Polymer Surface Research Articles

Engineering Nanoclusters of Cell Adhesive Ligands on Biomaterial Surfaces: Superior Cell Proliferation and Myotube Formation for Skeletal Muscle Tissue Regeneration.

Engineering biointerfaces with nanoscale clustering of integrin-binding cell adhesive peptides is critical for promoting receptor redistribution into signaling complexes. Skeletal muscle cells are exquisitely sensitive to integrin-mediated signaling, yet biomaterials supporting myogenesis through control of the density and nanodistribution of ligands have not been developed. Here, materials are developed with tailorable cell adhesive ligands distribution at the interface by independently controlling their global and local density to enhance myogenesis, by promoting myoblast growth and myotube formation. To this end, RGD-functionalized low-fouling polymer surfaces with global ligand densities (G) from 0-7µg peptide/mg polymer and average local ligand densities (L) from 1-6.3 ligands/cluster, are generated and characterized. Cell studies demonstrate improvements in cell adhesion, spreading, growth, and myotube formation up to a density of 7µg peptide/mg polymer with 4 ligands/cluster. Optimizing ligand density and distribution also promotes early myofiber maturation, identified by increased MF20 marker protein expression and sarcomere-forming myotubes. At higher ligand densities, these cell properties are decreased, indicating that ligand multivalency is a critical parameter for tailoring cell-material interactions, to a certain threshold. The findings provide new insights for designing next-generation biomaterials and hold promise for improved engineering of skeletal muscle.

Nanoimprinting of Crosslinked Polyurethane / Polycaprolactone Blends: Scratch Recovery of Surface Topographies.

Scratch recovery of micro-nano-patterned polymer surfaces extends the service life of products that require tunable surface properties and contributes to more sustainable development. Scratch recovery has been widely studied in bulk and 4D-printed polymers via intrinsic self-healing mechanisms. Existing studies on self-healing of micro/nano-scale polymeric surfaces are limited to the recovery of controlled tensile or compressive strain. Scratch recovery requires material transport to close the gap created by a scratch. Here, for the first time, scratch recovery of thermally nanoimprinted polymer surfaces in a heterogeneous polymer is reported. A blend of Polyurethane (TPU) and poly(caprolactone) (PCL) with selectively crosslinked TPU imparts shape-memory properties, and the uncrosslinked PCL retains chain mobility for molecular diffusion during scratch recovery. Scratch recovery of nanoimprinted micro-pillars has been achieved spontaneously and completely by heat and without any pressure input. The healing temperature is determined to be the melting point of PCL at 60°C. Rapid recovery is also achieved at 60 s with complete closure of scratch width of 5µm and topography recovery of the nanoimprinted micro-pillars.

The use of interphacial energies to estimate the spreading coefficients of organic liquids by the solid polymer surface of polytetrafluoroethylene

In the article, using equations previously obtained by the author, calculations were made of the interfacial energies of a solid polymer – polytetrafluoroethylene in contact with organic liquids and their vapors. Based on the calculation results, the spreading coefficients in the studied systems were calculated. Since Young’s derivation of the equation for the cosine of the contact angle, many researchers have attempted to determine the surface energy of solids, which would, in turn, make it possible to determine the interfacial energy at the solid-melt (liquid) interface. However, on the way to solving this problem there were obstacles associated with various processes that accompany phenomena occurring on the surface of a solid body in the presence of a liquid (melt) of another body on its surface. This is not the place to list all types of processes. They are well known to specialists in the field of surface phenomena. Here are just a few of them that affect the surface properties of bodies: chemical reactions, mutual dissolution of components of solid and liquid phases, deformation of solid phases, etc. In the case of contact of the polymer with organic liquids, such obstacles do not exist. Also, since it is impossible to dwell on all publications devoted to the determination of the surface energy of solids, the article discusses specific works on determining the interfacial energy at contact angles close to or equal to zero. Since the question of the behavior of interfacial energy at a contact angle equal to zero is of fundamental importance, and there are conflicting opinions in the literature on this matter, giving the correct answer to this question is an urgent task. Using examples of calculations of interfacial energies of homologous series of organic liquids on a solid surface of polytetrafluoroethylene, we have shown that only at zero contact angle the interfacial energy is zero. In this article, using interfacial energy values, we are the first to calculate the spreading coefficients of organic liquids over the surface of a solid polymer, which, in our opinion, is also an urgent task.

Thin-film electrodes of dielectric elastomer-based actuators for an active vibration control system

Precision research and technological equipment, as a rule, is not able to provide its specification characteristics without a high-quality vibration protection system. Active vibration control of an object is provided with the help of an additional source of movement, an actuator. The most promising high accuracy actuators are based on smart materials, such as materials with shape memory, piezoelectric and magnetostrictive materials, electro- and magnetic active fluids and elastomers. Dielectric elastomer is one of the types of electroactive polymers. Actuators based on a dielectric elastomer show high performance in terms of accuracy and speed and operate due to the controllable deformation of the elastomer under the action of a high voltage electric field. The paper provides a comparison of actuators based on sheet and thin film control electrodes. The influence of the quality of the polymer surface and the type of electrodes on the travel range of the actuator and maximum amplitude of vibrations the system can suppress on the basis of a dielectric elastomer is estimated. The formation of the electrode by magnetron sputtering in vacuum makes it possible to create a thin-film layer of copper that covers the elastomer, despite the developed surface. The effect of ion treatment of an elastomer before coating on the quality of the formed electrode is considered. After the ion treatment, the surface of the elastomer acquires a more uniform regular structure. A thin-film electrode layer is formed according to the topology of the elastomer to an accomplished standard.

Insights into the phase behavior at interfaces using vibrational sum frequency generation spectroscopy.

Phase separation is ubiquitous at the interface between two distinct phases. Physical transformation during phase separation often plays a crucial role in many important mechanisms, such as lipid phase separation, which is fundamental for transport through biological membranes. Phase separation can be complex, involving changes in the physical state and the reorganization of molecular structures, influencing the behavior and function of materials and biological systems. Surface-sensitive vibrational sum frequency generation (VSFG) spectroscopy provides a powerful tool for investigating these interfacial processes. As a non-linear optical technique, VSFG spectroscopy is sensitive to changes in molecular orientation and interactions at interfaces, making it an ideal method for studying phase separation processes. Here, we review the molecular interaction mechanisms underlying phase separation. We also explore the application of VSFG spectroscopy in studying phase separation processes at different interfaces. In particular, we focus on oil-water interfaces, which are relevant in environmental and industrial contexts; polymer and lipid surfaces, important for materials science and biological membranes; and intrinsically disordered protein systems, which play key roles in cellular function and disease.

Development of Functionalized Polylactide Thin Films Using Poly(methylhydrogenosiloxane) Sol-Gel Process with Improved Antifouling Properties.

Biobased polylactide (PLA) films were modified with low reticulate polysiloxane gel acting as a scalable platform for the hydrophilization of polymeric film surface. The PLA thin film was first coated with poly(methylhydrogenosiloxane) (PMHS) by the sol-gel transition via the condensation of diethoxymethylsilane (DH) and triethoxysilane (TH) using trifluoromethanesulfonic acid as a catalyst. Then, hydrosilylation of Si-H bonds in the presence of Karstedt's catalyst allowed the covalent grafting of hydrophilic alkene-containing molecules, i.e., triethylene glycol monomethyl allyl (TEGMEA) and a new zwitterionic allylcarboxybetaine (ACB) synthesized for the first time by the quaternization of dimethyl allyl amine (DMAA) with β-propiolactone. PMHS coating on the PLA film was evidenced by Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The observation by atomic force microscopy (AFM) revealed a homogeneous coating with low roughness (RMS = 0.29 nm). The hydrophilicity of functionalized PLA films was determined by water contact angle (WCA) measurements using the captive bubble method. A large increase in wettability properties was observed for both grafting with TEGMEA (WCA = 38°) and ACB (WCA = 42°) in comparison with the native PLA film (WCA = 80°). Moreover, the biocompatibility and antifouling efficiency of functionalized PLA films were evaluated by protein adsorption, bacterial adhesion, and cytotoxicity tests. The results indicate that the grafting of the two types of hydrophilic compounds does not affect the biocompatibility of PLA while significantly reducing protein adsorption and bacterial adhesion, thus showing the great potential of this surface functionalization strategy for applications in the medical field.

Catalytic Hydrolysis of Paraoxon by Immobilized Copper(II) Complexes of 1,4,7-Triazacyclononane Derivatives.

Organophosphate neuroactive agents represent severe security threats in various scenarios, including military conflicts, terrorist activities and industrial accidents. Addressing these threats necessitates effective protective measures, with a focus on decontamination strategies. Adsorbents such as bentonite have been explored as a preliminary method for chemical warfare agent immobilization, albeit lacking chemical destruction capabilities. Chemical decontamination, on the other hand, involves converting these agents into non-toxic or less toxic forms. In this study, we investigated the hydrolytic activity of a Cu(II) complex, previously studied for phosphate ester hydrolysis, as a potential agent for chemical warfare decontamination. Specifically, we focused on a ligand featuring a thiophene anchor bound through an aliphatic spacer, which exhibited high hydrolytic activity in its Cu(II) complex form in our previous studies. Paraoxon, an efficient insecticide, was selected as a model substrate for hydrolytic studies due to its structural resemblance to specific chemical warfare agents and due to the presence of a chromogenic 4-nitrophenolate moiety. Our findings clearly show the hydrolytic activity of the studied Cu(II) complexes. Additionally, we demonstrate the immobilization of the studied complex onto a solid substrate of Amberlite XAD4 via copolymerization of its thiophene side group with dithiophene. The hydrolytic activity of the resultant material towards paraoxon was studied, indicating its potential utilization in organophosphate neuroactive agent decontamination under mild conditions and the key importance of surface adsorption of paraoxon on the polymer surface.

Integration of nanomaterials in FDM for enhanced surface properties: Optimized manufacturing approaches

This article presents a comprehensive review of advanced techniques for integrating nanomaterials into fused deposition modeling (FDM) processes, addressing prevalent challenges such as limited surface quality and wear resistance in traditional FDM-printed parts. The integration of nanomaterials offers potential solutions to these issues by enhancing surface properties. This review explores key methodologies, including direct nanoparticle mixing with polymer filaments, in-situ polymerization, and surface coating techniques, and demonstrates their impact on improving surface roughness and wear resistance. Specifically, nanomaterial-enhanced composites achieve up to a 30% reduction in surface roughness and a 40% improvement in wear resistance compared to conventional materials. To optimize manufacturing processes, we apply the Taguchi method to identify critical process parameters such as extrusion temperature, print speed, layer thickness, and nanoparticle concentration that influence surface properties. Our simulations and analysis of variance (ANOVA) indicate that optimal settings can enhance surface quality by 25% and improve wear resistance by 35%. The proposed methodologies and theoretical framework lay the groundwork for experimental validation, which will involve testing the optimized parameters and assessing their practical impact. This research advances the field of additive manufacturing by providing novel insights into nanomaterial integration, paving the way for improved FDM technology with applications spanning aerospace, biomedical engineering, and beyond. The findings contribute significantly to overcoming existing limitations and enhancing the performance of FDM-printed parts.

Treatment of polyethylene microplastics degraded by ultraviolet light irradiation causes lysosome-deregulated cell death

BackgroundMicroplastics (MPs), plastic particles < 5 mm in size, are prevalent in the environment, and human exposure to them is inevitable. To assess the potential risk of MPs on human health, it is essential to consider the physicochemical properties of environmental MPs, including polymer types, size, shape, and surface chemical modifications. Notably, environmental MPs undergo degradation due to external factors such as ultraviolet (UV) rays and waves, leading to changes in their surface characteristics. However, limited knowledge exists regarding the health effects of MPs, with a specific focus on their surface degradation. This study concentrates on cytotoxic MPs with surface degradation through UV irradiation, aiming to identify the mechanisms underlying their cell toxicity.ResultsPolyethylene (PE) and surface-degraded PE achieved through UV light irradiation were employed as model MPs in this study. We explored the impact of PE and degraded PE on cell death in murine macrophage cell line RAW264.7 cells and human monocyte cell line THP-1 cells. Flow cytometric analysis revealed that degraded PE induced programmed cell death without activating caspase 3, while non-degraded PE did not trigger programmed cell death. These findings suggest that degraded PE might induce programmed cell death through mechanisms other than caspase-driven apoptosis. To understand the mechanisms of cell death, we investigated how cells responded to degraded PE-induced cellular stress. Immunofluorescence and western blotting analyses demonstrated that degraded PE induced autophagosome formation and increased p62 expression, indicating inhibited autophagy flux after exposure to degraded PE. Furthermore, degraded PE exposure led to a decrease in acidic lysosomes, indicating lysosomal dysregulation. These results imply that degraded PE induces lysosomal dysfunction, subsequently causing autophagy dysregulation and cell death.ConclusionsThis study unveils that UV-induced degradation of PE results in cell death attributed to lysosomal dysfunction. The findings presented herein provide novel insights into the effects of surface-degraded MPs on biological responses.

Effects of atmospheric pressure plasma treatment and its aging behaviors on interfacial strength of PI/PEEK composite film

AbstractSince the properties of surface roughness with time and the wettability pattern of polymer surfaces transformed by plasma remain unclear. In order to understand the mechanism of aging effect on film properties, this paper analyzes the aging of plasma‐treated PI films. The optimal treatment conditions were first explored by adjusting the plasma treatment power. Based on the effect of plasma treatment power on the surface physicochemical properties and mechanical properties of PI films. It was found that the content of oxygen‐containing functional groups on the surface of the film was highest at a plasma treatment power of 800 W, and the surface energy reached a maximum value of 67.71 mJ/m2. As the treatment power increases, the surface etching of the PI film increases significantly, as does the roughness. However, if the power is too high, it can cause excessive etching, resulting in peeling of the film surface. In addition, the mechanical properties of the films decreased with increasing plasma treatment power. Based on the effect of plasma treatment power on the surface physicochemical and mechanical properties of PI films, the best overall modification effect of PI films was determined when the treatment power was 800 W and the speed was 6 mm/s. And at 800 W, the peel strength of the PI/PEEK composite film reached a maximum value of 9.55 N/cm, which was 77.84% higher than that of the untreated composite film. However, plasma‐treated PI films can experience surface remodeling after being exposed to air for a period of time. In this paper, the wettability as well as the mechanical properties of the films are analyzed for different aging times. The results showed that after 30 days of plasma treatment, the O/C and N/C contents on the surface of the PI film decreased, and the wettability performance decreased by 19.45% compared with that of the recently treated film.

Rational design of pH-responsive nano-delivery system with improved biocompatibility and targeting ability from cellulose nanocrystals via surface polymerization for intracellular drug delivery

Cellulose nanocrystals (CNCs), derived from diverse sources and distinguished by their inherent biodegradability, excellent biocompatibility, and facile cellular engulfment due to their rod-like structure, hold great promise as carriers for the development of nano-delivery systems. In this work, highly efficient rod-like CNCs were employed as substrates for grafting glycidyl onto their surfaces through ring-opening polymerization, forming hyperbranched polymers with superior cell uptake properties. Subsequently, 4-vinylbenzeneboronic acid (VB) and poly (ethylene glycol) methyl ether methacrylate (PEGMA) were employed as monomers in the polymerization process to fabricate a pH-responsive targeted nano-delivery system, denoted as CNCs-VB-PEGMA, via single electron transfer reactive radical polymerization (SET-LRP) reaction. The CNCs-VB-PEGMA was successfully prepared and used for the loading of curcumin (Cur) to form a pH-responsive nano-delivery system (CNCs-VB-PEGMA-Cur), and the loading rate of Cur was as high as 70.0 %. Studies showed that this drug delivery system could actively targeting liver cancer cells with the 2D cells model and 3D tumor microsphere model, showing efficient liver cancer cell-killing ability. Collectively, the CNCs-VB-PEGMA drug delivery system has potential applications in liver cancer therapy as an actively targeting and pH-responsive drug delivery system.

Temporal evolution of mechanical properties in PDMS: A comparative study of elastic modulus and relaxation time for storage in air and aqueous environment

Polydimethylsiloxane (PDMS) is a soft, biocompatible polymer extensively employed in biomedical research, notable for its tunable mechanical properties achieved through cross-linking. While many studies have assessed the mechanical properties of PDMS utilizing macroscopic and microscopic methods, these analyses are often limited to freshly prepared samples. However, the mechanical properties of PDMS can be expected to change during prolonged exposure to water or air, such as interface polymer chain loosening or surface hardening, which are critical considerations in applications like cell culture platforms or microfluidic devices. This paper presents a comprehensive 10-day investigation of the evolution of PDMS surface mechanical properties through AFM-based nano-indentation. We focused on the most commonly utilized crosslinker-to-base ratios of PDMS, 1:10 (r10) and 1:20 (r20), under conditions of air and deionized water storage. For r10 samples, a hardening process was detected, peaking at 2.12 ± 0.35 MPa within five days for those stored in air and 1.71 ± 0.16 MPa by the third day for those immersed in water. During indentation, the samples displayed multiple contact points, suggesting the formation of distinct regions with varying mechanical properties. In contrast, r20 samples exhibited better stability, with an observed elastic modulus averaging 0.62 ± 0.06 MPa for air-stored and 0.74 ± 0.06 MPa for water-stored samples. Relaxation experiments, interpreted via the General Maxwell Model featuring two distinct component responses, a relatively consistent fast response τ1 (on the order of 10−1 s), and a more variable, slower response τ2 (on the order of 10 s), throughout the study period. The identification of two distinct relaxation times suggests the involvement of two disparate material property regimes in the relaxation process, implying changes in the surface material composition at the interface with air/water. These variations in mechanical properties could significantly influence the long-term functionality of PDMS in various biomedical applications.

Bacterial Degradation of Low-Density Polyethylene Preferentially Targets the Amorphous Regions of the Polymer.

Low-density polyethylene (LDPE) is among the most abundant synthetic plastics in the world, contributing significantly to the plastic waste accumulation problem. A variety of microorganisms, such as Cupriavidus necator H16, Pseudomonas putida LS46, and Pseudomonas chlororaphis PA2361, can form biofilms on the surface of LDPE polymers and cause damage to the exterior structure. However, the damage is not extensive and complete degradation has not been achieved. The changes in polymer structure were analyzed using Time-domain Nuclear Magnetic Resonance (TD-NMR), High-Temperature Size-Exclusion Chromatography (HT-SEC), Differential Scanning Calorimetry (DSC), and Gas Chromatography with a Flame Ionization Detector (GC-FID). Limited degradation of the LDPE powder was seen in the first 30 days of incubation with the bacteria. Degradation can be seen in the LDPE weight loss percentage, LDPE degradation products in the supernatant, and the decrease in the percentage of amorphous regions (from >47% to 40%). The changes in weight-average molar mass (Mw), number-average molar mass (Mn), and the dispersity ratio (Đ) indicate that the low-molar mass fractions of the LDPE were preferentially degraded. The results here confirmed that LDPE degradation is heavily dependent on the presence of amorphous content and that only the amorphous content was degraded via bacterial enzymatic action.

Peeling-induced interfacial roughness and charging for enhanced triboelectric power generation

To date, there have been a lot of efforts to enhance the conversion efficiency of triboelectric nanogenerators (TENGs) via physical and chemical modifications of the polymer surface. Herein, we report that a facile peeling of polymer from a substrate can enhance the triboelectric power output. The peeling of spin-coated polydimethylsiloxane (PDMS) from glass and polytetrafluoroethylene (PTFE) substrates has revealed a considerable increase in interfacial roughness and lateral friction. Surface-sensitive X-ray photoemission spectroscopy and non-contact current measurements have also revealed the transfer of counter-material and interfacial charging. The surface roughness of peeled PDMS is significant for the PTFE substrate, while the surface charge is significant for the glass substrate. The triboelectric output power density for peeled PDMS from the substrate is similar, 10.3 µW/cm2, but significantly larger than that for as-grown PDMS (2.2 µW/cm2). The peeling strength of PDMS significantly increases for glass compared to PTFE after the oxygen plasma treatment of substrates. The triboelectric charge of peeled PDMS from a plasma-treated glass substrate is almost 1.3 times larger than that from a PTFE substrate. This work implies that peeling polymer from a rough substrate with a large adhesion force would be a facile and effective way to increase the triboelectric power output, without any delicate surface treatments.

Studying the Feasibility of Creating Anisotropic Highly Hydrophobic Polymer Surfaces by Ion-Track Technology

Studying the Feasibility of Creating Anisotropic Highly Hydrophobic Polymer Surfaces by Ion-Track Technology

Density Functional Theory analysis and molecular dynamic simulation to understand the mechanism of hazardous dyes adsorption onto cellulose in aqueous solution

This work examines the use of cellulose in the elimination of anionic dye, indigo carmine and methyl red, from aqueous media. Theoretical analyses revealed that the examined compounds had several reactive sites that encouraged dyes to adhere to the cellulose surface, and molecular dynamics simulations demonstrated that this adsorption occurred flat-lying on the cellulose (200) surface. However, it has been discovered that the reactivity of individual molecules is limited in its ability to foretell the effectiveness and characteristics of compound adsorption on cellulose. The capacity to model dye adsorption on polymeric surfaces in the presence of a simulated aqueous solution is one of the key benefits of molecular dynamics modeling, and it can reveal valuable information regarding the selected molecules' adsorption configuration and its competitiveness. Both dyes exhibit high adsorption on the cellulose adsorbent, indicating that chemical bonds play a major role in the adsorption capacity of the dyes. The order of adsorption energy indicates a clear selective adsorption tendency. The radial distribution function analysis shows that both dyes are chemisorbed at the cellulose surface. Quantum and dynamic descriptors have validated the experimental results in the literature. This offers valuable insights into the adsorption mechanism of anionic dyes on cellulose.

Plasma-chamber wall interaction and its impact on polymer deposition in inductively-coupled C4F8/Ar plasmas

Plasma processing chambers, key tools in semiconductor device fabrication, must be meticulously maintained to ensure tool-to-tool matching. Processing chamber walls are liable to contamination with fluorocarbon (CxFy) film, which acts as a source and/or sink for active species during plasma processes. This contamination potentially affects processing quality and alters the plasma properties, increasing deviations between processing chambers. However, quantitative studies on the impact of wall contamination on the substrate deposition outcomes have been limited. Additionally, spatially resolved investigations are crucial for understanding the plasma-wall interaction. Therefore, this study evaluated the influence of polymer (CxFy) film wall contamination on plasma deposition via various plasma diagnostics and surface analyses. When the chamber inner wall was coated with polymer film, the thickness, surface roughness, and chemical composition of the deposited film on the bottom substrate were more uniform. These results were linked to alterations in the uniformity of active species in the plasma, such as CF2 and F, resulting from interaction with the polymer film on the wall's surface. The C–Fx and C–CFx composition ratios in the wall-coated films dramatically reduced, indicating that this film supplied the depositing precursors to the plasma. These results suggest that controlling the chamber wall conditions is important to maintain tool-to-tool matching and modulate the processing performance.

Fine carbonyl iron particles grafted with poly(2-isopropenyl-2-oxazoline): A potential embolization agent for cancer therapy

Despite the significant success of clinical trials on cancer patients using the therapy with carbonyl iron (CI) particles, this topic laid dormant for over two decades. In this context, we developed a CI particle-based embolization agent via polymer surface engineering and tested its biocompatibility and behavior in contact with human blood. The finest grade of the CI particles was controllably grafted with poly(2-isopropenyl-2-oxazoline) (PiPOx) using surface-initiated atom transfer radical polymerization (ATRP) to achieve a system combining the properties of suitable size, high magnetization, and advantages at the cellular level connected to the presence of PiPOx. The cell viability of 3T3 fibroblasts and P388.D1 macrophages was investigated after treatment with particle extracts and was found to be concentration-dependent but generally demonstrated no or mild cytotoxicity. The PiPOx-grafted particles showed negligible effect on the breakdown of human erythrocytes and significantly improved hydrophilic-hemophilic properties when compared to bare CI. The magnetorheological (MR) activity of the particles dispersed in human blood was studied in vitro under shear mode conditions showing slightly decreased shear stresses but improved sedimentation stability. Moreover, the effect of PiPOx molecular weight on the studied parameters was monitored across the whole range of tests. The study demonstrates the potential of prepared core-shell structures in biomedical and related fields of application.

Robust superhydrophobic copper oxide layer with high-low staggered structure on polymers for strong anti-icing and all-day de-icing

Recently, superhydrophobic materials with photothermal and electrothermal conversion functions have received much attention in solving icing problems. However, the currently emerging methods still suffer from the complexity of the preparation method, poor hydrophobicity, or poor abrasion resistance. Herein, a robust copper oxide layer with a high-low staggered structure was prepared on the polymer surface by laser-induced selective metallization (LISM), which can be used for anti-icing and all-day (daytime and night) de-icing. The high-low staggered structure of the superhydrophobic copper oxide surface gives the surface excellent hydrophobicity, light trapping capability, and high electrical resistance, resulting in the surface with superior delayed icing, photothermal de-icing, and electrothermal de-icing capabilities. The copper oxide layer has a water contact angle (CA) of up to 161.3° and a surface delayed icing time of 1374 s, which is 8.23 times longer than the conventional copper layer prepared by LISM. In addition, the surface temperatures of the copper oxide layer are 67.6 °C and 57.3 °C, respectively, under 1.0 sun irradiation or at 5 V applied voltage. Under these conditions, the copper oxide surface’s photothermal and electrothermal de-icing times are 159 and 186 s. In addition, the high-low staggered structure of the prepared superhydrophobic copper oxide surface makes the surface less susceptible to abrasion, resulting in excellent mechanical robustness of the copper oxide layer surface. The proposed method is suitable for low-cost large-scale manufacturing, which guides the preparation of copper oxide superhydrophobic materials for anti-icing and all-day de-icing, and has good application prospects.

POLYETHYLENE TEREPHTHALATE (PET) COATED WITH CHITOSAN AND CYCLOSPORINE A LAYERS AS A POTENTIAL STENT MATERIAL AND DRUG-DELIVERY SYSTEM

The aim of this paper was to design, prepare and characterise chitosan (Ch) and cyclosporine A (CsA) mixed films deposited on a plasma-activated polyethylene terephthalate (PET) polymer surface to be used as a cover for implantable blood vessel stents. The PET polymer coated with Ch and CsA layers was immersed in simulated body fluid (SBF) to examine how the obtained layers can behave in the environment of human body fluids. Time-of-flight secondary ion mass spectrometry was employed to determine the chemical composition of the deposited films and to analyse the spatial distribution of molecules on the PET surface. The results showed the controlled release of CsA from the chitosan matrix. It can be concluded that the modification of the PET polymer with layers of chitosan and CsA has great application potential in the tissue engineering as a biocompatible stent of blood vessels with therapeutic properties.