Does silver diammine fluoride concentration influence on bonding to carious dentinal lesions in primary teeth?

PURPOSE: This in vitro study evaluated the microshear bond strength (µSBS) of a universal adhesive after silver diammine fluoride (SDF) application at different concentrations on carious dentinal lesions in primary teeth. METHODS: Flat dentin carious-induced surfaces from 40 primary molars were randomly assigned to four experimental groups: without SDF treatment (control), 12% SDF, 30% SDF, or 38% SDF application. After 14 days of storage in artificial saliva at 37 °C, a universal adhesive system (Scotchbond Universal, 3 M ESPE) was applied in the etch-and-rinse mode and resin composite cylinders were built (0.72 mm2). After 24 h of water storage, the µSBS test was performed and the failure mode was determined. Data were analysed using one-way ANOVA and Tukey's post hoc tests (α = 0.05). RESULTS: The application of 38% SDF resulted in higher µSBS mean than control and use of 12% SDF (p = 0.006). No significant differences were observed among control, 12% SDF, and 30% SDF. All specimens tested showed adhesive/mixed failure. CONCLUSION: The use of SDF does not jeopardise the bonding of a universal adhesive applied in the etch-and-rinse mode to carious dentinal lesions in primary teeth, irrespective of the product concentration.

Fatty acid composition of vegetable oil blend and in vitro effects of pharmacotherapeutical skin care applications.

Vegetable oils have been used for a plethora of health benefits by their incorporation in foods, cosmetics, and pharmaceutical products, especially those intended for skin care. This study aimed to investigate the cutaneous benefits of a vegetable oil blend (VOB) formulation and its fatty acid composition. The anti-inflammatory activity was studied in macrophages of RAW 264.7 cells by investigating the release of nitric oxide (NO), superoxide anion generation (O2-), tumor necrosis factor-alpha (TNF-α), and interleukin 6 (IL-6). ABTS cation radical scavenging capacity assay, ferric reducing antioxidant potential (FRAP), 2,2-diphenyl-1-picrylhydrazyl (DPPH), and NO free radical scavenging assays were used to evaluate the antioxidant activity. VOB was tested for its ability to stimulate fibroblast proliferation and migration using the scratch assay, and antibacterial activity by the microdilution test. The fatty acid profile of a freshly prepared VOB formulation was determined by gas chromatography before and after accelerated stability testing. Chemical composition of VOB revealed the presence of oleic acid (C18:1n-9; 63.3%), linoleic acid (C18:2n-6; 4.7%), and linolenic acid (C18:3n-6; 5.1%) as major mono- and polyunsaturated fatty acids. No changes in the organoleptic characteristics and fatty acid composition were observed after the accelerated stability test. VOB 100 µg/mL reduced the healing time by increasing the total number of cells in the wounded area by 43.0±5.1% compared to the negative control group. VOB also suppressed the pro-inflammatory TNF-α and IL-6 cytokines, and NO and O2- production in lipopolysaccharide-stimulated macrophage cells. In conclusion, the VOB formulation contributed to the improvement of current therapeutic strategies for cutaneous applications in skin care.

Fatty acid composition of vegetable oil blend and in vitro effects of pharmacotherapeutical skin care applications

Vegetable oils have been used for a plethora of health benefits by their incorporation in foods, cosmetics, and pharmaceutical products, especially those intended for skin care. This study aimed to investigate the cutaneous benefits of a vegetable oil blend (VOB) formulation and its fatty acid composition. The anti-inflammatory activity was studied in macrophages of RAW 264.7 cells by investigating the release of nitric oxide (NO), superoxide anion generation (O2-), tumor necrosis factor-alpha (TNF-α), and interleukin 6 (IL-6). ABTS cation radical scavenging capacity assay, ferric reducing antioxidant potential (FRAP), 2,2-diphenyl-1-picrylhydrazyl (DPPH), and NO free radical scavenging assays were used to evaluate the antioxidant activity. VOB was tested for its ability to stimulate fibroblast proliferation and migration using the scratch assay, and antibacterial activity by the microdilution test. The fatty acid profile of a freshly prepared VOB formulation was determined by gas chromatography before and after accelerated stability testing. Chemical composition of VOB revealed the presence of oleic acid (C18:1n-9; 63.3%), linoleic acid (C18:2n-6; 4.7%), and linolenic acid (C18:3n-6; 5.1%) as major mono- and polyunsaturated fatty acids. No changes in the organoleptic characteristics and fatty acid composition were observed after the accelerated stability test. VOB 100 µg/mL reduced the healing time by increasing the total number of cells in the wounded area by 43.0±5.1% compared to the negative control group. VOB also suppressed the pro-inflammatory TNF-α and IL-6 cytokines, and NO and O2- production in lipopolysaccharide-stimulated macrophage cells. In conclusion, the VOB formulation contributed to the improvement of current therapeutic strategies for cutaneous applications in skin care.

Discovering and quantifying nontrivial fixed points in multi-field models.

We use the functional renormalization group and the [Formula: see text]-expansion concertedly to explore multicritical universality classes for coupled [Formula: see text] vector-field models in three Euclidean dimensions. Exploiting the complementary strengths of these two methods we show how to make progress in theories with large numbers of interactions, and a large number of possible symmetry-breaking patterns. For the three- and four-field models we find a new fixed point that arises from the mutual interaction between different field sectors, and we establish the absence of infrared-stable fixed-point solutions for the regime of small [Formula: see text]. Moreover, we explore these systems as toy models for theories that are both asymptotically safe and infrared complete. In particular, we show that these models exhibit complete renormalization group trajectories that begin and end at nontrivial fixed points.

Stability of fixed points and generalized critical behavior in multifield models.

We study models with three coupled vector fields characterized by O(N_{1})⊕O(N_{2})⊕O(N_{3}) symmetry. Using the nonperturbative functional renormalization group, we derive ß functions for the couplings and anomalous dimensions in d dimensions. Specializing to the case of three dimensions, we explore interacting fixed points that generalize the O(N) Wilson-Fisher fixed point. We find a symmetry-enhanced isotropic fixed point, a large class of fixed points with partial symmetry enhancement, as well as partially and fully decoupled fixed-point solutions. We discuss their stability properties for all values of N_{1},N_{2}, and N_{3}, emphasizing important differences to the related two-field models. For small numbers of field components, we find no stable fixed-point solutions, and we argue that this can be attributed to the presence of a large class of possible (mixed) couplings in the three-field and multifield models. Furthermore, we contrast different mechanisms for stability interchange between fixed points in the case of the two- and three-field models, which generically proceed through fixed-point collisions.

Sustained and complete hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) degradation in zero-valent iron simulated barriers under different microbial conditions.

Flow-through columns packed with "aged" zero-valent iron (ZVI) between layers of soil and sand were constructed to mimic a one-dimensional permeable reactive iron barrier (PRB). The columns were continuously fed RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine, ca. 18 mg l(-1)) for over one year. Two columns were bioaugmented with dissimilatory iron reducing bacteria (DIRB) Shewanella algae BrY or Geobacter metallireducens GS-15 to investigate their potential to enhance the reactivity of aged iron by reductive dissolution of passivating iron oxides or via production of biogenic reactive minerals. A third column was not bioaugmented to evaluate colonization by indigenous soil microorganisms. [14C]-RDX was completely removed in all columns at the start of the iron layer, and concentration profiles showed rapid and sustainable RDX removal over one year; however, a phylogenetic profile conducted after one year using DGGE analysis of recovered DNA did not detect S. algae BrY or G. metallireducens in their respective columns. Bacterial DNA was recovered from within the ZVI. Several unidentified 14C-labeled byproducts were present in the effluent of all columns. Dissolved 14C removal and the detection of dissolved inorganic 14C in these columns (but not in the sterile control) suggest microbial-mediated mineralization of RDX and sorption/precipitation of degradation products. Enhanced RDX mineralization in bioaugmented columns was temporary relative to the indigenously colonized column. However, shorter acclimation periods associated with bioaugmented PRBs may be desirable for rapid RDX mineralization, thereby preventing breakthrough of potentially undesirable byproducts. Overall, these results show that high RDX removal efficiency by ZVI-PRBs is achievable and sustainable and that the efficacy and start-up of ZVI-PRBs might be enhanced by bioaugmentation.

Kinetics of Cr(VI) reduction by carbonate green rust.

The kinetics of Cr(VI) reduction to Cr(III) by carbonate green rust were studied for a range of reactant concentrations and pH values. Carbonate green rust, [FeII4FeIII2(OH)12][4H2O x CO3], was synthesized by induced hydrolysis (i.e., coprecipitation) of an Fe(ll)/Fe(III) solution held at a constant pH of 8. An average specific surface area of 47 +/- 7 m2 g(-1) was measured for five separate batches of freeze-dried green rust precipitate. Heterogeneous reduction by Fe(II) associated with the carbonate green rust appears to be the dominant pathway controlling Cr(VI) loss from solution. The apparent stoichiometry of the reaction between ferrous iron associated with green rust ([Fe(II)GR]) and Cr(VI) was slightly higherthan the expected 3:1 ratio, possibly due to the presence of other oxidants, such as oxygen, protons, or interlayer carbonate ions. The rate of Cr(VI) reduction was proportional to the green rust surface area concentration, and psuedo-first-order rate coefficients (kobs) ranging from 1.2 x 10(-3) to 11.2 x 10(-3) s(-1) were determined. The effect of pH was small with a 5-fold decrease in rate with increasing pH (from 5.0 to 9.0). At low Cr(VI) concentrations (<200 microM), the rate of reaction was first order with respect to Cr(VI) concentration, whereas, at high Cr(VI) concentrations, rates appearto deviate from first-order kinetics and approach a constant value. Estimated amounts of surface Fe(II) and total Fe(II) suggest that the deviation from first-order kinetics observed at higher Cr(VI) concentrations and the 50-fold decrease in rate observed upon three sequential exposures to Cr(VI) is due to exhaustion of available Fe(II).

Mass transport effects on the kinetics of nitrobenzene reduction by iron metal.

To evaluate the importance of external mass transport on the overall rates of contaminant reduction by iron metal (Fe0), we have compared measured rates of surface reaction for nitrobenzene (ArNO2) to estimated rates of external mass transport in a permeable reactive barrier (PRB). The rate of surface reaction was measured at a polished Fe0 rotating disk electrode (RDE) in an electrochemical cell, and the rate of mass transport was estimated from a correlation for mass transport in packed-bed reactors. The kinetics of ArNO2 reduction were studied in pH 8.4 borate buffer at a potential below which an oxide film would form. The cathodic current measured in this system was dependent on the electrode rotation rate, and the measured first-order heterogeneous rate coefficient for surface reaction [krxn = (1.7 +/- 0.2) x 10(-3) cm s-1] was about 10 times faster than the first-order mass transport rate coefficient (kmt approximately 2 x 10(-4) cm s-1) estimated for PRBs. The similarity between rates of surface reaction and mass transport suggest that it may be important to consider mass transport processes in the design of PRBs for contaminants such as nitroaromatics that are highly reactive with Fe0.

Effects of natural organic matter, anthropogenic surfactants, and model quinones on the reduction of contaminants by zero-valent iron.

Recent studies of contaminant reduction by zero-valent iron metal (Fe0) have highlighted the role of iron oxides at the metal-water interface and the effect that sorption has at the oxide-water interface on contaminant reduction kinetics. The results suggest that a variety of organic surface-active substances might enhance or inhibit contaminant degradation, depending on the degree to which they promote solubilization, sorption. and/or reaction. Of particular interest is the effect of natural organic matter (NOM), because of its ubiquitous presence in natural waters and amphiphilic properties; anthropogenic surfactants, because of their use in groundwater remediation; and certain quinones, which represent the redox-active functional groups associated with NOM. In this study, no well-defined effects of these substances were found on the reduction of nitro benzene by Fe0, but the reduction of carbon tetrachloride and trichloroethylene (TCE) was inhibited by NOM. Results with carbon tetrachloride showed that the inhibitory effect of humic acids was greater than fulvic acids, but that several quinonoid NOM model compounds (juglone, lawsone. and anthraquinone disulfonate) increased the rate of reduction by Fe0. Isotherms for adsorption of TCE and NOM onto Fe0 showed evidence of competition for surface sites.

Chemistry and microbiology of permeable reactive barriers for in situ groundwater clean up.

Permeable reactive barriers (PRBs) are receiving a great deal of attention as an innovative, cost-effective technology for in situ clean up of groundwater contamination. A wide variety of materials are being proposed for use in PRBs, including zero-valent metals (e.g., iron metal), humic materials, oxides, surfactant-modified zeolites (SMZs), and oxygen- and nitrate-releasing compounds. PRB materials remove dissolved groundwater contaminants by immobilization within the barrier or transformation to less harmful products. The primary removal processes include: (1) sorption and precipitation, (2) chemical reaction, and (3) biologically mediated reactions. This article presents an overview of the mechanisms and factors controlling these individual processes and discusses the implications for the feasibility and long-term effectiveness of PRB technologies.