l-Lactic acid biosensor based on multi-layered graphene

Pristine graphene platelets and graphene oxide were used as electrode modifiers, aiming the investigation of their electrochemical efficacy towards β-nicotinamide adenine dinucleotide (NADH). The electrochemical detection of NADH is one of the most studied areas of bioelectroanalysis because of the ubiquity of NAD(P)H-based enzymatic reactions in nature. Commercially available graphene and laboratory prepared graphene oxide were used to modify glassy carbon electrodes and the behaviour of such modified electrodes against potassium ferricyanide (III) and NADH was reported. Relying on the graphene-modified transducer, l-lactic dehydrogenase (l-LDH) was successfully immobilised in a 1 % Nafion^® membrane. The developed biosensor, working at +250 mV versus Ag/AgCl reference electrode, was used to assess l-lactic acid in four different types of yogurts, revealing an l-lactic acid concentration ranging between 0.3 and 0.6 %.     

IrO2–SnO2 mixtures as electrocatalysts for the oxygen reduction reaction in alkaline media

In this work, SnO₂ + IrO₂ mixed oxides are studied as electrocatalysts for the oxygen reduction reaction (ORR) in alkaline media by means of voltammetric techniques under controlled mass transfer conditions thanks to the use of rotating (ring) disk electrodes (RDE/RRDE). The oxides, prepared by sol–gel methodology, are supported on the disk electrodes using a thin layer of anionic exchange polymer as gluing agent. The amount of deposited polymer was optimized to avoid any limitation due to the diffusion of reactant/products across the film thickness. The mixed oxides were prepared at the following mole fractions of IrO₂: $ x_{{{\text{IrO}}_{ 2} }} $  = 0.15, 0.31, 0.55, 0.73, and 1. The role of composition was studied in terms of the reaction pathways and the relevant fraction of H₂O₂ production, together with the potentials of the onset of ORR. The fraction of sites able to give proton/hydroxyl and electron transfers is also determined and discussed. The results point to the best performance of low-Ir containing mixtures and to their low sensitivity to the presence of methanol, a key feature in the case of crossover in alkaline direct alcohol fuel cells.     

A novel electron beam-based method for the immobilization of trypsin on poly(ethersulfone) and poly(vinylidene fluoride) membranes

A novel technique for the covalent immobilization of trypsin in a one-step reaction using low-energy electron beam is described. The enzyme immobilization was applied on poly(ethersulfone) and poly(vinylidene fluoride) microfiltration membranes. For this purpose, the membranes were dipped in an aqueous solution of trypsin followed by electron beam treatment.The effect of irradiation conditions on the immobilization was investigated, as well as the resulting membrane properties with respect to enzymatic activity, immobilized enzyme concentration, pure water flux, scanning electron microscopy, and porosimetry. This technique shall provide a simple, inexpensive method for enzyme immobilization on various polymer membranes and offer a tool for the application in enzymatic membrane reactors.     

A transcultural study on stirred strawberry yogurt: consumer acceptability versus sensory quality with trained panel

The present work was designed in order to obtain the cut off point, to be used in a shelf life study on whole stirred strawberry yogurt. The study was simultaneously carried out in Argentina, Chile and Costa Rica, assaying the same kind of product, elaborated in each one of the countries. The sensory quality parameters obtained from trained panelists and the consumers acceptability, were correlated by using the cut off point methodology through a quality evaluation by the Karlsruhe scale. According to preliminary studies, the storage at 42 degrees C produced considerable damage on parameters such as pH, acidity (volumetric assay), viscosity and sensory quality. For each sample, the cut off point was determined. This value corresponds to the threshold score for the sensory quality, where the consumer starts to perceive negative changes in the product, when comparing with the fresh product. The rejection percentage was also calculated according to the cut off point. The cut off points and the percentage of rejection obtained by the three participating countries were similar. Data obtained from Costa Rica showed changes in color, acidity and rancidity. Argentinean yogurts developed acidity that had a negative effect on texture, appearance and residual flavors. Chilean samples presented a sensory quality that remains almost without change through the studied time. The differences of the deterioration pattern amongst the three countries, demonstrates that the products are different in formulation and elaboration process, in spite of been the same kind of yogurt. This could be explained by differences specified in the regulation of each country.     

Resins containing amino and carboxylic acid groups. Synthesis,characterization, and metal ion retention properties

The crosslinked poly[3‐(methacryloylamino)propyl]dimethyl(3‐sulfopropyl)ammonium hydroxide], P(MAPDSA), and poly[3‐(methacryloylamino)propyl]dimethyl(3‐sulfopropyl)ammonium hydroxide‐co‐acrylic acid], P(MAPDSA‐co‐AA), were synthesized by radical polymerization. The resins were completely insoluble in water. Due to the lower metal ion retention of P(MAPDSA), the metal ions investigated under competitive and noncompetitive conditions for Cu(II), Cd(II), Hg(II), Zn(II), Pb(II), and Cr(III) ions by batch and column equilibrium procedures were carried out only for P(MAPDA‐co‐AA), particularly for Hg(II). The resin–Hg(II) ion equilibrium was achieved before 15 min. The resin showed a maximum retention capacity value for Hg(II) at pH 2 of 1.89 meq/g. The resin showed a high selectivity to Hg(II) ions. The recovery of the resin was investigated at 25°C with different concentrations of HNO₃ and HClO₄. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 525–530, 2005     

Gemini and Bicephalous Surfactants: A Review on Their Synthesis,Micelle Formation,and Uses

The use of surfactants in polymerization reactions is particularly important, mainly in emulsion polymerizations. Further, micelles from biocompatible surfactants find use in pharmaceutical dosage forms. This paper reviews recent developments in the synthesis of novel gemini and bicephalous surfactants, micelle formation, and their applications in polymer and nanoparticle synthesis, oil recovery, catalysis, corrosion, protein binding, and biomedical area, particularly in drug delivery.     

The Urinary Level of Injury Biomarkers Is Not Univocally Reflective of the Extent of Toxic Renal Tubular Injury in Rats

Nephrotoxicity is a major cause of intrinsic acute kidney injury (AKI). Because renal tissue damage may occur independently of a reduction in glomerular filtration rate and of elevations in plasma creatinine concentration, so-called injury biomarkers have been proposed to form part of diagnostic criteria as reflective of tubular damage independently of renal function status. We studied whether the urinary level of NGAL, KIM-1, GM2AP, t-gelsolin, and REGIIIb informed on the extent of tubular damage in rat models of nephrotoxicity, regardless of the etiology, moment of observation, and underlying pathophysiology. At a time of overt AKI, urinary biomarkers were measured by Western blot or ELISA, and tubular necrosis was scored from histological specimens stained with hematoxylin and eosin. Correlation and regression studies revealed that only weak relations existed between biomarkers and tubular damage. Due to high interindividual variability in the extent of damage for any given biomarker level, urinary injury biomarkers did not necessarily reflect the extent of the underlying tissue injury in individual rats. We contended, in this work, that further pathophysiological contextualization is necessary to understand the diagnostic significance of injury biomarkers before they can be used for renal tubular damage severity stratification in the context of nephrotoxic and, in general, intrinsic AKI.     

Steric and electronic effects on mesophase stability of segmented liquid crystalline polymers with arylazomethine pendant groups

Summary The kinetics of DL-lactide polymerization was studied in CH₂Cl₂ at 25°C and in toluene at 70°C with HAPENAlOMe, a new Schiff's base complex derived from 2-hydroxyacetophenone and ethylenediamine. A higher polymerization rate is observed with this initiator as compared to other previously reported Al-alkoxides complexes. The polymerization with HAPENAlOMe is also shown to be a living process in both solvents. Moreover, the polymerization proceeds to quite high conversion without significant occurrence of transesterification reactions as confirmed from ¹³C NMR and SEC analysis. Received: 4 October 1999/Accepted: 6 December 1999     

Phenol degradation by Fenton's process using catalytic in situ generated hydrogen peroxide

The recent reported pathway using oxygen and formic acid at ambient conditions has been utilized to generate hydrogen peroxide in situ for the degradation of phenol. An alumina supported palladium catalyst prepared via impregnation was used for this purpose. Almost full destruction of phenol was carried out within 6 h corresponding to the termination of 100 mM formic acid at the same time. In addition, a significant mineralization (60%) was attained. A simulated conventional Fenton process (CFP) using continuous addition of 300 ppm H₂O₂ displayed maximum 48% mineralization. Study of different doses of formic acid showed that decreasing the initial concentration of formic acid caused faster destruction of phenol and its toxic intermediates. The catalytic in situ generation of hydrogen peroxide system demonstrated interesting ability to oxidize phenol without the addition of Fenton's catalyst (ferrous ion). Lower Pd content catalysts (Pd1/Al and Pd0.5/Al) despite of producing higher hydrogen peroxide amount for bulk purposes, did not reach the same efficiency as the Pd5/Al catalyst in phenol degradation. The later catalyst showed a remarkable repeatability so that more than 90% phenol degradation along with 57% mineralization was attained by the used catalyst after twice recovery. Higher temperature (45 °C) gave rise to faster degradation of phenol resulting to almost the same mineralization degree as obtained at ambient temperature. Meanwhile, Pd leaching studied by atomic adsorption proved excellent stability of the catalysts.