Plasma-deposited AgOx-doped TiOx coatings enable rapid antibacterial activity based on ROS generation

Abstract To enable a rapid-acting antibacterial mechanism without the release of biocidal substances, TiO2 catalysts have been considered based on the generation of reactive oxygen species (ROS). Doping with dissimilar metals generates electron-hole pairs with narrow band gaps promoting the production of ROS. Here, plasma technology is investigated to deposit Ag nano islets on defective TiOx films, stabilized by plasma postoxidation suppressing Ag ion release. Importantly, ROS generation is maintained upon storage in the dark yet with diminishing efficacy; however, it can be restored by exposure to visible light. The rapid-acting antibacterial properties are found to strongly correlate with ROS generation, which can even be maintained by functionalization with hydrophobic plasma polymer films. The cytocompatible coatings offer promising applications for implants and other medical devices

Dissolution and transformation of cerium oxide nanoparticles in plant growth media

From environmental modeling of engineered nanomaterial (ENM) release, it is clear that ENMs will enter soils, where they interact with soil compounds as well as plant roots. We analyzed three different size groups of cerium dioxide nanoparticles (CeO2-NPs) in respect to chemical changes in the most common plant growth medium, Hoagland solution. We created a simple environmental model using liquid dispersions of 9-, 23-, and 64-nm-uncoated CeO2-NPs. We found that CeO2-NPs release dissolved Ce when the pH of the medium is below 4.6 and in the presence of strong chelating agents even at pH of 8. In addition, we found that in reaction with Fe2+-ions, equimolar amounts of Ce were released from NPs. We could elucidate the involvement of the CeO2-NPs surface redox cycle between Ce3+ and Ce4+ to explain particle transformation. The chemical transformation of CeO2-NPs was summarized in four probable reactions: dissolution, surface reduction, complexation, and precipitation on the NP surface. The results show that CeO2-NPs are clearly not insoluble as often stated but can release significant amounts of Ce depending on the composition of the surrounding medium

Extraction of Biofilms From Ureteral Stents for Quantification and Cultivation-Dependent and -Independent Analyses

Ureteral stenting is a common surgical procedure, which is associated with a high morbidity and economic burden, but the knowledge on the link between biofilms on these stents, morbidity, and the impact of the involved microbiota is still limited. This is partially due to a lack of methods that allow for a controlled extraction of the biofilms from stents. Development of an appropriate in vitro model to assess prevention of biofilm formation by antimicrobial coatings and biomaterials requires a profound understanding of the biofilm composition, including the involved microbiota. This work describes an analytical pipeline for the extraction of native biofilms from ureteral stents for both cultivation-dependent and -independent analysis, involving a novel mechanical abrasion method of passing stent samples through a tapered pinhole. The efficiency of this novel method was evaluated by quantifying the removed biofilm mass, numbers of cultivable bacteria, calcium content, and microscopic stent analysis after biofilm removal using 30 clinical stent samples. Furthermore, the extraction of in vitro formed Escherichia coli biofilms was evaluated by universal 16S quantitative PCR, a cultivation-independent method to demonstrate efficient biofilm removal by the new approach. The novel method enables effective contamination-free extraction of the biofilms formed on ureteral stents and their subsequent quantification, and it represents a useful tool for comprehensive examinations of biofilms on ureteral stents

Interaction of graphene-related materials with human intestinal cells: an in vitro approach

Graphene-related materials (GRM) inherit unique combinations of physicochemical properties which offer a high potential for technological as well as biomedical applications. It is not clear which physicochemical properties are the most relevant factors influencing the behavior of GRM in complex biological environments. In this study we have focused on the interaction of GRM, especially graphene oxide (GO),and Caco-2 cells in vitro. We mimiked stomach transition by acid-treatment of two representative GRM followed by analysis of their physicochemical properties. No significant changes in the material properties or cell viability of exposed Caco-2 cells in respect to untreated GRM could be detected. Furthermore, we explored the interaction of four different GO and Caco-2 cells to identify relevant physicochemical properties for the establishment of a material property–biological response relationship. Despite close interaction with the cell surface and the formation of reactive oxygen species (ROS), no acute toxicity was found for any of the applied GO (concentration range 0–80 μg ml−1) after 24 h and 48 h exposure. Graphene nanoplatelet aggregates led to low acute toxicity at high concentrations, indicating that aggregation, the number of layers or the C/O ratio have a more pronounced effect on the cell viability than the lateral size alone

Dissolution and transformation of cerium oxide nanoparticles in plant growth media

From environmental modeling of engineered nanomaterial (ENM) release, it is clear that ENMs will enter soils, where they interact with soil compounds as well as plant roots. We analyzed three different size groups of cerium dioxide nanoparticles (CeO2-NPs) in respect to chemical changes in the most common plant growth medium, Hoagland solution. We created a simple environmental model using liquid dispersions of 9-, 23-, and 64-nm-uncoated CeO2-NPs. We found that CeO2-NPs release dissolved Ce when the pH of the medium is below 4.6 and in the presence of strong chelating agents even at pH of 8. In addition, we found that in reaction with Fe2+-ions, equimolar amounts of Ce were released from NPs. We could elucidate the involvement of the CeO2-NPs surface redox cycle between Ce3+ and Ce4+ to explain particle transformation. The chemical transformation of CeO2-NPs was summarized in four probable reactions: dissolution, surface reduction, complexation, and precipitation on the NP surface. The results show that CeO2-NPs are clearly not insoluble as often stated but can release significant amounts of Ce depending on the composition of the surrounding medium.ISSN:1388-0764ISSN:1572-896

Recent Development in Phosphonic Acid-Based Organic Coatings on Aluminum

Research on corrosion protection of aluminum has intensified over the past decades due to environmental concerns regarding chromate-based conversion coatings and also the higher material performance requirements in automotive and aviation industries. Phosphonic acid-based organic and organic-inorganic coatings are increasingly investigated as potential replacements of toxic and inefficient surface treatments for aluminum. In this review, we have briefly summarized recent work (since 2000) on pretreatments or coatings based on various phosphonic acids for aluminum and its alloys. Surface characterization methods, the mechanism of bonding of phosphonic acids to aluminum surface, methods for accessing the corrosion behavior of the treated aluminum, and applications have been discussed. There is a clear trend to develop multifunctional phosphonic acids and to produce hybrid organic-inorganic coatings. In most cases, the phosphonic acids are either assembled as a monolayer on the aluminum or incorporated in a coating matrix on top of aluminum, which is either organic or organic-inorganic in nature. Increased corrosion protection has often been observed. However, much work is still needed in terms of their ecological impact and adaptation to the industrially-feasible process for possible commercial exploitation