDS analyses were performed on sterile bandages coated with the formulation AV-PVP-Thyme-I 2 (Figure 4 and Supplementary File S4). Figure 2b and c shows the SEM of the braided surgical PGA suture coated with AV-PVP-Thyme-I2.These can be compared to our previous investigation showing the same, uncoated, plain PGA suture (Figure 2a) [34].The coated suture has clear patches of semicrystalline nature distributed all over.These patches are covering the braids of the suture homogenously.The EDS reveals again carbon (53%), oxygen (40%), iodine (2%), and chlorine (0.2%) (Figure 2d and Supplementary File S2).Cupper with 4% originates from the suture itself.The homogenously coated PGA sutures have a potential to be used in surgical operations to prevent surgical-site infections.Figure 3 depicts the SEM analysis of impregnated surgical facemasks (Supplementary File S3).The medical face masks consisted of two layers.The white inner layer, which is directed towards the face, and the blue outer layer.The morphology of the two layers under the microscope differs from each other completely.The white layer shows a dense structure of entangled thin fibers (Figure 3a), while the blue outer layer shows a net-like structure with robustly ordered fibers next to each other (Figure 3c). Figure 3b,d shows semi-crystalline depositions of small, cube-like or spherical moieties on the surface of the face mask tissues.Figure 3c,d reveals a thin layer of coating on the tissue surface, while Figure 3b shows hives of title bio-material on the originally white, thin, entangled fibers.The thin, homogenous layer on the blue face mask tissues indicates successful adsorption.As a conclusion, the formulation AV-PVP-Thyme-I2 is homogenously distributed on the face mask tissues and does not compromise breathability or air movement (Figure 3a,b).Therefore, our impregnated face mask tissues could be used to mitigate viral load and inflammatory processes in the upper respiratory tract.However, further studies are needed to confirm the antiviral activity of our formulation, which will be part of our future investigations.SEM and EDS analyses were performed on sterile bandages coated with the formulation AV-PVP-Thyme-I2 (Figure 4 and Supplementary File S4).The cotton bandage is homogenously coated by the title biohybrid (Figure 4a,b).In Figure 4b, the same pattern of small-sized, almost spherical or cube-like patches is seen as previously confirmed in the face mask tissue in Figure 3d.Additionally, the whole surface is uniformly coated by these small circular or cube-like patches.Figure 4c depicts the EDS The cotton bandage is homogenously coated by the title biohybrid (Figure 4a,b).In Figure 4b, the same pattern of small-sized, almost spherical or cube-like patches is seen as previously confirmed in the face mask tissue in Figure 3d.Additionally, the whole surface is uniformly coated by these small circular or cube-like patches.Figure 4c depicts the EDS of the title formulation on the bandage.Carbon with 65.1% is followed by oxygen with 31.8, and finally iodine with 3.1%.Again, gold appears as a result of the gold coating.The homogenous deposition of AV-PVP-Thyme-I 2 on the bandage is a good indicator for the potential use of our impregnated bandages as antimicrobial dressings.The cotton bandage is homogenously coated by the title biohybrid (Figure 4a,b).In Figure 4b, the same pattern of small-sized, almost spherical or cube-like patches is seen as previously confirmed in the face mask tissue in Figure 3d.Additionally, the whole surface is uniformly coated by these small circular or cube-like patches.Figure 4c depicts the EDS of the title formulation on the bandage.Carbon with 65.1% is followed by oxygen with 31.8, and finally iodine with 3.1%.Again, gold appears as a result of the gold coating.The homogenous deposition of AV-PVP-Thyme-I2 on the bandage is a good indicator for the potential use of our impregnated bandages as antimicrobial dressings.
The weak, broad shifts at 141 and 145 cm −1 belong to unsymmetrical triiodide units made up of molecular I 2 and iodide ions in the form of (I-I• • • I − ) as overtones (Figure 5 and Table 1) [29,[34][35][36]111].These are distorted, unsymmetrical, and nonlinear triiodide units (I-I• • • I − ) and are also confirmed by UV-spectral analysis in the next part of this investigation (Figure 5 and Table 1) [29,[34][35][36].The Raman spectrum does not indicate the presence of any other iodine moieties.The absence of strong absorption bands between 140 and 175 cm −1 , as well as the missing absorption bands around 166 cm −1 confirms definitely the lack of pentaiodide ions within the title bio-material (Figure 5 and Table 1) [29,[34][35][36].The absence of other Raman shifts confirms the purity of AV-PVP-Thyme-I 2 .The UV-vis spectral analysis reveals interesting information when the samples AV-PVP-Thyme, AV-PVP-Thyme-I 2 , AV-PVP-Thyme-I 2 (after 18 months), pure Thyme macerated for 3 months, and PVP-I 2 are compared (Figure 6a-c).As witnessed in our previous investigations, similar patterns of high-intensity, broad absorptions appear around 200-240, 250-320, and 325 to 420 nm in the iodinated samples (Figure 6) [29,[34][35][36].The absorptions of AVand Thyme-bio-compounds, PVP, and iodine units overlap with each other and cause broad bands [29,[34][35][36].Thyme and AV-bio-compounds are clearly over-dominated by the stronger intensity absorptions of PVP and iodine moieties, which makes the spectral analysis challenging [29,[34][35][36].Therefore, additional UV spectra of pure Thyme extract, which was macerated in ethanol for 3 months, and its main bio-constituents thymol, and carvacrol were added to the investigation.The comparison with these and the previously studied AV-PVP-Sage-I 2 allows better predictions on the composition of the title formulation since Sage contains thymol and carvacrol (Table 2) [34].

UV-Vis Spectroscopy
The formulation AV-PVP-Thyme-I 2 shows in the UV-visible spectrum strong absorption bands related to I 2 at 204 nm, I − at 201 nm, and "smart" triiodide ions in the form of symmetrical, linear [I-I-I − ] units at 289 and nonlinear [I-I• • • I − ] moieties at 359 nm, in agreement with our previous studies (Figure 6 and Table 2) [24][25][26][27][28][29][30][32][33][34][35][36].After storing the AV-PVP-Thyme-I 2 for 18 months (blue curve), the UV-vis spectrum reveals almost similar absorptions without change.It is suggested that the triiodide absorption intensities, as well as their increased band broadness, indicate not only enhanced hydrogen bonding within the formulation but also a predominance of symmetrical [I-I-I − ] in comparison to asymmetrical triiodide [I-I• • • I − ] moieties.This assumption is supported by the Raman spectrum, which shows a strong absorption peak at 112 cm −1 for "smart" triiodides and a broad, weak absorption band at 141 and 145 cm −1 for asymmetric [I-I• • • I − ] units (Figure 5 and Table 1) [29,30,[34][35][36].The absence of pentaiodide ions in the title biohybrid is not only confirmed by the Raman spectrum but also in the UV-spectral analysis.The purple curve for PVP-I 2 reveals a broad band around 444 nm as an indicator for I 5 − units, while it is lacking in AV-PVP-Thyme-I 2 (red curve) and AV-PVP-Thyme-I 2 (after 18 months, blue curve) (Figure 6 and Table 2).
Adding iodine increases the absorption of triiodide moieties highly (Figure 6, red curve).This curtails the follow-up of the Thyme-and AV-biocomponents whereabouts through overlap with the strong, broad, high-intensity bands of the triiodide units around 289 and 359 nm in the red curve.Further, increased absorption around 289 and 359 nm occurs after storing AV-PVP-Thyme-I 2 for 18 months (blue curve) (Figure 6 and Table 2).The 18 months old title bio-formulation and its fresh counterpart demonstrate interesting behavior.The ongoing processes can be elucidated by comparing PVP-I 2 (purple curve) with AV-PVP-Thyme-I 2 (Figure 6 and Table 2).
UV-spectral analysis of PVP-I 2 (purple curve) reveals iodide ions at 202 nm, molecular iodine at 205 nm, triiodide ions at 290 and 360 nm, and pentaiodide ions at 444 nm (Figure 6, purple curve) [29,30,[34][35][36].Once AV and Thyme are added to form AV-PVP-Thyme-I 2 (red curve), the absorption pattern changes.The pentaiodide ions, which consist of actually (I 2 • • • I 3 − ), disappear in the red curve (Figure 6 and Table 2).Adding the plant extracts leads to destabilization and loss of pentaiodide ions: Breaking apart into iodine molecules and triiodide ions.This alone should be a reason to record higher intensity absorptions of molecular iodine and triiodide anions in the red curve of the title bio-material.However, only higher intensity absorption of I 3 − is observed in AV-PVP-Thyme-I 2 , while I 2 and even I − absorption bands show reduced intensities.This can be explained by: Iodine and iodide ions form more triiodide anions, hence again increasing the triiodide absorption intensities and at the same time decreasing their own.In this case, the concentration of molecular iodine should not decrease much because there was already a surplus in the sample.However, the redox reaction: Reduction: May explain how the surplus of molecular iodine is used up to produce iodide ions, which will in turn increase the triiodide concentration, according to Equation (2).The oxidation reaction in Equation (3) refers to the hydroxyl groups in the AV-and Thyme bio-compounds.Accordingly, -C=O vibrational absorption intensities increase after adding AV-and Thyme extracts to the FTIR analysis, confirming the assumption in Equation (3).
Initially, AV-and Thyme bio-constituents could compete against triiodides being complexed by PVP through hydrogen bonding.Suitable plant biocomponents may interfere and hydrogen bond instead of triiodide ions, leading to their release from PVP.This would hamper the antimicrobial properties of the title formulation.The results of the antimicrobial testing are remarkable and even show higher inhibitory action after a storage period of 18 months.In conclusion, the competition between AV-and Thyme bio-compounds in AV-PVP-Thyme-I 2 does not scale down the inhibitory action in the fresh sample or after storing it for 18 months.PVP protects triiodide ions within AV-PVP-Thyme-I 2 through hydrogen bonding and acts as a sustained-release reservoir by inhibiting I 3 − decomposition [34][35][36]128].In contrast, this would have resulted in iodine release, decolorization of the formulation, and reduced antimicrobial properties after 18 months of storage.Instead, our results from the UV-spectral analysis and the antimicrobial testing confirm the absence of decolorization of the formulation; however, only a decrease in iodine and iodide ion concentrations and augmented antimicrobial properties were found.
Another interesting fact is related to the vibrational band absorptions of -C=O in PVP at 210, 218, and 221 (C=O) nm in the purple curve [34][35][36].These shift to shorter wavelengths towards 208, 213, and 217 nm in combination with decreased absorption intensities in AV-PVP-Thyme-I 2 (red curve), respectively (Figure 6a and Table 2).The blue shift with reduced absorption intensities implies more hydrogen bonding, encapsulation, and removal of conjugated systems by changing PVP-related C=O groups to C-O [34][35][36].
As a conclusion, AV-and Thyme polyphenols are not able to remove triiodide ions from PVP through hydrogen bonding completely.Triiodide ions are protected by PVP even after 18 months within the formulation without releasing them.The analytical results show no change in the composition, while the antimicrobial testing showed even higher inhibition by the 18 months older sample in comparison to the fresh AV-PVP-Thyme-I 2 .Therefore, the longer the sample is stored, the more triiodide ions are available and encapsulated by PVP within a sustained-release reservoir [34][35][36]128].

Fourier-Transform Infrared (FTIR) Spectroscopy
FTIR analysis of Thymol, PVP-I 2 , and AV-PVP-Thyme-I 2 confirms the purity of the title formulation and its composition (Figure 7 and Supplementary File S2).
As a conclusion, AV-and Thyme polyphenols are not able to remove triiodide ions from PVP through hydrogen bonding completely.Triiodide ions are protected by PVP even after 18 months within the formulation without releasing them.The analytical results show no change in the composition, while the antimicrobial testing showed even higher inhibition by the 18 months older sample in comparison to the fresh AV-PVP-Thyme-I2.Therefore, the longer the sample is stored, the more triiodide ions are available and encapsulated by PVP within a sustained-release reservoir [34][35][36]128].

Fourier-Transform Infrared (FTIR) Spectroscopy
FTIR analysis of Thymol, PVP-I2, and AV-PVP-Thyme-I2 confirms the purity of the title formulation and its composition (Figure 7 and Supplementary File S2).[34][35][36].The addition of AV and Thyme extract leads to a broadening of the bands between 3700 and 3500 cm −1 due to an increase in hydrogen bonding by the added AV-and Thyme-biocomponents through their hydroxyl-and carboxylic acid groups (Figure 7).The FTIR spectrum also shows higher absorption intensities between 3300 and 3100, 1850 and 1450 cm −1 , and in the fingerprint region (Figure 7).The band related to asymmetric -C=O stretching vibrations at 1658 cm −1 in PVP-I2 (B, purple curve) is blue shifted towards 1653 cm −1 (A, red curve), with an additional broadening and increased absorption intensity in AV-PVP-Thyme-I2 (Figure 7 and Table 3) [34][35][36].[34][35][36].The addition of AV and Thyme extract leads to a broadening of the bands between 3700 and 3500 cm −1 due to an increase in hydrogen bonding by the added AV-and Thyme-biocomponents through their hydroxyland carboxylic acid groups (Figure 7).The FTIR spectrum also shows higher absorption intensities between 3300 and 3100, 1850 and 1450 cm −1 , and in the fingerprint region (Figure 7).The band related to asymmetric -C=O stretching vibrations at 1658 cm −1 in PVP-I 2 (B, purple curve) is blue shifted towards 1653 cm −1 (A, red curve), with an additional broadening and increased absorption intensity in AV-PVP-Thyme-I 2 (Figure 7 and Table 3) [34][35][36].
Table 3. FTIR analysis of AV-PVP-Thyme-I 2 (A) and PVP-I 2 (B) in solvent ethanol (cm −1 ).These findings indicate that adding AV-and Thyme bio-compounds increased hydrogen bonding with the carbonyl groups of the PVP in competition to the complexed polyiodide moieties.This process is enabled by the release of PVP-complexed pentaiodide ions and their subsequent decomposition into triiodide ions and iodine molecules, according to Equation (1).Additionally, increased absorption of the carbonyl stretching vibration confirms the availability of the newly added -C=O groups within the AV-and Thyme extracts originating from aloin, acemannan, and trans-rosmarinic acid originating from carboxylic -COO and -C(=O)OCH 3 ester groups (Figure 7 and Table 3) [34][35][36]43,44,58,91,92].At the same time, an AV-based -OH stretching vibration from aloin, emodin, galacturonic acid, and mannose is available in AV-PVP-Thyme-I 2 at 3445 cm −1 , in agreement with previous studies (Table 3) [34][35][36]44,45].After adding AV and Thyme, the asymmetric and symmetric C-H stretching vibrations are red-shifted from 2947 to 2955 cm −1 and from 2862 to 2868 cm −1 , respectively (Table 3) [34][35][36]44].This finding confirms that incorporating AV and Thyme phenolic compounds like aloin, aloe emodin, rosmarinic acid, thymol, and carvacrol into the formulation increases the number of functional group conjugations and the solvent effect [34][35][36]43].The same is witnessed in the region between 3260 and 3130 cm −1 with new, high-intensity absorption bands at 3445, 3383, 3215, and 3148 cm −1 .These bands correspond to the hydroxyl and carboxylic groups of the bio-extracts Thyme and AV in AV-PVP-Thyme-I 2 (Figure 7 and Table 3).
The low absorption band at 1753 cm −1 in both samples reveals the low degree of acetylation of the -C=O groups asymmetrical stretching vibration in PVP.These vibrations indiscriminately increase in intensity when AV-and Thyme extracts are added (Figure 7 and Table 3) [34][35][36].The vibration of the -C=O group in the polymeric PVP matrix is assigned to the band at 1038 cm −1 in PVP-I 2 (Figure 7 and Table 3).Once AV-and Thyme extracts are added, this band is seen with less intensity and blue shifted towards 1036 cm −1 (Figure 7 and Table 3).Reduced absorption intensity coupled with a small blue shift indicates higher complexation around the PVP-carbonyl group [34][35][36].Another encapsulation process affects the bands of asymmetric stretching vibrations for -C-H groups and -CH 2 twisting at 2990 and 880 cm −1 , which show up with reduced intensities at 2990 and 881 cm −1 after adding AV-and Thyme-extracts, respectively [34][35][36].
In conclusion, incorporating AV-and Thyme extracts into PVP-I 2 resulted in broadening and increased absorption intensities by their -C=C-, -C=O-, and -COOH-groups in the formulation.Hydrogen bonding increased with the PVP polymetric matrix, which releases pentaiodide ions as part of the process.The PVP backbone composed of [-CH-CH 2 -] ngroups is more coiled through encapsulation of triiodide ions and further AV-and Thyme bio-compounds [34][35][36].The complexation of triiodide anions increases over time and results in a PVP polymeric matrix entangled or coiled around the triiodide moieties, acting as a protective, sustained-released reservoir around them [34][35][36]128].The coiled or entangled structure is confirmed in the SEM images of the bandages and the face mask in the form of small, circular, or cube-like patches covering the surface of the tissues (Figures 3d and 4b).

X-ray Diffraction (XRD)
The XRD analysis of AV-PVP-Thyme-I 2 confirms the purity of the sample with peaks from AV, Thyme, PVP, and iodine (Figure 8).
time and results in a PVP polymeric matrix entangled or coiled around the triiodide moieties, acting as a protective, sustained-released reservoir around them [34][35][36]128].The coiled or entangled structure is confirmed in the SEM images of the bandages and the face mask in the form of small, circular, or cube-like patches covering the surface of the tissues (Figures 3d and 4b).

X-ray Diffraction (XRD)
The XRD analysis of AV-PVP-Thyme-I2 confirms the purity of the sample with peaks from AV, Thyme, PVP, and iodine (Figure 8).The XRD analysis reveals almost the same peaks for AV-PVP-Thyme and AV-PVP-Thyme-I2.AV-PVP-Thyme-I2 reveals clearly lower intensities in the XRD pattern.The only peak with slightly higher intensity in the iodinated compound in relation to AV-PVP-Thyme is at 2θ = 30° (Figure 8).Previously, other investigators assigned 2Theta values around 24, 30, 37, and 46° to iodine, which confirms the composition of our title biomaterial (Figure 8 and Table 4) [120,121].
The decrease in weak intensities after iodination indicates strong encapsulation of iodine into the PVP backbone in the form of triiodide anions.The only shifts in maxima occur at 2θ = 45.81 • and 45.92 • in AV-PVP-Thyme (green curve) towards 2θ = 45.84 • and 45.95 • after iodination (red curve), indicating higher complexation of polyiodide moieties into the formulation AV-PVP-Thyme-I 2 (Figure 8 and Table 4) [81].
Additionally, the absence of new peaks in AV-PVP-Thyme-I 2 points to an amorphization of iodine during this process, as witnessed before in our previous study of AV-PVP-Sage-I 2 (Figure 8 and Table 4) [34].
The XRD analysis confirmed the purity of AV-PVP-Thyme-I 2 (Figure 8 and Table 4).

Antimicrobial Activities of AV-PVP-Thyme-I 2
The inhibitory action of the title bio-material AV-PVP-Thyme-I 2 was tested by disc diffusion assay (DD) against 10 reference microorganisms on sterile discs at concentrations of 11, 5.5, and 2.75 µg/mL.We impregnated sterile, braided, surgical PGA sutures, cotton bandages, surgical face masks, and KN95 face masks with a concentration of 11 µg/mL.The reference microorganisms included the fungus C. albicans WDCM 00054 Vitroids, the Gram-positive bacteria S. pneumonia ATCC 49619, S. aureus ATCC 25923, S. pyogenes ATCC 19615, E. faecalis ATCC 29212, and B. subtilis WDCM0003, as well as the Gram-negative E. coli WDCM 00013 Vitroids, P. mirabilis ATCC 29906, P. aeruginosa WDCM 00026 Vitroids, and K. pneumonia WDCM00097 Vitroids.The negative controls were ethanol and water, which had no inhibitory effect.These are not included in Table 5.
The common antibiotics gentamycin (G) and nystatin (NY) were utilized as positive controls (Table 5).After storing the title formulation for 18 months, we performed DD tests again and obtained surprisingly augmented antimicrobial properties in comparison to the fresh AV-PVP-Thyme-I 2 .Storing the sample did not result in the decomposition of the triiodide ions.During this time, the triiodide ions were protected by the polymeric PVP matrix, which acted successfully as a sustained-release reservoir.Such complexation prevents the decomposition and subsequent loss of iodine molecules before confronting the cell membranes of microorganisms (Table 5) [128].
Table 5 is arranged from up to down in decreasing inhibitory action against the 10 reference microorganisms.Accordingly, the pathogens were susceptible in decreasing order towards C. albicans WDCM 00054, followed by the Gram-positive bacteria (S. aureus ATCC 25923, B. subtilis WDCM 00003, S. pyogenes ATCC 19615, E. faecalis ATCC 29212, S. pneumoniae ATCC 49619), and lastly the Gram-negative pathogens (K.pneumoniae WDCM 00097, E. coli WDCM 00013, P. aeruginosa WDCM 00026, and P. mirabilis ATCC 29906) (Table 5).The DD tests revealed the highest ZOI for C. albicans WDCM 00054 and confirmed that AV-PVP-Thyme-I 2 is a strong antifungal agent.Our bio-formulation encompasses even the control antibiotic nystatin (NY) almost fivefold, with 61 mm compared to 16 mm, respectively (Table 1).The remarkable ZOI of 61 mm in the 18 months old sample is clearly an indicator of enhanced antimicrobial properties compared to the 50 mm ZOI in the fresh AV-PVP-Thyme-I 2 (Table 5).The DD studies against C. albicans WDCM 00054 resulted in ZOI = 50, 35, 30, and 15 for the concentrations of 11, 5.5, 2.75, and 1.38 µg/mL, respectively (Figure 9 and Table 5).
Table 5. Antimicrobial testing by disc dilution studies of antibiotics (A), AV-PVP-Thyme-I 2 long-term stability study after 18 months (L1), AV-PVP-Thyme-I 2 (1,2,3), suture (S), bandage (B), mask blue layer (M B ), and mask white layer (M W ). ZOI (mm) against microbial strains by diffusion assay.The common antibiotics gentamycin (G) and nystatin (NY) were utilized as positive controls (Table 5).After storing the title formulation for 18 months, we performed DD tests again and obtained surprisingly augmented antimicrobial properties in comparison to the fresh AV-PVP-Thyme-I2.Storing the sample did not result in the decomposition of the triiodide ions.During this time, the triiodide ions were protected by the polymeric PVP matrix, which acted successfully as a sustained-release reservoir.Such complexation prevents the decomposition and subsequent loss of iodine molecules before confronting the cell membranes of microorganisms (Table 5) [128].
As a conclusion, the bio-hybrid AV-PVP-Thyme-I 2 is a strong antifungal agent against C. albicans WDCM 00054.The Gram-positive bacteria S. aureus ATCC 25923 is also inhibited strongly in comparison to the common antibiotic gentamycin, while B. subtilis WDCM 00003 and S. pyogenes ATCC 19615 are intermediately susceptible.These findings enable the potential use of our title bio-formulation as an antifungal and antibacterial coating, as well as a surface contact agent against the mentioned pathogens.
As a conclusion, the bio-hybrid AV-PVP-Thyme-I2 is a strong antifungal agent against C. albicans WDCM 00054.The Gram-positive bacteria S. aureus ATCC 25923 is also inhibited strongly in comparison to the common antibiotic gentamycin, while B. subtilis WDCM 00003 and S. pyogenes ATCC 19615 are intermediately susceptible.These findings enable the potential use of our title bio-formulation as an antifungal and antibacterial coating, as well as a surface contact agent against the mentioned pathogens.
As a conclusion, surgical PGA sutures coated with our bio-formulation AV-PVP-Thyme-I2 may have potential as antimicrobial agents to prevent surgical-site infections against C. albicans WDCM 00054 and Gram-positive bacteria E. faecalis ATCC 29212, S. aureus ATCC 25923, and B. subtilis WDCM 00003.5).K. pneumoniae WDCM 00097 is the only susceptible Gram-negative pathogen on dip-coated surgical sutures with a ZOI of 2 mm (Table 5 and Figure 10c).
As a conclusion, surgical PGA sutures coated with our bio-formulation AV-PVP-Thyme-I 2 may have potential as antimicrobial agents to prevent surgical-site infections against C. albicans WDCM 00054 and Gram-positive bacteria E. faecalis ATCC 29212, S. aureus ATCC 25923, and B. subtilis WDCM 00003.
Face masks were confirmed as essential tools in mitigating opportunistic pathogens during the COVID-19 pandemic [2][3][4]36].They are pivotal as personal protective equipment to prevent the spread of microbes during normal flu or cold seasons in all public settings, including clinics, hospitals, elderly homes, emergency wards, and intensive care units [2][3][4]36].The last COVID-19 outbreak was marked by an inability to provide the pub-lic with high-quality face masks globally [2][3][4]36].Supply chains broke down, pharmacies and drug stores ran out of stocks, prices skyrocketed, while quality, safety, sustainability, and environmental concerns remained [2,4,36].Low-income communities worldwide had no adequate access to face masks.Re-using face masks by spraying them with antimicrobial surface contact agents can mitigate microbial proliferation, reduce environmental pollution, increase accessibility, and increase sustainability.
We coated surgical face masks (M) and KN95 masks with our bio-hybrid AV-PVP-Thyme-I 2 and studied the inhibitory action (Table 5.) The results reveal the same trends mentioned for discs, with the best results for C. albicans WDCM 00054, followed by strong inhibitory action against Gram-positive and intermediate susceptibility of Gram-negative bacteria (Table 5).C. albicans WDCM 00054 and the Gram-positive bacteria are highly susceptible against AV-PVP-Thyme-I 2 coated on KN95 face masks, then the white surgical face mask layer (M W ), and lastly the blue face mask layer (M B ) (Table 5).The inhibitory action against C. albicans WDCM 00054 is ameliorated when AV-PVP-Thyme-I 2 is impregnated on the KN95 mask (80 mm, Figure 11d), followed by the surgical facemask white layer (55 mm), and lastly the blue layer (45 mm) (Table 5 and Figure 11).
Face masks were confirmed as essential tools in mitigating opportunistic pathogens during the COVID-19 pandemic [2][3][4]36].They are pivotal as personal protective equipment to prevent the spread of microbes during normal flu or cold seasons in all public settings, including clinics, hospitals, elderly homes, emergency wards, and intensive care units [2][3][4]36].The last COVID-19 outbreak was marked by an inability to provide the public with high-quality face masks globally [2][3][4]36].Supply chains broke down, pharmacies and drug stores ran out of stocks, prices skyrocketed, while quality, safety, sustainability, and environmental concerns remained [2,4,36].Low-income communities worldwide had no adequate access to face masks.Re-using face masks by spraying them with antimicrobial surface contact agents can mitigate microbial proliferation, reduce environmental pollution, increase accessibility, and increase sustainability.
We coated surgical face masks (M) and KN95 masks with our bio-hybrid AV-PVP-Thyme-I2 and studied the inhibitory action (Table 5.) The results reveal the same trends mentioned for discs, with the best results for C. albicans WDCM 00054, followed by strong inhibitory action against Gram-positive and intermediate susceptibility of Gram-negative bacteria (Table 5).C. albicans WDCM 00054 and the Gram-positive bacteria are highly susceptible against AV-PVP-Thyme-I2 coated on KN95 face masks, then the white surgical face mask layer (M W ), and lastly the blue face mask layer (M B ) (Table 5).The inhibitory action against C. albicans WDCM 00054 is ameliorated when AV-PVP-Thyme-I2 is impregnated on the KN95 mask (80 mm, Figure 11d), followed by the surgical facemask white layer (55 mm), and lastly the blue layer (45 mm) (Table 5 and Figure 11).Among the Gram-positive reference strains, the antimicrobial action of AV-PVP-Thyme-I 2 is strongest on KN95 against B. subtilis WDCM00003 with 40 mm, then S. aureus ATCC 25932 with 38 mm, S. pyogenes ATCC 19615 with 30 mm, E. faecalis ATCC 29212 with 28 mm, and lastly S. pneumoniae ATCC 49619 with 26 mm (Table 5 and Figure 11).The title formulation exerted strong inhibitory properties in comparison to the common antibiotics against Gram-negative bacteria, but with mixed results (Table 5).K. pneumoniae WDCM 00097 was more susceptible to the title bio-formulation on M B with 28 mm, followed by KN95 with 24 mm and M W with 21 mm (Table 5 and Figure 11).E. coli WDCM 00013 and P. aeruginosa WDCM 00026 showed both higher susceptibilities on M W with ZOI = 25 in comparison to M B and KN95 with 24/16 and 20/23 mm, respectively (Table 5).
As a conclusion, the bio-hybrid AV-PVP-Thyme-I 2 exerts strong inhibitory action on KN95 face masks and surgical face masks against C. albicans WDCM 00054, the Grampositive microorganisms B. subtilis WDCM 00003, S. aureus ATCC 25923, S. pyogenes ATCC 19615, E. faecalis ATCC 29212, and S. pneumoniae ATCC 49619.Gram-negative pathogens K. pneumoniae WDCM 00097, E. coli WDCM 00013, and P. aeruginosa WDCM 00026 were more susceptible to the surgical face masks.P. mirabilis ATCC 29906 is only inhibited when AV-PVP-Thyme-I 2 is impregnated on KN95 masks.Antiviral tests were not performed and are planned to be investigated in future studies in our group.
Wound treatment needs a sophisticated approach to hasten the healing process successfully by preventing infection of the wound surroundings [15,36,39,40,42,46,48,52]. Impregnating cotton bandages with antimicrobial substances may mitigate the proliferation of harmful microorganisms on the wound and reduce treatment duration [15,39,40].Therefore, we coated sterile cotton bandages (B) with our bio-formulation AV-PVP-Thyme-I 2 and studied its action against our reference strains (Table 5).As expected, the same pattern of AV-PVP-Thyme-I 2 antimicrobial action is exerted, with the highest antimicrobial action towards C. albicans WDCM 00054, followed by Gram-positive and Gram-negative pathogens (Table 5).C. albicans WDCM 00054 reveals the highest inhibition zone (53 mm) in comparison to all other reference strains and the common antibiotics (Table 5 and Figure 12).
28 mm, and lastly S. pneumoniae ATCC 49619 with 26 mm (Table 5 and Figure 11).The title formulation exerted strong inhibitory properties in comparison to the common antibiotics against Gram-negative bacteria, but with mixed results (Table 5).K. pneumoniae WDCM 00097 was more susceptible to the title bio-formulation on M B with 28 mm, followed by KN95 with 24 mm and M W with 21 mm (Table 5 and Figure 11).E. coli WDCM 00013 and P. aeruginosa WDCM 00026 showed both higher susceptibilities on M W with ZOI = 25 in comparison to M B and KN95 with 24/16 and 20/23 mm, respectively (Table 5).
As a conclusion, the bio-hybrid AV-PVP-Thyme-I2 exerts strong inhibitory action on KN95 face masks and surgical face masks against C. albicans WDCM 00054, the Grampositive microorganisms B. subtilis WDCM 00003, S. aureus ATCC 25923, S. pyogenes ATCC 19615, E. faecalis ATCC 29212, and S. pneumoniae ATCC 49619.Gram-negative pathogens K. pneumoniae WDCM 00097, E. coli WDCM 00013, and P. aeruginosa WDCM 00026 were more susceptible to the surgical face masks.P. mirabilis ATCC 29906 is only inhibited when AV-PVP-Thyme-I2 is impregnated on KN95 masks.Antiviral tests were not performed and are planned to be investigated in future studies in our group.
Wound treatment needs a sophisticated approach to hasten the healing process successfully by preventing infection of the wound surroundings [15,36,39,40,42,46,48,52]. Impregnating cotton bandages with antimicrobial substances may mitigate the proliferation of harmful microorganisms on the wound and reduce treatment duration [15,39,40].Therefore, we coated sterile cotton bandages (B) with our bio-formulation AV-PVP-Thyme-I2 and studied its action against our reference strains (Table 5).As expected, the same pattern of AV-PVP-Thyme-I2 antimicrobial action is exerted, with the highest antimicrobial action towards C. albicans WDCM 00054, followed by Gram-positive and Gram-negative pathogens (Table 5).C. albicans WDCM 00054 reveals the highest inhibition zone (53 mm) in comparison to all other reference strains and the common antibiotics (Table 5 and Figure 12).The Gram-positive pathogens are also highly susceptible to impregnated bandages with a ZOI = 35, 32, 28, 24, and 23 mm against B. subtilis WDCM 00003, S. aureus ATCC 25932, S. pyogenes ATCC 19615, S. pneumoniae ATCC 49619, and E. faecalis ATCC 29212, respectively (Figure 12 and Table 5).
Even the Gram-negative bacteria showed high-to-intermediate inhibitory action.K. pneumoniae WDCM 00097 was highly susceptible with 28 mm ZOI, followed by E. coli WDCM 00013 with 23 mm and P. aeruginosa WDCM 00026 with 20 mm, respectively (Figure 12 and Table 5).
As a conclusion, cotton bandages enhance the antimicrobial properties of AV-PVP-Thyme-I2 against all the selected reference strains.The highest inhibition zones were recorded against C. albicans WDCM 00054, suggesting its use as an antifungal agent on  5).
Even the Gram-negative bacteria showed high-to-intermediate inhibitory action.K. pneumoniae WDCM 00097 was highly susceptible with 28 mm ZOI, followed by E. coli WDCM 00013 with 23 mm and P. aeruginosa WDCM 00026 with 20 mm, respectively (Figure 12 and Table 5).
As a conclusion, cotton bandages enhance the antimicrobial properties of AV-PVP-Thyme-I 2 against all the selected reference strains.The highest inhibition zones were recorded against C. albicans WDCM 00054, suggesting its use as an antifungal agent on bandage as well as on discs, face masks, and sutures.Our title bio-formulation has potential applications against Gram-negative and Gram-positive bacteria on face masks, bandages, discs, and sutures in descending order.
The general susceptibility pattern remains valid for all the tested carrier materials (suture, disc, bandage, surgical face mask, and KN95).The material, which allows a dense, homogenous coating by small, spherical, or cube-like patches of AV-PVP-Thyme-I 2 , seems to be the most suitable carrier, enhancing the antimicrobial properties.Table 5 is arranged in order of highest to lowest susceptibility, starting with C. albicans WDCM 00054, Grampositive, and finally Gram-negative microorganisms.The arrangement of Gram-positive pathogens is ruled by different factors in accordance with our previous studies [34][35][36].Morphology, size, properties, structure, and motility of the microorganisms are a function of their susceptibility to our bio-hybrid AV-PVP-Thyme-I 2 .The main reason is the iodine release from the sustained-released reservoir PVP, followed by the antimicrobial actions of the monoterpenes Thymol and Carvacrol (Figure 13).
bandage as well as on discs, face masks, and sutures.Our title bio-formulation has potential applications against Gram-negative and Gram-positive bacteria on face masks, bandages, discs, and sutures in descending order.
The general susceptibility pattern remains valid for all the tested carrier materials (suture, disc, bandage, surgical face mask, and KN95).The material, which allows a dense, homogenous coating by small, spherical, or cube-like patches of AV-PVP-Thyme-I2, seems to be the most suitable carrier, enhancing the antimicrobial properties.Table 5 is arranged in order of highest to lowest susceptibility, starting with C. albicans WDCM 00054, Grampositive, and finally Gram-negative microorganisms.The arrangement of Gram-positive pathogens is ruled by different factors in accordance with our previous studies [34][35][36].Morphology, size, properties, structure, and motility of the microorganisms are a function of their susceptibility to our bio-hybrid AV-PVP-Thyme-I2.The main reason is the iodine release from the sustained-released reservoir PVP, followed by the antimicrobial actions of the monoterpenes Thymol and Carvacrol (Figure 13).These monoterpenes and AV components are complexed by PVP through hydrogen bonding.The analytical results suggest a firm PVP-I2 complex even after a storage period of 18 months and point at the availability of smart triiodides protected within the PVPsustained reservoir over that long period.
Molecular iodine is a small, lipophilic molecule.This property enables its diffusion through the cell membranes of the studied microorganisms.Phenolic acids originating from the AV-and Thyme extract pass also through the cell membranes.Gram-positive pathogens, with their lipophilic peptidoglycan layers, accelerate diffusion and cell death.Gram-negative pathogens are affected less by molecular iodine and phenolic acids.Nevertheless, depending on the carrier (KN95, surgical face mask, and bandage), high inhibition zones are recorded.However, porin channels in Gram-negative bacteria allow hydrophilic triiodide ions and iodide ions, as well as small phenolic acid diffusion through the outer membranes.However, the porin channel diffusion is successful in KN95, surgical face masks, and bandages.Cell membrane diffusion remains the major mechanism ameliorating Gram-positive bacteria inhibition on KN95, surgical face masks, and bandages as well.
The morphology of the microorganisms characterizes their inhibition by the title bioformulation AV-PVP-Thyme-I2.The susceptibility of the Gram-positive pathogens is highest in S. aureus ATCC 25932, which consists of clusters of non-motile cocci.The pattern continues with non-motile chains and pairs of cocci.Gram-negative bacteria inhibition is These monoterpenes and AV components are complexed by PVP through hydrogen bonding.The analytical results suggest a firm PVP-I 2 complex even after a storage period of 18 months and point at the availability of smart triiodides protected within the PVPsustained reservoir over that long period.
Molecular iodine is a small, lipophilic molecule.This property enables its diffusion through the cell membranes of the studied microorganisms.Phenolic acids originating from the AV-and Thyme extract pass also through the cell membranes.Gram-positive pathogens, with their lipophilic peptidoglycan layers, accelerate diffusion and cell death.Gramnegative pathogens are affected less by molecular iodine and phenolic acids.Nevertheless, depending on the carrier (KN95, surgical face mask, and bandage), high inhibition zones are recorded.However, porin channels in Gram-negative bacteria allow hydrophilic triiodide ions and iodide ions, as well as small phenolic acid diffusion through the outer membranes.However, the porin channel diffusion is successful in KN95, surgical face masks, and bandages.Cell membrane diffusion remains the major mechanism ameliorating Gram-positive bacteria inhibition on KN95, surgical face masks, and bandages as well.
The morphology of the microorganisms characterizes their inhibition by the title bio-formulation AV-PVP-Thyme-I 2 .The susceptibility of the Gram-positive pathogens is highest in S. aureus ATCC 25932, which consists of clusters of non-motile cocci.The pattern continues with non-motile chains and pairs of cocci.Gram-negative bacteria inhibition is directly proportionate to their motility.The swarming bacteria P. mirabilis ATCC 29906 is only inhibited on KN95.Therefore, homogenously coated carriers with small, spherical, cube-like patches of AV-PVP-Thyme-I 2 ensure even inhibition of motile Gram-negative bacteria.
In general, the results on discs, surgical PGA sutures, cotton gauze bandages, and face masks enable the potential use of the title bio-formulation AV-PVP-Thyme-I 2 in many applications.AV-PVP-Thyme-I 2 may be utilized to prevent inflammatory processes, to curb microbial proliferation, to reduce wound and surgical-site infections, to prevent airborne transmission of microbes, and as a surface killing agent (Figure 14).

bacteria.
In general, the results on discs, surgical PGA sutures, cotton gauze bandage face masks enable the potential use of the title bio-formulation AV-PVP-Thyme-I2 in applications.AV-PVP-Thyme-I2 may be utilized to prevent inflammatory proces curb microbial proliferation, to reduce wound and surgical-site infections, to p airborne transmission of microbes, and as a surface killing agent (Figure 14).The biohybrid can be potentially used in oral care products or dental treatm facilitate the removal of colonizing oral pathogens like S. aureus, E. faecalis, S. pyog coli, P. aeruginosa, and C. albicans.These opportunistic pathogens form biofilms cavities surrounding teeth and gingiva and can even reach the dentin walls of root [131][132][133] (Figure 15).The biohybrid can be potentially used in oral care products or dental treatment to facilitate the removal of colonizing oral pathogens like S. aureus, E. faecalis, S. pyogenes, E. coli, P. aeruginosa, and C. albicans.These opportunistic pathogens form biofilms in oral cavities surrounding teeth and gingiva and can even reach the dentin walls of root canals [131][132][133] (Figure 15).C. albicans and E. faecalis colonize oral cavities and form dental biofilm in and around teeth (Figure 14).The biofilm leads progressively to inflammation, plaque formation, dental caries, periodontal disease, and other dangerous systemic infections like rheumatoid arthritis, chronic kidney disease, and inflammatory bowel disease [131][132][133].Throat and oral cavity infections caused by S. pyogenes from dental plaque can lead to serious illnesses like pneumonia, endocarditis, or encephalitis [133].Such colonizers could be stopped by using our bio-formulation as mouthwash or gargle due to its high C. albicans and E. faecalis colonize oral cavities and form dental biofilm in and around teeth (Figure 14).The biofilm leads progressively to inflammation, plaque formation, dental caries, periodontal disease, and other dangerous systemic infections like rheumatoid arthritis, chronic kidney disease, and inflammatory bowel disease [131][132][133].Throat and oral cavity infections caused by S. pyogenes from dental plaque can lead to serious illnesses like pneumonia, endocarditis, or encephalitis [133].Such colonizers could be stopped by using our bio-formulation as mouthwash or gargle due to its high inhibitory action on C. albicans and further oral pathogens (Table 5 and Figure 14).Future investigations should include cytotoxicity, cell culture, in vivo, and antiviral studies to verify the suitability of the mentioned applications.

Preparation of Aloe Vera (AV) Extract and Thyme Extract
Fresh Thyme plants were purchased in August from a local store in Jordan.They were washed several times with distilled water to remove dust and soil, and then twice with absolute ethanol.The leaves were dried for 1 h at ambient temperature, and then 100 mg of a fresh Thyme plant consisting of leaves and stems was cut into pieces.These pieces were immediately transferred into a sterile, brown glass bottle with a screw cap.We added 100 mL of absolute ethanol, sealed the glass bottle, and stored it at ambient temperature in darkness for 3 months as part of a maceration.The macerate extract was then stored in a fridge at 3 • C under darkness for further use.
The leaves of the Aloe Vera (Aloe barbadensis Miller) plant were harvested during December from the botanical garden of Ajman University in the morning hours [34][35][36].Within 10 min, the leaves with lengths of 35 to 50 cm were washed with water, then rinsed many times with distilled water, followed by absolute ethanol, then several times with ultrapure water, and finally left to dry for 1 h.After being dried, the AV leaves were cut with a sterile knife to be able to collect the mucilaginous gel in a sterile beaker.Then, the gel was transferred to a sterile mixer, mixed for 20 min until the gel was homogenized, and finally centrifuged at 4000 rpm for 40 min (3K 30; Sigma Laborzentrifugen GmbH, Osterode am Harz, Germany).The supernatant had a light-yellow color, was transferred immediately into a sterile brown bottle with a screw cap, and was stored in the fridge at 3 • C in darkness.

Preparation of AV-PVP-Thyme-I 2
AV-PVP-Thyme-I 2 is prepared by a simple one-pot synthesis.For this, 2 mL of pure AV gel is filled into a sterile beaker.Then, we added 2 mL of a freshly prepared solution of 1 g polyvinylpyrrolidone K-30 (PVP) in 10 mL of distilled water at ambient temperature under continuous stirring.In this mixture, we added 2 mL of Thyme extract while stirring at ambient temperature.Finally, 2 mL of freshly prepared iodine solution (0.05 g of iodine in 3 mL of absolute ethanol) was added at ambient temperature with continuous stirring.The formulation AV-PVP-Thyme-I 2 was immediately placed into a sterile glass sample tube with a screw cap and stored in the fridge for further use at 3 • C in darkness.The formulation was kept for 18 months under these conditions and characterized in comparison to the fresh sample.Scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS) analyses were performed using VEGA3 from TESCAN (Brno, Czech Republic) at 15 kV.One drop of the formulation AV-PVP-Thyme-I 2 was diluted with distilled water, placed on the carbon-coated copper grid, and dried.This sample was gold-coated using the Quorum Technology Mini Sputter Coater.The SEM analysis allowed a glimpse of the morphology, while the EDS analysis confirmed the purity of the title formulation.

UV-Vis Spectrophotometry (UV-Vis)
The biohybrid AV-PVP-Thyme-I 2 was analyzed using a UV-Vis spectrophotometer model 2600i from Shimadzu (Kyoto, Japan) in the wavelength range of 195 to 800 nm.

Raman Spectroscopy
The formulation AV-PVP-Thyme-I 2 was analyzed at ambient temperature on a REN-ISHAW (Gloucestershire, UK), equipped with an optical microscope.The sample was transferred into a cuvette (1 cm × 1 cm) and placed in front of the laser beam with an excitation of 785 nm.The beam was directed within a spot diameter of 2micron onto the sample by a 50× objective of a confocal microscope.A CCD-based monochromator collected the scattered light with a spectral range between 50 and 3400 cm −1 with a spectral resolution of −1 cm −1 , output power of 0.5%, and integration time of 30 s.

Fourier-Transform Infrared Spectroscopy (FTIR)
The formulation AV-PVP-Thyme-I 2 underwent a FTIR analysis in the range between 400 and 4000 cm −1 on an ATR IR spectrometer with a diamond window (Shimadzu, Kyoto, Japan).The liquid sample was diluted with absolute ethanol and analyzed by FTIR.

X-ray Diffraction (XRD)
AV-PVP-Thyme-I 2 was analyzed using XRD from BRUKER (D8 Advance, Karlsruhe, Germany) by Cu radiation with a wavelength of 1.54060, coupled two theta/theta, time/step of 0.5 s, and a step size of 0.03.

Determination of Antimicrobial Activities of AV-PVP-Thyme-I 2
AV-PVP-TCA-I 2 was tested against a selection of 10 microbial strains (C.albicans WDCM 00054 Vitroids, S. aureus ATCC 25923, S. pneumoniae ATCC 49619, E. faecalis ATCC 29212, S. pyogenes ATCC 19615, Bacillus subtilis WDCM 0003 Vitroids, K. pneumoniae WDCM 00097 Vitroids, E. coli WDCM 00013 Vitroids, P. aeruginosa WDCM 00026 Vitroids, and P. mirabilis ATCC 29906).The positive controls were the common antibiotics gentamicin and nystatin (for C. albicans WDCM 00054 Vitroids only).Pure ethanol and ultrapure water were the negative controls and did not inhibit anything.All the tests were repeated three times, and the average was presented in this study.The formulation was impregnated and also tested on sterile discs, sterile PGA sutures, cotton gauze bandages, surgical facemasks, and KN95 masks against the same reference strains.

Procedure for Zone of Inhibition Plate Studies
We utilized the zone of inhibition plate method to study the susceptibility of the 10 reference microbial strains against AV-PVP-Thyme-I 2 [134].The selected bacterial reference strains were suspended in 10 mL of MHB and incubated for 2 to 4 h at a temperature of 37 • C. The fungus C. albicans WDCM 00054 was incubated at 30 • C in Sabouraud Dextrose broth.All microbial cultures were adjusted to the 0.5 McFarland standard.We used sterile cotton swabs to seed disposable, sterilized Petri dishes with MHA uniformly with 100 µL of microbial culture.After drying for 10 min the plates were ready for antimicrobial testing of AV-PVP-Thyme-I 2 .

Disc Diffusion Method (DD)
We followed the antimicrobial testing as per the recommendations of the Clinical and Laboratory Standards Institute (CLSI) [135].Sterile filter paper discs were impregnated for 24 h by 2 mL of AV-PVP-Thyme-I 2 at concentrations of 11 µg/mL, 5.5 µg/mL, 2.75, and 1.38 µg/mL.Then, these discs were dried for 24 h under ambient conditions.The antibiotic discs of gentamycin and nystatin were used as positive controls.A ruler was utilized to measure the diameter of the zone of inhibition (ZOI) to the nearest millimeter, which is the clear area around the disc.No clear inhibition zone means that the reference microbial strain was not inhibited.The sterile, braided surgical PGA sutures with a length of 2.5 mL were impregnated for 24 h in a 50 mL solution of AV-PVP-Thyme-I 2 at ambient temperature.The blue sutures became brown-blue and were then dried for 24 h under ambient conditions.The cotton gauze bandages, surgical face masks, and KN95 masks were cut with a sterile scissor into square pieces measuring 5 cm x 5 cm.These squares were impregnated in 50 mL of AV-PVP-Thyme-I 2 for 24 h and dried for 24 h at ambient temperatures.All the impregnated materials were tested by disc diffusion methods against the same selection of 10 reference microbial strains.

Statistical Analysis
We used SPSS software (version 17.0, SPSS Inc., Chicago, IL, USA) for the statistical analysis and represented the data in mean values.The statistical significance between groups was calculated by a one-way ANOVA.Values of p < 0.05 were treated as statistically significant.

Conclusions
AMR is a continuous threat to health and quality of life.Pathogens evolve by using different mechanisms to outsmart attempts to curb their proliferation.Multi-drug-resistant ESKAPE microorganisms (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter spp., and Escherichia coli) cause globally increasing rates of morbidity and mortality.New approaches are pivotal because they are cost-effective, sustainable, and facile.Natural antimicrobial formulations consisting of synergistic medicinal plant extracts seem to offer alternatives to AMR.Plants developed defense systems based on their synergistically combined plethora of bio-compounds.As an alternative approach, we add molecular iodine to the mixture of biocomponents.Iodine is a known microbicide, and until now, there have been no known resistance mechanisms to iodine.Therefore, adding iodine enhances the antimicrobial activities of the plant bio-materials originating from AV and Thyme.Iodine must be complexed within PVP to prevent its untimely and fast release, mitigate its stability, and ensure its long-term use.Polymeric complexes of PVP and iodine are already used in many products with cosmeceutical, oral health, and pharmaceutical backgrounds, as well as being excellent antimicrobial agents.Our group used AV gel and Thyme extracts together within the sustained-release reservoir PVP-I 2 .Our formulation, AV-PVP-Thyme-I 2 , is confirmed to be a strong antifungal agent against C. albicans WDCM 00054 on sterile discs, sutures, cotton gauze bandages, surgical face masks, and KN95 face masks.Five Gram-positive microorganisms, including the notorious S. aureus ATCC 25923, were strongly susceptible to the title bio-formulation even at a low concentration of 11 µg/mL, especially on cotton gauze bandages and face masks.Three out of four Gram-negative pathogens, including reference strains of the dangerous ESKAPE pathogens K. pneumoniae WDCM 00097, P. aeruginosa WDCM 00026, and E. coli WDCM 00013, were strongly inhibited by the same low concentration of 11 µg/mL AV-PVP-Thyme-I 2 .P. mirabilis ATCC 29906 was only susceptible with a ZOI of 25 mm on KN95 masks.Face masks and cotton bandages allow homogenous coating by AV-PVP-Thyme-I 2 with small, spherical, cube-like patches and guarantee the high susceptibility of the selected reference strains.
The microbicidal formulation AV-PVP-Thyme-I 2 could be potentially applied in oral treatments and surgery because it inhibits the oral cavity-related opportunistic pathogens (S. aureus ATCC 25923, E. faecalis ATCC 29212, S. pyogenes ATCC 19615, E. coli WDCM 00013, P. aeruginosa WDCM 00026, and C. albicans WDCM 00054) colonizing oral cavities, which in the worst-case scenario lead to dangerous systemic infections.They also cause throat and oral cavity infections, resulting in potentially fatal illnesses like pneumonia and others.Further applications could be skin antiseptics or inanimate surface disinfectants against communityand hospital-acquired infections.Impregnated face masks with AV-PVP-Thyme-I 2 strongly inhibited all 10 reference strains.This application could enable the re-use of face masks as a sustainable solution for the planet and low-income populations.The results on cotton gauze bandages encourage the use of AV-PVP-Thyme-I 2 in wound dressing materials.Further investigations are needed to evaluate the in vivo biological activities.

Figure 5 Figure 4 .
Figure 5 is the result of the Raman spectroscopic analysis of the title bio-material AV-PVP-Thyme-I 2 .

Figure 6
Figure 6 depicts the UV-vis spectra of fresh AV-PVP-Thyme-I 2 in comparison to AV-PVP-Thyme-I 2 after 18 months of storage, AV-PVP-Thyme, PVP-I 2 , and pure Thyme macerated for 3 months.

Figure 7
Figure7reveals similarities in the FTIR spectrum of AV-PVP-Thyme-I2 and PVP-I2, in comparison to our previous investigations[34][35][36].The addition of AV and Thyme extract leads to a broadening of the bands between 3700 and 3500 cm −1 due to an increase in hydrogen bonding by the added AV-and Thyme-biocomponents through their hydroxyl-and carboxylic acid groups (Figure7).The FTIR spectrum also shows higher absorption intensities between 3300 and 3100, 1850 and 1450 cm −1 , and in the fingerprint region (Figure7).The band related to asymmetric -C=O stretching vibrations at 1658 cm −1 in PVP-I2 (B, purple curve) is blue shifted towards 1653 cm −1 (A, red curve), with an additional broadening and increased absorption intensity in AV-PVP-Thyme-I2 (Figure7and Table3)[34][35][36].

Figure 7
Figure 7 reveals similarities in the FTIR spectrum of AV-PVP-Thyme-I 2 and PVP-I 2 , in comparison to our previous investigations[34][35][36].The addition of AV and Thyme extract leads to a broadening of the bands between 3700 and 3500 cm −1 due to an increase in hydrogen bonding by the added AV-and Thyme-biocomponents through their hydroxyland carboxylic acid groups (Figure7).The FTIR spectrum also shows higher absorption intensities between 3300 and 3100, 1850 and 1450 cm −1 , and in the fingerprint region (Figure7).The band related to asymmetric -C=O stretching vibrations at 1658 cm −1 in PVP-I 2 (B, purple curve) is blue shifted towards 1653 cm −1 (A, red curve), with an ν (C-N) 1099 vs ν (C-O) 1038 vs ν (C-O) ν = vibrational stretching, δ = deformation, s = symmetric, a = asymmetric; absorption intensity: vs = very strong, s = strong, m = medium, vw = very weak, sh = shoulder.

Figure 12 .
Figure 12.Impregnated sterile bandages with AV-PVP-Thyme-I 2 , with the positive control antibiotics nystatin (100 IU) and gentamicin (30 µg/disc).From left to right: AV-PVP-Thyme-I 2 (11 µg/mL) against (a) C. albicans WDCM 00054, (b) B. subtilis WDCM 00003, and (c) E. coli WDCM 00013.The Gram-positive pathogens are also highly susceptible to impregnated bandages with a ZOI = 35, 32, 28, 24, and 23 mm against B. subtilis WDCM 00003, S. aureus ATCC 25932, S. pyogenes ATCC 19615, S. pneumoniae ATCC 49619, and E. faecalis ATCC 29212, respectively (Figure12and Table5).Even the Gram-negative bacteria showed high-to-intermediate inhibitory action.K. pneumoniae WDCM 00097 was highly susceptible with 28 mm ZOI, followed by E. coli WDCM 00013 with 23 mm and P. aeruginosa WDCM 00026 with 20 mm, respectively (Figure12and Table5).As a conclusion, cotton bandages enhance the antimicrobial properties of AV-PVP-Thyme-I 2 against all the selected reference strains.The highest inhibition zones were recorded against C. albicans WDCM 00054, suggesting its use as an antifungal agent on bandage as well as on discs, face masks, and sutures.Our title bio-formulation has potential applications against Gram-negative and Gram-positive bacteria on face masks, bandages, discs, and sutures in descending order.The general susceptibility pattern remains valid for all the tested carrier materials (suture, disc, bandage, surgical face mask, and KN95).The material, which allows a dense, homogenous coating by small, spherical, or cube-like patches of AV-PVP-Thyme-I 2 , seems to be the most suitable carrier, enhancing the antimicrobial properties.Table 5 is arranged

Figure 15 .
Figure 15.Bacterial colonization in the oral cavity.