Curcumin associated magnetite nanoparticles inhibit in vitro melanoma cell growth

Curcumin is a natural product possessing therapeutic properties but the low water solubility of this compound limits its use. We have successfully incorporated curcumin into a bilayer of dodecanoic acid attached to magnetite nanoparticles in an effort to maximize solubility and delivery efficiency. Curcumin/magnetite nanoparticles were characterized using diffused reflectance infra-red fourier transform spectroscopy (DRIFTS) and X-ray powder diffraction (XRD). Moreover curcumin associated magnetite nanoparticles inhibited in vitro melanoma cell growth. An inhibitory concentration (IC50) of 66.0 +/- 3.0 microM (48 +/- 2.2 microg-iron/mL) was observed for the curcumin/magnetite nanoparticles. Fluorescent microscopy revealed that curcumin associated magnetite nanoparticles were internalized by the melanoma cells and remained in the cytoplasm. The curcumin/magnetic nanoparticles synthesized in this study possess magnetic and water solubility properties making this a novel curcumin formulation with therapeutic potential.     

Catalytic Performance of Ce1−x Ni x O2 Catalysts for Propane Oxidative Steam Reforming

The model, proposed by Peskov et al. (Catal Today 105:223, 2005) to describe kinetic oscillations observed in the N₂O + H₂ reaction on Ir(110), is used to illustrate the effect of periodic perturbation of the reactant pressures on oscillations. The attention is focused on the conversion of natural period-1 oscillations to period-1 oscillations with the imposed frequency. For this conversion, simultaneous perturbation of both reactant pressures is found to be much more efficient compared to perturbation of one of the pressures.     

LaCoO3 nanosystems by a hybrid CVD/sol-gel approach

LaCoO3 nanosystems are receiving increasing attention for the development of innovative fuel cells and heterogeneous catalysts. In this report, we describe the synthesis of nanophasic LaCoO3 thin films by a hybrid chemical vapor deposition (CVD)/sol-gel (SG) approach. The adopted strategy consists in the CVD of La-O-based systems on SG cobalt oxide xerogels CoOx(OH)y at temperatures as low as 200 degrees C and in the subsequent thermal treatment in air (400-800 degrees C, 2-8 h). In this context, particular attention is devoted to achieving an intimate La/Co intermixing already in the as-prepared systems, in order to favor reactions yielding a single La-Co-O phase with uniform composition. The obtained results point out to the formation of pure and structurally homogeneous LaCoO3 nanosystems after annealing at 700 degrees C, 2 h, with a typical grain-like morphology. More severe thermal treatment resulted in the thermal decomposition of LaCoO3 nanocrystallites.     

Apoptogenic effect of the lipophilic <i>o</i>-naphthoquinone CG 10-248 on rat hepatocytes: light and electron microscopy studies

CG 10-248 (3,4-dihydro-2,2-dimethyl-9-chloro-2H-naphtho[1,2b]pyran- 5,6-dione; CG-NQ), a β-lapachone analogue, modified the ultrastructure of rat hepatocytes, as demonstrated by light and electron microscopy. After 4 h incubation with 100 µM CG-NQ, the following effects were observed: (a) nuclear chromatin condensation; (b) chromatin fragmentation; (c) displacement of mitochondria, concentrated around the nucleus; (d) disruption or expansion of mitochondrial outer or inner membranes, respectively; (e) displacement and alteration of endoplasmic reticulum (rough and smooth); (f) decrease of microvilli; (g) blebbing of plasma membrane and production of apoptotic bodies formed by folding of plasma membrane fragments around mitochondria or peroxysomes; and (h) production of hydrogen peroxide. Expression of such effects varied according to hepatocyte samples and taken together strongly support an apoptotic action of CG-NQ dependent on “reactive oxygen species”.     

Wheat gluten-based materials plasticised with glycerol and water by thermoplastic mixing and thermomoulding

BACKGROUND: Gluten has been investigated as a source for biodegradable polymeric materials because it is a renewable, available and low‐cost raw material. The aim of this study was to evaluate the influence of some variables involved in the two stages of protein/plasticiser thermo‐mechanical processing, where a mixture of glycerol and water was used as the plasticiser. RESULTS: Gluten/glycerol/water blends mixed under different thermal conditions (adiabatic starting at 25 °C and isothermal at 60 and 90 °C) exhibited shear thinning capillary flow behaviour, where a marked increase in flow properties was obtained at the highest temperature. Two thermal events, glass transitions related to the plasticiser blend and gluten, were detected by Modulated Differential Scanning Calorimetry (MDSC) and Dynamic Mechanical Analysis (DMA) tests. Moderate moulding temperature led to less resistant materials showing higher ductility, whereas higher mixing and moulding temperatures led to bioplastics with higher mechanical properties. CONCLUSION: A moulding temperature of 130 °C (close to the denaturation temperature) was found to be suitable for the thermomoulding process. In addition, the use of moderate mixing temperature seems to be convenient for those applications that required materials exhibiting high water absorption behaviour and suitable mechanical properties. Protein extractability results reflect the benefits of combining high shear and high temperature during processing to improve cross‐linking reactions. Copyright © 2010 Society of Chemical Industry     

Decamethylosmocene-catalyzed efficient oxidation of saturated and aromatic hydrocarbons and alcohols with hydrogen peroxide in the presence of pyridine

Decamethylosmocene, (Me₅C₅)₂Os (1), is a pre-catalyst in a very efficient oxidation of alkanes with hydrogen peroxide in acetonitrile at 20–60 °C. The reaction proceeds with a substantial lag period that can be reduced by the addition of pyridine in a small concentration. The lag period can be removed if 1 is incubated with pyridine and/or H₂O₂ in MeCN prior to the alkane oxidation. Alkanes, RH, are oxidized primarily to the corresponding alkyl hydroperoxides, ROOH. Turnover numbers attain 51,000 in the case of cyclohexane (maximum turnover frequency was 6000 h^?1) and 3600 in the case of ethane. The oxidation of benzene and styrene also occurs with a lag period to afford phenol and benzaldehyde, respectively. A kinetic study of cyclohexane oxidation and selectivity parameters (measured in the oxidation of n-heptane, methylcyclohexane, isooctane, cis- and trans-dimethylcyclohexanes) indicates that the oxidation of saturated, olefinic, and aromatic hydrocarbons proceeds with the participation of hydroxyl radicals. The 1/H₂O₂/py/MeCN system also oxidizes 1-phenylethanol to acetophenone.     

The effect of Cs ions on codeposition of SiC particles with nickel

Electrodeposition of SiC particles (technical powder) with nickel matrix in the presence of cesium ions (0–37.6 mM) was investigated. The influence of Cs⁺ concentration on cathodic polarization curves was determined in galvanostatic and potentiodynamic measurements. The presence of Cs⁺ in the solution enhanced in some extent adsorption of Ni²⁺ ions on SiC, but preferential cesium adsorption occurred simultaneously. The last phenomenon resulted in cesium incorporation in the composite coating. The particle content in the deposits (16–24 vol%) was governed by the amount of nickel ions adsorbed on SiC. Structure of the composite coatings was studied by microscopic observations. At highest Cs⁺ concentrations, incorporation of small SiC grains was inhibited. Microhardness of deposits (390–800 HV) was directly dependent on the SiC content in the coatings.     

Design,Spectroscopy, and Assessment of Cholinesterase Inhibition and Antimicrobial Activities of Novel Coumarin–Thiadiazole Hybrids

A novel series of coumarin–thiadiazole hybrids, derived from substituted coumarin-3-carboxylic acids was isolated and fully characterized with the use of a number of spectroscopic techniques and XRD crystallography. Several of the novel compounds showed intensive fluorescence in the visible region, comparable to that of known coumarin-based fluorescence standards. Moreover, the new compounds were tested as potential antineurodegenerative agents via their ability to act as acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhibitors. Compared to the commercial standards, only a few compounds demonstrated moderate AChE and BuChE activities. Moreover, the novel derivatives were tested for their antimicrobial activity against a panel of pathogenic bacterial and fungal species. Their lack of activity and toxicity across a broad range of biochemical assays, together with the exceptional emission of some hybrid molecules, highlights the possible use of a number of the novel hybrids as potential fluorescence standards or fluorescence imaging agents.     

Effects of genetic polymorphisms CYP1A1, GSTM1, GSTT1 and GSTP1 on urinary 1-hydroxypyrene levels in sugarcane workers

Sugarcane workers in Brazil are exposed to various genotoxic compounds, including polycyclic aromatic hydrocarbons (PAHs), derived from an incomplete combustion process of burnt sugarcane fields. The effects of the occupational exposure to sugarcane fields burning were measured in urine samples of sugarcane workers from the northwest of the State of S?o Paulo when exposed (harvesting) and when non-exposed (non-harvesting). The urinary levels of 1-hydroxypyrene (1-OHP) and the influence of the genetic polymorphisms CYP1A1, GSTM1, GSTT1 and GSTP1 were evaluated. Our results showed that the 1-OHP levels were significantly higher (P<0.0000) in the exposed sugarcane workers (0.318 mumol mol(-1) creatinine) than in the non-exposed workers (0.035 mumol mol(-1) creatinine). In an unvaried analysis, no influence regarding the polymorphisms was observed. However, multivariate regression analysis showed that the CYP1A1()4 polymorphism in the exposed group, and age and the GSTP1 polymorphism in the non-exposed group significantly influenced urinary 1-OHP excretion levels (P<0.10). The same group of sugarcane workers was significantly more exposed to PAHs during the harvesting period than during the non-harvesting period.