Synthesis and Characterization of Mesoporous Mg- and Sr-Doped Nanoparticles for Moxifloxacin Drug Delivery in Promising Tissue Engineering Applications.

Mesoporous silica-based nanoparticles (MSNs) are considered promising drug carriers because of their ordered pore structure, which permits high drug loading and release capacity. The dissolution of Si and Ca from MSNs can trigger osteogenic differentiation of stem cells towards extracellular matrix calcification, while Mg and Sr constitute key elements of bone biology and metabolism. The aim of this study was the synthesis and characterization of sol-gel-derived MSNs co-doped with Ca, Mg and Sr. Their physico-chemical properties were investigated by X-ray diffraction (XRD), scanning electron microscopy with energy dispersive X-ray analysis (SEM/EDX), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), X-ray fluorescence spectroscopy (XRF), Brunauer Emmett Teller and Brunauer Joyner Halenda (BET/BJH), dynamic light scattering (DLS) and ζ-potential measurements. Moxifloxacin loading and release profiles were assessed with high performance liquid chromatography (HPLC) cell viability on human periodontal ligament fibroblasts and their hemolytic activity in contact with human red blood cells (RBCs) at various concentrations were also investigated. Doped MSNs generally retained their textural characteristics, while different compositions affected particle size, hemolytic activity and moxifloxacin loading/release profiles. All co-doped MSNs revealed the formation of hydroxycarbonate apatite on their surface after immersion in simulated body fluid (SBF) and promoted mitochondrial activity and cell proliferation.

Concentration, fractionation, and ecological risk assessment of heavy metals and phosphorus in surface sediments from lakes in N. Greece.

The presence of phosphorus (P) and heavy metals (HMs) in surface sediments originating from lakes Volvi, Kerkini, and Doirani (N. Greece), as well as their fractionation patterns, were investigated. No statistically significant differences in total P content were observed among the studied lakes, but notable differences were observed among sampling periods. HM contents in all lakes presented a consistent trend, i.e., Mn > Cr > Zn > Pb > Ni > Cu > Cd, while the highest concentrations were recorded in Lake Kerkini. Most of the HMs exceeded probable effect level value indicating a probable biological effect, while Ni in many cases even exceeded threshold effects level, suggesting severe toxic effects. P was dominantly bound to metal oxides, while a significant shift toward the labile fractions was observed during the spring period. The sum of potentially bioavailable HM fractions followed a downward trend of Mn > Cr > Pb > Zn > Cu > Ni > Cd for most lakes. The geoaccumulation index Igeo values of Cr, Cu, Mn, Ni, and Zn in all lakes characterized the sediments as "unpolluted," while many sediments in lakes Volvi and Kerkini were characterized as "moderately to heavily polluted" with regard to Cd. The descending order of potential ecological risk [Formula: see text] was Cd > Pb > Cu > Ni > Cr > Zn > Mn for all the studied lakes. Ni and Cr presented the highest toxic risk index values in all lake sediments. Finally, the role of mineralogical divergences among lake sediments on the contamination degree was signified.

Effect of ethanol/TEOS ratios and amount of ammonia on the properties of copper-doped calcium silicate nanoceramics.

Calcium magnesium silicate glasses could be suggested for the synthesis of scaffolds for hard tissue regeneration, as they present a high residual glassy phase, high hardness values and hydroxyapatite-forming ability. The use of trace elements in the human body, such as Cu, could improve the biological performance of such glasses, as Cu is known to play a significant role in angiogenesis. Nano-bioceramics are preferable compared to their micro-scale counterparts, because of their increased surface area, which improves both mechanical properties and apatite-forming ability due to the increased nucleation sites provided, their high diffusion rates, reduced sintering time or temperature, and high mechanical properties. The aim of the present work was the evaluation of the effect of different ratios of Ethanol/TEOS and total amount of the inserted ammonia to the particle size, morphology and bioactive, hemolytic and antibacterial behavior of nanoparticles in the quaternary system SiO2-CaO-MgO-CuO. Different ratios of Ethanol/TEOS and ammonia amount affected the size and morphology of bioactive nanopowders. The optimum materials were synthesized with the highest ethanol/TEOS ratio and ammonia amount as verified by the enhanced apatite-forming ability and antibacterial and non-hemolytic properties.

In vitro evaluation of the shear bond strength and bioactivity of a bioceramic cement for bonding monolithic zirconia.

STATEMENT OF PROBLEM: Adhesive cementation is the most common bonding strategy for zirconia restorations. Although cementation with a bioactive luting agent has been proposed as an alternative, how the bond strength compares is unclear. PURPOSE: The purpose of this in vitro study was to evaluate shear bond strength after cementing a monolithic zirconia ceramic to human dentin with a bioceramic cement, compare it with a traditional cement, and evaluate its bioactive properties. MATERIAL AND METHODS: A total of 120 dentin specimens and 120 yttria-stabilized tetragonal zirconia polycrystal (Y-TZP) (BruxZir) cylindrical specimens were used. Zirconia and dentin specimens were randomly divided into 8 study groups (n=15) based on 2 luting cement types (a bioceramic cement or glass ionomer cement as control), 2 airborne-particle abrasion protocols (50 µm or 110 µm), and 2 water storage durations (24 hours or 30 days). After the shear bond strength test using a universal machine at a crosshead speed of 1 mm/min, fracture patterns were evaluated under a stereomicroscope and a scanning electron microscope. Strength values were statistically analyzed with a 3-factor ANOVA model (α=.05). Bioactivity was evaluated in simulated body fluid (SBF). RESULTS: The control glass ionomer cement achieved significantly greater shear bond strength compared with the tested bioceramic cement. Mean bond strength values ranged from 2.52 MPa to 5.23 MPa for the bioceramic cement tested and from 4.20 MPa to 6.61 MPa for the control cement. The duration of water storage played a significant role in the bond strength, with groups stored for 30 days reaching higher bond strength values, whereas the particle size of airborne-particle abrasion did not have a significant effect. Failure types were primarily mixed. No apatite formation was recorded on the surface of the specimens even after 30 days of immersion in SBF. CONCLUSIONS: The evaluated cement did not develop apatite in SBF, and its bond strength values were below the control glass ionomer cement.

Color stability of lithium disilicate ceramics after aging and immersion in common beverages.

STATEMENT OF PROBLEM: The color of an esthetic restoration and its color stability are important for long-term success. However, the impact of common beverages on lithium disilicate ceramic is not well known. PURPOSE: The purpose of this in vitro study was to investigate color variations of lithium disilicate ceramics after thermocycling (TC) and immersion in commonly consumed beverages. MATERIAL AND METHODS: A total of 288 specimens (1×10×10 mm) were fabricated from IPS e-max computer-aided design (CAD) (n=72), IPS e-max CERAM ([CER] n=72), IPS e-max Press with glazing ([PG] n=72), and IPS e-max Press without glazing ([PNG] n=72) according to the manufacturer's instructions. Each group was divided into 4 subgroups (n=18): TC, coffee, black tea, and red wine. Thermocycling was performed at 21 900 cycles at 5°C, 37°C, 55°C, and 37°C (3 years' clinical simulation), whereas the specimens were soaked in the staining solutions for up to 54 hours (3 years' clinical simulation). Color parameters L*, a*, and b* were assessed with an ultraviolet-visible spectroscopy recording spectrophotometer. Color difference (ΔE) was calculated using the equation [ΔΕ= [(ΔL*)2 + (Δa*)2 + (Δb*)2]½]. Intraexaminer reliability was assessed by using the intraclass correlation coefficient. Two-way analysis of variance was used for the analysis of ΔΕ, and the parameters L*, a*, and b* were analyzed with linear mixed models for repeated measurements and the Bonferroni pair-wise comparison test (α=.05). RESULTS: Parameters ΔΕ, L*, a*, and b* were significantly affected by the interaction between material and treatment (P<.001). A ΔΕ >1 was recorded for PG with tea, wine, and coffee, PG after TC and CER after TC. For L*, greater reduction was observed for PNG with tea and CER after TC, whereas for a* significant changes were positive (to red shades), except for PNG with TC, where PNG with wine showed the greatest positive change. For b*, significant changes were negative (to blue shades) except for PNG with tea and coffee and CAD with tea. CONCLUSIONS: All groups demonstrated color changes below the clinically perceptible level (ΔΕ<3.7), except PNG in tea which showed statistically significant color differences (ΔΕ>4). CAD presented higher color stability compared with the nonglazed Press specimens.

Odontogenic differentiation and biomineralization potential of dental pulp stem cells inside Mg-based bioceramic scaffolds under low-level laser treatment.

This study aimed to investigate the potential of low-level laser irradiation (LLLI) to promote odontogenic differentiation and biomineralization by dental pulp stem cells (DPSCs) seeded inside bioceramic scaffolds. Mg-based, Zn-doped bioceramic scaffolds, synthesized by the sol-gel technique, were spotted with DPSCs and exposed to LLLI at 660 nm with maximum output power of 140 mw at fluencies (a) 2 and 4 J/cm2 to evaluate cell viability/proliferation by the MTT assay and (b) 4 J/cm2 to evaluate cell differentiation, using real-time PCR (expression of odontogenic markers) and a p-nitrophenylphosphate (pNPP)-based assay for alkaline phosphatase (ALP) activity measurement. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis were used for structural/chemical characterization of the regenerated tissues. Exposure of the DPSCs/scaffold complexes to the proposed LLLI scheme was associated with statistically significant increase of odontogenesis-related markers (bone morphogenetic protein 2 (BMP-2): 22.4-fold, dentin sialophosphoprotein (DSPP): 28.4-fold, Osterix: 18.5-fold, and Runt-related transcription factor 2 (Runx2): 3.4-fold). ALP activity was significantly increased at 3 and 7 days inside the irradiated compared to that in the non-irradiated SC/DPSC complexes, but gradually decreased until 14 days. Newly formed Ca-P tissue was formed on the SC/DPSC complexes after 28 days of culture that attained the characteristics of bioapatite. Overall, LLLI treatment proved to be beneficial for odontogenic differentiation and biomineralization of DPSCs inside the bioceramic scaffolds, making this therapeutic modality promising for targeted dentin engineering.

Characterization, heavy metal content and health risk assessment of urban road dusts from the historic center of the city of Thessaloniki, Greece.

In the present study, an investigation of the mineralogy and morphology, the heavy metal content and the health risk of urban road dusts from the second largest city of Greece was conducted. For this reason road dust samples from selected sites within the city core area were collected. No differences were observed in the mineralogy of road dusts coming from different sampling sites, and they were mainly consisted of quartz and calcite, while an elevated amorphous content was detected. Morphologically road dusts presented Ca-rich, Fe-rich and silicates particles with various shapes and sizes. The mean concentrations of Cd, Cr, Cu, Mn, Ni, Pb and Zn in road dust were 1.76, 104.9, 662.3, 336.4, 89.43, 209 and 452.8 µg g-1, respectively. A series of spatial distribution patterns revealed that the hotspot areas were tended to associate with major road junctions and regions with high traffic. Combination of pollution indexes and statistical analyses (correlation analysis, cluster analysis and principal component analysis) revealed that road dusts have a severe influence by anthropogenic activities. In attempt to identify the source of metals through geostatistical and multivariate statistical analyses, it was concluded as follows: Cr, Cu, Fe and Zn mainly originated from tire/break wear and vehicle abrasions, while Cd, Mn and Pb were mainly related to fuel/oil leakage from automobiles along with oil lubricants and vehicle abrasion. Hazard quotient values for children based on total metal concentrations for the road dust ingestion route were lower than safe level (=1). However, the fact that the Hazard Index value for Pb (0.459) which is a particularly toxic metal, was close to safe level, renders essential further investigation in order to provide more reliable characterizations of potential health risks.

Airborne 210Pb, Si, Zn and Pb as tracers for atmospheric pollution in Helsinki metropolitan area.

This study analyzed 16070 daily and 608 weekly air filter samples from the Helsinki metropolitan area collected between 1962 and 2005. The aim was to use the Potential Source Contribution Function (PSCF) to determine potential sources of silicon (Si), zinc (Zn), lead (Pb), and radioactive isotope 210Pb. The main sources for Si and Pb were industrial activities, particularly mining, metal industry, and traffic. Common source areas for Zn and 210Pb were identified in the eastern and southeastern parts of the measuring site.

Viability and Proliferation Assessment of Gingival Fibroblasts Cultured on Silver Nanoparticle-Doped Ti-6Al-4V Surfaces.

PURPOSE: To investigate the biocompatibility of silver nanoparticle (AgNP)-doped Ti-6Al-4V surfaces by evaluating the viability and proliferation rate of human gingival fibroblasts (HGFs)-as the dominant cells of peri-implant soft tissues-seeded on the modified surfaces. MATERIALS AND METHODS: AgNPs (sizes 8 nm and 30 nm) were incorporated onto Ti-6Al-4V specimen surfaces via electrochemical deposition, using colloid silver dispersions with increasing AgNP concentrations of 100 ppm, 200 ppm, and 300 ppm. One control and six experimental groups were included in the study: (1) control (Ti-6Al-4V), (2) 8 nm/100 ppm, (3) 8 nm/200 ppm, (4) 8 nm/300 ppm, (5) 30 nm/100 ppm, (6) 30 nm/200 ppm, and (7) 30 nm/300 ppm. HGF cell primary cultures were isolated from periodontally healthy donor patients and cultured in direct contact with the group specimens for 24 and 72 hours. The cytotoxicity of AgNP-doped Ti-6Al-4V specimens toward HGF was assessed by the MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) and BrdU (5-bromo-2'-deoxyuridine) assay tests. Calcein AM and ethidium homodimer (EthD-1) fluorescent stains were used to determine the live and dead cells. The morphology and attachment properties of the HGFs were determined via scanning electron microscopy (SEM). RESULTS: Energy dispersive x-ray (EDX) analysis confirmed the presence of AgNPs on the specimens. The MTT test revealed that AgNPs of both sizes and all concentrations presented a decreased cellular metabolic activity compared to the control discs. All concentrations of both sizes of AgNPs affected the cell proliferation rate compared to the control group, as revealed by the BrdU assay. Overall, cytotoxicity of the modified Ti-6Al-4V surfaces depended on cell exposure time. Observation via confocal microscopy confirmed the results of the MTT and BrdU assay tests. Specifically, most cells remained alive throughout the 72-hour culture period. SEM images revealed that adjacent cells form bonds with each other, creating confluent layers of conjugated cells. CONCLUSIONS: The findings of the present study indicate that Ti-6Al-4V surfaces modified with 8 nm and 30 nm AgNPs at concentrations of 100 ppm, 200 ppm, and 300 ppm do not produce any serious cytotoxicity toward HGFs. The initial arrest of the HGF proliferation rate recovered at 72 hours. These results on the antibacterial activity against common periodontal pathogens, in combination with the results found in a previous study by the same research group, suggest that AgNP-doped Ti-6Al-4V surfaces are potential candidates for use in implant abutments for preventing peri-implant diseases.

Removal of Bromine from Polymer Blends with a Composition Simulating That Found in Waste Electric and Electronic Equipment through a Facile and Environmentally Friendly Method.

The increasing volume of plastics from waste electric and electronic equipment (WEEE) nowadays is of major concern since the various toxic compounds that are formed during their handling enhance the difficulties in recycling them. To overcome these problems, this work examines solvent extraction as a pretreatment method, prior to thermochemical recycling by pyrolysis. The aim is to remove bromine from some polymeric blends, with a composition that simulates WEEE, in the presence of tetrabromobisphenol A (TBBPA). Various solvents-isopropanol, ethanol and butanol-as well as several extraction times, were investigated in order to find the optimal choice. Before and after the pretreatment, blends were analysed by X-ray fluorescence (XRF) to estimate the total bromine content. Blends were pyrolyzed before and after the soxhlet extraction in order to evaluate the derived products. FTIR measurements of the polymeric blends before and after the soxhlet extraction showed that their structure was maintained. From the results obtained, it was indicated that the reduction of bromine was achieved in all cases tested and it was ~34% for blend I and ~46% and 42% for blend II when applying a 6 h soxhlet with isopropanol and ethanol, respectively. When using butanol bromine was completely eliminated, since the reduction reached almost 100%. The latter finding is of great importance, since the complete removal of bromine enables the recycling of pure plastics. Therefore, the main contribution of this work to the advancement of knowledge lies in the use of a solvent (i.e., butanol) which is environmentally friendly and with a high dissolving capacity in brominated compounds, which can be used in a pretreatment stage of plastic wastes before it is recycled by pyrolysis.

Composite PLGA-Nanobioceramic Coating on Moxifloxacin-Loaded Akermanite 3D Porous Scaffolds for Bone Tissue Regeneration.

Silica-based ceramics doped with calcium and magnesium have been proposed as suitable materials for scaffold fabrication. Akermanite (Ca2MgSi2O7) has attracted interest for bone regeneration due to its controllable biodegradation rate, improved mechanical properties, and high apatite-forming ability. Despite the profound advantages, ceramic scaffolds provide weak fracture resistance. The use of synthetic biopolymers such as poly(lactic-co-glycolic acid) (PLGA) as coating materials improves the mechanical performance of ceramic scaffolds and tailors their degradation rate. Moxifloxacin (MOX) is an antibiotic with antimicrobial activity against numerous aerobic and anaerobic bacteria. In this study, silica-based nanoparticles (NPs) enriched with calcium and magnesium, as well as copper and strontium ions that induce angiogenesis and osteogenesis, respectively, were incorporated into the PLGA coating. The aim was to produce composite akermanite/PLGA/NPs/MOX-loaded scaffolds through the foam replica technique combined with the sol-gel method to improve the overall effectiveness towards bone regeneration. The structural and physicochemical characterizations were evaluated. Their mechanical properties, apatite forming ability, degradation, pharmacokinetics, and hemocompatibility were also investigated. The addition of NPs improved the compressive strength, hemocompatibility, and in vitro degradation of the composite scaffolds, resulting in them keeping a 3D porous structure and a more prolonged release profile of MOX that makes them promising for bone regeneration applications.

Flexural strength and the probability of failure of cold isostatic pressed zirconia core ceramics.

STATEMENT OF PROBLEM: The flexural strength of zirconia core ceramics must predictably withstand the high stresses developed during oral function. The in-depth interpretation of strength parameters and the probability of failure during clinical performance could assist the clinician in selecting the optimum materials while planning treatment. PURPOSE: The purpose of this study was to evaluate the flexural strength based on survival probability and Weibull statistical analysis of 2 zirconia cores for ceramic restorations. MATERIAL AND METHODS: Twenty bar-shaped specimens were milled from 2 core ceramics, IPS e.max ZirCAD and Wieland ZENO Zr, and were loaded until fracture according to ISO 6872 (3-point bending test). An independent samples t test was used to assess significant differences of fracture strength (α=.05). Weibull statistical analysis of the flexural strength data provided 2 parameter estimates: Weibull modulus (m) and characteristic strength (σ(0)). The fractured surfaces of the specimens were evaluated by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS). The investigation of the crystallographic state of the materials was performed with x-ray diffraction analysis (XRD) and Fourier transform infrared (FTIR) spectroscopy. RESULTS: Higher mean flexural strength (P<.001) and σ(0) were recorded for WZ ceramics. However IZ ceramics presented a higher m value and a microstructure with fewer voids and pores. The fractured surfaces presented similar fractographic properties (mirror regions followed by hackle lines zones). Both groups primarily sustained the tetragonal phase of zirconia and a negligible amount of the monoclinic phase. CONCLUSIONS: Although both zirconia ceramics presented similar fractographic and crystallographic properties, the higher flexural strength of WZ ceramics was associated with a lower m and more voids in their microstructure. These findings suggest a greater scattering of strength values and a flaw distribution that are expected to increase failure probability.

Effect of brominated flame retardant on the pyrolysis products of polymers originating in WEEE.

Chemical recycling is an environmentally friendly method, which is often used for the recycling of plastics included in waste electric and electronic equipment (WEEE), since fuels and secondary valuable materials can be produced. Brominated flame retardants (BFRs) are usually added into these plastics to reduce their flammability; but they are toxic substances. The aim of this work is to examine the thermal behaviour and the products obtained after pyrolysis of polymer blends that consist of acrylonitrile-butadiene-styrene (ABS), high-impact polystyrene (HIPS), polycarbonate (PC) and polypropylene (PP) with composition that simulates real WEEE, in the absence and presence of a common BFR, tetrabromobisphenol A (TBBPA), in order to investigate its effect on pyrolysis products. Blends were prepared via the solvent casting method and the melt-mixing in an extruder; it was revealed that the latter method may be a better choice for blends preparation, since it did not affect the products obtained. The chemical structure of each polymeric blend was identified by Fourier transform infrared spectroscopy (FTIR). Thermal degradation of the blends was evaluated by thermogravimetric (TG) experiments performed using a thermal analyser (TGA) and a pyrolyser for evolved gas analysis (EGA). It was observed that blends had a similar behaviour during their thermal degradation; and in most cases, they followed a one-step mechanism. Pyrolysis products were identified by the pyrolyser combined with a gas chromatographer/mass spectrometer (GC/MS), and comprised various useful compounds, such as monomers, aromatic hydrocarbons and phenolic compounds that could be used as chemical feedstock. Furthermore, it was found that TBBPA affected products distribution by enhancing the formation of phenolic compounds and on the other hand by resulting in brominated compounds, such as dibromophenol.

Effect of different zirconia surface pretreatments on the flexural strength of veneered Y-TZP ceramic before and after in vitro aging.

PURPOSE: The investigation of zirconia core surface pretreatments on the flexural strength of bilayered zirconia ceramics before and after artificial accelerating aging. METHODS: Ninety bar-shaped specimens were manufactured from Yttria Stabilized Tetragonal Zirconia Polycrystal (Y-TZP) and divided in three groups depending on zirconia surface pretreatment before veneering: layering with liner, pretreatment with silane-containing gas flame (SGF) with the Silano-Pen device and alumina air-abrasion. Half of the veneered specimens in each group (n=15) underwent artificial accelerating aging. A 4-point bending test was performed to determine flexural strength. Three specimens from each group were further analyzed using Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FTIR) before veneering and after fracture (aged and non-aged subgroups). RESULTS: Alumina air-abrasion was correlated to increased phase transformation from tetragonal to monoclinic zirconia phase. Qualitative analysis revealed that with the majority of the specimens pretreated with the silane-containing gas flame, areas of the veneering material remained firmly attached to the zirconia core after flexural strength testing. There was no statistically significant difference on the flexural strength among the groups before or after aging. Artificial accelerating aging resulted in statistically significant higher flexural strength of the specimens after aging. CONCLUSION: SGF pretreatment can be an acceptable and feasible alternative method before the veneering of Y-TZP zirconia as it presented slightly higher bond strength compared with alumina air-abrasion which was associated with higher tetragonal to monoclinic (t→m) phase transformation. Accelerating aging leads to an increase of the mechanical properties under in vitro conditions.

Novel Femto Laser Patterning of High Translucent Zirconia as an Alternative to Conventional Particle Abrasion.

BACKGROUND: currently applied surface treatments for zirconia bonding may create undesired microcracks and surface flaws. The aim of the present study was to evaluate the efficacy of alternative surface treatments on the shear bond strength of high translucency zirconia to 10-Methacryloyloxydecyl dihydrogen phosphate (MDP)-containing resin-based cement. METHODS: fifty disk-shaped specimens (10 mm × 5 mm) were fabricated from a commercial yttria-stabilized zirconia with 5 mole% yttrium oxide tetragonal zirconia polycrystal (5Y-TZP), and underwent air-abrasion with alumina particles (50 µm-AL50 and 90 µm-AL90), glass beads (GB 10-60 µm), and ablation with femtosecond laser (FEMTO). Shear bond strength was evaluated with a universal testing machine under a crosshead speed of 0.5 mm/min until fracture. Fracture type was evaluated with an optical stereomicroscope. Differences among groups were evaluated by one-way ANOVA and Bonferroni pairwise comparison tests (p < 0.05). RESULTS: the highest shear bond strength values were presented by the laser treated group (23.97 ± 3.7 MPa). No statistically significant differences were found among the Cl, Al50, Al90 and FEMTO groups. The lowest mean value was presented by the glass-beads treated group (11.93 ± 2.88 MPa) which was significantly lower compared to all other groups (p < 0.001). CONCLUSIONS: under the limitations of this in vitro study, femtosecond laser treatment of High-translucent monolithic zirconia (HTZ) ceramics is a promising alternative method for the mechanical retention of resin cements.

In vitro assessment of oral and respiratory bioaccesibility of trace elements of environmental concern in Greek fly ashes: Assessing health risk via ingestion and inhalation.

Fly ash engender significant environmental and human health problems due to enhanced contents of potentially harmful trace elements (TrElems). This study aims to evaluate human exposure to TrElems via a combined ingestion (i.e., oral bioaccessibility) and inhalation (i.e., respiratory bioaccessibility) pathway. Five fly ash samples were collected from power plants operating in the main lignite basins of Greece, while the ingestible (<250 µm) and inhalable (<10 µm) particle size fractions were utilized. The Unified Bioaccessibility Method (UBM) was utilized to assess the oral bioaccessibility, while the respiratory bioaccessible fractions were extracted using the Artificial Lysosomal Fluid (ALF). All studied FAs exhibited significantly higher contents in Ba, Cr, Ni, V and Zn. Cadmium was presented relative enriched in the finer size fraction (<10 µm), while Ba, Co, Cr, Cu, Mn, Ni and V were depleted. The UBM-extractable concentrations fluctuated greatly among the studied FAs, while notably lower bioaccessible contents were recorded in the gastrointestinal phase. On the other hand, ALF-extractable concentrations were surprisingly higher than the corresponding UBM-extractable ones in the gastric phase. The oral bioaccessibility of the studied TrElems ranged from 12.5 to 100%, while respiratory bioaccessibility presented high values exceeding 45% on average. A significant effect of fly ash type on human bioaccessibility was revealed. Thus, high-Ca FAs exhibited significantly higher bioaccessibility of the studied TrElems via ingestion, while a relatively higher bioaccessibility via inhalation was observed for high-Si FAs. Regarding non-carcinogenic health risk via ingestion and inhalation, Cr and Co exhibited the highest HQing and HQinh values, however there were significantly lower than safe level (HQ < 1). On the contrary, Cr was the dominant contributor to carcinogenic risk with CR values being well above threshold or even tolerable risk levels.

Design, characterisation and drug release study of polymeric, drug-eluting single layer thin films on the surface of intraocular lenses.

To design, develop and study a novel drug delivery system for intraocular applications. The spin coating technique was applied to develop a polymeric, drug-eluting thin film consisting of a blend of organic polymers [poly (D, L lactide coglycolide) lactide: glycolide 75: 25, PLGA and polycaprolactone, PCL] and dexamethasone on the surface of intraocular lenses (IOLs). The initial durability of the IOLs during spinning was assessed. Information about the structural and optical properties of the modified IOLs was extracted using atomic force microscopy, scanning electron microscopy and spectroscopic ellipsometry. A drug release study was conducted for 8 weeks. The IOLs were durable in spinning speeds higher than the ones used to develop thin films. Single-layer thin films were successfully developed on the optics and the haptics of the lenses. The films formed nanopores with encapsulated aggregates of dexamethasone. The spectroscopic ellipsometry showed an acceptable optical transparency of the lenses regardless of the deposition of the drug-eluting films on their surface. The drug release study demonstrated gradual dexamethasone release over the selected period. In conclusion, the novel drug-eluting IOL system exhibited desired properties regarding its transparency and drug release rate. Further research is necessary to assess their suitability as an intraocular drug delivery system.

The effect of different aging protocols on the flexural strength and phase transformations of two monolithic zirconia ceramics.

INTRODUCTION: The aim of the present study was to investigate how different aging protocols can affect the flexural strength and phase transformations of yttrium-stabilized zirconia ceramics (Y-TZP) for monolithic restorations. MATERIALS AND METHODS: Bar-shaped specimens from two zirconia ceramics bars were divided into three groups: a. no treatment (c), b. aging in an autoclave (a), and c. thermal cycling (t). The flexural strength was determined by the 3-point bending test and statistical analysis was performed to determine significant differences (p< 0.05). Weibull statistics was used to analyze the dispersion of strength values while surface microstructural analysis was performed through X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). RESULTS: Aging did not significantly affect the flexural strength but differences were recorded between the two groups, with group A presenting higher strength values and m-phase percentages. CONCLUSIONS: The observed differences between the two ceramics could be attributed to variations in composition and processing.

Morphological and geochemical characterization of the particulate deposits and the black crust from the Triumphal Arch of Galerius in Thessaloniki, Greece: Implications for deterioration assessment.

In the present study, 12 particulate deposits and one black crust sample were collected from the Triumphal Arch of Galerius in Thessaloniki, Greece and characterized by employing a multi-analytical approach including chemical analysis of trace elements and ionic species, as well as scanning electron microscopy coupled with energy dispersive X-ray spectrometry (SEM-EDS) to gain information about the micromorphology and the chemical composition in terms of major elements. In addition, one unaltered marble sample, e.g. the marble directly beneath the black crust, was examined by microscopic and isotopic methods to characterize its texture and origin. The particulate deposits consist mainly of calcite, quartz, aluminosilicate mineral phases, several metal oxides of Fe, Ti and FeCr with Mn and Cu. They also include bird droppings enriched in P and S, and plant residuals. The black crust has a similar mineral composition and is dominated by calcite with traces of quartz and halite, whereas P- and S-enriched particles are common. In both cases a coating on calcite crystals with a thin crust rich in Ca, Ba and S is commonly observed and is attributed to the previous conservation works. Concentrations of As, Zn, Pb, Cu, nitrate, sulfate, chloride and acetate were significantly higher in particle deposits than in the black crust as opposed to Fe, Co, Ni and formates that were at the same level. The traffic-related trace elements Pb, Zn and Cu and most ions were significantly higher in low-altitude deposition samples. The current marble deterioration is induced by a combination of factors, including mechanical, physico-chemical and biological processes.

Mechanical and thermal properties of PMMA resin composites for interim fixed prostheses reinforced with calcium ß-pyrophosphate.

Interim restorations are essential in fixed prosthodontics as they provide temporary protection of teeth before the insertion of the permanent restoration. Poly(methyl methacrylate) (PMMA) is widely used in the fabrication of interim-fixed restorations as it is a biocompatible material with a lot of convenient properties. However, it exhibits low impact and tensile strength and therefore it is necessary to be reinforced. Calcium ß-pyrophosphate (ß-CPP) is considered a promising reinforcing material for dental applications, especially for enamel regeneration due to its stability at low pH and its low wear rate. The aim of this study was to manufacture PMMA/ß-CPP composites suitable for fixed-interim restorations and to study their mechanical and thermal properties. In order to enhance ß-CPP dispersion into PMMA matrix, ball-milling was performed for 1 or 6 h. Three-point bending test was performed to study flexural strength, Dynamic Mechanical Analysis (DMA) to reveal the elastic and viscous moduli along with Tg, Fourier Transform Infrared Spectroscopy (FTIR) and X-Ray Diffraction Analysis (XRD) to investigate the structure of the materials and SEM for the morphological evaluation of both composite powders and polymerized specimens. Thermogravimetric Analysis (TGA) and Differential Scanning Calorimetry (DSC) experiments were performed to study their thermal properties. A statistically significant increase in flexural strength was found in the 0.5, 0.75 and 1% composite groups after 6 h ball-milling, relative to the control, with the 6 h ball milling mixed specimens, presenting the highest flexural strength values. The brittle fracture type was common to all groups. An obvious improvement of the mechanical properties and a slight improvement in the thermal stability of the composite materials values were also observed as ß-CPP content was increased, while Tg values were statistically not-affected.