Color evaluation of a dielectric mirror coating using porcine tissue and prosthetic gingival material: a comparison of two models.

AIM: The aim of this study was to firstly evaluate the esthetics of a dielectric multilayer coating on titanium below porcine tissue (in vitro porcine model). Secondly, a polymer model was used to investigate the same samples to compare the models to each other and discuss their validity for optical assessment of esthetic coatings for implant applications. MATERIALS & METHODS: A dielectric mirror coating was deposited on titanium substrates (Ti- Bragg) and tested below porcine tissue and polymer platelets of three test thicknesses (1 mm, 2 mm and 3 mm). Titanium without coating (Ti) was used as a negative control. Furthermore, the substrates were subjected to three different surface treatments (polished, machined and sand-blasted). The color difference values ΔL, Δa, Δb and ΔE were calculated for each sample. In total, six samples were tested in both models. Statistical analysis of the data (one sample Wilcoxon test, Kruskal-Wallis with Bonferroni-Holm corrected Mann-Whitney post hoc tests for multiple testing) was conducted for each sample in both evaluation methods. RESULTS: In the in vitro porcine model, sand-blasted Ti-Bragg and Ti samples showed ΔE values significantly above the threshold value of 3.70, indicating a dark appearance of the 1 mm thick covering tissue. As the test thickness increased, polished and machined Ti-Bragg samples were significantly invisible (ΔE < 3.70 with P < 0.05). Excessive brightening effects from Ti-Bragg samples were not observed from the in vitro porcine model, but below polymer platelets the samples exhibited significantly high ΔL values, which also resulted in a significant and visible color change (ΔE >> 3.70 with P < 0.05). CONCLUSION: Ti-Bragg was suggested to be an appropriate coating system for dental implants to improve the soft tissue esthetics. The design of this coating system can be adjusted by varying different parameters to satisfy the requirements of an esthetic coating. The polymer model is valid for test thicknesses of 2 and 3 mm, however, one might have to increase the thickness to 1.5 mm or alter the composition of the resin for 1 mm thick platelets to increase the opacity and therefore adapt to the soft tissue situation.

Fracture toughness of esthetic dental coating systems by nanoindentation and FIB sectional analysis.

Improving the esthetics of Ti-based dental implants is the last challenge remaining in the optimization process. The optical issues were recently solved by the application of highly and selectively reflective coatings on Ti implants. This work focuses on the mechanical durability of these esthetic ceramic based coating systems (with and without adhesion layers). The coating systems (Ti-ZrO2, Ti-Al-ZrO2, Ti-Ti-Al-ZrO2, Ti-Ag-ZrO2, Ti-Ti-Ag-ZrO2, Ti-Bragg and Ti-TiO2-Bragg) were subjected to nanoindentation experiments and examined using scanning electron microscopy and focused ion beam cross sectional analysis. Three coating systems contained adhesion layers (10nm of Ti or 60nm of TiO2 layers). The fracture toughness of selected samples was assessed applying two different models from literature, a classical for bulk materials and an energy-based model, which was further developed and adjusted. The ZrO2 based coating systems (total film thickness<200nm) followed a circumferential cracking behavior in contrast to Bragg coated samples (total film thickness around 1.5µm), which showed radial cracking emanating from the indent corners. For Ti-ZrO2 samples, a fracture toughness between 2.70 and 3.70MPam(1/2) was calculated using an energy-based model. The classical model was applied to Bragg coated samples and their fracture toughness ranged between 0.70 and 0.80MPam(1/2). Furthermore, coating systems containing an additional layer (Ti-Ti-Al-ZrO2, Ti-Ti-Ag-ZrO2 and Ti-TiO2-Bragg) showed an improved adhesion between the substrate and the coating. The addition of a Ti or TiO2 layer improved the adhesion between substrate and coating. The validity of the models for the assessment of the fracture toughness depended on the layer structure and fracture profile of the samples investigated here (classical model for thick coatings and energy-based model for thin coatings).

In vitro color evaluation of esthetic coatings for metallic dental implants and implant prosthetic appliances.

OBJECTIVES: The aim of this study was to characterize the optical properties of newly developed esthetic coatings for metallic implants and components for an improved peri-implant soft tissue appearance. MATERIAL AND METHODS: Pig maxillae (n = 6) were used for the in vitro color evaluation of coated and uncoated samples. Three different coating systems (Ti-ZrO(2), Ti-Al-ZrO(2), and Ti-Ag-ZrO(2)) were deposited on titanium substrates, which exhibited different roughness (polished, machined, and sand-blasted) and interference colors (pink, yellow, and white). Spectrophotometric measurements were made of samples below three different mucosa thicknesses (1 mm, 2 mm, and 3 mm) and titanium served as negative control. Color difference ΔE was calculated using ΔL, Δa, and Δb values for each sample (in total 30 samples). RESULTS: ΔE values were significantly above the threshold value of 3.70 for sand-blasted Ti and Ti-ZrO(2) samples when tested below 1 mm thick soft tissue, hence resulted in a dark appearance of the soft tissues. In contrast, Ti-Al-ZrO(2) and Ti-Ag-ZrO(2) samples showed significant ΔL values below 1 mm, which indicates a brightening of the covering tissue. In general, ΔE values decreased with increasing thickness of the tissue. At 3 mm thick tissue, ΔE values were significantly below 3.70 for Ti-Al-ZrO(2) and Ti-Ag-ZrO(2) samples. The preferable substrate surface should be machined due increased color brightness, good soft tissue integration and improved adhesion between coating and substrates. Improvement of the optical appearance of the metal was achieved with the coating systems Ti-Al-ZrO(2) and Ti-Ag-ZrO(2). Darkening effects could not be observed for these systems, and partially light brightening of the tissue was observed. Advantageous colors were suggested to be pink and yellow.

Non-targeted analysis of wastewater treatment plant effluents by high performance liquid chromatography-time slice-solid phase extraction-nuclear magnetic resonance/time-of-flight-mass spectrometry.

Extracts of effluents from two different wastewater treatment plants (WWTP) in Switzerland taken during the application period of pesticides were examined by coupling an HPLC-MS system to a nuclear magnetic resonance spectrometer using a post column peak trapping device. By trapping 1 min portions of the chromatogram onto post column solid phase extraction cartridges (time slice-SPE-NMR) a comprehensive overview of proton carrying constituents could be achieved. Non-supervised statistical analysis of the NMR spectra obtained by this approach revealed NMR resonances pointing to contaminants present in decreasing proton concentration in the extracts. Comparison of exact mass data acquired during the trapping process to these NMR resonances enabled the identification of the pesticides Linuron, Metazachlor, Ethofumesate, Isoproturon, Metamitron, Propazine and Chloridazon. Desaminometamitron, a known transformation product of Metamitron could also be identified together with unexpected highly concentrated C8, C10 and C12 fatty acids and their glycerol mono- and di esters. Other compounds identified were a drug metabolite (3-Carboxymefenamic acid), a sun screen agent (Ensulizole: 2-Phenyl-1H-1,3-benzodiazole-6-sulfonic acid) and industrial chemicals (Benzotriazole, N-Benzyl-indole). In addition, a number of well-resolved proton spectra cannot be attributed to a mass response showing the need of further investigations using 2D-NMR and different ionization techniques.

Comprehensive non-targeted analysis of contaminated groundwater of a former ammunition destruction site using 1H-NMR and HPLC-SPE-NMR/TOF-MS.

The aim of the present study was to explore the capabilities of the combination of 1H NMR (proton nuclear magnetic resonance) mixture analysis and HPLC-SPE-NMR/TOF-MS (high-performance liquid chromatography coupled to solid-phase extraction and nuclear magnetic resonance and time-of-flight mass spectrometry) for the characterization of xenobiotic contaminants in groundwater samples. As an example, solid-phase extracts of two groundwater samples taken from a former ammunition destruction site in Switzerland were investigated. 1H NMR spectra of postcolumn SPE enriched compounds, together with accurate mass measurements, allowed the structural elucidation of unknowns. This untargeted approach allowed us to identify expected residues of explosives such as 2,4,6-trinitrotoluene (2,4,6-TNT), Hexogen (RDX) and Octogen (HMX), degradation products of TNT (1,3,5-trinitrobenzene (1,3,5-TNB), 2-amino-4,6-dinitrotoluene (2-A-4,6-DNT), 3,5-dinitrophenol (3,5-DNP), 3,5-dinitroaniline (3,5-DNA), 2,6-dinitroanthranite, and 2-Hydroxy-4,6-dinitrobenzonitrile), benzoic acid, Bisphenol A (a known endocrine disruptor compound), and some toxicologically relevant additives for propelling charges: Centralite I (1,3-diethyl-1,3-diphenylurea), DPU (N,N-diphenylurethane), N,N-diphenylcarbamate (Acardite II), and N-methyl-N-phenylurethane. To our knowledge, this is the first report of the presence of these additives in environmental samples. Extraction recoveries for Centralite I and DPU have been determined. Contaminants identified by our techniques were quantified based on HPLC-UV (HPLC-ultraviolet detection) and 1H NMR mixture analysis. The concentrations of the contaminants ranged between 0.1 and 48 microg/L assuming 100% recovery for the SPE step.