10 research outputs found

    Influence of magnesium and strontium substitutions in the structure of hydroxyapatite lattice on the deposition rate and properties of the CaP coatings formed via RF-sputtering of the powder targets

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    This work is dedicated to studying of the properties of the calcium phosphate (CaP) coatings deposited on Ti substrates by radio-frequency magnetron sputtering (RFMS) of three hydroxyapatite-based powder targets: pure hydroxyapatite (HA), Mg-substituted HA (Mg-HA, Mg = 0.93 ± 0.13 at.%) and Sr-substituted HA (Sr-HA, Sr ∼ 0.47 at.%). The influence of ionic substitutions in the structure of the sputtered targets on the surface morphology, physicochemical properties of the coatings and their wettability were studied. It is revealed that Mg and Sr ionic substitutions in the crystal lattice of HA at these concentrations don't affect deposition rate, however, it influences morphology, wettability and elemental and phase composition of deposited coatings

    Comparison study on the properties of the CaP coatings formed by RF-magnetron sputtering of the Mg- and Sr-substituted ß-tricalcium phosphate and hydroxyapatite

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    This article describes the influence of Mg and Sr substitutions in the structure of -tricalcium phosphate and hydroxyapatite powder targets on the deposition rate of coatings formed via RF-magnetron sputtering and their properties. It was revealed that even low doses of ionic substitutions in -tricalcium phosphate significantly affect deposition rate, morphology and physico-chemical properties of respective coatings. Similar doses of these substitutions in hydroxyapatite are not enough to influence the deposition rate, but they affect coating properties

    Composite biphase coatings formed by hybrid technology for biomedical applications

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    Calcium-phosphate (CaP) coatings were formed via combining methods of microarc oxidation (MAO) and radiofrequency magnetron sputtering (RFMS). SEM, XPS, XRD and nanoindentation methods were used to study physico-chemical and mechanical properties of the coatings. It was revealed that the upper CaP layer changes the morphology of the coatings at the microscale and increases the Ca/P ratio of biphasic coatings

    Shape stabilization and laser triggered shape transformation of magnetic particle functionalized liquid metal motors

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    Liquid metal motors made from biologically benign gallium are promising candidates for various applications ranging from drug delivery to targeting and killing cancer cells directly. One of the main problems with this novel technology is the need to utilize a membrane, making it possible to maintain a defined shape in order to perform the required functions. For magnetic remote guidance, liquid metal motors can be doped with magnetic iron microparticles, forming a transition magnetic liquid. In an alternative approach liquid metal structures are coated with magnetite nanoparticles. We hereby present an approach to laminate biologically benign gallium-based magnetic liquid metal motors with a biodegradable and biocompatible macromolecular thin film to retain the initial shape. Thanks to the polymer lamination and by the help of magnetic fields, the presented liquid metal motors can be remotely guided. The shape retaining macromolecular thin film can be liquefied by photothermal effects such as laser irradiation in order to change the shape of the liquid metal motor into a droplet due to surface energy minimization, allowing for penetration of structures smaller than the initial motor size. This work uses a relatively large technical demonstrator to show the technical realization and properties of this novel system, which opens up new paths and potential applications

    Reactive magnetron plasma modification of electrospun PLLA scaffolds with incorporated chloramphenicol for controlled drug release

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    Surface modification with the plasma of the direct current reactive magnetron sputtering has demonstrated its efficacy as a tool for enhancing the biocompatibility of polymeric electrospun scaffolds. Improvement of the surface wettability of materials with water, as well as the formation of active chemical bonds in the near-surface layers, are the main reasons for the described effect. These surface effects are also known to increase the release rate of drugs incorporated in fibers. Herein, we investigated the effect of plasma modification on the chloramphenicol release from electrospun poly (lactic acid) fibrous scaffolds. Scaffolds with high—50 wt./wt.%—drug content were obtained. It was shown that plasma modification leads to an increase in the drug release rate and drug diffusion coefficient, while not deteriorating surface morphology and mechanical properties of scaffolds. The materials’ antibacterial activity was observed to increase in the first day of the experiment, while remaining on the same level as the unmodified group during the next six days. The proposed technique for modifying the surface of scaffolds will be useful for obtaining drug delivery systems with controlled accelerated release, which can expand the possibilities of local applications of antibiotics and other drugs

    Modification of the Ceramic Implant Surfaces from Zirconia by the Magnetron Sputtering of Different Calcium Phosphate Targets: A Comparative Study

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    In this study, thin calcium phosphate (Ca-P) coatings were deposited on zirconia substrates by radiofrequency (RF) magnetron sputtering using different calcium phosphate targets (calcium phosphate tribasic (CPT), hydroxyapatite (HA), calcium phosphate monobasic, calcium phosphate dibasic dehydrate (DCPD) and calcium pyrophosphate (CPP) powders). The sputtering of calcium phosphate monobasic and DCPD powders was carried out without an inert gas in the self-sustaining plasma mode. The physico-chemical, mechanical and biological properties of the coatings were investigated. Cell adhesion on the coatings was examined using mesenchymal stem cells (MSCs). The CPT coating exhibited the best cell adherence among all the samples, including the uncoated zirconia substrate. The cells were spread uniformly over the surfaces of all samples

    Polyether Ether Ketone Coated with Ultra-Thin Films of Titanium Oxide and Zirconium Oxide Fabricated by DC Magnetron Sputtering for Biomedical Application

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    Recently, polyether ether ketone has raised increasing interest in research and industry as an alternative material for bone implants. This polymer also has some shortcomings, as it is bioinert and its surface is relatively hydrophobic, causing poor cell adhesion and therefore slow integration with bone tissue. In order to improve biocompatibility, the surface of polyether ether ketone-based implants should be modified. Therefore, polished disc-shaped polyether ether ketone samples were surface-modified by direct current magnetron sputtering with ultrathin titanium and zirconium coatings (thickness < 100 nm). The investigation results show a uniform distribution of both types of coatings on the sample surfaces, where the coatings mostly consist of titanium dioxide and zirconium dioxide. Differential scanning calorimetry revealed that the crystalline structure of the polyether ether ketone substrates was not changed by the coating deposition. Both coatings are amorphous, as shown by X-ray diffraction investigations. The roughness of both coating types increases with increasing coating thickness, which is beneficial for cell colonization. The coatings presented and investigated in this study improve wettability, increasing surface energies, in particular the polar component of the surface energies, which, in turn, are important for cell adhesion

    Improvement of the Surface Properties of Polyether Ether Ketone via Arc Evaporation for Biomedical Applications

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    Polyether ether ketone is a bioinert polymer, that is of high interest in research and medicine as an alternative material for the replacement of bone implants made of metal. The biggest deficit of this polymer is its hydrophobic surface, which is rather unfavorable for cell adhesion and thus leads to slow osseointegration. In order to address this drawback, 3D-printed and polymer extruded polyether ether ketone disc samples that were surface-modified with titanium thin films of four different thicknesses via arc evaporation were investigated and compared with non-modified disc samples. Depending on the modification time, the thickness of the coatings ranged from 40 nm to 450 nm. The 3D-printing process does not affect the surface or bulk properties of polyether ether ketone. It turned out that the chemical composition of the coatings obtained did not depend on the type of substrate. Titanium coatings contain titanium oxide and have an amorphous structure. Microdroplets formed on the sample surfaces during treatment with an arc evaporator contain a rutile phase in their composition. Surface modification of the samples via arc evaporation resulted in an increase in the arithmetic mean roughness from 20 nm to 40 nm for the extruded samples and from 40 nm to 100 nm for the 3D-printed samples, with the mean height difference increasing from 100 nm to 250 nm and from 140 nm to 450 nm. Despite the fact that the hardness and reduced elastic modulus of the unmodified 3D-printed samples (0.33 GPa and 5.80 GPa) are higher than those of the unmodified extruded samples (0.22 GPa and 3.40 GPa), the surface properties of the samples after modification are approximately the same. The water contact angles of the polyether ether ketone sample surfaces decrease from 70° to 10° for the extruded samples and from 80° to 6° for the 3D-printed samples as the thickness of the titanium coating increases, making this type of coating promising for biomedical applications

    Modification of the Ceramic Implant Surfaces from Zirconia by the Magnetron Sputtering of Different Calcium Phosphate Targets: A Comparative Study

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    In this study, thin calcium phosphate (Ca-P) coatings were deposited on zirconia substrates by radiofrequency (RF) magnetron sputtering using different calcium phosphate targets (calcium phosphate tribasic (CPT), hydroxyapatite (HA), calcium phosphate monobasic, calcium phosphate dibasic dehydrate (DCPD) and calcium pyrophosphate (CPP) powders). The sputtering of calcium phosphate monobasic and DCPD powders was carried out without an inert gas in the self-sustaining plasma mode. The physico-chemical, mechanical and biological properties of the coatings were investigated. Cell adhesion on the coatings was examined using mesenchymal stem cells (MSCs). The CPT coating exhibited the best cell adherence among all the samples, including the uncoated zirconia substrate. The cells were spread uniformly over the surfaces of all samples

    Antibacterial Calcium Phosphate Coatings for Biomedical Applications Fabricated via Micro-Arc Oxidation

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    A promising method for improving the functional properties of calcium-phosphate coatings is the incorporation of various antibacterial additives into their structure. The microbial contamination of a superficial wound is inevitable, even if the rules of asepsis and antisepsis are optimally applied. One of the main problems is that bacteria often become resistant to antibiotics over time. However, this does not apply to certain elements, chemical compounds and drugs with antimicrobial properties. In this study, the fabrication and properties of zinc-containing calcium-phosphate coatings that were formed via micro-arc oxidation from three different electrolyte solutions are investigated. The first electrolyte is based on calcium oxide, the second on hydroxyapatite and the third on calcium acetate. By adding zinc oxide to the three electrolyte solutions, antibacterial properties of the coatings are achieved. Although the same amount of zinc oxide has been added to each electrolyte solution, the zinc concentration in the coatings obtained vary greatly. Furthermore, this study investigates the morphology, structure and chemical composition of the coatings. The antibacterial properties of the zinc-containing coatings were tested toward three strains of bacteria—Staphylococcus aureus, methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa. Coatings of calcium acetate and zinc oxide contained the highest amount of zinc and displayed the highest zinc release. Moreover, coatings containing hydroxyapatite and zinc oxide show the highest antibacterial activity toward Pseudomonas aeruginosa, and coatings containing calcium acetate and zinc oxide show the highest antibacterial activities toward Staphylococcus aureus and methicillin-resistant Staphylococcus aureus
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