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1.
Sci Rep ; 11(1): 15034, 2021 Jul 22.
Article in English | MEDLINE | ID: mdl-34294856

ABSTRACT

New angle-resolved photoelectron spectroscopy (ARPES) data, recorded at several different photon energies from the Si(111)(7 × 7) surface, show that the well-known S1 and S2 surface states that lie in the bulk band gap are localised at specific (adatom and rest atom) sites on the reconstructed surface. The variations in the photoemission intensity from these states as a function of polar and azimuthal emission angle, and incident photon energy, are not consistent with Fermi surface mapping but are well-described by calculations of the multiple elastic scattering in the final state. This localisation of the most shallowly bound S1 state is consistent with the lack of significant dispersion, with no evidence of Fermi surface crossing, implying that the surface is not, as has been previously proposed, metallic in character. Our findings highlight the importance of final state scattering in interpreting ARPES data, an aspect that is routinely ignored and can lead to misleading conclusions.

2.
Nanotechnology ; 23(38): 385703, 2012 Sep 28.
Article in English | MEDLINE | ID: mdl-22947695

ABSTRACT

We have investigated the geometry and electronic structure of two different types of self-aligned silicon nanoribbons (SiNRs), forming either isolated SiNRs or a self-assembled 5 × 2/5 × 4 grating on an Ag(110) substrate, by scanning tunnelling microscopy and high resolution x-ray photoelectron spectroscopy. At room temperature we further adsorb on these SiNRs either atomic or molecular hydrogen. The hydrogen absorption process and hydrogenation mechanism are similar for isolated or 5 × 2/5 × 4 ordered SiNRs and are not site selective; the main difference arises from the fact that the isolated SiNRs are more easily attacked and destroyed faster. In fact, atomic hydrogen strongly interacts with any Si atoms, modifying their structural and electronic properties, while molecular hydrogen has first to dissociate. Hydrogen finally etches the Si nanoribbons and their complete removal from the Ag(110) surface could eventually be expected.


Subject(s)
Crystallization/methods , Hydrogen/chemistry , Nanostructures/chemistry , Nanostructures/ultrastructure , Silicon/chemistry , Silver/chemistry , Adsorption , Electron Transport , Macromolecular Substances/chemistry , Materials Testing , Molecular Conformation , Particle Size , Surface Properties
3.
Phys Rev Lett ; 94(18): 187601, 2005 May 13.
Article in English | MEDLINE | ID: mdl-15904410

ABSTRACT

High resolution core level photoemission spectroscopy, photoelectron diffraction, and x-ray magnetic circular dicroism (XMCD) have been used to characterize the structural and magnetic properties of bcc-cobalt films grown on GaAs(110) substrates by using Sb as a surfactant. We have unambiguously disentangled the surfactant role played by the Sb which improves the crystallinity and reduces the lattice distortion of the metallic films as well as changes the interdiffusion process at the interface compared to the Co/GaAs(110) system. As a consequence of these combined effects, an improvement on the magnetic response of the grown Co thin films has been observed by XMCD measurements.

4.
J Am Soc Nephrol ; 10(8): 1681-8, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10446935

ABSTRACT

In the hypothyroid kidney, exogenous adenosine (ADO) produces vasodilation and restores renal function to near-normal values. This study evaluates whether this response is mediated by nitric oxide synthesis stimulated by adenosine. GFR and urinary excretion of NO2-/NO3- (UNO2-/NO3-) were measured in normal (NL) and hypothyroid (HTX) rats under basal conditions and during infusion of: intra-aortic ADO, intravenously, 1,3-dipropyl-8p-sulfophenylxanthine (DPSPX), 8-cyclopentyl-1,3-dipropyl xanthine (DPCPX), N(omega)-nitro-L-arginine methylester (L-NAME) + ADO, L-NAME + PSPX, L-NAME + DPCPX, and intrarenal (IR) ADO or DPCPX + IR ADO. Intra-aortic ADO induced a fall in GFR and increased UNO2-/NO3- slightly in NL rats; in HTX rats, both GFR and UNO2-/NO3- increased significantly. DPSPX and DPCPX increased UNO2-/NO3- excretion in NL animals with minor changes in GFR; the blockers increased both GFR and UNO2-/ NO3- in HTX rats. L-NAME completely blocked the increase in NO2-/NO3- induced by ADO, DPSPX, and DPCPX. The intrarenal infusion of ADO at 1, 10, and 35 nmol/kg per min progressively decreased GFR with a slight increase in UNO2-/ NO3- in NL rats; in the HTX, GFR increased with the highest dose and UNO2-/NO3- progressively increased. DPCPX prevented the fall in GFR induced by intrarenal ADO in NL rats, with no further changes in UNO2-/NO3-; in HTX rats, intrarenal ADO under A1 blockade further increased GFR and UNO2-/NO3-. Arterial and venous ADO concentrations were lower in the HTX rats. In the HTX kidney, NO production was stimulated by ADO, most likely through activation of A2 or A3 receptors, whereas A1 receptors had an inhibitory effect. Thus, ADO receptors are involved in the regulation of kidney function in pathophysiologic conditions.


Subject(s)
Adenosine/physiology , Hypothyroidism/metabolism , Kidney/metabolism , Nitric Oxide/biosynthesis , Adenosine/antagonists & inhibitors , Adenosine/pharmacology , Animals , Aorta/physiopathology , Hormone Antagonists/pharmacology , Hypothyroidism/physiopathology , Injections , Injections, Intra-Arterial , Kidney/drug effects , Kidney/physiopathology , Male , Nitric Oxide/antagonists & inhibitors , Purinergic P1 Receptor Antagonists , Rats , Rats, Wistar , Xanthines/pharmacology
5.
Acta odontol. venez ; 36(3): 35-40, 1998. tab, graf
Article in Spanish | LILACS | ID: lil-258386

ABSTRACT

El propósito de este estudio fue determinar la prevalencia e intensidad de fluorosis dental en escolares de 10 a 13 años de edad residentes en áreas fluoruradas y áreas no fluoruradas de la ciudad de Mérida, Venezuela. El índice de Dean fue utilizado para estimar la severidad de fluorosis dental en una muestra de 834, los cuales fueron examinados en 8 escuelas seleccionadas aleatoriamente. Se confirmó el lugar de residencia mediante un cuestionario de fluoruro que recogió información acerca de los factores de riesgo secundarios: lugar de residencia anterior, tipo de agua de consumo, prescripción de tabletas, gotas o enjuagues con fluoruro, hábitos de cepillado, uso de dentífricos y su ingestión en el momento del cepillado. La prevealencia de fluorosis fue del 36 por ciento. La asociación entre fluorosis y lugar de residencia fue significativa, pues la razón de proporcionalidad fue de 2.39. La categoría de fluorosis mayormente encontrada fue la forma "muy leve"


Subject(s)
Humans , Male , Female , Adolescent , Drinking Water , Fluorosis, Dental/epidemiology , Fluorosis, Dental/etiology , Fluorosis, Dental/pathology , Fluoridation/adverse effects , Risk Factors , Age Distribution , Chi-Square Distribution , Dental Enamel/pathology , Dentifrices/metabolism , Fluorides/metabolism , Fluoridation/methods , Odds Ratio , School Dentistry/methods , Data Interpretation, Statistical , Surveys and Questionnaires
6.
J Public Health Manag Pract ; 3(3): 43-51, 1997 May.
Article in English | MEDLINE | ID: mdl-10186723

ABSTRACT

This study evaluated the outcome of a targeted dental sealant program by comparing the survival probabilities of sealed high-risk first molar tooth sites to unsealed low-risk tooth sites in 1,122 children enrolled in a school-based sealant program. A comparison of the survival probabilities between low-risk first molar teeth that did not receive sealants and the sealed high-risk first molar teeth did not show significant differences. The results suggest that the protocol used by the program provides a satisfactory method for identification of children who could best benefit from sealants in a school-based situation.


Subject(s)
Dental Caries/prevention & control , Pit and Fissure Sealants/therapeutic use , School Health Services , Adolescent , Child , Humans , Life Tables , Molar , New York , Pilot Projects
7.
J Nutr ; 115(11): 1488-97, 1985 Nov.
Article in English | MEDLINE | ID: mdl-4056944

ABSTRACT

This study was initiated to explore the quantitative and qualitative differences in milk total fatty acids and milk retinyl esters when either hydrogenated or nonhydrogenated fat is fed during pregnancy and lactation. Rats were fed diets containing 10% by weight of corn oil or partially hydrogenated corn oil. Milk was collected on d 1, 8 and 14 of lactation and analyzed for protein, total fatty acids, fatty acid pattern, and retinyl ester pattern. Whereas diet produced no quantitative differences in milk protein or total fatty acids, the pattern of milk fatty acids varied significantly. Rats fed corn oil produced milk having more medium-chain saturated fatty acids, less long-chain monoenoic fatty acids, and more polyunsaturated fatty acids compared to those fed hydrogenated corn oil. Rats fed hydrogenated corn oil produced milk fat having 21-26% of the trans fatty acid, elaidic acid. Significant differences were also observed with duration of lactation: medium-chain fatty acids increased three to fourfold between d 1 and 8, where cis-monoenes and polyunsaturated fatty acids declined. The pattern of milk retinyl esters strongly reflected, but was not identical to, that of total milk fat. Comparing d 14 milk from rats fed corn oil with that from rats fed hydrogenated corn oil, medium-chain esters of retinol constituted 24 and 11% of total retinyl esters, whereas saturated long-chain fatty acid esters constituted 52 and 44%, respectively. trans Fatty acid esters of retinol comprised 24% of vitamin A esters in milk of rats fed hydrogenated fat. These data provide evidence that the composition of milk retinyl esters, as well as that of total milk fat, is determined both by the type of fatty acids from diet and from diet-related differences in de novo synthesis of fatty acids within the mammary gland and other tissues.


Subject(s)
Dietary Fats/metabolism , Fatty Acids/analysis , Milk/analysis , Administration, Oral , Animals , Chromatography, Gas , Corn Oil , Fatty Acids/biosynthesis , Female , Milk/drug effects , Milk Proteins/analysis , Oils/pharmacology , Pregnancy , Rats , Rats, Inbred Strains , Vitamin A/metabolism , Vitamin A/pharmacology
8.
J Nutr ; 115(8): 1033-41, 1985 Aug.
Article in English | MEDLINE | ID: mdl-4020482

ABSTRACT

We have investigated the effects of maternal vitamin A intake during pregnancy and lactation or during lactation alone on the concentration of vitamin A in rat's milk and on vitamin A levels in plasma and liver of dams and their pups. Groups of Sprague-Dawley rats were fed diets having either a high vitamin A content [15 retinol equivalents (R.E.)/g diet] or a low vitamin A content (0.6 R.E./g) for 42 d, including 7-8 d prior to pregnancy, pregnancy, and for 14 d of lactation. The concentration of vitamin A in milk on d 14 of lactation was significantly greater on the high vitamin A diets [114 +/- 16 micrograms/dl (mean +/- SEM; n = 8) versus 52 +/- 7.3 micrograms/dl (n = 11), P less than 0.005]. However, milk vitamin A concentration on d 1 of lactation did not vary with maternal vitamin A intake during pregnancy. In a second study in which supplementation with vitamin A (30 R.E./g diet) was begun on d 1 postpartum, the milk vitamin A content increased progressively with duration of lactation. Maternal plasma vitamin A concentrations did not differ between rats fed the higher or lower vitamin A diets. However, liver vitamin A concentrations both of dams and of their 14-d-old pups were significantly higher when dams were fed the higher vitamin A diets during pregnancy and/or lactation. The results of these studies indicate that the transfer of vitamin A from mother to offspring by milk and the vitamin A status of dams and their suckling neonates is influenced by maternal vitamin A intake during lactation.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Animal Population Groups/metabolism , Animals, Suckling/metabolism , Lactation , Milk/metabolism , Vitamin A/administration & dosage , Animals , Body Weight , Female , Liver/metabolism , Pregnancy , Rats , Rats, Inbred Strains , Vitamin A/blood , Vitamin A/metabolism
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