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1.
Int. j. morphol ; 42(3): 698-708, jun. 2024. ilus, tab
Article in English | LILACS | ID: biblio-1564638

ABSTRACT

SUMMARY: Tissue engineering aims to fabricate a scaffold that exhibits a suitable surface topography for a desired cellular response. Therefore, a study analyzing the characteristics of bone grafts is important for future research directions. This work aims to analyze the physical-chemical characteristics of commercially available bone grafts of human and bovine origin for dental use, using morphological analysis of the surface and chemical composition by variable pressure scanning electron microscope (VP-SEM) and energy-dispersive x-ray (EDX) spectrometry. In addition, pore diameter and surface area were analyzed by degassing method using a porosimeter, and particle size by laser diffraction. The analyzed allograft and xenograft particles differ in morphological characteristics and chemical composition. The allograft particles present a cuboidal and prismatic geometric morphology with angled edges and the absence of macropores. On the contrary, the xenograft particles present an irregular morphology with macropores in their structure. There is a statistically significant difference in C, P, and Ca between the xenograft and allografts (p < 0,05). The analyzed composition of allografts showed mainly the presence of C and O. In contrast, the composition of the xenograft was mainly Ca. These differences could influence the osteogenic properties of allografts and xenografts. This analysis provides basic information to understand the physicochemical properties of allografts and xenografts that facilitate cell-graft interaction.


La ingeniería de tejidos tiene como objetivo fabricar un andamio que muestre una topografía de superficie adecuada para una respuesta celular deseada. Por tanto, un estudio que analice las características de los injertos óseos es importante para futuros enfoques de investigación. Este trabajo tiene como objetivo analizar las características físico-químicas de injertos óseos de origen humano y bovino disponibles comercialmente para uso odontológico, mediante análisis morfológico de la superficie y composición química mediante microscopio electrónico de barrido de presión variable (VP-SEM) y x-dispersivo de energía. espectrometría de rayos (EDX). Además, el diámetro de los poros y el área superficial se analizaron mediante el método de desgasificación utilizando un porosímetro y el tamaño de las partículas mediante difracción láser. Las partículas de aloinjerto y xenoinjerto analizadas difieren en características morfológicas y composición química. Las partículas del aloinjerto presentan una morfología geométrica cúbica y prismática con bordes angulados y ausencia de macroporos. Por el contrario, las partículas de xenoinjerto presentan una morfología irregular con macroporos en su estructura. Existe una diferencia estadísticamente significativa en C, P y Ca entre el xenoinjerto y los aloinjertos (p < 0,05). La composición analizada de los aloinjertos mostró principalmente la presencia de C y O. Por el contrario, la composición del xenoinjerto fue principalmente Ca. Estas diferencias podrían influir en las propiedades osteogénicas de los aloinjertos y xenoinjertos. Este análisis proporciona información básica para comprender las propiedades fisicoquímicas de aloinjertos y xenoinjertos que facilitan la interacción célula-injerto.


Subject(s)
Humans , Animals , Cattle , Allografts/anatomy & histology , Allografts/chemistry , Spectrometry, X-Ray Emission , Bone Regeneration , Microscopy, Electron, Scanning , Porosity , Bone Transplantation , Heterografts/anatomy & histology , Heterografts/chemistry
2.
Int. j. morphol ; 42(2): 530-537, abr. 2024. ilus, tab
Article in English | LILACS | ID: biblio-1558130

ABSTRACT

SUMMARY: Even though morphometric and mineral studies related to the guinea pig (Cavia porcellus) skull have been carried out, this study is the first attempt to evaluate all developmental stages of male and female guinea pigs. This study aims to this study is to create 3D modeling of CT images obtained from the skulls of male and female guinea pigs during the developmental period (prepuberty and the period between puberty and adulthood) and following periods (young adulthood and old adulthood), to analyze some biometric bone data such as volume, surface area and length, and to assess the developmental analysis of the mineral matter change in their skulls. The CT-scanned skulls were transferred to 3D Slicer (5.0.2), which is used for 3D modeling. The surface area and volume were calculated by measuring the measurement points on the models. In addition, the XRF device was used to show elemental ratio changes during different developmental stages. According to metric measurements, a gradual increase was observed during the life period. The metric measurements of the skull bone had a higher measurement value in male guinea pigs than in their female counterparts. While Ca/P ratio increased up to the third group and partially decreased in the fourth group in males, it gradually increased from the first group to the fourth group in females. This study revealed that puberty, adulthood and sex were effective in the physical and chemical characterization of skull bone structure in guinea pigs.


Aunque se han realizado estudios morfométricos y de minerales relacionados con el cráneo del cobayo (Cavia porcellus), esta investigación es el primer intento de evaluar las etapas de desarrollo de cobayos machos y hembras. El objetivo de este estudio fue crear un modelado 3D de imágenes de tomografía computarizada obtenidas de los cráneos de cobayos machos y hembras durante el período de desarrollo (prepubertad y el período entre la pubertad y la edad adulta) y los períodos siguientes (edad adulta joven y edad adulta mayor), para analizar algunos datos biométricos de los huesos, como el volumen, la superficie y la longitud, y además, analizar el cambio de materia mineral en sus cráneos durante el desarrollo. Los cráneos escaneados se transfirieron a 3D Slicer (5.0.2), que se utiliza para el modelado 3D. El área de superficie y el volumen se calcularon midiendo los puntos de medición en los modelos. Además, se utilizó el dispositivo XRF para mostrar los cambios en las proporciones elementales durante diferentes etapas de desarrollo. Según mediciones métricas, se observó un aumento gradual durante el período de vida. Las medidas métricas del hueso del cráneo tuvieron un valor de medición más alto en los cobayos machos que en las hembras. Mientras que la relación Ca/P aumentó hasta el tercer grupo y disminuyó parcialmente en el cuarto grupo en los machos y aumentó gradualmente del primer grupo al cuarto grupo en las hembras. Este estudio reveló que la pubertad, la edad adulta y el sexo fueron efectivos en la caracterización física y química de la estructura ósea del cráneo en cobayos.


Subject(s)
Animals , Male , Female , Guinea Pigs , Skull/chemistry , Skull/diagnostic imaging , Tomography, X-Ray Computed , Imaging, Three-Dimensional , Skull/anatomy & histology , Spectrometry, X-Ray Emission , Minerals/analysis
3.
Braz. j. oral sci ; 22: e231303, Jan.-Dec. 2023. ilus
Article in English | LILACS, BBO | ID: biblio-1442844

ABSTRACT

Aim: To evaluate the potential of inducing mineral density changes of indirect pulp capping materials applied to demineralized dentin. Methods: A total of 50 cavities were prepared, 5 in each tooth, in extracted ten molars without caries, impacted or semi-embedded. The cavities were scanned by microcomputed tomography (µ-CT) after creating artificial caries by microcosm method (pre-treatment). Each cavity was subjected to one of 5 different experimental conditions: control (dental wax), conventional glass ionomer cement (Fuji IX GP Extra), resin-modified calcium silicate (TheraCal LC), resin-modified calcium hydroxide (Ultra-Blend Plus), MTA (MM-MTA) and the samples were kept under intrapulpal pressure using simulated body fluid for 45 days. Then, the second µ-CT scan was performed (post-treatment), and the change in dentin mineral density was calculated. Afterward, elemental mapping was performed on the dentinal surfaces adjacent to the pulp capping agents of 5 randomly selected samples using energy dispersive X-ray spectroscopy (EDS) apparatus attached to a scanning electron microscope (SEM). The Ca/P ratio by weight was calculated. Friedman test and Wilcoxon Signed Ranks test were used to analyze the data. Results: There was a significant increase in mineral density values of demineralized dentin after treatment for all material groups (p<0.05). Resin-modified calcium silicate had similar efficacy to MTA and conventional glass ionomer cement, but was superior to resin-modified calcium hydroxide in increasing the mineral density values of demineralized dentin. Conclusions: Demineralized dentin tissue that is still repairable can be effectively preserved using materials with remineralization capability


Subject(s)
Spectrometry, X-Ray Emission , Calcium Hydroxide , Silicates , Calcium Compounds , X-Ray Microtomography , Glass Ionomer Cements
4.
Int. j. high dilution res ; 21: 67-84, June 20, 2022.
Article in English | LILACS, HomeoIndex | ID: biblio-1396376

ABSTRACT

Homeopathy is highly controversial. The main reason for this is its use of very highly dilute medicines (high homeopathic potencies, HHP), diluted beyond the Avogadro/Loschmidt limit. Research using Nano Tracking Analysis has demonstrated the presence of particles in HHPs. This study aims to verify the results of a previous publication that identified the ionic composition of these particles in all dilutions. We used Scanning Electron Microscopy & Energy Dispersive X-Ray Spectroscopy (SEM-EDX) to examine dilutions of a commonly used homeopathic medicine, an insoluble metal, Cuprum metallicum, for the presence of particles (NPs). The homeopathic medicines tested were specially prepared according to the European pharmacopoeia standards. We compared the homeopathic dilutions/dynamizations of copper with simple dilutions and dynamized lactose controls. We observed an ionic diversity common to all preparations including HHPs but also significant differences in the relative quantity of each ion between manufacturing lines of homeopathic copper and lactose controls. The probability that the observed differences could have occurred chance alone (especially above Avogadro limit) can be rejected at p < 0.001. The essential component of these homeopathic medicines is sodium hydrogen carbonate, modulated by some other elements and by its quantity, size and shape. Homeopathic medicines made of Cuprum metallicum do contain material with a specific ionic composition even in HHPs diluted beyond the Avogadro/Loschmidt limit. This specificity can be attributed to the manufacturing process. This material demonstrates that the step-by-step process (dynamized or not) does not match the theoretical expectations of a dilution process. The starting material and dilution/dynamization method influences the nature of these NPs. Further measurements are needed on other raw materials using the same controls (solvent and simply diluted manufacturing lines) to support these findings. The role of sodium bicarbonate must be carefully studied in the future.


Subject(s)
Dynamization , Homeopathic Pharmacy Techniques , Nanoparticles , Spectrometry, X-Ray Emission , Microscopy, Electron, Scanning , Cuprum , Sodium Bicarbonate , Copper , Lactose
5.
Int. j. morphol ; 40(2): 530-539, 2022. ilus, tab
Article in Spanish | LILACS | ID: biblio-1385613

ABSTRACT

RESUMEN: En salmonicultura se utilizan imágenes de rayos X, para evaluar la columna vertebral y las aletas, pero estas no permiten cuantificar los minerales que constituyen el hueso, para esto se utilizan otras técnicas que son destructivas. La Microscopía Electrónica de Barrido de presión variable (VP SEM) acoplada al detector espectroscopia de rayos X de energía dispersiva (EDX) acoplado, nos permite analizar la microestructura y a la vez determinar elementos químicos, porcentaje y distribución presentes en puntos específicos en una muestra. Se utilizaron 5 truchas control y 5 con deformidad mandibular, de agua dulce en etapa de smolt, se analizó la estructura y mineralización del hueso, se eligieron en promedio 6 puntos de cuantificación por región de interés y se analizaron mediante Microscopía Electrónica de Barrido (VP SEM-EDX). Los datos obtenidos muestran porcentaje en masa de Ca promedio en hueso articular de truchas fueron de 8.07 % y de 14.48 % en truchas con deformidad mandibular y control respectivamente y el porcentaje en masa promedio de P es de 4.07 % y 7.60 %, en truchas con deformidad mandibular y control respectivamente. Se identificó además otros elementos presentes en la muestra como Mg, Na, C, O, N, S, F, Zn, Al y Fe, con especial interés en el aumento de carbono en las muestras analizadas con deformidad mandibular y la presencia de aluminio en todas las muestras. La Técnica de VP SEM-EDX, permite evaluar de forma directa, sin destrucción de la muestra y con una preparación mínima de la muestra. En el hueso, la aplicación más frecuente de SEM-EDX es la medición del contenido de Ca y P y la relación que existe entre estos elementos Ca/P, en la muestra. Paralelamente la técnica nos permite la detección de otros microelementos provenientes del agua o de la alimentación y que eventualmente pueden provocar alteraciones en los peces, confirmando la hipótesis que el microanálisis elemental tiene utilidad para la salmonicultura.


SUMMARY: In salmon farming systems, X-ray images are used to evaluate the spine and fins, but these do not allow quantifying the minerals that make up the bone, for different techniques that are destructive are used. Variable Pressure Scanning Electron Microscopy (VP SEM) coupled to an Energy Dispersive X-ray spectroscopy detector (EDX), allows us to analyze the microstructure and at the same time determine chemical elements, percentages, and distribution present at specific points in a sample. Five control and five jaw deformity trout, from freshwater and in the smolt stage were used. The structure and mineralization of the bone were analyzed, an average six quantification points were chosen per region of interest (ROI) and then they were analyzed by Scanning Electron Microscopy (VP SEM-EDX). The data obtained have shown the average mass percentage of calcium in trout joint bone was 8.07 % and 14.48 % in jaw deformity and control trout, respectively; and the average mass percentage of phosphorus is 4.07 % and 7.60 %, in jaw deformity and control trout, respectively. Other elements present in the sample were also identified, such as magnesium, sodium, carbon, oxygen, nitrogen, sulphur, fluorine, zinc, aluminium, and iron, with special interest the increase of carbon in the analyzed samples with mandibular deformity and the presence of aluminum in all samples. The VP SEM-EDX Technique allows direct evaluation, without destruction of the sample and with minimal sample preparation. In bone, the most frequent application of SEM-EDX is the measurement of the content of calcium (Ca) and phosphorus (P) and the relationship that exists between these elements, calcium/phosphorus (Ca/P), in the sample. At the same time, the technique allows us to detect other microelements from water or food that can eventually cause alterations in fish, confirming the hypothesis that elemental microanalysis is useful for salmon farming.


Subject(s)
Animals , Tooth/chemistry , Oncorhynchus mykiss , Mandible/chemistry , Minerals/analysis , Spectrometry, X-Ray Emission , Tooth/ultrastructure , Microscopy, Electron, Scanning , Mandible/ultrastructure
6.
Natal; s.n; 29 dez. 2021. 93 p. tab, ilus, graf.
Thesis in Portuguese | LILACS, BBO | ID: biblio-1532968

ABSTRACT

Introdução: Os fios Copper Ni-Ti (CuNiTi) possuem indicações de uso clínico específicas, permanecendo no ambiente bucal por um longo período. Por esse motivo suas características mecânicas, termodinâmicas e estruturais devem ser preservadas durante todo o período de uso. Objetivos: Investigar se ocorrem alterações no comportamento mecânico, termodinâmico, estrutura e composição química superficial em fios CuNiTi 35°C submetidos ao envelhecimento in vivo (uso clínico) e in vitro (termociclagem), evidenciando as possíveis diferenças entre os métodos de envelhecimento. Material e Métodos: A amostra total foi constituída de 30 arcos pré-contornados 0.016", termodinâmicos com adição de cobre, e temperatura austenítica final (Af) de 35°C, da marca Ormco®. As análises destes fios resultaram em dois capítulos. Para o experimento clínico, 10 unidades de fios foram instaladas em 05 pacientes e permaneceram em meio bucal durante 30, 60 e 90 dias, e 05 fios foram analisados como recebidos (CR). A cada período, um hemiarco completo mais 1/3 (um terço) do hemiarco inferior direito foi retirado para análises. Para o experimento in vitro os 15 fios restantes foram submetidos à termociclagem para simulação do envelhecimento em ambiente oral durante 30 (600 ciclos), 60 (1200 ciclos) e 90 dias (1800 ciclos) com variação de temperatura entre 5°C e 55°C, com banhos de 90 segundos em cada temperatura, e transição de 15 segundos entre os banhos. Após cada período de envelhecimento in vivo e in vitro, os fios foram submetidos a um teste de padronização das suas dimensões através da medição dos diâmetros com paquímetro, Microscopia Eletrônica de Varredura (MEV), Espectrometria por Raios X Fluorescentes (FRX), ensaios de tração uniaxial e ensaio de Varredura Diferencial de Calorimetria (DSC). Resultados: No capítulo 1 a comparação entre os fios CR e os envelhecidos revelou que não houve diferença significativa entre os diâmetros das amostras, das forças obtidas ou mesmo das temperaturas Af, independentemente do tempo de permanência em boca. Foram encontrados predominantemente Ni, Ti, Cu e Al nas amostras, além de outros elementos químicos em concentrações variadas. No capítulo 2 não houve diferença significativa entre os diâmetros das amostras, das forças obtidas ou mesmo das temperaturas Af entre as amostras, independentemente do tempo ou do método de envelhecimento. Conclusão: As análises laboratoriais dos fios envelhecidos in vivo e in vitro foram comparadas, evidenciando que as características mecânicas, termodinâmicas e químicas dos fios permanecem estáveis mesmo até 90 dias de uso clínico ou 1800 ciclos de termociclagem. O método de envelhecimento in vitro se mostra uma alternativa viável para a análise destes parâmetros, em substituição aos métodos in vivo (AU).


Introduction: Copper Ni-Ti wires (CuNiTi) have specific indications for clinical use, remaining in the oral environment for a long period. For this reason, their mechanical, thermodynamic and structural characteristics must be preserved throughout the period of use of these materials. Objectives: To investigate whether there are changes in the mechanical, thermodynamic, structure and surface chemical composition of CuNiTi 35°C wires subjected to in vivo aging (clinical use) and in vitro (thermocycling), highlighting the possible differences between the aging methods. Material and Methods: The total sample was obtained from 30 pre-contoured Ormco® 0.016 thermodynamic archwires with copper addition and austenitic final temperature (Af) of 35°C. The analysis of these archwires resulted in two articles. For the clinical experiment, 10 units of wires were installed in 05 patients and remained in the oral environment for 30, 60 and 90 days, and 05 wires were analyzed as received. At each period, a complete hemiarch plus 1/3 of the right lower hemiarch was removed for analysis. For the in vitro experiment, the 15 remaining wires underwent thermocycling to simulate the aging of the oral environment for 30 (600 cycles), 60 (1200 cycles) and 90 days (1800 cycles) with a temperature range between 5°C and 55°C, with 90 second baths at each temperature, and 15 second transition between baths. After each in vivo and in vitro aging period, the wires underwent to a standardization test of their dimensions, by defining the diameters with a caliper, Scanning Electron Microscopy (SEM), Fluorescent X-Ray Spectrometry (FRX), tests of Uniaxial traction and Differential Scanning Calorimetry (DSC) test. Results: In chapter 1, the comparison between CR and aged wires revealed that there was no significant difference between the sample diameters, the forces obtained or even the temperatures Af, regardless the time spent in the mouth. Predominantly Ni, Ti, Cu and Al were found in the samples, in addition to other chemical elements in different concentrations. In chapter 2 there was no significant difference between the diameters of the samples, the forces obtained or even the temperatures Af between the samples, regardless of time or aging method. Conclusion: The comparison of the laboratoral analyzes of the archwires aged in vivo and in vitro showed that the mechanical, thermodynamic and the surface chemical characteristics were stable, even up to 90 days of clinical use or 1800 thermocycling cycles. The in vitro aging method is a viable alternative for the analysis of these parameters, replacing the in vivo methods (AU).


Subject(s)
Orthodontic Wires , Orthodontics , Spectrometry, X-Ray Emission/instrumentation , Smart Materials , Calorimetry, Differential Scanning , Microscopy, Electron, Scanning/instrumentation
7.
Int. j. odontostomatol. (Print) ; 15(2): 381-386, jun. 2021. ilus, tab, graf
Article in Spanish | LILACS | ID: biblio-1385772

ABSTRACT

Los instrumentos rotatorios utilizados en el tratamiento de conductos dentales necesitan cumplir con ciertas características físicas que le confieran un uso correcto, adecuado y seguro para su uso clínico. En el mercado comercial existen una serie de instrumentos importados que dejan en duda la autenticidad de estos debido a sus bajos costos. En este estudio evaluamos física, química y morfológicamente dos kits de instrumentos rotatorios Protaper universal (Dentsply) mediante análisis de MEB, EDX, microdureza y EDS. Uno de los kits (grupo 1) se adquirió directamente de la casa comercial y otro kit importado que a simple vista no parecía cumplir con los estándares de calidad de un correcto empaquetado (grupo 2). En el análisis de MEB se observaron características morfológicas muy diferentes entre ambos kits, el grupo 2 presentó diversas irregularidades en la superficie de las limas, sin embargo, en el EDS no se encontró diferencia alguna. En cuanto al análisis de microdureza se observó una estadística estadísticamente significativa y en el EDS se observaron mayores picos de intensidad en cuanto a la aleación de Ni-Ti en el grupo 2. Estos resultados sugieren que existen instrumentos rotatorios importados que a pesar de su bajo costo pueden presentar ciertas características muy similares a los kits auténticos, sin embargo, física y químicamente pueden resultar en un riesgo para su uso clínico debido a la diferencia entre estos.


Rotatory files are instruments used in the treatment of dental canals roots. These instruments need to comply with certain physical characteristics for a correct, adequate and safe use for clinical use. In the commercial market there are a series of imported instruments that cast doubt on their authenticity due to their low costs. In this study we physically, chemically and morphologically evaluated two Protaper universal rotary instrument kits (Dentsply) using SEM, EDX, microhardness and EDS analysis. One of the kits (group 1) was purchased directly from the commercial house and another imported kit that a simple view did not seem to meet the quality standards of a correct packaging (group 2). In the SEM analysis, very different morphological characteristics were observed between both kits, group 2 presented various irregularities on the surface of the files, however, no difference was found in the EDS. Regarding the microhardness analysis, a statistically significant statistic was observed and in the EDS, higher intensity peaks were observed in terms of the Ni-Ti alloy in group 2. These results suggest that there are imported rotary instruments that despite their low cost can present characteristics very similar to authentic kits, however, physically and chemically they can result in a risk for their clinical use due to the difference between them.


Subject(s)
Root Canal Filling Materials/chemistry , Root Canal Obturation/instrumentation , Dental Instruments , Rotation , Spectrometry, X-Ray Emission , Materials Testing , Root Canal Preparation/instrumentation , Equipment Design
8.
Rev. biol. trop ; Rev. biol. trop;69(supl. 2)mar. 2021.
Article in English | LILACS, SaludCR | ID: biblio-1507768

ABSTRACT

Introduction: Echinoderm coelomocytes have traditionally been investigated through a morphological approach using light microscopy, which relies on the idea of constant cell shape as a stable character. However, this can be affected by biotic or abiotic conditions. Objective: To analyze if the consistency in cell morphology offered by the cytocentrifugation method, might be used as a convenient tool to study echinoderm coelomocytes. Methods: Cells of Echinaster (Othilia) brasiliensis (Asteroidea), Holothuria (Holothuria) tubulosa (Holothuroidea), Eucidaris tribuloides, Arbacia lixula, Lytechinus variegatus, and Echinometra lucunter (Echinoidea) were spread on microscope slides by cytocentrifugation, stained, and analyzed through light microscopy. Additionally, fluorescence microscopy, scanning electron microscopy, and energy-dispersive x-ray spectroscopy were applied to cytospin preparations, to complement the analysis of granular and colorless spherulocytes of Eucidaris tribuloides. Results: Altogether, 11 cell types, including phagocytes, spherulocytes, vibratile cells, and progenitor cells were identified in the samples analyzed. The granular spherulocyte, a newly-described cell type, was observed in all Echinoidea and was very similar to the acidophilic spherulocytes of Holothuria (Holothuria) tubulosa. Conclusions: Cytocentrifugation proved to be versatile, either as the main method of investigation in stained preparations, or as a framework on which other procedures may be performed. Its ability to maintain a constant morphology allowed accurate correspondence between live and fixed/stained cells, differentiation among similar spherulocytes as well as comparisons between similar cells of Holothuroidea and Echinoidea.


Introducción: Los celomocitos de equinodermos se han investigado tradicionalmente a través de un enfoque morfológico utilizando microscopía óptica, que se basa en la idea de la forma celular constante como un carácter estable. Sin embargo, esto puede verse afectado por condiciones bióticas o abióticas. Objetivo: Analizar si la consistencia en la morfología celular que ofrece el método de citocentrifugación podría utilizarse como una herramienta conveniente para estudiar los celomocitos de equinodermos. Métodos: Células de Echinaster (Othilia) brasiliensis (Asteroidea), Holothuria (Holothuria) tubulosa (Holothuroidea), Eucidaris tribuloides, Arbacia lixula, Lytechinus variegatus y Echinometra lucunter (Echinoidea) se esparcieron en portaobjetos de microscopio por citocentrifugación, se tiñeron y analizaron mediante microscopía óptica. Adicionalmente, se aplicó microscopía de fluorescencia, microscopía electrónica de barrido y espectroscopía de rayos X con dispersión de energía a las preparaciones de citoespina, para complementar el análisis de los esferulocitos granulares e incoloros de Eucidaris tribuloides. Resultados: En total, se identificaron en las muestras analizadas 11 tipos de células, incluidos fagocitos, esferulocitos, células vibrátiles y células progenitoras. El esferulocito granular, un tipo de célula recién descrito, se observó en todos los Echinoidea y fue muy similar a los esferulocitos acidófilos de Holothuria (Holothuria) tubulosa. Conclusiones: La citocentrifugación demostró ser un método bastante versátil, ya sea como el método principal de investigación en preparaciones teñidas o como un marco en el que se pueden realizar otros procedimientos. Su capacidad para mantener una morfología constante permitió una correspondencia precisa entre las células vivas y las células fijas/teñidas, la diferenciación entre esferulocitos similares, así como comparaciones entre células similares de Holothuroidea y Echinoidea.


Subject(s)
Animals , Spectrometry, X-Ray Emission/methods , Echinodermata/microbiology , Centrifugation/instrumentation , Cell Nucleus Shape
9.
Araçatuba; s.n; 2021. 38 p. ilus, graf, tab.
Thesis in Portuguese | BBO, LILACS | ID: biblio-1435696

ABSTRACT

O objetivo do presente estudo foi sintetizar e caracterizar ciclotrifosfato de sódio (NaTMP) contendo cálcio, e verificar seu efeito utilizando modelo de lesões iniciais de erosão do esmalte. Os ciclotrifosfatos contendo cálcio (CaNaTMP) foram sintetizados utilizando coluna para cromatografia e adição de sobrenadante de solução contendo hidróxido de cálcio e analisados por meio de microscopia eletrônica de varredura e espectroscopia de raios-X por dispersão de energia. Para determinar o efeito sobre lesões erosivas iniciais, blocos de esmalte bovino sadios (n=96) foram selecionados por dureza de superfície inicial e divididos em 8 grupos experimentais (12 blocos/grupo): controle (água deionizada), 0,24% NaF (1100 ppm F), 0,25%, 0,5% e 1% de NaTMP e CaNaTMP nas mesmas concentrações. Os blocos de esmalte foram imersos em 4 mL das soluções experimentais durante 2 minutos, seguidos por 4 desafios erosivos (ácido cítrico, 0,75%, pH 3,5, por 1 minuto, sob agitação). A porcentagem de perda da dureza de superfície (%SH) foi calculada após cada desafio ácido. Os dados foram submetidos à análise de variância de medidas repetidas a dois critérios, seguida pelo teste de Tukey (p< 0,05). O processo de síntese levou a substituição de átomos de Na por átomos de Ca e as partículas apresentaram tamanhos homogêneos. As soluções contendo 0,25%, 0,5% e 1% CaNaTMP apresentaram menor %SH quando comparadas as suas contrapartes sem cálcio (p< 0,001), após os quatro desafios erosivos. Quando comparado a solução contendo 1100 ppm F, as soluções 0,5% e 1% CaNaTMP promoveram redução na perda de dureza (p< 0,001). Concluiu-se que soluções contendo CaNaTMP promoveram efeitos protetores superiores em comparação ao grupo 1100 ppm F sobre lesões iniciais do esmalte(AU)


The objective of the present study was to synthesize and characterize sodium cyclotriphosphate (NaTMP) containing calcium and verify its effect using an initial enamel erosion model. Cyclotriphosphate containing calcium (CaNaTMP) was synthesized using column chromatography, and addition of a solution with calcio hydroxide supernatant and analyzed by scanning electron microscopy and energydispersive X-ray spectroscopy. To determine the effect on enamel initial erosion, sound bovine enamel blocks (n=96) were selected by initial surface hardness and divided into to 8 experimental groups (12 blocks/group): control (deionized water), 0.24% NaF (1100 ppm F), 0.25%, 0.5% and 1% NaTMP and CaNaTMP at the same concentrations. The enamel blocks were immersed in 4 mL of the experimental solutions for 2 minutes followed by 4 erosive challenges (citric acid, 0.75%, pH 3.5, for 1 minute, under stirring). The percentage of surface hardness variation (%SH) was calculated after each acid challenge. Data were subjected to two-way repeated measures analysis of variance, followed by Tukey's test (p< 0.05). The synthesis process led to the replacement atoms of Na by atoms of Ca with particles having, homogeneous sizes. The solutions containing 0.25%, 0.5% and 1% CaNaTMP promoted lower %SH when compared to their counterparts without calcium (p< 0.001), after the four erosive challenges. When compared to the solution containing 1100 ppm F, the 0.5% and 1% CaNaTMP solutions were superior in reducing hardness loss (p< 0.001). It was concluded that solutions containing CaNaTMP led to superior protective effects compared to the 1100 ppm F group on initial enamel erosion(AU)


Subject(s)
Phosphates , Tooth Erosion , Calcium , Dental Enamel/injuries , Spectrometry, X-Ray Emission , Tooth Erosion/prevention & control , Microscopy, Electron, Scanning , Dental Enamel
10.
Braz. dent. sci ; 24(1): 1-10, 2021. tab, ilus
Article in English | BBO, LILACS | ID: biblio-1145375

ABSTRACT

Objectives: This study aimed to assess the effect of the polishing procedure and surface sealant application on the fluoride release of restorative materials. Material and Methods: The groups were consisted of using five different restorative materials were employed: Beautifil II, GCP Glass Fill, Amalgomer CR, Zirconomer and Fuji IX GP. 30 disk-shaped specimens (8x2 mm) were prepared from each material. Each group was subdivided into three groups considering finishing procedures: Mylar strip, polishing with Super-Snap discs, G-Coat Plus application after polishing with Super-Snap discs. The amount of fluoride released into distilled water was measured using a fluoride ion-selective electrode and ion analyzer after 24 hours, followed by measurement on days 3, 7, 15, 21, and 28. Surface analysis of the materials was performed with SEM (Scanning Electron Microscopy) and EDS (Energy Dispersive X-ray Spectroscopy). The data were statistically analyzed using two-way repeated measure ANOVA and LSD test (p=0.05). Results: The highest amount of fluoride released was measured after the first 24 h for all materials. Beautifil II released less fluoride than other materials in all measurement periods (p<0.05). After polishing, the amount of fluoride released from all materials except Beautifil II increased (p<0.05). The application of G-Coat Plus did not impact the amount of fluoride release of any materials (p>0.05). EDS analysis showed the most percentage of oxygen in all materials. Conclusion: The polishing procedure might induce an increase in fluoride release of glass ionomer-based materials, and the application of G-Coat Plus cannot affect the amount of fluoride release. (AU)


Objetivos: Este estudo teve como objetivo avaliar o efeito do procedimento de polimento e aplicação de selante superficial na liberação de flúor de materiais restauradores. Material e Métodos: Os grupos consistiram na utilização de cinco materiais restauradores diferentes: Beautifil II, GCP Glass Fill, Amalgomer CR, Zirconomer e Fuji IX GP. Trinta espécimes em forma de disco (8x2 mm) foram preparados a partir de cada material. Cada grupo foi subdividido em três grupos considerando os procedimentos de acabamento: tira Mylar, polimento com discos Super-Snap, aplicação de G-Coat Plus após polimento com discos Super-Snap. A quantidade de flúor liberada na água destilada foi medida usando um eletrodo íon-seletivo de fluoreto e analisador de íons após 24 horas, seguido pela medição nos dias 3, 7, 15, 21 e 28. A análise da superfície dos materiais foi realizada com MEV (Microscopia Eletrônica de Varredura) e EDS (Espectroscopia de Energia Dispersiva de Raios-X). Os dados foram analisados estatisticamente usando ANOVA de dois fatores com medidas repetidas e teste LSD (p = 0,05). Resultados: A maior quantidade de flúor liberado foi medida após as primeiras 24 horas para todos os materiais. O Beautifil II liberou menos flúor do que outros materiais em todos os períodos avaliados (p <0,05). Após o polimento, a quantidade de flúor liberada de todos os materiais, exceto Beautifil II, aumentou (p <0,05). A aplicação de G-Coat Plus não afetou a quantidade de liberação de flúor de nenhum material (p> 0,05). A análise por EDS revelou a maior porcentagem de oxigênio em todos os materiais. Conclusão: O procedimento de polimento pode induzir um aumento na liberação de flúor de materiais à base de ionômero de vidro, e a aplicação de G-Coat Plus não pode afetar a quantidade de liberação de flúor (AU)


Subject(s)
Spectrometry, X-Ray Emission , Fluorides , Glass Ionomer Cements
11.
Araçatuba; s.n; 2021. 137 p. ilus, graf, tab.
Thesis in English, Portuguese | LILACS, BBO | ID: biblio-1436158

ABSTRACT

O objetivo deste estudo in vitro foi avaliar o efeito da aplicação de agentes antioxidantes após o clareamento dentário e previamente à cimentação de laminados cerâmicos na estabilidade cromática do conjunto restaurador, assim como nas propriedades mecânicas de nanodureza (HIT), módulo de elasticidade (Eit*), grau de conversão, resistência de união e morfologia da interface adesiva. Ademais, a neutralização de peróxido de hidrogênio e a caracterização superficial do esmalte, como ângulo de contato, energia de superfície, energia livre total de interação, microscopia eletrônica de varredura e espectroscopia de energia dispersiva do substrato submetido à ação das soluções antioxidantes e do agente clareador também foram analisados. Duzentos e quarenta e dois blocos de esmalte dentário (7x8x0,6mm) foram utilizados para o processo de cimentação e distribuídos em grupos experimentais de acordo com os métodos de procedimentos (grupo não clareado, grupo clareado com Whiteness HP Maxx 35%), tipos de antioxidantes adotados (controle; ácido ascórbico 10% e α-tocoferol 10%) e períodos de cimentação (após 24 horas e 14 dias do processo de cimentação) (n = 22). Foi utilizado o sistema adesivo Tetric N Bond Universal e o cimento resinoso Variolink Esthetic LC (Ivoclar Vivadent) como agentes cimentantes. Os dados foram submetidos a testes estatísticos de normalidade e analisados por ANOVA e teste de Tukey (α = 0,05). Os dados da morfologia da interface adesiva, obtidas pela microscopia confocal a laser, foram submetidas ao teste Kappa inter-examinadores e os dados foram submetidos aos testes Kruskal-Wallis e Dunn (α = 0,05). Os resultados mostraram que, de modo geral, a utilização da solução antioxidante α-tocoferol 10% pós-clareamento no período mediato promoveu resultados satisfatórios com relação à estabilidade cromática do conjunto restaurador, assim como para as propriedades mecânicas, grau de conversão, resistência de união e morfologia da interface adesiva comparado ao grupo clareado sem associação dos agentes antioxidantes, tanto para o período mediato, quanto para o período de 14 dias (p< 0,05). A solução de αtocoferol 10% apresentou maiores valores de neutralização do peróxido de hidrogênio e maiores valores de molhabilidade do esmalte em relação aos grupos controle e ácido ascórbico (p< 0,05). A energia de superfície e energia livre total de interação do esmalte dentário foi significativamente influenciada pelo tratamento clareador (p< 0,05). Dessa forma, conclui-se que o emprego da solução antioxidante α-tocoferol 10% promoveu resultados promissores, sugerindo que o mesmo poderia ser utilizado mediatamente após o clareamento dental na cimentação de laminados cerâmicos(AU)


The aim of this in vitro study was to evaluate the effect of antioxidant agents application after tooth bleaching and prior to luting of ceramic veneers on color stability of the restorative set, as well as on mechanical properties of nanohardness (HIT), elastic modulus (Eit*), degree of conversion, bond strength and morphology of the adhesive interface. Furthermore, the hydrogen peroxide neutralization and surface characterization of enamel, such as contact angle, surface energy, total free energy of interaction, scanning electron microscopy and energy-dispersive spectroscopy of the substrate submitted to the action of antioxidant solutions and bleaching agent were also analyzed. Two hundred forty two dental enamel blocks (7 x 8 x 0.6 mm) were used for the luting process and distributed into experimental groups according to the procedure methods (unbleached group, bleached group with Whiteness HP Maxx 35%), types of antioxidants adopted (control; 10% ascorbic acid and 10% α-tocopherol) and the luting periods (24 hours and 14 days after the luting process) (n = 22). Tetric N Bond Universal adhesive system and Variolink Esthetic LC resin cement (Ivoclar Vivadent) were used as luting agents. Data were submitted to statistical tests of normality and analyzed by ANOVA and Tukey tests (α = 0.05). The adhesive interface morphology data, obtained by confocal laser microscopy, were submitted to the interexaminer Kappa test and the data were submitted to Kruskal-Wallis and Dunn´s tests (α = 0.05). The results showed that, in general, the use of 10% α-tocopherol antioxidant solution after bleaching in mediate period promoted satisfactory results regarding the color stability of the restorative set, as well as for the mechanical properties, degree of conversion, shear bond strength and adhesive interface morphology compared to the bleached group without antioxidant agents association, both for the mediate and 14-day period (P < 0.05). The 10% αtocopherol solution showed higher hydrogen peroxide neutralization values and higher enamel wettability values compared to the control and ascorbic acid groups (P < 0.05). Surface energy and total free energy of interaction of tooth enamel were significantly influenced by the bleaching treatment (P < 0.05). Thus, it is concluded that the use of 10% αtocopherol antioxidant solution promoted promising results, suggesting that it could be used mediately after tooth bleaching on luting of ceramic laminates(AU)


Subject(s)
Tooth Bleaching , Ceramics , Cementation , Antioxidants , Ascorbic Acid , Spectrometry, X-Ray Emission , Surface Properties , Oxidative Stress , Resin Cements , Tocopherols , Dental Cements , Dental Enamel , Shear Strength , Elastic Modulus , Hardness , Hydrogen Peroxide
12.
Braz. oral res. (Online) ; 34: e005, 2020. tab, graf
Article in English | LILACS | ID: biblio-1055521

ABSTRACT

Abstract The purpose of this study was to evaluate the effect of ionizing radiation from high energy X-ray on fluoride release, surface roughness, flexural strength, and surface chemical composition of the materials. The study groups comprised five different restorative materials: Beautifil II, GCP Glass Fill, Amalgomer CR, Zirconomer, and Fuji IX GP. Twenty disk-shaped specimens (8x2 mm) for fluoride release and 20 bar-shaped specimens (25 x 2x 2 mm) for flexural strength were prepared from each material. Each material group was divided into two subgroups: irradiated (IR) and non-irradiated (Non-IR). The specimens from IR groups were irradiated with 1.8 Gy/day for 39 days (total IR = 70.2 Gy). The amount of fluoride released into deionized water was measured using a fluoride ion-selective electrode and ion analyzer after 24 hours and on days 2, 3, 7, 15, 21, 28, 35, and 39 (n = 10). The flexural strength was evaluated using the three-point bending test (n = 10). After the period of measurement of fluoride release, seven specimens (n = 7) from each group were randomly selected to evaluate surface roughness using AFM and one specimen was randomly selected for the SEM and EDS analyses. Data were analyzed with two-way ANOVA and Tukey tests (p = 0.05). The irradiation significantly increased fluoride release and surface roughness for Amalgomer CR and Zirconomer groups (p < 0.05). No significant change in flexural strength of the materials was observed after irradiation (p > 0.05). The ionizing radiation altered the amount of fluoride release and surface roughness of only Amalgomer CR and Zirconomer. The effect could be related to the chemical compositions of materials.


Subject(s)
Apatites/radiation effects , Radiation, Ionizing , Bisphenol A-Glycidyl Methacrylate/radiation effects , Composite Resins/radiation effects , Fluorides/chemistry , Glass Ionomer Cements/radiation effects , Apatites/chemistry , Reference Values , Spectrometry, X-Ray Emission , Surface Properties/radiation effects , Time Factors , Zirconium/radiation effects , Zirconium/chemistry , Materials Testing , Microscopy, Electron, Scanning , Reproducibility of Results , Analysis of Variance , Bisphenol A-Glycidyl Methacrylate/chemistry , Statistics, Nonparametric , Composite Resins/chemistry , Flexural Strength , Glass Ionomer Cements/chemistry
13.
Braz. J. Pharm. Sci. (Online) ; 56: e18440, 2020. tab, graf
Article in English | LILACS | ID: biblio-1249159

ABSTRACT

In this study, naftifine (a topical antifungal drug) loaded poly(vinyl) alcohol (PVA)/sodium alginate (SA) nanofibrous mats were prepared using the single-needle electrospinning technique. The produced nanofibers were crosslinked with glutaraldehyde (GTA) vapor. The morphology and diameter of the electrospun nanofibers were studied by scanning electron microscopy (SEM). SEM images showed the smoothness of the nanofibers and indicated that the fiber diameter increased with crosslinking and drug loading. Atomic force microscopy (AFM) images confirmed the uniform production of the scaffolds, and elemental mapping via energy dispersive X-ray spectroscopy (EDS) showed the uniform distribution of the drug within the nanofibers. An attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy study demonstrated that naftifine has sufficient secondary interactions with the polymer blend. The crosslinking treatment decreased the burst drug release effectively and the release mechanism followed Korsmeyer-Peppas Super Case-II transport. Overall, these findings suggest the potential use of naftifine-loaded PVA/SA nanofibers as a topical antifungal drug delivery system.


Subject(s)
Administration, Topical , Nanofibers/analysis , Spectrometry, X-Ray Emission/instrumentation , Spectrum Analysis/instrumentation , Pharmaceutical Preparations/administration & dosage , Drug Delivery Systems , Spectroscopy, Fourier Transform Infrared/methods , Microscopy, Atomic Force/instrumentation , Alginates/adverse effects , Drug Liberation
14.
Pesqui. vet. bras ; Pesqui. Vet. Bras. (Online);39(12): 933-941, Dec. 2019. tab, ilus
Article in English | VETINDEX, LILACS | ID: biblio-1056925

ABSTRACT

Bovine periodontitis is a multifactorial disease primarily associated with a potentially pathogenic microbiota housed in the oral biofilm of animals. Biofilms are organized structures, in which the constituents coexist in symbiosis, already described as a predisposing factor to periodontitis in other species. The objective of the present study was to characterize the structure and chemical aspects of the bovine black pigmented supragingival biofilm using scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS), respectively, and determine its relationship with bovine periodontitis. Eleven premolar teeth from different animals were evaluated; five non-pigmented samples and six samples with black pigmented biofilms were initially submitted to SEM, and three areas of these samples were selected for EDS. The structure of the pigmented biofilm was more complex and irregular because of a higher content of mineral elements. The semi-quantitative EDS data indicated an association of iron (p<0.014) and magnesium (p<0.001) with the occurrence of periodontitis, whereas carbon, phosphorus, calcium, manganese, sodium, and potassium were not associated with the disease. Carbon (p<0.039), manganese (p<0.007), and iron (p<0.015) were associated with pigmentation, whereas phosphorus, calcium, and magnesium were not associated with it. Spearman correlation test showed the relationships between calcium and phosphorus, and iron and silicon. The strong association of iron in the pigmented supragingival biofilm and with the occurrence of periodontitis suggests the presence of microorganisms that use this element in their metabolism and that are also associated with bovine periodontitis. This study suggests that the pigmented deposits in the crown of the teeth of cattle are an true biofilm with the deposition of iron, and it indicates that the presence of iron and magnesium in these formations may be involved in the metabolism of some microorganisms associated with the etiology of bovine periodontitis.(AU)


A periodontite bovina é uma infecção multifatorial associada primariamente à microbiota potencialmente patogênica presente no biofilme bucal. Biofilmes são estruturas organizadas, nas quais os constituintes convivem em simbiose, descritos em outras espécies como um fator predisponente à periodontite. O objetivo do presente estudo foi caracterizar estrutural e quimicamente o biofilme supragengival pigmentado de preto em bovinos, utilizando-se as técnicas de microscopia eletrônica de varredura (MEV) e espectroscopia de dispersão de energia (EDS), respectivamente, correlacionando os elementos identificados à ocorrência de periodontite e pigmentação. Foram avaliados 11 dentes primeiro-molares; cinco amostras sem pigmentação visível e seis amostras com biofilme pigmentado de preto, que foram submetidas inicialmente à MEV; posteriormente foram selecionadas três áreas aleatórias de cada dente para realização da EDS. A estrutura do biofilme pigmentado revelou formações irregulares e mais complexas, provavelmente devido ao maior acúmulo de elementos minerais. Os resultados semi-quantitativos da EDS apontaram associações entre a presença de ferro (p<0,014) e magnésio (p<0,001) com a ocorrência de periodontite. Carbono, fósforo, cálcio, manganês, sódio e potássio não apresentaram associação com a periodontite. Em relação à pigmentação, carbono (p<0,039), manganês (p<0,007) e ferro (p<0,015) foram os elementos estatisticamente significantes, enquanto fósforo, cálcio e magnésio não apresentaram associação com a pigmentação. O teste de correlação de Spearman demonstrou associações entre os elementos cálcio e fósforo, e ferro e silício. A forte associação do ferro presente no biofilme supragengival com a ocorrência de periodontite, sugere a presença de micro-organismos que utilizam este elemento em seu metabolismo e que possivelmente tenham envolvimento com o desenvolvimento da periodontite bovina. Os resultados inéditos do presente trabalho sugerem que os depósitos pigmentados que se formam na coroa dos dentes de bovinos são um biofilme verdadeiro com deposição de ferro, e indicam que a presença de ferro e magnésio nestas formações pode estar envolvida no metabolismo de alguns dos principais micro-organismos associados à etiologia da periodontite bovina.(AU)


Subject(s)
Animals , Cattle , Periodontitis/etiology , Periodontitis/veterinary , Dental Plaque/etiology , Dental Plaque/veterinary , Dental Plaque/chemistry , Periodontitis/microbiology , Spectrometry, X-Ray Emission/veterinary , Microscopy, Electron, Scanning/veterinary , Iron , Magnesium
15.
Rev. chil. radiol ; 25(3): 94-102, oct. 2019. tab, ilus
Article in Spanish | LILACS | ID: biblio-1058206

ABSTRACT

Resumen: Se presenta una aplicación basada en Microsoft Excel llamada Xpektrin para el cálculo de dosis en radiología general. La aplicación permite simular espectros de rayos X en radiología general utilizando el modelo TASMICS a partir de mediciones del kerma en aire (Kair) y de la capa Hemirreductora (HVL). Tiene implementado el cálculo de magnitudes radiométricas y dosimétricas, como el kerma en aire en la superficie de entrada (Ke) y la dosis en piel (Dskin), en función de la elección arbitraria de los factores de exposición, el tipo y grosor de filtro, la distancia foco-piel y el tamaño de campo. Xpektrin fue validado con la herramienta computacional SPEKTR 3.0, utilizando mediciones de dosis y de HVL de tubos de rayos X de tres recintos hospitalarios. Se encontró buena correlación en ambas aplicaciones entre las mediciones experimentales y los valores calculados de HVL y con coeficientes de Pearson R² ≥ 0.99 en todos los casos. Sin embargo, se obtuvo mejor concordancia con los valores experimentales de HVL con Xpektrin (mediana de diferencias -0.43%, -0.04% y 0.01%) que con SPEKTR 3.0 (mediana de diferencias -3.31%, 0.10% y -7.85%), en particular para el tubo con mayor filtración. Xpektrin está optimizada para ser utilizada en los departamentos de radiología para la determinación de dosis de pacientes individuales en función de los parámetros utilizados durante la exposición, por lo que puede ser utilizada como parte de un sistema de registro dosimétrico o como apoyo para el establecimiento de niveles de referencia para diagnóstico (NRD), siendo particularmente útil en servicios con equipos sin registros automáticos de dosis. Además, debido a sus características de simulador, puede ser útil como herramienta pedagógica. El uso de Excel permite que sea altamente distribuible y fácil de usar, sin necesidad de conocimientos de programación.


Abstract: Xpektrin, an easy to use and highly distributable X-Ray Spectra Simulator in General Radiography. An application based on Microsoft Excel called Xpektrin is presented for dose calculation in general radiology. The application was developed to simulate X-ray spectra in general radiography using the TASMICS model. Using as inputs air kerma (Kair) and Half-value layer (HVL) measurements, Xpektrin allows the calculation of several radiometric and dosimetric quantities, such as the entrance surface air kerma (Ke) and the skin dose (Dskin), depending on the exposure factors, filter material type, filter thickness, focus-skin distance and field size. Xpektrin was validated against the Matlab toolkit SPEKTR 3.0, using dose and HVL measurements of X-ray tubes from three different hospitals. It was found good correlation in both applications between the experimental measurements and the calculated HVL and Kair values with Pearson coefficients R² ≥ 0.99 in all cases. However, experimental and calculated HVL have better agreement with Xpektrin (median percent difference -0.43%, -0.04% and 0.01%) than SPEKTR 3.0 (median percent difference -3.31%, 0.10% and -7.85%), particularly for the tube with greater filtration thickness. Xpektrin is optimized to be used in radiology departments for patient dose determination depending on the exposure parameters and may be used as part of a dosimetric record system or as a support for the determination of Diagnostic Reference Levels, which may be useful when no automatic dose records are available. In addition, due to its simulator characteristics, it can be useful as a pedagogical tool. Using Excel allows Xpektrin to be highly distributable and easy to use, without the need for programming skills.


Subject(s)
Humans , Radiology/methods , Spectrometry, X-Ray Emission/methods , Computer Simulation , Spectrometry, X-Ray Emission/standards , Software , Monte Carlo Method , Diagnostic Reference Levels
16.
J. appl. oral sci ; J. appl. oral sci;27: e20180233, 2019. tab, graf
Article in English | LILACS, BBO | ID: biblio-975899

ABSTRACT

Abstract Objective: To analyze color change, microhardness and chemical composition of enamel bleached with in-office bleaching agent with different desensitizing application protocols. Materials and Methods: One hundred and seventeen polished anterior human enamel surfaces were obtained and randomly divided into nine groups (n = 13). After recording initial color, microhardness and chemical composition, the bleaching treatments were performed as G1: Signal Professional White Now POWDER&LIQUID FAST 38% Hydrogen peroxide(S); G2: S+Flor Opal/0.5% fluoride ion(F); G3: S+GC Tooth Mousse/Casein Phosphopeptide-Amorphous Calcium Phosphate (CPP-ACP) paste(TM); G4: S+UltraEZ/3% potassium nitrate&0.11% fluoride(U); G5: S+Signal Professional SENSITIVE PHASE 1/30% Nano-Hydroxyapatite (n-HAP) suspension(SP); G6: S-F mixture; G7: S-TM mixture; G8: S-U mixture; G9: S-SP mixture. Color, microhardness and chemical composition measurements were repeated after 1 and 14 days. The percentage of microhardness loss (PML) was calculated 1 and 14 days after bleaching. Data were analyzed with ANOVA, Welch ANOVA, Tukey and Dunnett T3 tests (p<0.05). Results: Color change was observed in all groups. The highest ΔE was observed at G7 after 1 day, and ΔE at G8 was the highest after 14 days (p<0.05). A decrease in microhardness was observed in all groups except G6 and G7 after 1 day. The microhardness of all groups increased after 14 days in comparison with 1 day after bleaching (p>0.05). PML was observed in all groups except G6 and G7 after bleaching and none of the groups showed PML after 14 days. No significant changes were observed after bleaching at Ca and P levels and Ca/P ratios at 1 or 14 days after bleaching (p>0.05). F mass increased only in G2 and G6, 1 day after bleaching (p<0.05). Conclusions: The use of desensitizing agents containing fluoride, CPP-ACP, potassium nitrate or n-HAP after in-office bleaching or mixed in bleaching agent did not inhibit the bleaching effect. However, they all recovered microhardness of enamel 14 days after in-office bleaching.


Subject(s)
Humans , Tooth Bleaching/methods , Dental Enamel/drug effects , Dentin Desensitizing Agents/chemistry , Tooth Bleaching Agents/chemistry , Reference Values , Saliva, Artificial/chemistry , Spectrometry, X-Ray Emission , Spectrophotometry , Surface Properties/drug effects , Time Factors , Materials Testing , Calcium Phosphates/chemistry , Microscopy, Electron, Scanning , Caseins/chemistry , Random Allocation , Reproducibility of Results , Analysis of Variance , Potassium Compounds/chemistry , Color , Statistics, Nonparametric , Dental Enamel/chemistry , Hardness Tests , Hydrogen Peroxide/chemistry , Nitrates/chemistry
17.
Braz. oral res. (Online) ; 33: e015, 2019. tab, graf
Article in English | LILACS | ID: biblio-989477

ABSTRACT

Abstract We assessed the effect of a new coating material based on resin-modified glass-ionomer with calcium (Ca) in inhibiting the demineralization of underlying and adjacent areas surrounding caries-like lesions in enamel. The measures used were surface hardness (SH) and cross-sectional hardness (CSH). Thirty-six bovine enamel specimens (3 × 6 × 2 mm) were randomly allocated into three groups (n = 12): No treatment (NT); resin-modified glass-ionomer with Ca (Clinpro XT Varnish, 3M ESPE) (CL), and fluoride varnish (Duraphat, Colgate) (DU). The specimens were subjected to alternated immersions in demineralizing (6 h) and remineralizing solutions (18 h) for 7 days. SH measurements were conducted at standard distances of 150, 300, and 450 µm from the treatment area. CSH evaluated the mean hardness profile over the depth of the enamel surface and at standard distances from the materials. The energy-dispersive X-ray spectroscopy analysis was conducted to evaluate the demineralization bands created on the sublayer by % of calcium (Ca), phosphorus (P), and fluoride (F). Ca/P weight ratio was also calculated. Based on SH and CSH measurements, there was no difference between groups at the distances 150 µm (p = 0.882), 300 µm (p = 0.995), and 450 µm (p = 0.998). Up to 50 µm depth (at 150 µm from the treatment area), CL showed better performance than DU ( p< 0.05). NT presented higher loss of Ca and P than CL and DU (p < 0.05). There was no significant difference in the % of F ion among the three groups. The new coating material was similar to F varnish in attenuating enamel demineralization.


Subject(s)
Animals , Cattle , Calcium/chemistry , Resin Cements/chemistry , Dental Enamel/drug effects , Glass Ionomer Cements/chemistry , Reference Values , Sodium Fluoride/chemistry , Spectrometry, X-Ray Emission , Surface Properties/drug effects , Time Factors , Materials Testing , Cariostatic Agents/chemistry , Random Allocation , Fluorides, Topical/chemistry , Reproducibility of Results , Tooth Demineralization/prevention & control , Hardness Tests , Hydrogen-Ion Concentration
18.
Korean J. Ophthalmol ; Korean J. Ophthalmol;: 8-15, 2019.
Article in English | WPRIM | ID: wpr-741304

ABSTRACT

PURPOSE: To investigate the clinical manifestations and properties of remnant particles in the subconjunctival space after high-frequency radio-wave electrosurgery for conjunctivochalasis. METHODS: We performed a retrospective, observational case series with in vitro experimental imaging in nine eyes from eight patients who presented with small dark-gray lesions during follow-up after high-frequency radio-wave electrosurgery for conjunctivochalasis. General examination including slit-lamp examination and visual acuity testing was performed preoperatively and postoperatively. During follow-up, we evaluated remnant particles and any other complications including granuloma or conjunctival injection with slit-lamp photography and anterior optical coherence tomography. Coagulation tips were investigated with scanning electron microscope and energy dispersive X-ray spectroscopy to analyze the insulating electrode and assess changes to tips after repeated use. RESULTS: None of the patients included in this study experienced any change in visual acuity or major complications postoperatively. Small dark-gray lesions (0.3 to 0.5 mm in size) were observed in the inferior bulbar sub-conjunctival space in the location where high-frequency radio-wave electrosurgery had been performed. Cirrus high-definition optical coherence tomography images revealed focal hyper-reflection with a posterior shadow, suggesting foreign particles. Scanning electron microscopy and energy dispersive X-ray spectroscopy imaging analysis revealed peaks of carbon and fluorine complexes, consistent with the polytetrafluoroethylene coating on the electrode. CONCLUSIONS: There were no instances of inflammatory reaction, particle migration, or major complications due to particles. Physicians should be aware of the possibility of remnant polytetrafluoroethylene particles in subconjunctival tissue when using insulated coagulation tips subjected to repeat sterilization.


Subject(s)
Humans , Carbon , Electrodes , Electrosurgery , Fluorine , Follow-Up Studies , Granuloma , In Vitro Techniques , Microscopy, Electron, Scanning , Photography , Polytetrafluoroethylene , Retrospective Studies , Spectrometry, X-Ray Emission , Sterilization , Tomography, Optical Coherence , Visual Acuity
19.
Annals of Dermatology ; : 666-668, 2019.
Article in English | WPRIM | ID: wpr-762389

ABSTRACT

Localized cutaneous argyria is a rare condition in which the skin changes into blue-grey spots due to the absorption of silver. The lesions need to be differentiated from other pigmentary disorders and require radiographic and histological examination for more accurate diagnosis. Scanning electron microscopy and energy dispersive x-ray spectroscopy can be a confirmatory tool in the evaluation of silver elements in biopsy tissue. This report shows the localized cutaneous argyria in earlobe of a 21-year-old woman who wears silver earrings for 10 years.


Subject(s)
Female , Humans , Young Adult , Absorption , Argyria , Biopsy , Diagnosis , Ear , Microscopy, Electron, Scanning , Nevus, Blue , Silver , Skin , Spectrometry, X-Ray Emission
20.
Article in English | WPRIM | ID: wpr-764043

ABSTRACT

In the present study, rutile phase titanium dioxide nanoparticles (R-TiO₂ NPs) were prepared by hydrolysis of titanium tetrachloride in an aqueous solution followed by calcination at 900℃. The composition of R-TiO₂ NPs was determined by the analysis of X-ray diffraction data, and the characteristic features of R-TiO₂ NPs such as the surface functional group, particle size, shape, surface topography, and morphological behavior were analyzed by Fourier-transform infrared spectroscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy, transmission electron microscopy, dynamic light scattering, and zeta potential measurements. The average size of the prepared R-TiO₂ NPs was 76 nm, the surface area was 19 m²/g, zeta potential was −20.8 mV, and average hydrodynamic diameter in dimethyl sulfoxide (DMSO)–H₂O solution was 550 nm. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and morphological observations revealed that R-TiO₂ NPs were cytocompatible with oral cancer cells, with no inhibition of cell growth and proliferation. This suggests the efficacy of R-TiO₂ NPs for the aesthetic white pigmentation of teeth.


Subject(s)
Dimethyl Sulfoxide , Dynamic Light Scattering , Hydrodynamics , Hydrolysis , Microscopy, Electron, Scanning , Microscopy, Electron, Transmission , Mouth Neoplasms , Nanoparticles , Particle Size , Pigmentation , Spectrometry, X-Ray Emission , Spectrum Analysis , Titanium , Tooth , X-Ray Diffraction
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