Il est généralement accepté que les lits vasculaires oculaires auraient la faculté d’autoréguler leur apport sanguin afin de contrebalancer les variations de pression de perfusion oculaire (PPO). Plusieurs études ont tenté d’évaluer ce mécanisme en mesurant les effets d’une variation de la PPO - induite par un exercice ou par une augmentation de la pression intra-oculaire (PIO) à l’aide d’une suction sclérale - sur le débit sanguin oculaire (DSO). Or, les méthodes de mesure du DSO utilisées jusqu'à maintenant présentent de nombreux désavantages et limites, ce qui rend difficile leur usage clinique. De récents développements dans le domaine des investigations non-invasives des paramètres sanguins oculaires proposent un modèle capable de mesurer en temps réel la concentration en oxygène, un autre paramètre important du métabolisme rétinien. Dans le cadre de la présente étude, ce nouveau modèle est utilisé afin de mesurer les effets d’un effort physique dynamique sur la concentration d’oxygène dans les capillaires de la tête du nerf optique (COTNO) de sujets jeunes et en santé. Six jeunes hommes non fumeurs ont participé à l’étude. L’effort physique dynamique consistait en une séance de bicyclette stationnaire de 15 minutes menant à une augmentation du pouls à 160 battements par minute. La COTNO était mesurée avant et immédiatement après la séance d’exercice. La pression artérielle (PA) et la PIO étaient mesurées ponctuellement alors que le pouls et la saturation sanguine en oxygène (SpO2) au niveau digital étaient mesurés tout au long de l’expérience. L’effort physique a entrainé une réduction de la PIO chez tous les sujets, une réduction de la COTNO chez tous les sujets sauf un tandis que la SpO2 demeura constante chez tous les sujets. Une corrélation quadratique entre les variations de la PIO et de la COTNO a pu être notée. Ces résultats suggèrent une corrélation directe entre les variations de la COTNO et celles de la PPO et de la PA. Les résultats de la présente étude suggèrent que les variations de la COTNO chez un sujet en santé suite à un effort physique dynamique pourraient représenter sa capacité à compenser un tel effort. De plus, les changements métaboliques sanguins induits par l’effort physique dynamique pourraient représenter une cause commune aux variations de la PIO et de la COTNO. / It is generally accepted that ocular vascular beds have the ability to autoregulate their blood flow to counter balance the variations in the ocular perfusion pressure (OPP). Many studies have tried to evaluate this mechanism by quantifying the effects of a variation in OPP on the ocular blood flow (OBF). This was induced by either exercise or scleral suction which increases intra-ocular pressure (IOP). However, the methods used for these measurements have many disadvantages and limitations, which deters their clinical use. Recent developments in the field of non-invasive investigation of ocular blood parameters propose a model for the measurement, in real-time, of oxygen concentration in the blood streams, another important parameter of the retinal metabolism. In the present study, this new model is used to evaluate the effects of dynamic physical efforts on the blood oxygenation in the optic nerve head capillary structures (BOONH) in young healthy subjects. Six non-smoking young men participated in the study. 15-minute sessions of stationary bicycle leading to a heart rate of 160bpm were performed as dynamic physical effort. The BOONH was measured before and immediately after the exercise. The blood pressure (BP) and the IOP were measured periodically while the heart rate and the oxygen saturation in blood (SpO2) were measured in a finger throughout the exercise. The physical effort led to a reduction of the IOP in all subjects, a decrease in the BOONH in all but one subjects and a constant SpO2 in all subjects. A quadratic correlation was observed between the variations in IOP and in BOONH. These results suggest a direct correlation between the variations in BOONH and those of the OPP and the BP. The results of the present study suggest that the variations in BOONH in a healthy subject following a physical dynamic effort could indicate his/her capacity to compensate for such an effort. Moreover, the metabolic changes in the blood due to physical dynamic efforts could be a common cause of the variations in IOP and BOONH.

This Diploma Thesis is focused on study of electrochemical behavior of 2,4,6-trinitrotoluene (TNT) and 2,4,6-trinitrophenol (picric acid) on finding the optimum conditions for their determination using direct current voltammetry (DCV) and differential pulse voltammetry (DPV) at a mercury meniscus modified silver solid amalgam electrode (m-AgSAE) in the solution of Britton-Robinson (BR) and on finding of the limit of quantification (LQ) for these substances. Practical applicability of the newly developed methods was verified on direct determination of TNT and picric acid in model samples of drinking and river water. Moreover, the electrochemical behaviors of TNT and picric acid was studied using cyclic voltammetry (CV). Optimum medium for the determination of TNT at m-AgSAE was: methanol-BR buffer pH 4.0 (1:9). Upon the DCV it is proper to apply regeneration potentials Ereg,1= 0 mV and Ereg,2= -1100 mV and upon the DPV was apply regeneration potentials Ereg,1= 0 mV and Ereg,2= -600 mV were applied. The concentration dependence of the peak current was found to be linear for both techniques over the concentration range of 1·10-6 -1·10-4 mol/l with LQ of 0.54 µmol/l (for DCV) and 0.46 µmol/l (for DPV). The method developed for the determination of TNT were verified on the model samples of drinking...

The aim of presented Diploma Thesis was to study an electrochemical behavior of nitroimidazole drugs metronidazole and ornidazole and to find optimal conditions for their voltammetric determination at a mercury meniscus modified silver solid amalgam electrode using DC voltammetry (DCV) and differential pulse voltammetry (DPV). Voltammetric behavior of selected drugs was investigated in dependence on the pH of the medium used (realized using a Britton-Robinson buffer (BR buffer)) and a mechanism of the reduction of both drugs was investigated using cyclic voltammetry (CV). The optimum medium for voltammetric determination of studied nitroimidazole drugs at the m-AgSAE in a region of cathodic potentials was found to be the BR buffer of pH 8.0. Then, the concentration dependences were measured in this optimum medium in the concentration range from 2·10-7 mol/L to 1·10-4 mol/L. The limits of quantification (LQs) for both metronidazole and ornidazole were found in the concentration order of 10-7 mol/L by using DCV and DPV at the m-AgSAE. The applicability of the newly developed voltammetric methods of the determination of nitroimidazole drugs was verified on the model samples of drinking and river water, with LQ ≈ 2·10-7 mol/L for both DC voltammetry and differential pulse voltammetry at the m-AgSAE....

This thesis deals with the analysis of nano-structured layers deposited by high-frequency magnetron sputtering on the monocrystalline silicon surface. The content of the work focuses on the magnetron sputtering application as an alternative method for passivation and antireflection layers deposition of silicon solar cells. The procedure of pre-deposite silicon surface cleaning by plasma etching in the Ar/H2 gas mixture atmosphere is suggested. In the next step the silicon nitride and aluminum nitride layers with hydrogen content in Ar/N2/H2 gas mixture by magnetron sputtering are deposited. One part of the thesis describes an experimental pseudo-carbide films deposition from a silicon target in the atmosphere of acetylene (C2H2). An emphasis is placed on the research of sputtered layers properties and on the conditions on the silicon-layer interface with the help of the standard as well as special measurement methods. Sputtered layers structure is analyzed by modern X-ray spectroscopy (XPS) and by Fourier infrared spectroscopy (FTIR). Optical ellipsometry and spectrophotometry is used for the diagnostic of the layers optical properties depending upon the wavelength of incident light. A special method of determining the surface lay-out of the charge´s carrier life in the volume and on the surface of silicon is employed to investigate the passivating effects of the sputtered layers.

O objetivo desta pesquisa foi desenvolver e validar métodos analíticos para o fármaco besilato de anlodipino (ABC) em comprimidos. O método espectrofotométrico no ultra violeta e o método por cromatografia líquida de alta eficiência (CLAE) desenvolvidos foram considerados simples, exatos e precisos. Foram analisadas amostras contendo 5 mg,10 mg e uma amostra formulada de 5mg de ABC/comprimido. Para o método espectrofotométrico, a primeira diluição das amostras foi feita em metanol e as subseqüentes em água. A leitura foi efetuada a 364,4 nm. A linearidade para ABC foi estabelecida na faixa de 41,0-61,0 mg/mL e o coeficiente de correlação foi R= 0,9996. O limite de detecção e o de quantificação foram respectivamente 0,54 e 1,8 mcg/mL. A exatidão e a precisão foram 98,99% e 0,37%, respectivamente. Nas análises por cromatografia líquida de alta eficiência (CLAE), foram utilizadas as seguintes condições: coluna LiChrospher ® 100 RP-18 Merck ® (250 mm x 4,6 mm, 5µm), fase móvel constituída por metanol: água: (35:65) com 1% de TEA e pH ajustado para 5.0 com ácido fosfórico; fluxo de 1,0 mL/min; detecção UV a 238 nm e temperatura de 22 ±1°C.Tempo de retenção (RT) ABC foi de 3,7 min. Foi obtida linearidade no intervalo de 50 a 350 mcg/mL e coeficiente de correlação = 0,9999. O limite de detecção e o de quantificação foram respectivamente de 2,26 mcg/mL e 7,52 mcg/mL. A exatidão foi de 100,18% e a precisão foi de 0,37% para a CLAE. Ambos os métodos podem ser usados na rotina de análise para o controle de qualidade de comprimidos contendo ABC. / The objective of this research was to develop and validate analytical methods for the amlodipine besylate (ABC) determination in tablets. Simple, accurate and precise spectrophotometric and HPLC methods were validate for ABC determination in samples containing 5.0 and 10.0 mg of ABC / tablet. For the spectrophotometric method, the first dilutions of samples were made in methanol and the consecutive in distilled water. Determination was made at 364.4 nm. Linearity was in the range of 41.0-61.0 µg/mL and r= 0.9996. The detection and quantitation limits were respectively, 0.54 µg/mL and 1.80 µg/mL. Accuracy and precision were respectively, 98.99% and 0.37%. For HPLC analysis, the following conditions were used: a LiChrospher ® 100 RP-18 Merck® (250 mm x 4,6 mm, 5µm) column; methanol: water with 1% of triethylamine adjusted to pH 5.0 with phosphoric acid (35:65), as mobile phase; a flow rate of 1.0 mL /min; UV detection at 238 nm and temperature of 22 ±1 °C . Retention time was 3.7 min. Linearity was in the range of 50.0 - 350.0 µg/mL and r = 0.9999. The detection and quantitation limits were respectively, 2.26 µg/mL and 7.52 µg/mL. Accuracy and precision were respectively, 100.18% and 0.37%. Both methods can be used in routine analysis for quality control of tablets containing ABC.

O cloridrato de ranitidina, um antagonista dos receptores H2 da histamina, foi determinado em comprimidos e injetáveis por espectrofotometria no ultravioleta, a 313nm, e por espectrofotometria no visível, a 615nm, utilizando o cloridrato da hidrazona da 3-metil-2-benzotiazolinona (MBTH) a 0,35% em HCl 0,M e cloreto férrico a 0,40% em HCl 0,1M, como reagentes de cor. Na espectrofotometria no ultravioleta a lei de Beer foi obedecida no intervalo de concentração de 5,0 a 18,0 µg/mL. Quatro amostras comerciais foram analisadas. Os coeficientes de variação foram 0,36% e 0,71% para comprimidos, e 0,51% e 0,24% para injetáveis. A média de recuperação foi 99,88%. Na espectrofotometria no visível a lei de Beer foi obedecida no intervalo de concentração de 1,44 a 5,76 µg/mL. Os coeficientes de variação foram 0,72% e 0,59% para comprimidos, e 0,53% e 0,61% para injetáveis. A média de recuperação foi 99,39%. Os resultados foram comparados estatisticamente e foram compatíveis para as amostras que se encontravam em bom estado de conservação. / Ranitidine hydrochloride, a histamine H2-receptor antagonist, was determined in tablets and injections by ultraviolet spectrophotometry at 313nm , and visible spectrophotometry using as color reagent 0,35% 3-methyl-2-benzothiazolinone hydrochloride in HCl 0,1M and 0,40% ferric chloride in HCl 0,1M. In ultraviolet spectrophotometry, Beer\'s law was obeyed in the range of concentration from 5,0 to 18,0 µg/mL. Four commercially available were analyzed. The coefficients of variation were 0,36% and 0,71% for tablets, and 0,51% and 0,24% for injections. The recovery average was 99,88%. In visible spectrophotometry, Beer\'s law was obeyed in the range of concentration from 1,44 to 5,76 µg/mL. The coefficients of variation were 0,72% and 0,59% for tablets, and 0,53% and 0,61% for injections. The recovery average was 99,39%. The results obtained by using the two methods were statistically compared and were compatible when samples were kept in good conditions of storage.

Les traitements antireflets (AR) sont très largement utilisés pour améliorer la transmission de systèmes optiques composés de hublots, lentilles, de lames séparatrices,… Dans cette thèse les gammes spectrales visées sont le visible étendu [400-1800nm] et le moyen infrarouge [3,7-4,8µm]. La méthode de nanostructuration par dépôts de films minces utilisant des techniques PVD en incidence oblique (Oblique Angle Deposition) a été choisie car elle permet d’envisager des AR hautes performances sur une large gamme de longueur d’onde, via un procédé industrialisable. L’introduction de porosité via le contrôle des angles de dépôt est utilisée pour nanostructurer l’architecture de chaque couche et de l’empilement ; méthode permettant de modifier et d’optimiser les propriétés optiques des couches constituantes en vue d’un design complet optimal. Une cartographie des indices effectifs accessibles par OAD a été dégagée concernant les trois matériaux déposés (TiO2, SiO2 et Ge). Mais les propriétés optiques de ces couches nanostructurées diffèrent largement de celles des couches denses du fait de la présence d’anisotropie, de gradient d’indice, de diffusion et d’absorption. A partir de caractérisations microstructurales, chimiques et optiques poussées (AFM, MEB, MET, tomographie FIB, tomographie MET, EDX, EELS, spectrophotométrie et ellipsométrie généralisée) un modèle optique analytique plus complexe et couplé à des analyses par éléments finis (FDTD) est présenté. L’ensemble du travail a permis d’élaborer par OAD de simples antireflet bicouches démontrant déjà de hauts niveaux de transmission, supérieurs aux traitements AR existants (interférentiel) ou en développement (Moth-eyes). / Anti-reflective (AR) coatings are widely used to improve the transmission of optical systems composed of window, lenses, separating filters,... In this thesis, the spectral ranges targeted are the extended visible [400-1800nm] and the mid infrared [3.7-4.8µm]. Thin film deposition nanostructuring method using oblique angle deposition (oblique angle deposition) PVD technique was chosen because it allows high performance AR to be considered over a wide wavelength range, by an industrial process. The introduction of porosity with the control of deposition angle is used to nanostructure the architecture of each layer and stack; a method for modifying and optimizing the optical properties of the constituent layers for optimal complete design. A mapping of the effective indices accessible by OAD has been identified for the three materials deposited (TiO2, SiO2 and Ge). However optical properties of these nanostructured layers differ greatly from those of dense layers due to the presence of anisotropy, index gradient, diffusion and absorption. Based on advanced microstructural, chemical and optical characterizations (AFM, SEM, TEM, FIB tomography, TEM tomography, EDX, EELS, spectrophotometry and generalized ellipsometry) a more complex analytical optical model coupled with finite element analyses (FDTD) is presented. All the work has enabled OAD to develop simple two-layer anti-reflective coatings that already demonstrate high levels of transmission, superior to existing (interferential) or work in progress (Moth-eyes) AR treatments.

O presente trabalho apresenta o desenvolvimento de metodologias baseadas no sistema de Análise por Injeção Seqüencial (SIA) para a determinação de fosfato e silicato, nitrito e nitrato, assim como a especiação de Fe(II) e Fe(III) em amostras de interesse ambiental, com ênfase para sistemas aquáticos. Para todas as determinações utilizou-se a espectrofotometria de absorção molecular na região do visível como técnica de detecção. A determinação de fosfato e silicato foi baseada na reação de ambos os ânions com molibdato de amônio em meio ácido e posterior redução do Mo(VI) à Mo(V) com ácido ascórbico. O procedimento SIA foi desenvolvido para contornar a interferência mútua das duas espécies explorando o efeito de complexação do molibdato pelo ácido oxálico. A determinação de nitrito foi baseada na reação de diazotação com sulfanilamida e diclorato de N-1 naftil etilenodiamina (NED), enquanto a determinação de Fe(II) baseou-se na sua complexação com 1,10 fenantrolina. A determinação de nitrato e Fe(III) foi efetuada pelas mesmas reações após a redução a nitrito e Fe(II) em colunas de cádmio e zinco amalgamado, respectivamente. A estabilidade das curvas analíticas foi avaliada em diferentes dias de trabalho, obtendo-se variações não superiores a 5% durante um período de 4 dias. O sistema de injeção seqüencial foi explorado também no sentido de regenerar as colunas redutoras no intervalo de tempo entre duas amostras. A estabilidade das curvas analíticas, a viabilidade de regeneração das colunas redutoras e a possibilidade de realizar a amostragem através de filtração tangencial, permitindo a realização de análises com características de tempo real, sugerem que o sistema de injeção seqüencial tem grande potencial para ser implementado em estações automáticas de monitoramento da fração solúvel de indicadores de poluição em águas naturais e residuais. / The present work presents the development of analytical methodologies based on Sequential Injection Analysis (SIA) for determination of phosphate and silicate, nitrite and nitrate, as well as speciation Fe(II)/Fe(III) in environmental samples with emphasis for aquatic environments. All determinations were performed using molecular absorption spectrophotometry at the visible range of the spectrum as the detection technique. The determination of phosphate and silicate was based on the reaction of both anions with ammonium molybdate in acidic medium, followed by reduction of Mo(VI) to Mo(V) with ascorbic acid. The SIA procedure was developed to avoid the mutual interference of both species exploiting the complexation of the molybdate by oxalic acid. The determination of nitrite was based on the diazotation reaction with sulfanilamide and N-l naphtyl ethylenediamine dihydrochlorine (NED), while the determination of Fe(II) were based on the complexation with 1,10 phenantroline. The determination of nitrate and Fe(III) were based on the same reactions, performed after their reduction to nitrite and Fe(II) in reducing columns containing cooperized cadmium and amalgamated zinc, respectively. The stability of the analytical curves was evaluated in different working days, in which no variations greater than 5% were observed during a period of 4 consecutive days. The sequential injection analysis was exploited to regenerate the reducing columns in the time interval between two sample. The stability of the analytical curves, the easy and automatic regeneration of the reducing columns, as well as the possibility to perform sampling through tangential filtration, which permits the analysis to be performed in real time, are characteristics that show the potential application of the sequential injection systems in automatic stations for monitoring the soluble fraction of pollution indicators in natural waste waters.

Bases científicas para o entendimento dos efeitos da poluição atmosférica sobre a saúde humana são ainda necessárias em todo o mundo, considerando que os dados locais devem ser utilizados como parâmetro para tomada de decisão e controle da poluição do ar. Países em desenvolvimento carecem de tecnologia para detecção e mensuração dos níveis de poluição do ar, o que dificulta a atualização de legislação sobre padrões da qualidade do ar para o controle das fontes emissoras. Diversas abordagens metodológicas tem sido sugeridas por agências internacionais, no entanto para o contexto local faz-se necessário adaptações que resulte em métodos replicáveis pelas agências brasileiras. No Brasil, o Ministério da Saúde, através da Vigilância em Saúde Ambiental, estimula o desenvolvimento de metodologias que possam viabilizar a implementação do programa de vigilância em saúde relacionada à qualidade do ar. O objetivo deste estudo foi aplicar a metodologia de análise de riscos para avaliar a qualidade do ar na cidade de Salvador e o impacto sobre a saúde, na perspectiva de implantação de ações da Vigilância em Saúde Ambiental. Este estudo se caracteriza como ciência no contexto da ação. Foram realizados dois estudos para aplicação da metodologia proposta. No primeiro estudo, em fase de identificação do perigo, os poluentes foram caracterizados em termos de sua composição química, utilizando a técnica de biomonitoramento como ferramenta alternativa para acessar as partículas presentes na atmosfera urbana. Para a detecção de metais no material particulado foram utilizadas técnicas analíticas de espectrofotometria de absorção atômica e para a análise morfológica destas partículas foram utilizadas técnicas de microscopia eletrônica de varredura convencional e micro análises de raios-x. A composição química do material particulado foi estudada para entendimento das emissões locais. No segundo estudo, além da identificação do contaminante e caracterização do risco foi também avaliado a exposição à saúde humana. Estratégias de comunicação de riscos foram utilizadas para o envolvimento de partes interessadas. Os resultados de contaminação atmosférica observados nesta tese sugerem que as ferramentas aplicadas no contexto da análise de riscos, em suas diversas etapas, são viáveis, apresentando evidências científicas aos tomadores de decisão, e assim contribuindo com novas tecnologias para o SUS, especialmente na implementação de programa em vigilância da saúde relacionada à qualidade do ar / Scientific bases for understanding the effects of atmospheric pollution on human health are still necessary in all parts of the world, considering that local data should be used as a parameter for decision-making and the control of air pollution. Developing countries lack the technology to detect and measure levels of air pollution, making it difficult to update legislation on air quality standards for the control of emission sources. Several methodological approaches have been suggested by international agencies, however for the local context it is necessary to make adjustments that will result in replicable methods across Brazilian agencies. In Brazil, the Ministry of Health, through the Environmental Health Surveillance, stimulates the development of methodologies that can facilitate the implementation of a health surveillance program related to air quality. The objective of this study was to apply risk analysis methods to evaluate the air quality of the city of Salvador and its impact on health, from the perspective of the Environmental Health Surveillance\'s regulatory actions. This study is characterized by science and decision. Two studies were conducted that applied the proposed methods. In the first study, during the hazard identification phase, pollutants were characterized in terms of their chemical composition using a biomonitoring technique as an alternative tool to access the particles present in the urban atmosphere. The analytic techniques of atomic absorption spectrophotometry were used for the detection of metals in the particulate matter, and for the morphologic analysis of these particles, conventional scanning electron microscopy and X-ray microanalysis techniques were used. The chemical composition of the particulate matter was then studied to understand local emissions. In the second study, in addition to contaminant identification and risk characterization, human health exposure was also evaluated. Risk communication strategies were used for the involvement of stakeholders. The observed results of atmospheric contamination in this thesis suggest that the applied tools within the context of risk analysis, in its diverse stages, are viable and present scientific evidence to decision-making, thus contributing new technologies for National Health System, particularly the implementation of a health surveillance program related to air quality

O cloridrato de ranitidina, um antagonista dos receptores H2 da histamina, foi determinado em comprimidos e injetáveis por espectrofotometria no ultravioleta, a 313nm, e por espectrofotometria no visível, a 615nm, utilizando o cloridrato da hidrazona da 3-metil-2-benzotiazolinona (MBTH) a 0,35% em HCl 0,M e cloreto férrico a 0,40% em HCl 0,1M, como reagentes de cor. Na espectrofotometria no ultravioleta a lei de Beer foi obedecida no intervalo de concentração de 5,0 a 18,0 µg/mL. Quatro amostras comerciais foram analisadas. Os coeficientes de variação foram 0,36% e 0,71% para comprimidos, e 0,51% e 0,24% para injetáveis. A média de recuperação foi 99,88%. Na espectrofotometria no visível a lei de Beer foi obedecida no intervalo de concentração de 1,44 a 5,76 µg/mL. Os coeficientes de variação foram 0,72% e 0,59% para comprimidos, e 0,53% e 0,61% para injetáveis. A média de recuperação foi 99,39%. Os resultados foram comparados estatisticamente e foram compatíveis para as amostras que se encontravam em bom estado de conservação. / Ranitidine hydrochloride, a histamine H2-receptor antagonist, was determined in tablets and injections by ultraviolet spectrophotometry at 313nm , and visible spectrophotometry using as color reagent 0,35% 3-methyl-2-benzothiazolinone hydrochloride in HCl 0,1M and 0,40% ferric chloride in HCl 0,1M. In ultraviolet spectrophotometry, Beer\'s law was obeyed in the range of concentration from 5,0 to 18,0 µg/mL. Four commercially available were analyzed. The coefficients of variation were 0,36% and 0,71% for tablets, and 0,51% and 0,24% for injections. The recovery average was 99,88%. In visible spectrophotometry, Beer\'s law was obeyed in the range of concentration from 1,44 to 5,76 µg/mL. The coefficients of variation were 0,72% and 0,59% for tablets, and 0,53% and 0,61% for injections. The recovery average was 99,39%. The results obtained by using the two methods were statistically compared and were compatible when samples were kept in good conditions of storage.