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Query: UMLS:C0432222 (SEM)
 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Humic substances (HS) are macromolecular products derived from a physical, chemical, and microbiological process called "humification." These substances play an important role in the mobility and bioavailability of nutrients and contaminants in the environment. Adsorption isotherms provide a macroscopic view of the retention phenomena. However, complementary techniques are needed in order to study the retention mechanism. The application of the classical models and some modern ones, based on humic substances chemistry, do not accurately describe these adsorption data. The aim of this paper is to model isotherms and combine adsorption data with spectroscopy and microscopy techniques to study the Cu(II) retention on a HS. The adsorption isotherms shape varies significantly with the solution pH from L-type (pH 2-6) to S-type (pH 8). FTIR shows that, when pH is 2 the retention of Cu(II), as [Cu(H(2)O)(6)](2+), is the preferred retention mechanism. The quantity of Cu(II) retained as [Cu(OH)(H(2)O)(6)](+) rises, as pH increases. At pH 4, Cu(II) begins to precipitate, which is the preferred mechanism at pH 8.02. The presence of HS has a great influence on the precipitation process of Cu(II), giving rise to amorphous precipitates. As it is shown by SEM-XRF, Cu(II) distributes heterogeneously on HS surface and accumulates on the humic phases. The presence of different anions (chloride and nitrate) slightly modifies the HS behavior as cation exchanger. When Cl(-) ions are present, part of the Cu(II) form [CuCl(4)](2-), which is stable in solution due to its negative charge; when the anion present is NO(3)(-) the formed complex, [CuNO(3)](+), is retained on the HS.
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PMID:Cu(II) retention on a humic substance. 1469 34

Nitrite (NO2) and nitrate (NO3) concentrations are usually measured as a marker of NO metabolism. The aim of this study was to validate and standardize a method for the quantification of these two metabolites (nitrite and nitrate) in urine. The sample (urine) were deproteinized with NaOH, zinc sulfate and reduced with cadmium granules. Analytical recovery of NO3 added to urine samples after reduction with cadmium granules was 96-105% (Griess reaction). Calibration curves for nitrite and nitrate were linear over the concentration range of 2.1 to 200 micromole/L in urine. The detection limit of the assay was 0.9 micromole/L and the quantification limit was 2.1 micromole/L. Usual values were determined for healthy subjects: the mean concentration of NO2/NO3 (Unox) was 51.1 +/- 5.3 micromole/mmol creatinine (mean +/- SEM) (n = 15). Within-run precision was 6.6% and between-day precision was 2.2%.
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PMID:[Analysis of nitrites and nitrates (Unox) in urine]. 1502 6

Nitrite (NO2-) and nitrate (NO3-) concentrations are usually measured as a marker of NO metabolism. The aim of this study was to validate and standardize the method for the quantification of these two metabolites (nitrite and nitrate) in serum. The samples (serum) were deproteinized with NaOH, zinc sulfate and reduced with cadmium granules. Analytical recovery of NO3- added to serum samples after reduction with cadmium granules was 96-105% (Griess reaction). Calibration curves for nitrate and nitrite were linear over the concentration range of 2.1 to 200 micromol/L in plasma. The detection limit of the assay was 0.9 micromol/L and the quantitation limit was 2.1 micromol/l. Usual values were determined from healthy subjects: the mean concentration of NO2-/NO3- (NOx) was 26.2 +/- 1.1 micromol/l (mean +/- SEM) (n = 39). Within-run precision was 6.8% and between-day precision was 2.1%.
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PMID:[Analysis of nitrites/nitrates (NOx) in serum]. 1510 30

The asymmetry introduced by a complex or nonspherical basis promotes photonic band gap formation in three-dimensional photonic crystals. However, relatively few techniques have been demonstrated to produce uniform nonspherical colloids for use as photonic crystal bases. Here we expand the menu of basis types with high refractive index by preparing nonspherical zinc sulfide colloids of uniform size and shape. Dimers, trimers, and planar tetramers were precipitated from aqueous solution by the thermal decomposition of thioacetamide in the presence of zinc nitrate, manganese nitrate, and nitric acid. The well-defined morphological types were obtained from suspensions aged for 4-6 h at 26-32 degrees C and then for 20-35 min at 85 degrees C. Stereological techniques were used to analyze SEM images and determine the percentage of each particle class. For example, the quantitative characterization of a particle population prepared at 29 degrees C for 6 h and 85 degrees C for 22 min had the composition 59+/-3% spheres, 31+/-2% dimers, 7+/-1% trimers, 0.4+/-0.2% tetramers, and 2.5+/-0.8% complex clusters (encompasses all other varieties of shape). X-ray diffraction and X-ray photoelectron spectroscopy confirmed the zinc blend crystal structure and the stoichiometric composition of the particles. The refractive index was estimated as 2.25 (413 nm) -2.09 (709 nm) by fitting experimental absorption spectra to curves derived from Mie scattering calculations. This indicated an average porosity approximately 24%. Such colloids offer the potential to form diamond-like lattices with large, stable photonic band gaps.
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PMID:Nonspherical ZnS colloidal building blocks for three-dimensional photonic crystals. 1512 Feb 83

The assessment of the postprandial state in diabetes mellitus has gained importance due to postprandial hyperglycemia being considered as an independent risk factor for cardiovascular disease. Hyperglycemia may contribute to vascular dysfunction through the alteration of the nitric oxide/cyclic guanosine monophosphate (NO/cGMP) pathway. The authors assessed the NO/cGMP pathway in the fasting and postprandial state in 20 type 1 diabetic patients (age: 34.1 +/- 2.6 years, body mass index (BMI): 24.1 +/- 1.3 kg/m (2), duration of diabetes: 16 +/- 2.2 years, HbA (1C): 8.3 +/- 0.4 %, [x +/- SEM], 10 without, 10 with late complications) and 20 matched control subjects (age: 39.7 +/- 1.9 years, BMI: 25.3 +/- 1.1 kg/m (2)). In the fasting state NO end product (nitrite/nitrate) levels did not differ between the diabetic and control group, cGMP levels were found to be significantly lower in the diabetic group (2.5 +/- 0.2 vs. 4.6 +/- 0.6 nmol/l, p = 0.01). A higher level of lipid peroxidation end products (TBARS) was found in diabetic subjects (6.7 +/- 0.4 vs. 5.0 +/- 0.3 micro mol/l, p = 0.004). The diabetic subgroup without late complications had significantly higher nitrite/nitrate levels compared to the patients with complications (57.8 +/- 6.6 vs. 30.4 +/- 4.3 micro mol/l, p = 0.006), their TBARS and cGMP levels were similar. The control subjects responded to the test meal with an increase in the cGMP levels (4.6 +/- 0.6 to 5.5 +/- 0.6 nmol/l, p = 0.02), while in the diabetic group no change was detected. Postprandial nitrite/nitrate levels decreased in both groups, they were significantly lower in the diabetic group. There was no difference between postprandial nitrite/nitrate, cGMP, or glucose levels in the diabetic subgroups. Postprandial glucose levels showed a significant negative correlation with cGMP levels in the diabetic group (r = - 0.50, p = 0.02). The results suggest that in subjects with type 1 diabetes mellitus NO might have an impaired ability to induce cGMP production in the fasting state prior to the development of late specific complications or microalbuminuria under hyperglycemic conditions. Postprandial hyperglycemia is suggested to interfere with endothelial NO action, as shown by the decreased nitrite/nitrate and unchanged cGMP plasma levels in the diabetic group. The impairment of the NO/cGMP pathway both in the fasting and postprandial state that was shown in patients without diabetic complications may be an early sign of hyperglycemia induced vascular damage in type 1 diabetes mellitus.
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PMID:Impairment of the NO/cGMP pathway in the fasting and postprandial state in type 1 diabetes mellitus. 1514 72

This study evaluated the effect of multiple consecutive adhesive resin coatings of adhesive bonded to human dentin on nanoleakage and resin-dentin bond strength. Resin bonded dentin specimens were prepared using a total-etch adhesive (One-Step Plus) applied as multiple consecutive coating, or using two self-etch adhesive systems (iBond or Fluoro Bond). For the total-etch adhesive, resin application and air evaporation were performed 1, 2, 3, or 4 times. The self-etch adhesives were applied according to manufacturers' instructions. Resin-dentin bonded beams were prepared and immersed in water (control) or ammoniacal silver nitrate. After storage, microtensile bond strengths were measured. The fractured surfaces were examined by scanning and transmission electron microscopy (SEM and TEM), and energy-dispersive X-ray spectrometry (EDX). No significant differences in bond strength were found between water and silver nitrate storage groups. Several types of silver depositions (spotted, reticular, or water trees) were found in adhesive joints. The bond strengths of the single coated specimens of the total-etch adhesive were significantly lower than those receiving 2-4 coatings. Single coats produced more nanoleakage than multiple coats. However, no correlation was found between the bond strengths and nanoleakage between the different adhesives (total-etch adhesive with different conditions or self-etch adhesives).
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PMID:In vitro effect of nanoleakage expression on resin-dentin bond strengths analyzed by microtensile bond test, SEM/EDX and TEM. 1515 72

A new approach to the formation of palladium nanoparticulate films with diameter between 6 and 50 nm by the solid-liquid interface reaction technique (SLIRT) has been presented. A solid film of palladium nitrate was formed by the modified spin coating method. This film is subsequently immersed in a reducing solution to initiate a reaction at the interface and ultimately transforms it to a palladium metal film. The kinetics of palladium reduction has been studied by UV-visible spectroscopy. The characterization of the palladium film has been performed by various physicochemical techniques such as XRD, ED, XPS, SEM, EDX, TEM, and UV-visible spectroscopy. The texture and morphology of the materials has been investigated by atomic force microscopy (AFM). At a constant palladium nitrate concentration, the average diameter of palladium nanoparticles decreases with an increase of hydrazine concentration. The effect of concentration of hydrazine on the particle size has been discussed. The palladium film formation mechanism has been proposed for the SLIRT.
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PMID:Preparation of thin films comprising palladium nanoparticles by a solid-liquid interface reaction technique. 1527 60

This study evaluated the effects of various cavity configurations on the bond strength, microleakage, flexural strength and elastic modulus of a hybrid (Clearfil AP-X) and a microhybrid (Esthet-X) composite restorative. After the specimens were made with C-factors of less than 1, 2.4 and 3.4, flexural strength and elastic modulus were evaluated in three-point bending using a mechanical testing machine. Fragments of the fractured specimens were selected randomly and the fracture surfaces were examined in SEM. To evaluate the microtensile bond strength and microleakage of composite restorations in bovine cavities, C-factors (ratio of bonded to non-bonded cavity surface) were controlled as 1.0, 2.3, 3.0 and 3.7. All specimens were stored in distilled water at 37 degrees C for 24 hours and tested in a universal testing machine (EZ Test, Shimadzu, Japan). For the microleakage test, teeth with restorations were stained with silver nitrate and examined by two examiners under a stereomicroscope at 40x magnification. The hybrid composite showed higher mechanical properties than the microhybrid composite. The flexural strength and elastic modulus of both composites decreased when polymerized under greater constraint, that is, with increasing C-factor. Mean microtensile bond strength to dentin was also decreased with increasing C-factor for both types of composites. Microleakage scores for the hybrid composite restorations were generally higher than the microhybrid composite.
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PMID:Effects of cavity configuration on composite restoration. 1527 88

Hydroxyapatite (HAp) coatings were deposited onto substrates of metal biomaterials (Ti, Ti6Al4V, and 316L stainless steel) by electrophoretic deposition (EPD). Only ultra-high surface area HAp powder, prepared by the metathesis method 10Ca(NO3)2 + 6(NH4)2HPO4 + 8NH4OH), could produce dense coatings when sintered at 875-1000degreesC. Single EPD coatings cracked during sintering owing to the 15-18% sintering shrinkage, but the HAp did not decompose. The use of dual coatings (coat, sinter, coat, sinter) resolved the cracking problem. Scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS) inspection revealed that the second coating filled in the "valleys" in the cracks of the first coating. The interfacial shear strength of the dual coatings was found, by ASTM F1044-87, to be approximately 12 MPa on a titanium substrate and approximately 22 MPa on 316L stainless steel, comparing quite favorably with the 34 MPa benchmark (the shear strength of bovine cortical bone was found to be 34 MPa). Stainless steel gave the better result since -316L (20.5 microm mK(-1)) > alpha-HAp (approximately 14 microm mK(-1)), resulting in residual compressive stresses in the coating, whereas alpha-titanium (approximately 10.3 microm mK(-1)) < alpha-HAp, resulting in residual tensile stresses in the coating.
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PMID:Interfacial bond strength of electrophoretically deposited hydroxyapatite coatings on metals. 1534 25

The antibacterial effect of addition of silver oxide to Na2O x CaO x 2SiO2 glass have been studied. Silver containing and silver free Na2O x CaO x 2SiO2 glasses have been prepared by sol-gel synthesis using tetramethil orthosilicate, sodium ethoxide, calcium nitrate tetrahydrate and silver nitrate as starting materials and methyl ethyl ketone as solvent. The gel was examined by differential thermal analysis, thermo gravimetric analysis, FTIR spectroscopy and X-ray diffraction analysis. Antibacterial and bioactive tests on gel glass powders, obtained after a heat treatment of 2 h at 600 degrees C of the dried gel, were carried out. High antimicrobial effects of samples against Escherichia coli and Streptococcus mutans were found. FTIR measurements and SEM micrographs have ascertained the formation of a hydroxyapatite layer on the surface of samples soaked in a simulated body fluid for different times.
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PMID:Antibacterial and bioactive silver-containing Na2O x CaO x 2SiO2 glass prepared by sol-gel method. 1538 20


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