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At least 865 records · Page 48Linked to original sources
PubMed2000

Human vascular smooth muscle cells but not endothelial cells express prostaglandin E synthase.

In a previous work, we postulated that endothelial cells possess only the following 2 enzymes involved in prostanoid synthesis: cyclooxygenase and prostacyclin synthase. The present work focused on investigating the expression of prostaglandin (PG) E synthase (PGES) in vascular cells. After incubation of vascular smooth muscle cells (SMCs) and human umbilical vein endothelial cells (HUVECs) with [(14)C]arachidonic acid, the profile of prostanoid synthesis was assessed by HPLC. Untransformed PGH(2) released by the cells was evaluated as the difference in the formation of PGF(2alpha) in the incubations performed in the presence and in the absence of SnCl(2). Resting SMCs and SMCs stimulated with phorbol 12-myristate 13-acetate (PMA), lipopolysaccharide (LPS), interleukin (IL)-1beta, and tumor necrosis factor (TNF)-alpha formed PGE(2) and PGI(2) (evaluated as 6-oxo-PGF(1alpha)), and in the presence of SnCl(2) only a small amount of PGE(2) was deviated toward PGF(2alpha). In contrast, resting and stimulated HUVECs produced PGI(2), PGE(2), PGF(2alpha), and PGD(2), and SnCl(2) completely diverted PGE(2) and PGD(2) toward PGF(2alpha). Reverse transcriptase-polymerase chain reaction analysis shows that mRNA encoding for PGES was not present in HUVECs and in endothelial cells from saphenous vein. Nevertheless, PGES was expressed in SMCs and induced by IL-1beta and TNF-alpha, and by PMA and LPS, although to a lesser extent. Whereas SMC stimulation led to an increase in the synthesis of PGE(2) and PGI(2) but not of untransformed PGH(2), stimulation of endothelial cells resulted in an enhanced release of the vasoconstricting prostanoid PGH(2).

Arachidonic Acid↗
PubMed2002

Regulation of cyclooxygenase- and cytochrome p450-derived eicosanoids by heme oxygenase in the rat kidney.

Heme oxygenase enzymes (HO-1 and HO-2) catalyze the conversion of heme to biliverdin, free iron, and carbon monoxide (CO). Heme and products derived from its metabolism potentially influence renal function and blood pressure by affecting the expression and/or activity of hemeproteins, including cytochrome P450 (CYP4A) monooxygenases and cyclooxygenases (COX-1 and COX-2). We studied HO isoform expression and examined the effect of HO-1 induction by SnCl(2) on CYP4A and COX expression and activity in the rat kidney. HO-1 protein levels in kidney tissues from untreated rats were barely detectable, whereas HO-2 protein was expressed in all kidney structures examined and its levels were higher in the outer medulla followed by the inner medulla/papilla and cortex. HO-2 expression along the nephron followed its regional distribution, ie, the highest levels were detected in the medullary thick ascending limb (mTAL) and inner medullary collecting ducts followed by proximal tubules. SnCl(2) Treatment did not significantly affect HO-2 expression or distribution; however, it markedly increased HO-1 protein in the inner and outer medulla, specifically, in the inner medullary collecting ducts and mTAL. CYP4A expression and 20-hydroxyeicosatetraenoic acid (20-HETE) synthesis were the highest in the outer medulla followed by the cortex and inner medulla/papilla. SnCl(2) treatment reduced cortical and inner medullary CYP4A protein levels by 60% and 50% and inhibited 20-HETE synthesis by 90% and 60%, respectively. Despite a significant induction of HO-1 protein in the outer medulla, CYP4A expression and 20-HETE synthesis were hardly affected. SnCl(2) treatment did not affect COX-1 expression but markedly reduced cortical and medullary COX-2 protein levels. We conclude that HO isoform expression is segmented within the kidney and along the nephron and that treatment with an HO-1 inducer suppressed the levels of CYP4A and COX-2 proteins in a tissue-specific manner with concomitant effects on their activity. Such interactions may play an important role in the regulation of renal function.

Animals↗
PubMed2001

Immobilization of acetylcholinesterase and choline oxidase in/on pHEMA membrane for biosensor construction.

In this study, acetylcholinesterase (AChE) and choline oxidase (ChO) were co-immobilized on poly(2-hydroxyethyl methacrylate) (pHEMA) membranes with the aim of using them in biosensor construction. pHEMA membranes were prepared with the addition of different salts in different HEMA: aqueous solution ratios and characterized in terms of porosity, thickness. permeability, and mechanical properties. Membranes prepared in the presence of SnCl4 were found to be superior in terms of porosity and permeability and were chosen as the immobilization matrix. Immobilization of the enzymes was achieved both by entrapment and surface attachment via epichlorohydrin (Epi) and Cibacron Blue F36A (CB) activation. The effect of immobilization on enzyme activity was evaluated by the comparison of Km and Vmax values for the free and immobilized bi-enzyme systems. The increase in Km was negligible (1.08-fold) for the bi-enzyme system upon immobilization on surface but was 2.12-fold upon entrapment. Specific activity of the free enzyme system was found to be 0.306 mV s(-1) microg(-1) ChO while it was 0.069 (4.43-fold decrease) for entrapped and 0.198 (1.54 fold decrease) for CB-Epi immobilized enzymes. The performance of immobilized enzymes in different buffer types, pH, and temperature conditions were evaluated. The best enzyme activity was obtained at pH 9.0. Activity of the enzymes was found to increase with increasing temperature (in the range 25-40 degrees C).

Acetylcholinesterase↗
PubMed2002

Raman studies of semiconducting oxide nanobelts.

Crystalline nanobelts of ZnO and SnO2 were prepared from a thermal evaporation of oxide powders inside an alumina tube in the absence of catalysts. Typical dimensions of the nanobelt samples ranged from approximately 10 to 100 microns in length, 30 to 300 nm in width, and 6 to 30 nm in thickness. Room temperature Raman spectra were obtained on pressed mats of nanobelt samples and compared with the corresponding spectra of the starting oxide powders and bulk materials. Collectively, our Raman data indicated that the as-prepared nanobelt samples used in this study were oxygen deficient. Upon annealing at 900 degrees C in flowing oxygen for 1 h, the nanobelt samples exhibited Raman features that corresponded to those expected in respective bulk semiconducting oxides. The dimensions of the nanobelts were a bit too large to expect significant quantum size effects on the phonon structure similar to those observed in carbon nanotubes and short-period semiconductor superlattices.

Aluminum↗
PubMed2001

Time-resolved luminescence in conducting polymer/antidot nanocomposites.

We report modification of the structure and properties of conjugated polymers through controlled embedding wide-gap nanocrystals (antidots) within the polymer matrix. Investigations were carried out by means of stationary and time-resolved photoluminescence. Antidots strongly modify the luminescence spectrum of poly(p-phenylene vinylene) but have almost no influence on the spectrum of poly(2-(6-cyano-6'-methylheptyloxy)-1, 4-phenylene. We explain this observation with respect to the different chain structure and electron density distribution in these two materials. The temporal evolution of luminescence spectra in polymer/antidot composites contains a series of characteristic times. The shortest of these (0.35-0.6 ns) are independent of antidot material and characterize processes in the polymer matrix. Larger times considerably exceeding 1 ns are composition-sensitive and attributable to carrier capture by nanocrystals. The qualitative character of the modification of luminescence spectra associated with the inclusion of antidots depends strongly on the characteristics of the polymer matrices and more weakly on the antidot material. This suggests that the predominant effect of the nanocrystals relates to the modification of the matrix near the polymer-inorganic interface.

Aluminum Oxide↗
PubMed2002

Nanocrystalline sensor-grade Sn1-xInxO2 (0 < or = x < or = 0.2).

Nanocrystalline Sn1-xInxO2 (0 < or = x < or = 0.2) has been successfully prepared by a solution chemical route. High-resolution transmission electron microscopy studies show that the average grain size of Sn0.8In0.2O2 heated at 310 degrees C, 500 degrees C, and 800 degrees C for 12 h is about 3-4 nm, 5-6 nm, and 7-10 nm, respectively. The corresponding values for pure SnO2 are 3-4 nm, 7-10 nm, and 50-90 nm, respectively. Powder X-ray diffraction and electron diffraction studies confirm the existence of solid solution only in the nanocrystalline state (the average particle size is in the range of 5-10 nm) with the solubility limited to 20% of In2O3. Indium ions stabilize the nanocrystalline nature of Sn1-xInxO2 (0 < or = x < or = 0.2) and prevent the grain growth by entering the SnO2 lattice. The thermal characteristics of nanocrystalline Sn1-xInxO2 (0 < or = x < or = 0.2) investigated by thermogravimetric (TG) and differential thermal analysis (DTA) show that the solid solution decomposes at 820 degrees C into SnO2 and In2O3, which is accompanied by a rapid crystal growth. The electrical conductivity and activation energy of Sn1-xInxO2 (0 < or = x < or = 0.2) undergo significant changes when the average grain size is less than or equal to 2 x the Debye length, LD.

Crystallization↗
PubMed2002

Synthesis of SnO2 nanoribbons by a carbothermal reduction process.

This communication describes, for the first time, the growth of SnO2 nanoribbons by a controlled carbothermal reduction process. An analysis of the transmission electron microscopy image revealed that these nanoribbons have a well-defined shape, with a typical width in the range of 70-300 nm. In general, the nanostructured ribbons were more than 100 microns in length. The results reported here support the hypothesis that this ribbon-like nanostructured material grows by a vapor-solid process. This study introduces two hypotheses to explain the SnO2 nanoribbon growth process.

Carbon↗
PubMedDate not supplied

Room temperature hydrogen gas sensitivity of nanocrystalline pure tin oxide.

Nanocrystalline (6-8 nm) tin oxide (SnO2) thin film (100-150 nm) sensor is synthesized via sol-gel dip-coating process. The thin film is characterized using focused ion-beam microscopy (FIB) and high-resolution transmission electron microscopy (HRTEM) techniques to determine the film thickness and the nanocrystallite size. The utilization of nanocrystalline pure-SnO2 thin film to sense a typical reducing gas such as hydrogen, at room temperature, is demonstrated in this investigation. The grain growth behavior of nanocrystalline pure-SnO2 is analyzed, which shows very low activation energy (9 kJ/mol) for the grain growth within the nanocrystallite size range of 3-20 nm. This low activation energy value is correlated, via excess oxygen-ion vacancy concentration, with the room temperature hydrogen gas sensitivity of the nanocrystalline pure-SnO2 thin film sensor.

Adsorption↗
PubMed2004

A simple and novel method to synthesize doped and undoped SnO2 nanocrystals at room temperature.

This work describes the synthesis, at room temperature, of doped and undoped SnO2 nanocrystals (particle size ranging from 1-3 nm) with no thermal or hydrothermal treatment. To the best of our knowledge, this is the first time that the synthesis, at room temperature, of doped and/or undoped SnO2 nanocrystals has been reported. This new synthesis method is based on the controlled oxidation, hydrolysis and polycondensation of tin ions in an ethanol solution. Another novel aspect of this method is the possibility of using surfactants, which may provide improved control over the particle size.

Antimony↗
PubMed2005

Large-scale hydrothermal synthesis of SnS2 nanobelts.

SnS2 nanobelts were successfully synthesized through a controllable solution-phase hydrothermal method on a large scale. The nanobelts have a very high yield, which is more than 95%, with widths ranging from 100 to 200 nanometers, lengths up to several micrometers and thicknesses ca. 10 nanometers. X-ray diffraction patterns, electronic diffraction, X-ray photoelectron spectra, field emission scanning electron microscopy images, transmission electron microscopy images and high-resolution transmission electron microscopy investigated the phase structures, compositions, and morphologies of SnS2 nanobelts. Dodecanethiol played important roles in the process of SnS2 nanobelts formation and growth. The formation mechanism of SnS2 nanobelts was investigated and discussed on the basis of the experimental results.

Crystallization↗
PubMed2005

Vapor phase growth of ZnO nanorod-nanobelt junction arrays.

By thermally evaporating a mixture of ZnO, SnO2, and graphite powders at 920 degrees C, large quantities of ZnO nanorods with typical diameters of 20-30 nm are grown secondarily from the surfaces of the ZnO nanobelts to form a nanorod-nanobelt junction array with interesting structural characteristics. A possible growth mechanism of the ZnO nanorod-nanobelt junction arrays with high surface-to-volume ratio is discussed. The ZnO nanorod-nanobelt junction arrays appear an enhanced visible emission due to the high quantity of the surface defects related to oxygen vacancies. The results reported in this paper would lead to new approaches to control the surface structures of ZnO nanomaterials that are critical for their applications, such as chemical sensors.

Crystallization↗
PubMed2005

Effect of air-pressure on room temperature hydrogen sensing characteristics of nanocrystalline doped tin oxide MEMS-based sensor.

Nanocrystalline indium oxide (In2O3)-doped tin oxide (SnO2) thin film sensor has been sol-gel dip-coated on a microelectrochemical system (MEMS) device using a sol-gel dip-coating technique. Hydrogen (H2) at ppm-level has been successfully detected at room temperature using the present MEMS-based sensor. The room temperature H2 sensing characteristics (sensitivity, response and recovery time, and recovery rate) of the present MEMS-based sensor has been investigated as a function of air-pressure (50-600 Torr) with and without the ultraviolet (UV) radiation exposure. It has been demonstrated that, the concentration of the surface-adsorbed oxygen-ions (which is related to the sensor-resistance in air), the ppm-level H2, and the oxygen (O2) partial pressure are the three major factors, which determine the variation in the room temperature H2 sensing characteristics of the present MEMS-based sensor as a function of air-pressure.

Air↗
PubMed2006

Structural and optical properties of tin oxide branched nanostructures.

Branched nanostructures of tin oxide (SnO2) have been synthesized by Vapor-Liquid-Solid (VLS) mechanism using a gold catalyst in the temperature range of 800-850 degrees C under an ambient gas flow of 200 sccm. The microstructural and the optical properties of the as prepared products have been studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), micro-Raman, and photoluminescence (PL) studies. SnO2 branches with a rutile phase are found to have a preferential orientation along (101). Typical lengths of these branches are found to be approximately 3-5 microm and diameters in the range of 50-100 nm. Selected area electron diffraction (SAED) pattern shows that the SnO2 branches have a tetragonal cross section with [101] crystal direction. A Raman line at 631 cm(-1) (Sn-O bond) is obtained in the micro Raman spectra. Low temperature PL spectrum shows a strong green emission band near 506 nm.

Crystallization↗
PubMed2006

Synthesis and mechanism study of mesoporous SnO2/SiO2 composites.

Mesoporous SnO2/SiO2 composite particles (Si/Sn < or = 0.25) sustainable to calcination up to 600 degrees C have been fabricated using a stepwise sol-gel technique on nonionic surfactant template (tetradecylamine, TDA). The newly designed preparation method involved the pre-formation of SnO2 sol solution from SnCl4. Subsequently, SnO2 nanocrystals were covered by the silicate species (from the hydrolysis of tetraethylorthosilicate, TEOS) in a pH controlled colloidal solution. Upon mixing with the surfactant solution, mesophase composite was obtained. After the removal of templates at various temperatures (400 to 600 degrees C), worm-like mesoporous SnO2/SiO2 with large specific surface area and pore volume as high as 362 m2/g and 0.33 cc/g were obtained, respectively. High thermal stability is mainly due to the effective inhibition of SnO2 crystal growth (mean crystallite size <30 A) by the amorphous SiO2 species at the grain boundaries. Formation of mesoporous silicate skeleton such as M41S family material was prevented. The obtained materials maintain the relatively narrow pore size distribution typically in the range of 30 to 70 A. Relations between material properties and key synthesis parameters (i.e. TDA/Si/Sn molar ratio and calcination temperature) were investigated by TGA, wide/small-angle X-ray scattering, (HR)TEM, BET, and FTIR techniques. Mechanisms on the mesostructure formation and crystal growth inhibition were also proposed with detailed discussion.

Crystallization↗
PubMed2006

Synthesis of nanocrystalline tin oxide thin film by swift heavy ion irradiation.

Nanocrystals of tin oxide were formed in e-beam evaporated films by swift heavy ion (SHI) irradiation. The nucleation of nanocrystals occurred due to electronic excitation by swift heavy ion. Nanophase thin films are characterized systematically by HRTEM, GAXRD, EDX, and UV/NIS absorption techniques. Nanocrystals having size of 8 nm radius are synthesized in different substrates during swift heavy ion irradiation and without subsequent annealing. SHI induced nanocrystallization could be achieved in both crystalline and non-crystalline substrates.

Crystallization↗
PubMed1987

The color accuracy of the Kubelka-Munk theory for various colorants in maxillofacial prosthetic material.

The reflectance model developed by Kubelka and Munk was evaluated for agreement in color prediction of thick pigmented samples and for linearity of optical absorption and scattering coefficients with concentration of colorant in maxillofacial elastomer. The colorants tested were generic opacifiers, dry mineral earth pigments, and fibrous colorants. Significant linear relationships were commonly found between the optical coefficients and the concentration of the colorants. These relationships indicated occasional optical interaction between the colorants and the elastomer. Color differences between theoretical and observed colors of the thick samples averaged 2.96, 3.47, and 1.60 for the opacifiers, mineral earth pigments, and fibrous colorants, respectively, when measured using the CIELAB uniform-color space. The agreement between theoretical and observed colors was significantly closer for the fibrous colorants than for the dry mineral earth pigments of the same labeled color.

Color↗
PubMed1988

A new ion-coating surface treatment of alloys for dental adhesive resins.

4-META and new phosphate-methacrylate resins adhere strongly to dental alloys. However, for strengthening the water durability of the adhesive interface, the oxidation of the alloy surface is indispensable. A new oxidation method using ion-sputtering was developed, and the effectiveness of this surface treatment on two dental alloys--a type IV gold alloy and Ni-Cr-Be alloy--was investigated. As an endurance test, thermocycling for a maximum of 100,000 cycles was adopted, and the tensile adhesive bond strength was then measured. Ion-coating the surface of the alloys resulted in strong bonds with adhesive resins, and after 100,000 thermocycles, a bond strength of above 20 MPa was maintained.

Adhesiveness↗