Argon plasma improves the tissue integration and angiogenesis of subcutaneous implants by modifying surface chemistry and topography
Received 15 March 2018
Accepted for publication 11 July 2018
Published 8 October 2018 Volume 2018:13 Pages 6123—6141
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Thiruganesh Ramasamy
Peer reviewer comments 3
Editor who approved publication: Dr Thomas J Webster
Michelle Griffin,1–3 Robert Palgrave,4 Víctor G Baldovino-Medrano,5 Peter E Butler,1–3 Deepak M Kalaskar1,6
1UCL Centre for Nanotechnology and Regenerative Medicine, Division of Surgery and Interventional Science, University College London, London, UK; 2Royal Free London NHS Foundation Trust Hospital, London, UK; 3The Charles Wolfson Center for Reconstructive Surgery, Royal Free London NHS Foundation Trust Hospital, London, UK; 4Department of Chemistry, University College London, London, UK; 5Laboratory of Surface Science (SurfLab), School of Chemical Engineering, Piedecuesta, Colombia; 6UCL Institute of Orthopaedics and Musculoskeletal Science, Division of Surgery and Interventional Science, University College London, London, UK
Background: Tissue integration and vessel formation are important criteria for the successful implantation of synthetic biomaterials for subcutaneous implantation.
Objective: We report the optimization of plasma surface modification (PSM) using argon (Ar), oxygen (O2) and nitrogen (N2) gases of a polyurethane polymer to enhance tissue integration and angiogenesis.
Methods: The scaffold’s bulk and surface characteristics were compared before and after PSM with either Ar, O2 and N2. The viability and adhesion of human dermal fibroblasts (HDFs) on the modified scaffolds were compared. The formation of extracellular matrix by the HDFs on the modified scaffolds was evaluated. Scaffolds were subcutaneously implanted in a mouse model for 3 months to analyze tissue integration, angiogenesis and capsule formation.
Results: Surface analysis demonstrated that interfacial modification (chemistry, topography and wettability) achieved by PSM is unique and varies according to the gas used. O2 plasma led to extensive changes in interfacial properties, whereas Ar treatment caused moderate changes. N2 plasma caused the least effect on surface chemistry of the polymer. PSM-treated scaffolds significantly (P<0.05) enhanced HDF activity and growth over 21 days. Among all three gases, Ar modification showed the highest protein adsorption. Ar-modified scaffolds also showed a significant upregulation of adhesion-related proteins (vinculin, focal adhesion kinase, talin and paxillin; P<0.05) and extracellular matrix marker genes (collagen type I, fibronectin, laminin and elastin) and deposition of associated proteins by the HDFs. Subcutaneous implantation after 3 months demonstrated the highest tissue integration and angiogenesis and the lowest capsule formation on Ar-modified scaffolds compared with O2- and N2-modified scaffolds.
Conclusion: PSM using Ar is a cost-effective and efficient method to improve the tissue integration and angiogenesis of subcutaneous implants.
Keywords: tissue integration, angiogenesis, surface modification, biomaterials, implants
Corrigendum for this paper has been published
Subcutaneous synthetic implants are being used in several surgical settings surgery to restore anatomy following surgical resection including breast, facial, abdominal and pelvic reconstruction. However, unacceptable levels of infection and extrusion with subcutaneous synthetic materials cause significant patient morbidity and demands on health care resources. One main reason for the poor performance of synthetic materials is the poor integration and lack of angiogenesis with the surrounding subcutaneous tissue, which leads to a lack of anchorage and consequently infection and extrusion of the implant.1–3
To improve the outcome of synthetic biomaterials, the substrate should aim to guide desired cell responses by mimicking the extracellular matrix (ECM). With the recent advancements in nanotechnology, nanocomposites offer substrates with a dimension that mimics the native ECM, improving their biocompatibility.4–8 Our group is currently developing a subcutaneous implant using a nanocomposite polyurethane.4,5 This polyurethane polymer has been extensively tested and meets international standards (ISO 10993) for biocompatibility. Due to hydrophobic nature, it has been extensively investigated for hollow organs including a vascular graft9 and lacrimal duct,10 where flow of fluids is the primary requirement rather than tissue integration.
Several methods have been investigated to modify the tissue integration of synthetic materials, including the deposition of proteins, growth factors and chemical groups.9–16 Creating functional materials is critical to modify the biological processes that occur at the material interface as they are controlled by the physiochemical properties at the material surface. Notably, manipulation of the surface chemistry and wettability of biomaterials is the simplest path for controlling surface interactions and improving biocompatibility.17,18 Biomolecules including proteins and growth factors can simply be adsorbed onto the material surface or covalently linked via chemical reactions onto the surface.19 Many groups have illustrated that adsorption of ECM components onto material surfaces can direct cell behavior including fibronectin, laminin, collagen and elastin.19 Several binding motifs from such ECMs have been identified and manufactured into short linear sequence of amino acids including RGD motifs to improve cell attachment to the biomaterial surface.19 However, with covalent bonding or adsorption techniques, understanding the correct presentation and gaining sufficient binding of the peptides or protein to direct cell behavior is difficult.20 The delivery of growth factors to direct cell behavior has also been reported by trapping the biomolecules in the scaffolds during the manufacturing process.20 The release kinetics of the molecule can be controlled by the porosity of the scaffolds.20 However, often the growth factor loses its bioactivity due to the prolonged physical entrapment.20 Electrostatic binding is an alternative advantageous technique as it mimics the natural interactions of the growth factors and the ECM.20 However, the presentation of biomolecules via this technique may not always be uniform and thus may not influence downstream pathways effectively.20 To overcome the challenges with using molecules to create a biometric surface, a biomaterial’s surface chemistry can be altered to direct cell behavior.21 Several chemical groups have been shown to influence cell behavior including carboxyl (−COOH), amine (−NH2), methyl (−CH3) and hydroxyl (−OH) groups.21 Studies have shown −NH2 improves adhesion, growth and matrix formation.22,23 Carboxyl groups have been shown to improve the adsorption of proteins and allow for cell adhesion.24 Several techniques can introduce such chemical groups onto the material surface including ion beam implantation and ion beam exchange.25 However, these techniques require extensive training and high costs.26 To overcome these challenges, an alternative method of modifying the surface chemistry of implants is using plasma surface modification (PSM).
PSM is an economical and effective method to control the physiochemical properties of biomaterials surfaces.18 PSM can modify the surface’s wettability by altering the surface chemistry and topography. Such physiochemical changes have been shown to enhance cell adhesion and proliferation, guide cell responses and modify the blood–biomaterial interface with the result of improving materials applicability for clinical use.27–39 An important advantage of PSM is that the treatment can be used to tune the surface chemical composition and wettability without changing the material’s bulk properties.
Radiofrequency plasma is the most widely used source of plasma, which involves passing an electric current through a gas.18 Various gases have been used with PSM to impart specific surface chemistries or etching effects to alter surface topography in order to tune the surface composition. Despite the extensive exploration of PSM over the years for modifying the interfacial properties of materials, there are no comprehensive studies documenting the effect of various gaseous plasmas on the characteristics of the biomaterial surface, or extensive in vitro and in vivo evaluation to confirm their efficacy. The majority of studies reported have used a variety of gases, parameters and materials, so it is difficult to compare the efficiency of various PSM methods.18
This study aimed to compare three commonly used gases for PSM, including argon (Ar), oxygen (O2) and nitrogen (N2), to optimize the plasma process to enhance tissue integration and angiogenesis of polyurethane scaffolds. In this study, we optimized the PSM process by treating scaffolds for various length of time, to determine the effect on polyurethane’s surface and bulk properties. The study was then expanded by in vitro and in vivo studies to find the most efficient modification process to enhance tissue integration and angiogenesis. The method developed in this study can be easily translated to other biomaterial surfaces, offering a significant advancement in developing materials for surgical applications requiring long-term subcutaneous implantation.
Materials and methods
Polyurethane polymer synthesis
The polymer was synthesized using a 2-part method as described previously.11,12 In brief, polycarbonate polyol (2000 molecular weight [Mw]) and trans-cyclohexanechloroydrinisobutyl-silses-106 quioxane (Hybrid Plastics Inc., Hattiesburg, MI, USA) were mixed followed by Polydehral Oligomeric Silsesquioxane (POSS) cages being dissolved into the polyol solution at 70°C. Then, 4, 4′-methylenebis(phenyl isocyanate) was added to form a pre-polymer. Following this, dimethylacetamide (DMAC) was then added slowly with chain extension performed by cooling the solution to 40°C. This led to the synthesis of the POSS-modified polycarbonate urea-urethane (PU) in DMAC solution. The scaffolds were manufactured using a salt-leaching method as described previously.11,12 A 3:7 wt ratio of sodium chloride (NaCl) to PU was used in all experiments. The NaCl/PU mixture was first poured onto steel molds and then placed in an oven at 65°C for 4–5 hours until all the solvent had evaporated. Casted polymer was then placed into deionized water for 7 days to remove all NaCl to produce porous scaffolds. For cell culture analysis, scaffolds were cut into circular discs of 16 mm diameter for use in 24-well plates.
Plasma surface modification (PSM)
PSM was performed using a radio frequency plasma generator configured to 40 kHz at 100 W and a flow rate of 0.4 mbar. PSM was performed by subjecting the scaffolds to either O2, Ar or N2 gas, for 1, 2.5, 5, 7.5 or 10 minutes. Untreated (Con) scaffolds were used as the control.
Contact angle measurements
The static water contact angle was analyzed using the sessile drop method using the DSA 100 instrument (KRUSS, Hamburg, Germany) as described previously (n=6).11,12 The static contact angle was measured on six scaffolds after varying the length of time of plasma exposure from 1 to 10 minutes.
The mechanical properties of scaffolds after PSM were analyzed with a Instron-5565 tensile 224 tester as described previously.11,12 The Average Young’s modulus of elasticity was reported following analysis of six independent scaffolds (n=6).
Scanning electron microscopy (SEM)
The scaffold’s surface structure and architecture, specifically the pore size and porosity (n=3), were analyzed using SEM.11,12 In brief, the scaffolds were fixed with 2.5% w/v glutaraldehyde/PBS for 48 hours. Following this, the scaffolds were critically point dried using CO2. The scaffolds were then gold-coated using a sc500 (EMScope; Quorum Technologies, Lewes, UK) sputter coater before imaging using a FEI Quanta 200F Scanning Electron Microscope.
X-ray photoelectron spectroscopy (XPS) studies
The treated and untreated scaffold’s surface chemistry was evaluated using a Thermo Scientific K-Alpha spectrometer, as described previously (n=3).11,12 In brief, monochromatic Al Kα X-rays (h=1,486 eV) were focused to a 400-μm diameter spot on the scaffold surface, defining the analysis area. The analysis depth was at the photon energies 5–10 nm. Survey spectra demonstrated the elemental composition of the surface. High-resolution spectra of the principle core line of each element present were then acquired for chemical state identification. Then, high-resolution spectra were fitted with Gaussian–Lorentzian peaks using the CasaXPS software to deconvolute different chemical environments. Gaussian–Lorentzian peaks were fitted using CasaXPS software to deconvolute different chemical environments.
Atomic force microscopy (AFM)
The roughness of the scaffolds surface was evaluated using an AFM (TAP150A) in the tapping mode (spring constant 2.919 n/m) as described previously (n=3).11,12 In brief, the root mean square roughness was calculated from the 5 μm scan of three areas using the NanoScope® analysis software version 1.40 (Bruker Corporation, Billerica, MA, USA). The PeakForce quantitative nanomechanical mapping was used to obtain an FV modulus using the modified Hertzian model.
Gel permeation chromatography (GPC)
Molecular weight averages and polymer dispersity were determined by GPC analysis. Scaffolds were prepared to 1 mg/mL concentration and passed through a 0.22 μm nylon filter before measurement. GPC measurements were performed on an Agilent 1260 infinity system equipped with 2 PLgel 5 μm mixed-D columns (300×7.5 mm), a PLgel 5 mm guard column (50×7.5 mm), a differential refractive index (DRI) and variable wavelength detector. The temperature of the columns and DRI was maintained at 50°C. The system was eluted with DMF containing 5 mM ammonium tetrafluoroborate at a flow rate of 1 mL/min and the DRI detector was calibrated with linear narrow poly(methyl methacrylate) standards with narrow molecular weight distribution (n=3).
Differential scanning calorimetry (DSC)
The polymer’s glass transition temperature (Tg) was measured post-PSM at 5 and 10 minutes of treatment using a Q2000 DSC (TA Instruments Ltd., Elstree, UK). Scaffolds (5–10 mg) were weighed in hermetic Tzero aluminum pans. An empty pan, matched to the weight of the scaffold pan, was used as a reference. The scaffolds were heated from 0°C to 250°C at 20°C/min. Data were analyzed with Universal Analysis 2000 with N2 used as the purge gas. DSC thermograms were drawn with Origin Pro 9.1 software (n=3; OrginLab, Northampton, MA, USA).
Protein adsorption studies
Total protein adsorption study
Functional presentation of cell-binding domains of adsorbed fibronectin and vitronectin
The accessibility of cell-binding domains of bFN and bVN adsorbed on the scaffolds was examined by ELISA using monoclonal antibodies (mAbs) directed to epitopes of the RGD-containing domains as described by Barrias et al.16 In brief, the scaffolds were incubated in the protein solutions (bFN or bVN) of different concentrations at 37°C. After washing with PBS, all surfaces were blocked with 1% w/v BSA/PBS and then incubated with specific mouse anti-bovine mAbs at predetermined optimal concentrations (0.17 μg/mL antibFN and 1 μg/mL anti-bVN in 1% w/v BSA/PBS, Alpha Laboratories, Eastleigh, UK) for 1 hour at 37°C. After washing three times in PBS, scaffolds were incubated with horseradish peroxidase-conjugated anti-mouse IgG (H+L) secondary antibody (1:1,000 in 1% w/v BSA/PBS; Fisher Scientific, Loughborough, UK) for 1 hour at 37°C. After further washing, scaffolds were incubated in o-phenylenediamine dihydrochloride substrate (0.4 mg/mL in 0.05 M phosphate–citrate buffer, pH 5.0, with 0.012% v/v hydrogen peroxide). The OD of the supernatant was then read using a spectrophotometer at 450 nm with reference to 620 nm.
The role of specific integrin involved in the fibroblast adhesion to the plasma-modified scaffolds was investigated as described by Kalaskar et al.17 Human dermal fibroblasts (HDFs) cells were trypsinized, counted and incubated for 30 minutes in the presence or absence of integrin-blocking antibodies α5β1 and α5β3 (Abcam, Cambridge, UK) from 1 to 10 mg/mL in cell culture medium at 37°C. The cells (treated with and without blocking antibodies) were seeded at a density of 50,000 cells/cm3 on the scaffolds treated with different PSMs. The number of attached cells was counted after 3 hours and cell adhesion was calculated by counting the number of attached cells in three different random fields of view in triplicate cultures.
In vitro biocompatibility testing
Cell culture and cell seeding
HDFs obtained from the European Collection of Authenticated Cell Culture (ECACC) were maintained in Dulbecco’s Modified Eagle’s Medium with 10% fetal bovine serum and 1% antibiotic solutions (Sigma-Aldrich, St Louis, MO, USA) as described previously.11,12 For in vitro experiments, 16 mm scaffolds were placed into the 24-well plates, for 24 hours in complete medium before cell seeding. Each scaffold was seeded with 1×104 cells/cm2. Every three days, the medium was changed.
Cellular adhesion and morphology
To study HDF architecture seeded on the scaffolds, the cytoskeleton was stained with actin-phalloidin after 24 hours.11,12 HDF viability was evaluated using Alamar Blue™ assay (Sigma-Aldrich) and the Fluorescence Hoechst DNA Quantification Kit (Sigma-Aldrich) examined DNA content on days 1, 2, 4, 7, 14 and 21 as described previously (n=6).11,12
Gene expression by RT-qPCR
Real-time quantitative polymerase chain reaction (RT-qPCR) was performed as described previously.40 First, RNA was extracted using Tri-Reagent (Life Technologies, Waltham, MA, USA) at 7 and 14 days. Second, Moloney murine leukemia virus reverse transcriptase was used to retro-transcribe the RNA (Promega, Madison, WI, USA). Following this, RT-qPCR was completed using the ABI Prism 7500 sequence detection system (Thermo Fisher Scientific, Waltham, MA, USA) with QuantiTect SYBR Green PCR kit (Qiagen, Hilden, Germany). GAPDH was used as the housekeeping gene to normalize the data using the 2−ΔΔCt method. The primers used in the study are listed in Table 1.
Table 1 The RT-qPCR primer sequences used in this study
The expression of ECM and adhesion-related proteins was using a method as previously described.40 At 14 days, the medium was removed and the scaffolds were washed and fixed in 4% paraformaldehyde. Following overnight incubation, the scaffolds were further washed. Following permeablization (0.5% Triton X-100), the scaffolds were blocked (0.5% BSA). Following incubation with primary antibodies overnight at 4°C, further washing was done before the scaffolds were incubated in secondary antibody for 2 hours (488 Alexa secondary antibody, 1:500). Finally, the cell nuclei were stained with Hoechst 33258 (2.5 μg/mL final concentration). Antibodies used in this study for immunocytochemistry are shown in Table 2.
Table 2 Primary antibody details used in this study
Enzyme-linked immunosorbent assay (ELISA) of vascular endothelial growth factor (VEGF)
The VEGF secretion by the HDFs was assessed using ELISA analysis (Quantikine; R&D Systems, Inc., Minneapolis, MN, USA) according to manufacturer instructions. On days 4, 7, 10 and 14, the cell culture supernatant was taken and evaluated using ELISA as described previously.41
In vivo analysis
Following PSM treatment, two 4 mm (diameter) by 1 mm (thickness) discs were subcutaneously implanted in the dorsum of one 4-month-old BALB/c mice (Charles River Laboratories, Wilmington, MA, USA) as described previously (n=6).11 The disc was implanted via a small incision and closed with interrupted 5,0 monocryl. All experiments were approved by the local governmental animal care committee and performed according to animal welfare UK legislation. At 6 and 12 weeks, using CO2 asphyxiation, the animals were sacrificed and the scaffolds excised and fixed in 4% paraformaldehyde. The scaffolds were excised with approximately 0.5 cm surrounding circular dermis. Fixed scaffolds were then paraffin embedded and cut into 3 μm sections for histological analysis. H&E staining was conducted according to standard procedures to assess tissue integration and CD31 immunohistochemistry staining for endothelial cells detection as per a previous study.11 The study was approved and conducted according to the animal research UK Home Office Guidelines.
GraphPad (Prism) was used to conduct statistical analysis using one- or two-way ANOVA with Tukey HSD post hoc test. A P-value <0.05 was considered statistically significant.
Untreated scaffolds (Con) demonstrated a static water contact angle of 67°±7°. The contact angle of the scaffolds significantly (P<0.05) decreased after 1 minute of Ar (32.2°±2°), N2 (62.7°±4°) and O2 (14.8°±7°) treatment compared with unmodified scaffolds (Con; Figure 1A).
Roughness using AFM
PSM affected the surface roughness of the scaffolds following Ar, O2 and N2 treatment. Unmodified scaffolds (Con) had a roughness of 8±1 nm (Figure 1B). Changes in surface roughness following Ar and N2 were only significant compared with control after 5 minutes of treatment time (N2, 1 minute, 9±1 nm; N2, 5 minutes, 13±2 nm; Ar, 1 minute, 9±1 nm; Ar, 5 minutes, 11±2 nm). However, O2 plasma led to linear increase in surface roughness with treatment time (O2, 1 minute, 16±3 nm; O2, 10 minutes, 38±4 nm), suggesting it was the most aggressive plasma treatment, and such changes were confirmed using SEM (Figure S1).
Surface elastic modulus using AFM
Ar and N2 plasma treatment showed no change in the surface elastic modulus as the treatment time increased compared with control (Con; Figure 1C). However, with O2 treatment, the surface elastic modulus increased linearly as the treatment time increased (P<0.05).
For XPS analysis, the relative molar concentrations of C, N and O from all scaffolds were normalized and presented as shown in Figure 1D–F. The C/(N+O) ratio showed a stepwise decrease after treatment with Ar and O2. It is suggested that this trend may be related to the removal of residual carbon contamination from the surface (Figure 1D). Conversely, the C/(N+O) ratio did not follow any definite pattern after the N2 treatment. The observed trend suggests there is a cyclic removal and deposition of carbon from the surface of the material under such conditions.
On the other hand, the N/(C+O) ratio only showed small changes after treatment with all three gases (Figure 1E), suggesting no significant changes to surface N concentration for all the scaffolds. For the O/(C+N) ratio, a significant increase was observed during the O2 treatment after one minute (Figure 1F). Further scaffold treatment did not bring an increase of the O/(C+N) ratio. For the Ar treatment, the O/(C+N) ratio increased gradually until five minutes, which remained constant even after longer treatment times. N2 treatment did not follow any particular trend. The calculated ratio suggests a similar pattern as that observed for the C/(N+O) treated with N2 plasma. Overall, the C ratio decreases with Ar and O2 treatment, and in response, the O ratio increases with Ar and O2 treatment. N2 treatment, on other hand, does not seem to have a significant effect over the polymer chemistry during the treatment process.
Bulk properties including mechanical testing, DSC analysis and molecular weight analysis
The changes in bulk properties of the scaffolds after PSM were examined by the GPC, DSC and mechanical properties. After 5 minutes of treatment, irrespective of the type of gas, there were no significant changes found in average molecular number (Mn) or average molecular weight (Mw) using GPC (Figure S2). After modification with plasma treatment, there was no difference in the Young’s modulus of the scaffolds with either Ar, N2 or O2 compared with untreated scaffolds (Con; Figure S3). There were no significant changes in the Tg after different PSM techniques using DSC analysis (Figure S4).
For all the gaseous plasma, 5 minutes provided the highest cellular attachment (Figure 2A). However, among all the test gases for 5 minutes, the highest cell adhesion at 24 hours was observed on Ar-modified scaffolds compared with O2- and N2-modified scaffolds (P<0.05).
When cell morphology was examined by staining cytoskeleton of the cells, HDF cells demonstrated spreading on all plasma-modified scaffolds and unmodified scaffolds (Figure 2B). In addition to this, HDF vinculin expression was confirmed on all scaffolds by immunocytochemistry after 24 hours. The expression of vinculin, focal adhesion kinase (FAK), talin and paxillin was higher on the PSM scaffolds compared with unmodified scaffolds (P<0.05). Among the gases tested, the expression of adhesion-related genes was significantly higher (P<0.05) on Ar compared with unmodified, N2 and O2 scaffolds (Figure 2C).
HDF viability and growth
Short-term cellular viability, determined using Alamar Blue assay and DNA content analysis, was significantly higher on plasma-modified scaffolds compared with unmodified control scaffolds with all treatment gases (P<0.05; Figure 3). For all treatment gases, the greatest level of cell growth was observed after 5 minutes of treatment compared with other treatment times.
Total protein adsorption
The type, amount and conformation of the essential proteins at surface interface determine the cell adhesion, their attachment and long-term growth. In order to understand the increase in growth of HDF cells on the PSM scaffolds, total protein adsorption was quantified on all scaffolds (Figure 4A). PSM scaffolds showed significantly higher amount of total protein adsorption compared with unmodified scaffolds. Among various treatment times used, 5 minutes of treatment with all test gases plasma led to the highest protein adsorption from serum containing media compared with control. Furthermore, when various test gases are compared, Ar (5 minutes) showed the highest protein adsorption compared with N2 and O2. To analyze the role of specific proteins in cell adhesion, the most common ECM proteins, FN and VN, adsorption was quantified (Figure S5). FN adsorption was found to be the highest on N2- and O2-treated scaffolds along with tissue culture plate (TCP; Figure S5), which reached saturation after 5 μg/mL, whereas, VN adsorption was found to be the highest on Ar along with TCP (Figure S5). Blocking integrin receptors for VN and FN demonstrated that the fibroblasts adhered to the modified surfaces using different receptors (Figure 4B and C). Fibroblasts adhered to N2- and O2-modified surfaces using fibronectin receptor α5β1 but using vitronectin receptor αVβ3 on Ar-modified surfaces. Since 5 minutes of treatment showed the highest protein adsorption, followed by cell viability and growth with all the gases, this treatment time was further used to understand the mechanism of cellular interaction in terms of role of specific protein adsorption, interaction of cell surface receptors and their effect on tissue integration and angiogenesis.
ECM formation in vitro
The mRNA expression and release of ECM factors of collagen type I, elastin, laminin and fibronectin were greater on Ar-modified scaffolds than on N2- and O2-modified scaffolds (P<0.05; Figure 5). There was no difference in collagen type III expression by the HDFs between the scaffolds (Figure 5). The protein expression of collagen, elastin and fibronectin by the HDFs was confirmed on the scaffolds using immunocytochemistry after PSM with all gases, as well as on unmodified scaffolds (Figure S6).
Assessment of tissue integration and angiogenesis in vivo
To assess the ability of the scaffolds to support tissue integration in vivo, the scaffolds were subcutaneously implanted for 6 and 12 weeks in a mice model and levels of tissue integration and angiogenesis were compared. Figure 6A shows the histology and immunohistochemistry of the explanted scaffolds treated with the three different gases and unmodified scaffolds. Quantification of H&E staining confirms significantly higher level of tissue ingrowth in the Ar-modified scaffolds compared with O2-, N2-treated and unmodified scaffolds at 6 and 12 weeks (P<0.05; Figure 6B). The degree of capsule formation was also measured after 12 weeks and found to be significantly reduced after PSM compared with unmodified scaffolds (Figure S7). Vascularization in vivo was assessed using CD31 staining to identify capillaries growing into the scaffolds after different PSM (Figure 7A). Analysis indicated that Ar-modified scaffolds had greater vessel formation than other plasma-modified scaffolds and unmodified scaffolds (P<0.05; Figure 7B). Furthermore, in vitro quantification of the secretion and expression of angiogenic growth factors, vascular endothelial growth factor (VEGF) and basic fibroblast growth factor, was also higher on Ar-modified scaffolds compared with N2-and O2-modified scaffolds (Figure 7C).
Surgical implants fail due to poor integration and lack of vascularization with the surrounding tissue.2 In this study, we used a cytocompatible material polyurethane to overcome that challenge by modifying it with PSM. Even though the usefulness of PSM has been widely documented, there is a lack of information on the efficiency of various gases used in PSM and optimal process parameters, which can be used to enhance tissue integration and angiogenesis of synthetic implants.
From the surface and bulk analyses, it is clear that polymer bulk properties remain unaffected by plasma treatment for various length of time and only the surface interfacial properties were altered. This is in agreement with previous reports, which suggest, that PSM has no effect on the bulk properties of materials.11,42,43 Detailed surface analysis revealed that all treatment gases significantly decreased the surface wettability, and led to an increase in topography and surface elastic modulus of the PSM scaffolds compared with unmodified scaffolds (Figure 1; P<0.05). The O2-treated scaffolds demonstrated an increasing roughness and surface elastic modulus as treatment time increased. However, on the other hand, N2 and Ar treatment showed very small changes to the roughness and the surface elastic modulus over 10 minutes. The surface wettability of the scaffolds was reversed by PSM after 1 minute of Ar, N2 and O2 treatments. The O2 surface modification also showed a greater effect on decreasing the contact angle of the scaffolds after similar exposure rates of Ar and N2 PSM.
The decrease in the contact angle and the increase in the surface roughness following O2 plasma are consistent with previous reports.27 Pappa et al found that O2 plasma significantly decreased the contact angle and increased the surface roughness of polycaprolactone polymer surfaces due to the introduction of polar groups on the surface of the polymer.27 Shah et al also demonstrated similar decreases in contact angle findings following the Ar and N2 treatment of polylactic acid surfaces.30 N2 has been shown to cause hydrophilic surfaces due to the deposition of −NH2 chemical functional groups.36 Ar has been shown to create hydrophilic surfaces due to deposition of polar functional groups (−OH) groups.33 In this study, we found a small increase in roughness after 5 minutes of Ar and N2 plasma treatment. Previous studies have shown both an increase and decrease in surface roughness following Ar and N2 plasma treatment.30,32,37,39 The differences in the literature may be due to varying intensities of the plasma gases generated due to contrasting methodology within studies.30
The XPS analysis confirmed that Ar and O2 plasma treatment acted as an effective carbon remover. A decrease in the carbon ratio and increase in the N2 ratio seemed proportional with these two treatment gases. As carbon was removed, underlying N2 from scaffolds surface was possibly exposed. It should also be noted that part of detected carbon could be associated to adventitious contamination, which is commonly observed in XPS analysis. Ar and O2 plasma treatments also showed an increase in O2 deposition. On the other hand, N2 treatment showed a pattern that could be demonstrating cyclical N2 deposition, carbon removal and O2 deposition from the surface, suggesting that there was very little effect on surface chemistry. Furthermore, this also shows that N2 plasma caused the smallest change to the scaffold’s surface chemistry. Taking all surface analysis results into consideration, it is safe to suggest that among all three gases tested, O2 treatment brought the most significant changes, Ar showed moderate changes and N2 treatment had the least effect on the surface properties. These changes may be accounted for by the difference in the reactivity of the plasma gas.30 The treatment of reactive gases like O2 brings about more surface changes than less reactive gases such as Ar and N2.30
The changes in bulk properties post-PSM were investigated in terms of mechanical properties, Mw and Mn, and Tg after increasing exposure of Ar, O2 and N2 treatment. The tensile mechanical properties and Tg of the polymer did not change after 10 minutes of Ar, O2 or N2 treatments. However, GPC showed a decrease in the Mw and Mn after 10 minutes of O2 modification, suggesting a time less than 10 minutes should be used to prevent the degradation of nanocomposite materials when using this treatment gas. The surface elastic modulus increased after increasing exposure of O2 treatment, which could be due to oxidative degradation and repolymerization of polymer forming harder interfaces.44 Tiganis et al demonstrated that an increase in the Young’s modulus at the specimen surface of acrylonitrile butadiene styrene using micro-indentation measurements indicated degradation of the polymer causing the polymer to become brittle and fail.44 However, further analysis and reports into polymer degradation are needed to account for this observation.
To find optimum cell culture conditions, HDF cells were cultured on PSM-treated polymers for various treatment times. It was interesting to note that, after 5 minutes of exposure, all PSM treatments enhanced the adhesion (Figure 2A) and growth (Figure 3A and B) of HDFs on the scaffolds. Cells do not directly interact with synthetic materials but attach to the absorbed layer of proteins on the material surface. Protein adsorption was greater on the PSM surface, correlating with enhanced cell adhesion on modified compared with unmodified scaffolds (Figure 4A). It is hypothesized that although there was low protein adsorption on unmodified scaffolds, the conformation was correct allowing for spreading of the fibroblasts similar to plasma-modified scaffolds, but the lower protein adsorption resulted into low levels of cell attachment. However, when the surfaces were modified with Ar, O2 or N2, there was more protein available causing higher cell attachment and cell spreading (Figure 4A). Among three gases for treatment, Ar showed the highest protein adsorption and thus cell attachment. To understand the reason behind this, further analysis of the cell–protein interaction was undertaken.
Cells recognize adsorbed proteins via integrins, which are linked between the ECM and the actin cytoskeleton.45,46 Integrins form focal adhesion complexes when cells are adhered. Such complexes contain structural proteins including vinculin, α-actin and talin, and signaling molecules such as paxillin and FAK.46,47 We observed an increase in the expression of vinculin, paxillin, talin and FAK by the HDFs on Ar-modified scaffolds. This may have contributed to the increase in cell adhesion and long-term growth observed on Ar-modified scaffolds compared with other PSM scaffolds.
Interestingly, this study also found that adhesion of the HDFs to the plasma-modified scaffolds occurred through different integrins. The integrin-blocking experiment showed a selective decrease in cell attachment on O2 and N2 when anti-α5β1-integrin antibody was used. This observation confirms the role of fibronectin on these surfaces, which is known to interact with cells via its classical α5β1 integrin receptor.46 But the decrease in cell attachment was only observed on Ar-treated scaffolds, when anti-αVβ3-integrin antibody was used, suggesting a predominate role of vitronectin in cellular attachment on these scaffolds.47 However, as the percentage decrease in cell attachments was around 40% with anti-αVβ3-integrin antibody on Ar-treated scaffolds, role of other cell surface receptors cannot be overlooked.
The data presented in this study show that the PSM scaffolds provide an optimum interface in terms of chemistry and topography after 5 minutes of treatment. The changes in the interfacial surface of polymer facilitated an optimum concentration and conformation of selective adhesion proteins, which resulted in enhanced cell attachment, growth and cellular function. It is possible that these interfacial changes induced by Ar allowed the highest number of proteins to be adsorbed in their optimal conformation due to moderate changes in surface hydrophilicity, roughness and surface chemistry. These surface changes resulted in higher cell attachment, growth and cellular function compared with O2 and N2 treatments. Figure S8 schematically explains this concept in more detail.
The observed short-term cell behavior was maintained in the long-term culture. The long-term cell survival and growth of HDF cells also led to the upregulation of several ECM-related genes including collagen type I, fibronectin, elastin and laminin (Figure 5). HDFs on Ar-treated scaffolds continued to express the highest level of ECM-related genes and also deposit corresponding ECM proteins (Figure S6). This confirmed that PSM enhances cellular function not only in the short term but also in long-term in vitro culture. Previous studies using PSM also showed an increase in the ECM production for other anchorage-dependent cells such as osteoblasts and chondrocytes.48,49
To ascertain the observed cellular behavior is not an effect of in vitro culture, further in vivo studies were conducted using mice model. Histological analysis of explanted scaffolds after 6 and 12 weeks showed a significantly higher level of tissue integration on PSM scaffolds compared with untreated scaffolds. However, it was highest on Ar-modified scaffolds compared with O2- and N2-treated scaffolds. Fibrous capsule formation around synthetic implants during in vivo studies is a common phenomenon. Examining the extent of fibrous capsule thickness can serve as good indicator of tissue material reaction. This study showed that the thickness of fibrous capsule formation on PSM scaffolds is significantly reduced compared with untreated scaffolds (Figure S7), suggesting that PSM not only facilitates tissue integration but also minimizes the inflammatory reactions.
The development of new blood vessels after clinical implantation of a material for restoration of facial defects is a limiting factor in all three-dimensional bioengineered constructs. Many growth factors are responsible for angiogenesis. Ring et al illustrated that dermal substitutes and allogenic bone implants enhanced their vascularization after Ar/hydrogen and Ar/O2 plasma treatment, respectively, using a dorsal skinfold chamber assay.50,51 In the current study, all plasma treatments led to increase in angiogenesis compared with untreated scaffolds. Ar treatment revealed the highest vessel formation as shown by CD31 staining (Figure 7A and B). During in vitro culture, HDFs secreted the highest amounts of VEGF (Figure 7C), which might have supported a greater influx and proliferation of endothelial cells and allowing for greater vessel formation in vivo.
In summary, to the best of our knowledge, this study for the first time reports a detailed investigation into the effect of various gases used for PSM on polymer surfaces and their effect on the short- and long-term tissue integration and angiogenesis. PSM significantly affected the surface chemistry of the polyurethane polymer, without affecting its bulk properties. Optimal PSM time for the polyurethane polymer was found to be 5 minutes based on both in vitro and in vivo studies for all the gases tested (Ar, O2 and N2). However, Ar modification was optimal for the polyurethane scaffolds in this study for the enhancement of cellular integration and angiogenesis. This is due to the unique combination of surface chemistry and topographical modification this treatment gas imparts.
Ar PSM is a simple, fast and very effective method of surface modification that can improve tissue integration and angiogenesis of polyurethane implants. Future work will investigate the effect of Ar surface modification on further clinically approved biomedical materials to assess its effectiveness at the clinical bedside.
This work was funded by the Medical Research Council and Action Medical Research Charity who provided MG a clinical fellowship to conduct this work; GN 2339.
MG performed all experiments and wrote the manuscript. RP performed XPS experiments and analysis of XPS data. VGBM performed analysis of the XPS data. PEB supervised all experiments and wrote the manuscript. DMK supervised all experiments, performed analysis of the data and wrote the manuscript. All authors contributed toward data analysis, drafting and critically revising the paper, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.
The authors report no conflicts of interest in this work.
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