A Novel Surface Modification Strategy via Photopolymerized Poly-Sulfobetaine Methacrylate Coating to Prevent Bacterial Adhesion on Titanium Surfaces

Recent investigations on the anti-adhesive properties of polysulfobetaine methacrylate (pSBMA) coatings had shown promising potential as antifouling surfaces and have given the impetus for the present paper, where a pSBMA coating is applied via photopolymerization on a macro-roughened, sandblasted, and acid-etched titanium implant surface in order to assess its antifouling properties. Current emphasis is placed on how the coating is efficient against the adhesion of Enterococcus faecalis by quantitative assessment of colony forming units and qualitative investigation of fluorescence imaging and scanning electron microscopy. pSBMA coatings via photopolymerization of titanium surfaces seems to be a promising antiadhesion strategy, which should bring substantial benefits once certain aspects such as biodegradation and osseointegration were addressed. Additionally, commercial SAL-titanium substrates may be coated with the super-hydrophilic coating, appearing resistant to physiological salt concentrations and most importantly lowering E. faecalis colonization significantly, compared to titanium substrates in the as-received state. It is very likely that pSBMA coatings may also prevent the adhesion of other germs

Ascorbic Acid/Retinol and/or Inflammatory Stimuli’s Effect on Proliferation/Differentiation Properties and Transcriptomics of Gingival Stem/Progenitor Cells

The present study explored the effects of ascorbic-acid (AA)/retinol and timed inflammation on the stemness, the regenerative potential, and the transcriptomics profile of gingival mesenchymal stem/progenitor cells’ (G-MSCs). STRO-1 (mesenchymal stem cell marker) immuno-magnetically sorted G-MSCs were cultured in basic medium (control group), in basic medium with IL-1β (1 ng/mL), TNF-α (10 ng/mL) and IFN-γ (100 ng/mL, inflammatory-medium), in basic medium with AA (250 µmol/L) and retinol (20 µmol/L) (AA/retinol group) or in inflammatory medium with AA/retinol (inflammatory/AA/retinol group; n = 5/group). The intracellular levels of phosphorylated and total β-Catenin at 1 h, the expression of stemness genes over 7 days, the number of colony-forming units (CFUs) as well as the cellular proliferation aptitude over 14 days, and the G-MSCs’ multilineage differentiation potential were assessed. Next-generation sequencing was undertaken to elaborate on up-/downregulated genes and altered intracellular pathways. G-MSCs demonstrated all mesenchymal stem/progenitor cells characteristics. Controlled inflammation with AA/retinol significantly elevated NANOG (p < 0.05). The AA/retinol-mediated reduction in intracellular phosphorylated β-Catenin was restored through the effect of controlled inflammation (p < 0.05). Cellular proliferation was highest in the AA/retinol group (p < 0.05)

Data supporting polymerization of anti-fouling polymer brushes polymerized on the pore walls of porous aluminium and titanium oxides

The data presented in this article affords insight into the fabrication and ensuing microstructure of the supported porous anodic aluminum oxide (AAO) and TiO2-nanotubes (NT) films that are used for the subsequent grafting of antifouling poly(oligo ethyleneglycol) methylether methacrylate (POEGMA) and poly acrylamide (PAAm) brushes. The experimental procedure for the grafting of POEGMA and PAAm via atom transfer radical polymerization (ATRP) is described in Wassel et al. (2019) https://doi.org/10.1016/j.matdes.2018.107542 [1]. The FTIR spectra of the porous oxides before and after attachment of (3-Aminopropyl)trimethoxysilane (APTMS) are presented. Microscopic images of thick POEGMA films and PAAm on AAO are displayed, and an FTIR spectrum of AAO/PAAm is shown. An EDX mapping of carbon is shown on an AAO/POEGMA sample. The adsorption behavior of Fluorescein isothiocyanate (FITC) marked bovine serum albumin (BSA) on patterned porous TiO2-NT films is documented. Finally microscopic images are presented to compare the scratch resistance behavior of pristine porous films with those functionalized with POEGMA

On-substrate, self-standing Au-nanorod arrays showing morphology controlled properties

We use supported alumina templates and electrodeposition to fabricate self-standing Au-nanorods (Au-NR) arrays. Depending on electrolyte and deposition conditions two different NR morphologies with either corrugated or smooth topologies are fabricated. We show that the properties of the NR arrays, including amphiphilic and optical, very much depend on their morphology. Smooth NR arrays are hydrophobic while the corrugated ones are hydrophilic. Also the optical reflectance, though it shows plasmon resonances at very similar wave lengths, is much lower for the corrugated NR arrays. The activity of the NR arrays as substrates for molecular detection using Raman scattering, and Rhodamine 6G (R6G) as model dye, also strongly depends on their morphology. R6G concentrations down to 1 pM are detected on the corrugated arrays yielding an effective enhancement factor (EF) of approximately 1 × 109. In contrast an over-estimated (because of their hydrophobic character) EF of 6 × 106 is obtained for the smooth NR arrays. © 2010 Elsevier Ltd

Self-standing corrugated Ag and Au-nanorods for plasmonic applications

We use home-made Si-supported anodized alumina thin film templates for the electrodeposition of large area self-standing Ag- and Au-nanorod (Au-NR) arrays. The deposition conditions chosen, i.e. electrolyte composition and deposition voltage, lead to a corrugated rod morphology, particularly for Au-NRs. Instantaneous nucleation followed by diffusion-controlled growth are thought to be the dominating mechanism for the morphology observed. Diffuse reflectance spectra show specific behaviours of Ag- and Au-NRs with longitudinal and transverse plasmon resonance modes and additional modes for Ag-NRs. The activity of the NR arrays as substrates for molecular detection using Raman scattering and Rhodamine 6G (R6G) as a model dye strongly depends on noble metal. R6G concentrations down to 1 pM are detected on the corrugated arrays yielding an effective enhancement factor (EF) of approximately 2 × 1010 for Ag-NRs and 1 × 109 for Au-NRs. The latter is the highest ever obtained for Au-nanostructures. Both nanostructures provide an enhancement that is high enough to detect single molecules using Raman scattering. The results are rationalized in terms of morphology effects on electromagnetic field intensity. © 2011 The Royal Society of Chemistry

Investigating adhesion of primary human gingival fibroblasts and osteoblasts to orthodontic mini-implants by scanning electron microscopy

Abstract Miniscrews offer controlled anchorage and thus optimize tooth movement in orthodontic treatment. Nevertheless, failures such as soft tissue problems, instability due to loosening, partial osseointegration, or even device fracture can occur. While clinical technique can play a role in some of these problems, the manufacturer’s design and material choice influence how the implant interacts with the surrounding tissue. In some cases, the design and material may trigger unwanted bone and soft tissue responses. This in vitro study investigates how the implant surface affects cell adhesion and growth of human primary fibroblasts and osteoblasts on commercially available orthodontic TiAl6V4 miniscrews from three producers: tomas-pin SD N 08 (Dentaurum), OrthoEasy Pin (Forestadent), and Dual Top G2 (Promedia, Jeil Medical). Cell–implant interaction at the top, neck, and drilling part of the screws was assessed qualitatively by scanning electron microscopy. While both cell types adhered to and grew on all products, subtle differences in cell shape and spreading were detected, depending on the microstructure of the implant surface. This indicates that cell adhesion to implant surfaces can be controlled by manipulating the machining conditions

A Bacteria and Cell Repellent Zwitterionic Polymer Coating on Titanium Base Substrates towards Smart Implant Devices

Biofouling and biofilm formation on implant surfaces are serious issues that more than often lead to inflammatory reactions and the necessity of lengthy post-operation treatments or the removal of the implant, thus entailing a protracted healing process. This issue may be tackled with a biocompatible polymeric coating that at the same time prevents biofouling. In this work, oxygen plasma-activated silanized titanium substrates are coated with poly(sulfobetaine methacrylate), a zwitterionic antibiofouling polymer, using photopolymerization. The characterization of polymer films includes FT-IR, AFM, and adhesion strength measurements, where adhesion strength is analyzed using a cylindrical flat punch indenter and water contact angle (WCA) measurements. Both cytotoxicity analysis with primary human fibroblasts and fluorescence microscopy with fibroblasts and plaque bacteria are also performed is this work, with each procedure including seeding on coated and control surfaces. The film morphology obtained by the AFM shows a fine structure akin to nanoropes. The coatings can resist ultrasonic and sterilization treatments. The adhesion strength properties substantially increase when the films are soaked in 0.51 M of NaCl prior to testing when compared to deionized water. The coatings are superhydrophilic with a WCA of 10° that increases to 15° after dry aging. The viability of fibroblasts in the presence of coated substrates is comparable to that of bare titanium. When in direct contact with fibroblasts or bacteria, marginal adhesion for both species occurs on coating imperfections. Because photopolymerization can easily be adapted to surface patterning, smart devices that promote both osseointegration (in non-coated areas) and prevent cell overgrowth and biofilm formation (in coated areas) demonstrate practical potential

Mesoporous and Macroporous Brookite Thin Films Having a Large Thermal Stability Range

A sol–gel chemistry approach is employed to generate mesoporous and macroporous brookite thin films using Ag ions as dopant species whose thermal stability is well above previously reported literature values for thin films. The Ag ions not only induce the formation of brookite but also participate in its enhanced thermal stability. Despite brookite being metastable in nature, which renders it a challenge to synthesize, it has been prescribed as a potential competitor to anatase. We have used a layer-by-layer approach to generate a mesoporous Ag-doped brookite structure at 500 °C with 95% composition by XRD. This tightly packed mesoporous structure can be described as striated grains of brookite protruding from the surface to form an interlocked network whose thermal stability spans up to 800 °C. The open structure of brookite makes it an apt host for the intercalant Ag species, whose inclusion within the brookite framework is improved by the presence of a stabilizing agent. Both the morphology of the surface and the presence of a stabilization agent for Ag contribute to enhancing its thermal stability. This is in contrast to the thermal stability of the macroporous brookite thin film, which was found to be lower (<700 °C) than that of the mesoporous brookite thin film. The reagents are deliberately chosen to produce a macroporous film in the absence of a stabilizing agent. Ag nodules are observed to be formed at 700 °C, which implies their limited intercalation into the brookite structure, thus rendering them relatively less stable. Moreover, the macroporous film being relatively more relaxed is more susceptible to phase transformation at a higher calcination temperature. Our results provide a platform that paves the way toward better control, thereby leading to a broader technological application of brookite

Nanocomposite Films of Laponite/PEG-Grafted Polymers and Polymer Brushes with Nonfouling Properties

We explore the suitability of nanocomposite thin films based on laponite nanomaterial and grafted antiadhesive polymers as transparent nonfouling surfaces. For this purpose, two polymers were chosen: a linear poly­(ethylene glycol) (PEG) silane, 2-[methoxy­(polyethyleneoxy)­propyl]-trimethoxysilane), and thermoresponsive poly­(oligo ethylene glycol)-methyl ether-methacrylate (POEGMA) brushes. PEG silane was grafted on the laponite nanoparticles in solution yielding homogeneous and transparent thin films via a dip coating procedure on glass and silicon substrates. POEGMA was grafted on laponite-(3-Aminopropyl)­trimethoxysilane (APTMS) nanocomposite films that were processed similarly to PEG-silane using atom transfer radical polymerization (ATRP). Film characterization with, among others, Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), and atomic force microscopy (AFM) attests to successful grafting of the polymers to the laponite nanoparticles. In particular, evidence of basal plane expansion of laponite with increasing silane concentration are obtained using XRD, while patent morphological changes are revealed with AFM. The results are discussed in terms of the different grafting sites on laponite and compared with literature. While LP-PEG-silane is easily applied to a surface from a precursor solution via a dip coating procedure LP-APTMS-OEGMA requires lots more chemicals, a thorough control of reaction parameters, and longer reaction time in order to generate films with the desirable properties. We therefore also addressed the antifouling properties of the films. These were tested together with control samples of bare glass and laponite thin films for 30 days in an algae container. More tests were conducted with fibroblast cell cultures. Our preliminary results show that grafting of PEG containing polymers and polymer brushes alters the properties of the laponite films from fouling to nonfouling surfaces. As a first estimate, the adhesion of particles (diatoms, algae, etc.) to surfaces is reduced by approximately 85% in the case of LP-PEG-silane and up to 92% in the case of LP-APTMS-POEGMA, in comparison to the control surfaces. Furthermore, practically no cell adhesion on such surfaces could be observed