Enrica Calóa,
Joao M. S. de Barrosa,
Mar Fernández-Gutiérrezbc,
Julio San Románbc,
Lucy Ballamyd and
Vitaliy V. Khutoryanskiy*a
aReading School of Pharmacy, University of Reading, Reading, Berkshire, RG6 6AD, UK. E-mail: v.khutoryanskiy@reading.ac.uk
bInstitute of Polymer Science and Technology, CSIC, C/Juan de la Cierva 3, Madrid 28006, Spain
cCIBER-BBN, C/ Monforte de Lemos 3-5, Madrid 28029, Spain
dConvaTec UK Ltd, First Avenue-Deeside Industrial Park, Flintshire CH5 2NU, Wales, UK
First published on 1st June 2016
Novel antimicrobial hydrogels with good mechanical and physical properties were synthesized by autoclaving aqueous mixtures of poly(vinyl alcohol) and poly(methyl vinyl ether-alt-maleic anhydride). The structure of these materials was studied by infrared spectroscopy, scanning electron microscopy and solid state nuclear magnetic resonance. The swelling behavior, mechanical properties and adhesion of the hydrogels to porcine skin were evaluated. It was established that these hydrogels exhibited antimicrobial properties and inhibited bacteria growth against Staphylococcus aureus. The biocompatibility of the hydrogels was confirmed using an MTT assay (indirect cytotoxicity) and by monitoring cell proliferation in contact with the gels (direct cytotoxicity).
Hydrogels have drawn interest from the wound care industry because of their resemblance to living tissue as well as their ability to absorb and retain exudate which improves the balance of hydration of the wound bed.6,7 A major advantage of hydrogel products is their transparency which allows the user to visually monitor the wound without removing the dressing. Unlike traditional wound care products, such as common plain gauze, hydrogel dressings do not require daily changes.8,9 Their high water content facilitates vapour and oxygen diffusion to the wound which may accelerate the healing process.9 Hydrogels are also well known to promote autolytic debridement, which is a process in which the body breaks down and removes dead tissue, carried out by specific enzymes called matrix metalloproteinases which migrate to the wound site after injury.10
Hydrogel-based dressings can be designed as amorphous gels or as flat sheets ready to be applied. In both cases they conform and slightly adhere to the surface of the wound, therefore avoiding the formation of the so-called ‘dead space’ where bacteria can proliferate causing infections.11
Hydrogels are typically synthesized via three-dimensional polymerization of hydrophilic monomers. This method requires extensive purification of the hydrogel product from any unreacted monomers, which are often toxic. Purification is achieved by extraction using excess water and may take up to two weeks. An alternative method for the preparation of hydrogels is the cross-linking of water-soluble polymers. This is achieved by using ionizing radiation such as gamma rays or accelerated electrons.12 The advantage of this method is that the hydrogel formation and its sterilization are achieved in a single step. However, the application of radiation requires the use of expensive facilities.
Recently we pioneered the synthesis of hydrogels using microwave-mediated thermal cross-linking in aqueous mixtures of functional water-soluble polymers. This method offers the advantage of hydrogel formation with simultaneous sterilization without the need for their purification because no toxic monomers or cross-linkers are used.13 In microwave processing, energy is supplied by an electromagnetic field and results in rapid heating of aqueous solutions. The use of this method commercially is often limited because of the need for access to industrial microwave facilities. Autoclaving is a viable alternative to microwave processing and is a more common method of heating aqueous solutions at industrial scale. Autoclaving is widely used for sterilisation of medical devices.
The present work is the first report on the synthesis of ‘ready-to-use’ hydrogels by autoclaving aqueous mixtures of poly(vinyl alcohol) (PVA) and poly(methyl vinyl ether-alt-maleic anhydride) (Gantrez® AN or Gant). The hydrogels developed in this work have a unique combination of properties such as excellent swelling ability, good mechanical strength, adhesiveness to skin, as well as intrinsic antimicrobial activity.
SR = (Ws − Wi)/Wi | (1) |
Human dermal fibroblasts passage 3 were seeded at a density of 8 × 104 cells per mL in complete medium (10% fetal bovine serum (FBS), 2% L-glutamine and 50 μg mL−1 of gentamicin were added) in a sterile 96-wells culture plate and cultured until confluence was reached. The medium was then replaced with the hydrogel (and control) extracts and incubated at 37 °C and 5% CO2 for 24 h. The MTT solution was prepared in warm PBS (0.5 mg mL−1) and added to the plate (100 μL per well), which was incubated at 37 °C for 3 h. The MTT and medium was removed and 100 μL of DMSO were used to solubilize the formazan retained by the cells. The absorbance was measured with a Biotek Synergy HT detector at 570/630 nm.
Human fibroblasts were also seeded at the same density (8 × 104 cells per mL) in complete medium in the presence of ∼5 mg hydrogel samples for direct biocompatibility testing. A hydrogel sample prepared by autoclaving PVA–Gantrez® AN aqueous mixtures (1:
1) containing 0.05%v/v Triton® was used as a positive control; this sample is expected to cause significant cytotoxicity. A commercial Aquacel® Ag (ConvaTec Ltd) dressing was used as a negative control. The cells were cultured and the media changed every day. Culture growth was monitored and the cells were stained for nuclei fluorescence using Hoescht 33342 and the Zeiss A1 Inverted Epifluorescent Microscope with Nikon NIS Elements photo-capturing system was used to take images of the cultures.
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Fig. 1 FTIR spectra of Gant powder (purple), PVAm powder (red) and freeze-dried PVAm–Gant (1![]() ![]() |
In the FTIR spectrum of Gantrez® AN the absorption peak of the anhydride carbonyl group is clearly visible in the region 1760–1820 cm−1; OH stretch peak (3300–2500 cm−1) and CO stretch peak typical for carboxylic acids (1320–1000 cm−1) are visible as well as the OH bend peak characteristic for carboxylic groups at 950–910 cm−1; C–O–C stretch peak of the methyl vinyl ether unit is visible at 1092 cm−1.20 In the PVA spectrum it is possible to observe the characteristic peaks of the hydroxyl groups (3200–3400 cm−1), CH stretch (3000–2850 cm−1), CH bend (1470–1450 cm−1) and CO stretch peak of alcohol groups (1320–1000 cm−1). The peaks present in the freeze-dried hydrogel spectrum result from the spectral features of both polymers. For instance, in the hydrogel's spectrum the peak attributable to the carbonyl of the maleic anhydride is shifted to lower wavelengths, typical for the carbonyl of the carboxylic acid (1710 cm−1) or the ester (1735 cm−1). The peak typical for the hydroxyl groups of the PVA is present in the same region 3200–3400 cm−1 in the hydrogel's spectrum as well, even if less pronounced. The peak at 1172–1177 cm−1 could support the esterification reaction between the COOH formed after the ring opening and the OH groups of PVA.20 A peak at 2400–2300 cm−1 is visible in all the three spectra and it is attributable to carbon dioxide present in the atmosphere.13 Fig. 2 shows the solid state 13C CP-MAS NMR spectra of Gantrez® AN, PVA and freeze-dried hydrogel sample with related assignments.
In the spectrum of Gantrez® AN: C1 and C2 of the two carbonyl groups of the anhydride cycle give a single peak at 190–170 ppm; C3 and C4 of the maleic anhydride cycle give a double peak at 35–55 ppm; C5 and C7 of the lateral chain give signals at 85–70 and 25–35 ppm, respectively; C6 of the methyl group gives a peak at 60–50 ppm. In the PVA spectrum: C8 gives a double peak at 70–60 ppm and C9 a single one at 50–40 ppm.
Moving on to the hydrogel's spectrum: C1 and C2 of the now open maleic cycle give a single peak in the same region (190–170 ppm) as in the spectrum of Gantrez® AN, as well as C3 and C4 that in this case give a higher peak at 55–35 ppm (for the contribution of C9), C5 (85–70 ppm), C6 (60–50 ppm) and C7 (25–35 ppm). The peak given by C8 in the hydrogel's spectrum is still found at 70–60 ppm (as in PVA) but is now single.
Since the spectroscopy did not provide a conclusive evidence on the formation of covalent linkages between Gantrez® AN and PVA, additional experiments were conducted with PVA–Gantrez® AN hydrogels cross-linked via non-covalent interactions through the formation of hydrogen bonds and crystalline domains. These physically cross-linked samples were prepared using freeze–thawing procedure, well-known for the preparation of hydrogels from PVA.21 For this purpose solution mixtures of Gantrez® AN and PVA, containing 0.25% w/v of NaOH, were frozen for a period of 9 hours and then thawed at room temperature leading to opaque hydrogels. Immersion of hydrogels produced via the freeze–thaw technique into boiling water results in completely different phenomena to the hydrogels produced via the autoclaving technique. The physically cross-linked freeze–thaw hydrogels undergo quick dissolution within 20 seconds due to disruption of intermolecular hydrogen bonds at high temperatures (Fig. 3). On the other hand, the autoclaved hydrogels are not dissolved upon immersion into boiling water and only minor additional swelling occurred within two hours. The results of the boiling experiments clearly demonstrate that autoclaving leads to the formation of stable bonds between Gantrez® AN and PVA, whose nature is likely to be covalent. We propose that autoclaving leads to the formation of ester bonds between the carboxylic groups of Gantrez® AN and hydroxyl groups of PVA. These bonds are not detected by spectroscopic techniques because their concentration in the hydrogels is very low. This is also consistent with our previous report on the synthesis of hydrogels using microwave processing.13 Typically 1–2 ester bonds per macromolecule will be sufficient to make a network and the concentration of these new bonds will be very low and impossible to detect by spectroscopic techniques. The presence of these bonds is further confirmed by degradation and complete dissolution of autoclaved hydrogels in boiling 10% NaOH solution within approximately 45 minutes.
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Fig. 3 Comparison between the behaviors of chemically and physically cross-linked PVAm–Gant (1![]() ![]() |
It should also be noted that autoclaving solutions of individual PVA and Gantrez® AN does not result in formation of hydrogels. Autoclaving-mediated cross-linking is only possible when two polymers are present in an aqueous mixture, which further confirms the formation of ester bonds between carboxylic groups of Gantrez® AN and hydroxyl groups of PVA.
Depending on the nature of cross-linking, the same mixture of polymers can be used to produce hydrogels with completely different properties (Fig. 4). For instance, physically cross-linked hydrogels produced by freeze–thaw technique are not fully transparent, have reversible properties and form at low temperatures, making them promising for tissue engineering and drug delivery due to their excellent mechanical strength.22 Chemically cross-linked autoclaved hydrogels, on the contrary, are less suitable for tissue engineering applications because of high temperatures used for their preparation; but they are highly promising for wound care. The properties of these hydrogels and their applicability for wound care shall be discussed in detail.
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Fig. 4 Proposed structure of chemically cross-linked autoclaved hydrogels (a) and physically cross-linked freeze–thaw hydrogels (b) based on PVA–Gant mixtures. |
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Fig. 5 Swelling kinetics for PVAm–Gant (1![]() ![]() |
No statistically significant effects of the polymer ratios of PVA molecular weights on the swelling ratios were observed (p < 0.05). It should be noted that all the values have high standard deviations because of the high amount of surface water present which was impossible to fully remove during the gravimetric measurements.
The mechanical behaviour of the autoclaved hydrogels was evaluated using a tensile test (Table 1). The exemplary strength–strain curves are shown in Fig. S3.† Young's modulus is commonly defined as the slope of stress (the force applied) versus strain (the deformation occurred in the material) curve. It is considered as the most relevant mechanical property of biomaterials.24 The ultimate strength is the maximum stress that a material can withstand. The elongation to break is the deformation (strain) measured at fracture.25
Composition (mol mol−1) | Young's modulus (N mm−2) | Tensile stress at break (N mm−2) | Ultimate strength (N mm−1) | Elongation to break (%) |
---|---|---|---|---|
aPVAm–Gant (1![]() ![]() |
(4.6 ± 1.2) × 10−5 | (3.1 ± 0.3) × 10−3 | (6.4 ± 0.8) × 10−2e | 110 ± 17 |
bPVAm–Gant (1![]() ![]() |
(1.3 ± 1.5) × 10−4 | (2.6 ± 0.2) × 10−3 | (5.1 ± 0.5) × 10−2d | 79 ± 13d |
cPVAm–Gant (2![]() ![]() |
(1.2 ± 1.5) × 10−4 | (9.7 ± 12.0) × 10−3 | (4.9 ± 1.3) × 10−2d | 96 ± 32 |
d PVAh–Gant (1![]() ![]() |
(3.0 ± 2.0) × 10−5 | (4.7 ± 0.1) × 10−3 | (9.3 ± 2.0) × 10−2e | 159 ± 6e |
ePVAh–Gant (1![]() ![]() |
(2.3 ± 1.1) × 10−5 | (1.4 ± 1.0) × 10−3 | (2.8 ± 2.0) × 10−2f | 87 ± 44 |
fPVAh–Gant (2![]() ![]() |
(4.3 ± 0.5) × 10−5 | (3.3 ± 0.2) × 10−3 | (6.8 ± 0.4) × 10−2 | 101 ± 2 |
The autoclaved hydrogels exhibited suitable mechanical properties for the proposed application. Similar materials designed for wound dressing or other biomedical applications, already described in the literature, exhibit higher stiffness compared with these hydrogels.26,27 For instance, the Young's modulus of the bacterial cellulose (nf-BC)–PVA composite hydrogels proposed by Qiao et al.26 are between 0.5 and 1 MPa. Hydrogels have often been compared to living biological tissue for their elasticity and flexibility and are considered for this reason as a very good temporary scaffold for tissue repair.28,29 All samples tested, showed more desirable values of elongation to break than the normal human skin itself, which goes from 75% at birth to 60% in the elderly.30 Young's modulus and tensile stress at break data are similar for all samples tested (Table 1). 1 to 1 molar ratio compositions exhibited higher strength values, with the gel containing high Mw PVA being the most elastic among the formulations considered (with an elongation to break of 159 ± 6%).
The porous structure of freeze-dried hydrogels was studied using SEM (Fig. 6). We observed highly porous structures with different pore sizes, wall thickness and distribution. Both large and small pores are clearly visible in these samples, indicating their inhomogeneous nature.
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Fig. 6 SEM images of freeze-dried hydrogels: (a and c) PVAh–Gant (1![]() ![]() ![]() ![]() |
At the same time, it is convenient to have a dressing capable of remaining in place for a number of days in order to protect the wound from bacteria and other pathogens. Porcine skin was used as a model to test the adhesion of the autoclaved hydrogels. The study of hydrogel detachment from skin surface can provide several characteristics of adhesion, including the force of detachment, the work of adhesion and cohesiveness.14
Fig. 7 shows the summary of detachment characteristics for the hydrogels prepared with different polymer ratios and from different PVA samples. The results of the detachment force, work of adhesion and adhesiveness are in agreement with each other and indicate that the hydrogels prepared with different polymer ratios have difference in their adhesive characteristics.
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Fig. 7 Adhesion of hydrogels to porcine skin: force of detachment values (a), work of adhesion value (b) and cohesiveness values (c) for autoclaved hydrogels. Asterisk (*) indicates significant statistical difference (p < 0.05). Typical detachment profile can be seen in Fig. S4.† |
The samples prepared from lower molecular weight PVA (51.3 kDa) show greater adhesion when they contain an excess of PVA. On the contrary, the hydrogels composed of higher molecular weight PVA (66.3 kDa) showed the greatest adhesion when the 1:
1 polymer ratio was used.
Adhesion is a complex phenomenon that is still not completely understood. It has been suggested that adhesion is directly related to the formation of non-covalent bonds, such as hydrogen bonds, between two surfaces in contact.35 Additionally, it is believed that the diffusion of unbound or loosely bound macromolecules, such as free linear polymer present, into the outer layer of the epithelium could also contribute to the adhesion. Therefore by increasing the degree of cross-linking which results in fewer loose macromolecules with potential to diffuse should decrease the adhesion to skin. Skin condition is expected to substantially affect adhesion of hydrogels. In this work, a healthy intact porcine skin was used as a substrate to study adhesive properties of hydrogels. The measurements of hydrogel adhesion using intact skin provide better reproducibility of results; therefore, this model is more common in characterisation of wound care products. If the skin was damaged, completely different adhesion results are expected as the wound surface will have substantially different nature and the results are expected to be less reproducible.
The antimicrobial properties of the PVAm–Gant and PVAh–Gant hydrogels were tested in a 24 h growth inhibition assay against a suitable Gram positive strain, Staphylococcus aureus. This pathogen is widely present in the environment and is responsible for many skin infections.45 Commercial wound dressing Aquacel® Ag was evaluated in parallel as a control. This method allows an easy and clear evaluation of antimicrobial activities of drugs or biomaterials and it is commonly used in microbiology, as it gives a correlation between concentration and bacterial inhibition.14,46
A clear bacteria growth inhibition zone (Fig. 8) was observed for all gel samples, confirming their intrinsic antimicrobial properties. As expected, it was higher when the bacteria concentration was lower (104 CFU mL−1). All hydrogel samples showed Staphylococcus aureus growth inhibition comparable to the control. The antimicrobial activity of hydrogels containing PVA has not been reported previously. However, Gantrez® AN has some documented antimicrobial properties.47 To establish the nature of the antimicrobial activity in autoclaved hydrogels we have prepared micronized dispersions of these samples and measured their pH. It was found that all samples exhibit pH of 3–4. This acidity may result from carboxylic groups formed by opening of maleic anhydride cycles and also from traces of acetic acid (>0.01% as estimated using 1H NMR spectroscopy) present in autoclaved samples. Acidic pH is known to inhibit the growth of Staphylococcus aureus, which is likely to explain the antimicrobial properties of these hydrogels.48
The tetrazolium salt is positively charged and can penetrate viable eukaryotic cells where it is converted into a colored product (formazan) with a maximum absorbance near 570 nm.49 The test was carried out using extracts collected from the gels in sterile conditions (Fig. 9). The MTT assay indicated that the extracts collected at 24 and 48 h from the hydrogels gave >70% cell viability. These levels of cell viability indicate that the hydrogels could be considered biocompatible for the application as medical devices.50
To assess the direct cytotoxicity human fibroblasts were seeded in the presence of the autoclaved hydrogels (Fig. 10). The gel produced in the presence of 0.05% Triton® served as a positive control and killed all the cells as expected. The cultures were stained for nuclei fluorescence and images were taken at 1, 2 and 7 days post-seeding. Cells growth and proliferation were comparable in the presence of the samples and the commercial product used as a control. Fibroblasts found favorable conditions to proliferate and did not show a modified behavior when seeded in the presence of PVA–Gantrez® AN autoclaved hydrogels.
The materials produced are proposed for the development of novel wound dressings. The antimicrobial properties of the autoclaved hydrogels, which therefore do not require the addition of any antimicrobial agents such as silver or iodine, represent a great advantage for application in wound management.
The full transparency of the hydrogels is an additional advantage allowing visual monitoring of the wound without removing the dressing so that it can be left in place for a longer period of time, reducing the risk of contamination to the wound from the environment.
Footnote |
† Electronic supplementary information (ESI) available: Exemplary stress–strain and detachment curves from porcine skin curve; additional swelling kinetics results. See DOI: 10.1039/c6ra08234c |
This journal is © The Royal Society of Chemistry 2016 |