Search Results (4)

Polypropylene (PP) nonwoven is widely used in biomedical textiles because of its lightweight and mechanical durability; however, its inherent hydrophobicity and chemical inertness limit further surface functionalization. In this study, a plasma-assisted UV grafting strategy was developed to fabricate thermo-responsive and antibacterial hydrogel coatings on PP nonwoven. Atmospheric-pressure plasma jet (APPJ) treatment was first employed to activate the PP nonwoven surface, followed by UV-induced graft polymerization of chitosan and N-isopropylacrylamide (NIPAAm), forming a chitosan-co-PNIPAAm hydrogel immobilized on the nonwoven substrate. Surface characterization using water contact angle measurement, Fourier transform infrared spectroscopy, and scanning electron microscopy confirmed effective plasma activation and successful hydrogel grafting. APPJ treatment significantly enhanced surface wettability, whereas subsequent UV grafting formed a continuous hydrogel on the PP nonwoven surface. The modified nonwoven exhibited distinct thermo-responsive swelling behavior in aqueous and simulated physiological environments, associated with the temperature-sensitive characteristics of the PNIPAAm component. In addition, the incorporation of chitosan imparted pronounced antibacterial activity against Escherichia coli, with inhibition zone diameters ranging from 14 to 16.5 mm, indicating high antibacterial sensitivity. Preliminary cytocompatibility evaluation further demonstrated favorable cell viability on the modified surfaces. This study demonstrates a scalable and low-temperature surface engineering approach for integrating stimuli-responsive and antibacterial hydrogel functionality into nonwoven polymer substrates, offering potential for advanced biomedical textile applications. Full article

The development of rapid analysis of human serum for the presence of allergen-specific Immunoglobulin E (IgE) is currently important. Consequently, we developed two types of three-dimensional (3D) protein biochips. The first one is a 3D hydrogel biochip containing hydrogel droplets with protein molecules (allergens, immunoglobulins and others). These droplets are disposed on elements consisting of short polymer brushes grafting from a surface of polybutylene terephthalate polymer. The immobilization of proteins was induced by short-wave ultraviolet (UV) radiation. On such a biochip, the kinetics of allergen–sIgE complex formation reached 60% of saturation for 6 h. Also, we developed a 3D brush microchip containing on the surface of a polyethylene terephthalate polymer the brush elements with protein molecules covalently immobilized by opening oxirane cycles by amino and thiol nucleophilic groups contained in proteins. In the case of the 3D brush microchip, the kinetics of allergen–sIgE complex formation reached 100% of saturation for 3 h, and fluorescent signals were 2–3 times higher than those of the 3D hydrogel biochip for some allergens. Thus, the comparative analysis revealed that 3D brush biochips are more useful for further studies of protein–protein interaction than 3D hydrogel ones. Full article

We demonstrate a single-component hydrophilic photocrosslinkable copolymer system that incorporates all critical functionalities into one chain. This design allows for the creation of uniform functional organic coatings on a variety of substrates. The copolymers were composed of a poly(ethylene oxide)-containing monomer, a monomer that can release a primary amine upon UV light, and a monomer with reactive epoxide or cyclic dithiocarbonate with a primary amine. These copolymers are easily incorporated into the solution-casting process using polar solvents. Furthermore, the resulting coating can be readily stabilized through UV light-induced crosslinking, providing an advantage for controlling the surface properties of various substrates. The photocrosslinking capability further enables us to photolithographically define stable polymer domains in a desirable region. The resulting copolymer coatings were chemically versatile in immobilizing complex molecules by (i) post-crosslinking functionalization with the reactive groups on the surface and (ii) the formation of a composite coating by mixing varying amounts of a protein of interest, i.e., fish skin gelatin, which can form a uniform dual crosslinked network. The number of functionalization sites in a thin film could be controlled by tuning the composition of the copolymers. In photocrosslinking and subsequent functionalizations, we assessed the reactivity of the epoxide and cyclic dithiocarbonate with the generated primary amine. Moreover, the orthogonality of the possible reactions of the presented reactive functionalities in the crosslinked thin films with complex molecules is assessed. The resulting copolymer coatings were further utilized to define a hydrophobic surface or an active surface for the adhesion of biological objects. Full article

Photocatalytic remediation represents a potential sustainable solution to the abatement of xenobiotic pollutants released within the water environment. Aeroxide^® P25 titanium dioxide nanoparticles (TiO₂ NPs) are well-known as one of the most efficient photocatalysts in several applications, and have also been investigated in water remediation as suspended powder. Recently, their application in the form of thin films has been revealed as a potential alternative to avoid time-consuming filtration processes. Polymers represent suitable substrates to immobilize TiO₂ NPs, allowing further production of thin films that can be exploited as a photoactive coating for environmental remediation. Nevertheless, the methods adopted to immobilize TiO₂ NPs on polymer matrix involve time-consuming procedures and the use of several reactants. Here, titanium dioxide-based nanocomposites (NCx) were obtained through a new approach based on Methyl Methacrylate in situ bulk polymerization and were compared with a blended mixture (BL). Their morphology and chemical–physical properties were investigated through Thermogravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), UV–Vis, and Raman spectroscopies. It was revealed that the in situ approach deeply influences the chemical–physical interactions between the polymer matrix and TiO₂ NPs. Photocatalytic experiments revealed the boosted photodegradation activity of NCx thin films, induced by the in situ approach. The photodegradation of paraquat and acetaminophen was also ascertained. Full article