Estudio de envejecimiento de poliamida de alto impacto marca Deflex® en saliva artificial comercial / Deflex® brand high impact polyamide aging study in commercial artificial saliva

Este trabajo presenta los resultados de un estudio de envejecimiento natural y acelerado en saliva artificial, de un material para uso odontológico de la marca Deflex® a base de poliamida de alto impacto, según lo establece la norma UNE EN IS0 10993-13 (2009) (AU)

is work presents the results of the study of natural and accelerated aging in artificial saliva, of a material for dental use of the brand Deflex® based on high impact polyamide, as established by the standard UNE EN IS0 10993-13 (2009) (AU)

Corn starch-based coating enriched with natamycin as an active compound to control mold contamination on semi-hard cheese during ripening.

The effectiveness of natamycin supported in corn starch-based films to control environmental molds (mainly Penicillium spp) activity that could colonize the surface of semi-hard cheese during ripening, was evaluated. The starch amount was maximized, and this was achieved by adding polyvinyl alcohol (PVA) and also polyurethane (PU) to the formulation. The PU acted as plasticizer and also provided functional groups that interacted with the natamycin and affected its diffusion. When 5 % PU was added, the natamycin migration of the coating doped with 1% natamycin was reduced by half. The natamycin distribution on both sides of the film was also evaluated, concluding that, in line with the reduced migration, when polyurethane is included, the formulation presents high hydrophobicity and natamycin is left with a preferential distribution towards the air face (exterior). For microbiological tests, microorganisms were isolated from cheese factories. Natamycin solutions showed inhibitory effect against environmental molds including Penicillium spp. Accordingly, films loaded with 0.1 % natamycin showed a significant inhibitory effect against Penicillium spp. The polymer combination in this work was optimized to obtain an active coating with good physicochemical properties and enriched with natamycin that has proven to be available for acting against molds and preferentially on the surface exposed to potential mold attack during ripening.

Photophysical properties of blue - emitting silicon nanoparticles.

Silicon nanoparticles with strong blue photoluminescence were synthesized by electrochemical etching of silicon wafers and ultrasonically removed under N(2) atmosphere in organic solvents to produce colloids. Thermal treatment leads to the formation of colloidal Si particles of 3 ± 1 nm diameter, which upon excitation with 340 - 380 nm light exhibited room temperature luminescence in the range from 400 to 500 nm. The emission and the one- and two-photon excitation spectra of the particles are not sensitive to surface functionalization with methyl 2-methylprop-2-enoate. However, the derivatized particles show higher emission quantum yields in air-saturated suspensions (44%) than the underivatized particles (27%), as well as higher stability of its dispersions.FTIR and XPS spectra indicate a significant surface oxidation of the particles. The Si:O:C ratio at the surface of the derivatized particles estimated from XPS is Si(3)O(6)(C(5)O(2)H(y))(1), with y = 7 - 8. Vibronic spacing is observed in both the emission and excitation spectra. The information obtained from one-photon excitation experiments (emission and excitation spectra, photoluminescence quantum yields, luminescence decay lifetimes and anisotropy correlation lifetimes), as well as from two-photon excitation fluorescence correlation spectroscopy (brightness and diffusion coefficients) and TEM indicate that the blue-emitting particles are monodisperse and ball-shaped. Particle size clearly determines the emission and excitation spectral region, as expected from quantum confinement, but the presence and extent of Si-O species on the silicon networks seem crucial for determining the spectrum features and intensity of emission. The nanoparticles could hold great potential as quantum dots for applications as luminescence sensors in biology and environmental science.

Film-forming microgels for pH-triggered capture and release.

The pH-responsive behavior for a series of lightly cross-linked, sterically stabilized poly(tertiary amine methacrylate)-based latexes adsorbed onto mica and silica was investigated using in situ tapping mode AFM at room temperature. The adsorbed layer structure was primarily determined by the glass transition temperature, T(g), of the latex: poly[2-(diethylamino)ethyl methacrylate]-based particles coalesced to form relatively featureless uniform thin films, whereas the higher T(g) poly[2-(diisopropylamino)ethyl methacrylate] latexes retained their original particulate character. Adsorption was enhanced by using a cationic poly[2-(dimethylamino)ethyl methacrylate] steric stabilizer, rather than a nonionic poly(ethylene glycol)-based stabilizer, since the former led to stronger electrostatic binding to the oppositely charged substrate. Both types of adsorbed latexes acquired cationic microgel character and swelled appreciably at low pH, even those that had coalesced to form films. Fluorescence spectroscopy was used to study the capture of a model hydrophobic probe, pyrene, by these adsorbed latex layers followed by its subsequent release by lowering the solution pH. The repeated capture and release of pyrene through several pH cycles was also demonstrated. Since these poly(tertiary amine methacrylate) latexes are readily prepared by aqueous emulsion polymerization and adsorption occurs spontaneously from aqueous solution, this may constitute an attractive route for the surface modification of silica, mica and other oxides.