Preparation and drug‐release behavior of minocycline‐loaded poly[hydroxyethyl methacrylate‐co‐poly(ethylene glycol)–methacrylate] films

In this work, biocompatible hydrogel matrices for wound‐dressing materials and controlled drug‐release systems were prepared from poly[hydroxyethyl methacrylate‐co‐poly(ethylene glycol)–methacrylate] [p(HEMA‐co‐PEG–MA] films via UV‐initiated photopolymerization. The characterization of the hydrogels was conducted with swelling experiments, Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis (differential scanning calorimetry), and contact‐angle studies. The water absorbency of the hydrogel films significantly changed with the change of the medium pH from 4.0 to 7.4. The thermal stability of the copolymer was lowered by an increase in the ratio of poly(ethylene glycol) (PEG) to methacrylate (MA) in the film structure. Contact‐angle measurements on the surface of the p(HEMA‐co‐PEG–MA) films demonstrated that the copolymer gave rise to a significant hydrophilic surface in comparison with the homopolymer of 2‐hydroxyethyl methacrylate (HEMA). The blood protein adsorption was significantly reduced on the surface of the copolymer hydrogels in comparison with the control homopolymer of HEMA. Model antibiotic (i.e., minocycline) release experiments were performed in physiological buffer saline solutions with a continuous flow release system. The amount of minocycline release was shown to be dependent on the HEMA/PEG–MA ratio. The hydrogels have good antifouling properties and therefore are suitable candidates for wound dressing and other tissue engineering applications. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Synthesis and characterization of magnetic beads containing aminated fibrous surfaces for removal of Reactive Green 19 dye: kinetics and thermodynamic parameters

BACKGROUND: Poly(HEMA‐co‐MMA) beads were prepared from 2‐hydroxyethyl‐methacrylate (HEMA) and methylmethacrylate (MMA) in the presence of FeCl₃. Thermal co‐precipitation of Fe(III) ions containing beads with Fe(II) ions was carried out under alkaline conditions. The magnetic beads were grafted with poly(glycidylmethacrylate; p(GMA)), and the epoxy groups of the grafted p(GMA) brushes were converted into amino groups by reaction with ammonia. RESULTS: The magnetic beads were characterized by surface area measurement, electron spin resonance (ESR), Mössbauer spectroscopy and scanning electron microscopy (SEM). The maximum adsorption of Reactive Green‐19 (RG‐19) dye on the p(GMA) grafted and amine modified magnetic beads was around pH 3.0. The adsorption capacity of magnetic beads was 84.6 mg dye g^?1. The effects of adsorbent dosage, ionic strength and temperature have also been reported. Batch kinetic sorption experiments showed that a pseudo‐second‐order rate kinetic model was applicable. CONCLUSION: The p(GMA) grafted and amine modified magnetic beads (adsorbent) were expected to have the advantage of mobility of the grafted chains in the removal of acidic dyes from aqueous solutions. The magnetic beads have potential as an adsorbent for removal of pollutants under various experimental conditions without significant reduction in their initial adsorption capacity. Copyright © 2011 Society of Chemical Industry     

A mixed integer linear programming formulation for optimal balancing of mixed-model U-lines

The mixed-model U-line balancing problem was first studied by Sparling and Miltenburg (Sparling, D. and Miltenburg, J., 1998. The mixed-model U-line balancing problem. International Journal of Production Research, 36(2), 485–501) but has not been mathematically formulated to date. This paper presents a mixed integer programming formulation for optimal balancing of mixed-model U-lines. The proposed approach minimises the number of workstations required on the line for a given model sequence. The proposed formulation is illustrated and tested on an example problem and compared with an existing approach. This paper also proposes a new heuristic solution procedure to handle large scale mixed-model U-line balancing problems. A comprehensive experimental analysis is also conducted to evaluate the performance of the proposed heuristic. The results show the validity and usefulness of the proposed integer formulation and effectiveness of the proposed heuristic procedure.     

Laser‐Textured Metal Substrates as Photoanodes for Enhanced PEC Water Splitting Reactions

We demonstrate the effect of femtosecond laser structuring of titanium substrates to increase the absorption, photoconversion, and overall photoelectrochemical water splitting (PEC) performance compared to pristine metal substrates, independent of any additional top coat layers. The influence of ultra short laser pulse patterning on PEC efficiency is investigated toward spectroscopic (UV‐Vis), microscopic (SEM), crystallographic (XRD), and compositional (XPS) properties. The beneficial effect of a periodically patterned substrate is attributed to enhanced specific surface area and improved in‐plane light trapping when compared to flat surfaces. Photoanodes for water splitting experiments fabricated by titanium and iron oxide films on laser pre‐patterned Ti substrates are also found to show enhanced PEC efficiency (0.057 mA cm^?2) when compared to unpatterened substrates (0.028 mA cm^?2). The lower absolute PEC efficiencies are due to extreme thin films.

     

The impact of toxicity of metals on the activity of ureolytic mixed culture during the precipitation of calcium

In this article, the inhibitory impact of metals on substrate utilization and microbial carbonate precipitation (MCP) by ureolytic mixed cultures (UMC) was investigated with glucose and mineral medium under batch conditions. The IC(50) (toxicant concentration eliciting 50% inhibitory effect) values were determined from the BOD values of samples. Inhibition, expressed as the value of 50% inhibitory effect (IC(50)), was evaluated by the decrease in substrate removal using BOD tests. The effect of toxicity of metals on substrate degradation, IC(50) values, was found to increase in the following order: Cd(II)>Cu(II)>Pb(II)>Cr(VI)>Ni(II)>Zn(II). Nitrification a possible phenomenon in the biocatalytic process was observed in several samples and this inhibited the precipitation of soluble calcium. During the removal of calcium from industrial calcium-rich wastewater, toxicity of metal at higher metal concentrations and possibility of nitrification at higher sludge ages should be considered.     

Enzymatic removal of phenol and p-chlorophenol in enzyme reactor: horseradish peroxidase immobilized on magnetic beads

Horseradish peroxidase was immobilized on the magnetic poly(glycidylmethacrylate-co-methylmethacrylate) (poly(GMA-MMA)), via covalent bonding and used for the treatment of phenolic wastewater in continuous systems. For this purposes, horseradish peroxidase (HRP) was covalently immobilized onto magnetic poly(GMA-MMA) beds using glutaraldehyde (GA) as a coupling agent. The maximum HRP immobilization capacity of the magnetic poly(GMA-MMA)-GA beads was 3.35 mg g(-1). The immobilized HRP retained 79% of the activity of the free HRP used for immobilization. The immobilized HRP was used for the removal of phenol and p-chlorophenol via polymerization of dissolved phenols in the presence of hydrogen peroxide (H(2)O(2)). The effect of pH and temperature on the phenol oxidation rate was investigated. The results were compared with the free HRP, which showed that the optimum pH value for the immobilized HRP is similar to that for the free HRP. The optimum pH value for free and immobilized HRP was observed at pH 7.0. The optimum temperature for phenols oxidation with immobilized HRP was between 25 and 35 degrees C and the immobilized HRP has more resistance to temperature inactivation than that of the free form. Finally, the immobilized HRP was operated in a magnetically stabilized fluidized bed reactor, and phenols were successfully removed in the enzyme reactor.     

Comparative characterization of monophenolase and diphenolase activities from a wild edible mushroom (Macrolepiota mastoidea)

In this study, Macrolepiota mastoidea, a wild edible mushroom, was evaluated for its polyphenol oxidase potential. Native electrophoresis, stained by l-dihydroxyphenylalanine, of the crude extracts from this species showed two bands having R_f values of 0.38 (minor) and 0.50 (major), supporting a polyphenol oxidase potential. The crude extracts showed monophenolase activity against 3-(4-hydroxyphenyl)-propionic acid and diphenolase activity against 4-methylcatechol as substrates. Monophenolase and diphenolase activities of enzyme extract prepared from M. mastoidea showed pH optimum values at pH 6.0 and pH 4.0, respectively. The extracts retained about 100% and 60% of their original monophenolase and diphenolase activities at their optimum pH values, respectively. It was estimated from thermodynamic data that M. mastoidea had a thermostable monophenolase activity. Thiourea and ascorbic acid were highly potential inhibitors for monophenolase, and ascorbic acid and sodium metabisulphite for diphenolase activity. It is clear from the present results that the enzyme extracts prepared from M. mastoidea possess polyphenol oxidase activities with interesting properties.     

Removal of toxic metal ions with magnetic hydrogels

Hydrogels, based on 2-acrylamido-2-methyl-1-propansulfonic acid (AMPS) were synthesized via photopolymerization technique and used for the preparation of magnetic responsive composite hydrogels. These composite hydrogels with magnetic properties were further utilized for the removal of toxic metal ions such as Cd(II), Co(II), Fe(II), Pb(II), Ni(II), Cu(II) and Cr(III) from aqueous environments. It was revealed that hydrogel networks with magnetic properties can effectively be utilized in the removal of pollutants. The results verified that magnetic iron particle containing p(AMPS) hydrogel networks provide advantageous over conventional techniques. Langmuir and Freundlich adsorption isotherms were applied for toxic metal removal and both isotherms were fit reasonably well for the metal ion absorptions.