Ex Vivo Analysis of MTA FLOW® Biomineralization and Push-Out Strength: A Pilot Study / Análisis ex vivo del proceso de biomineralización y resistencia al desplazamiento del MTA FLOW®: Estudio piloto

Abstract: This study evaluated the biomineralization processes and push-out strength of MTA Flow® with radicular dentine in three different consistencies. The push-out test was performed on an ex vivo model, using 2mm thick dentin discs from the middle third of the root with standardized cavities of 1.5 mm. Samples were filled with MTA-Angelus (Angelus Dental, Brazil), Biodentine (Septodont, France), MTA Flow® Putty (Ultradent, USA), MTA Flow® Thick or MTA Flow® Thin. The samples were divided into 3 groups: subgroup 1 (n=5), analysis of the biomineralization process; 2 (n=20), evaluation of the bonding strength and push-out resistance; and 3 (n=5), evaluation of the cement/ dentin interface. The samples filled with Biodentine had a higher precipitation of carbonate apatite. However, there was no significant difference between MTA-Angelus, MTA Flow® Putty, or Thick (p=0.0536), but there was a significant difference in the Thin group (P<0.05). The samples with Biodentine displayed the greatest release of calcium ions. The formation of a partially carbonated intermediate apatite layer was observed in all groups. Zones of biomineralization were observed at the interface but were not continuous. After 72 hours, a significant difference was found between the Biodentine and MTA Flow® Thin groups (p=0.0090) in the push-out test. The samples submerged in phosphate-buffered saline (PBS) for 15 days showed a significant difference between all groups and MTA Flow® Thin (p=0.0147). Putty or Thick consistencies presented a similar bonding strength to MTA-Angelus and Biodentine. MTA Flow® Putty and Thick consistencies show a good adaptation to dentin, similar to MTA-Angelus. However, the thickness of the interface was lower compared to that of Biodentine. MTA Flow® Thin, despite their tubular infiltration, results in gaps and a defective peripheral seal.Therefore, MTA Flow®, in Putty or Thick consistencies, presents a biomineralization process and push-out strength similar to MTA Angelus and Biodentine, however, both characteristics decreases considerably in Thin consistency.

Resumen: El objetivo de este estudio fue evaluar, en un modelo ex vivo, el proceso de biomineralización y fuerza de adhesión del MTA Flow® en sus tres diferentes consistencias por medio de la prueba de resistencia al desplazamiento (Push-out). Se utilizaron discos de dentina de 2mm de espesor del tercio medio radicular con cavidades estandarizadas de 1.5mm de diámetro, las cuales se obturaron con diferentes materiales entre ellos: MTA Angelus (Angelus Dental, Brasil), Biodentine (Septodont, Francia), MTA Flow® Consistencia Putty (Ultradent, E.E.U.U), MTA Flow® Consistencia Thick (Ultradent, E.E.U.U) y MTA Flow® Consistencia Thin (Ultradent, E.E.U.U). Las muestras se sometieron al proceso de biomineralización y a pruebas de Push-out. Las muestras obturadas con Biodentine promovieron una mayor precipitación de apatita carbonatada, sin embargo, no se presentó diferencia estadística significativa con respecto al MTA Angelus, MTA Flow® Putty ni Thick (p=0.0536). No obstante, si presentó una diferencia significativa con respecto al grupo de MTA Flow® consistencia Thin (P<0.05). Las muestras con Biodentine presentaron la mayor liberación de iones calcio. De acuerdo a las pruebas de resistencia al desplazamiento, a las 72 horas post-obturación, solamente se encontró diferencia significativa entre las muestras obturadas con Biodentine y las correspondientes al MTA Flow consistencia Thin (p=0.0090), sin embargo las muestras sumergidas 15 días en PBS presentaron diferencia significativa entre todos los grupos con respecto al MTA Flow Thin (p=0.0147). En general se observaron zonas de biomineralización en la interface, sin embargo, no fueron continuas. Se concluye que el MTA Flow en consistencia Putty o Thick presenta un proceso de biomineralización y una resistencia al desplazamiento similar al MTA Angelus y al Biodentine, sin embargo, esta última disminuye considerablemente en presentación Thin.

The effect of ionizing radiation on properties of fluoride-releasing restorative materials

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.

Desenvolvimento, caracterização e avaliação in vitro de cimento ósseo à base de nano hidroxiapatitas substituídas com magnésio, estrôncio e zinco / Development, characterization and in vitro evaluation of bone cement based on nano-hydroxyapatites substituted with magnesium, strontium and zinc

A incorporação de íons na estrutura da hidroxiapatita (HA) pode afetar sua estrutura, cristalinidade, solubilidade e citotoxicidade. Dentre os íons presentes na composição da apatita óssea, o magnésio (Mg2+), estrôncio (Sr2+) e zinco (Zn2+) são reconhecidos por promover a angiogênese e osteogênese. Portanto, as HAs substituídas podem apresentar melhor bioatividade, por fornecer íons com potencial de estimular a neoformação óssea nos locais enxertados. Nesse contexto, este estudo descreve a síntese, caracterização e comparação de uma série de nano-hidroxiapatitas (nHAs) substituídas e co-substituídas por Sr2+, Mg2+ ou Zn2+. Em seguida, foi desenvolvido um cimento ósseo à base das HAs com melhores resultados de citotoxicidade, associado ao DCPA, gelatina e quitosana. As nHAs foram caracterizadas físico-quimicamente usando diferentes técnicas. O método de co-precipitação foi eficaz para sintetizar HAs de dimensões nanométricas. Comparado a nHA pura, os difratogramas, espectros de FTIR e parâmetros de rede das nHAs substituídas e co-substituídas exibiram alterações, indicando que a incorporação de cátions resultou em distorções da rede da HA. Os testes de MTT demonstraram que as nHAs sintetizadas não foram citotóxicas, após contato direto com culturas de fibroblastos (L929) e pré-osteoblastos (MC3T3). Os resultados obtidos sugerem que as nHAs co-substituídas por Mg2+/Sr2+ e Zn2+/Sr2+ parecem induzir maior proliferação de células fibroblásticas e osteoblásticas, quando comparado a HA pura e substituída. Os cimentos ósseos desenvolvidos apresentaram capacidade de auto-endurecimento e resistência à lavagem. Além de possuírem alta molhabilidade e um perfil de liberação de íons Ca2+, Sr2+, Mg2+ e Zn2+, que está dentro das doses indicadas para estimular a proliferação de osteoblastos. Os cimentos exibiram excelente biocompatibilidade in vitro em culturas de células fibroblásticas, endoteliais e osteosblásticas. Os cimentos contendo nHAs co-substituídas por Mg2+/Sr2+ exibiram os melhores resultados de viabilidade celular. Após 24 horas de contato indireto com cultura de células fibroblásticas L929, o crescimento celular do grupo C2 foi maior que de todos os grupos em estudo (P < 0,01). Em cultura de células endoteliais EA.hy926, o percentual de células viáveis do grupo C3 foi significativamente maior que de todos os outros grupos, após 24 horas (p < 0,001). A citotoxicidade indireta em cultura de células pré-osteoblásticas MC3T3 revelou que após 48 horas, o grupo C3 apresentou maior viabilidade celular que todos os grupos em estudo (p < 0,01). O teste de formação de tubo sugere que todos os cimentos desenvolvidos possuem potencial angiogênico, sendo que os cimentos contendo nHAs co-substituídas por Zn2+/Sr2+ exibiram resultados significativamente superiores (p < 0,001). Apesar de ser necessário um maior número de testes de biocompatibilidade; a incorporação de íons na rede cristalina das nHAs, que são reconhecidos por afetar a angiogênese e a osteogênese, parece ter resultado no desenvolvimento de cimentos ósseos com potencial para promover a regeneração óssea.

The incorporation of ions into the HA lattice can affect its structure, crystallinity, solubility and cytotoxicity. From the ions present in the composition of bone apatite, Mg2+, Sr2+ and Zn2+ are recognized for promoting angiogenesis and osteogenesis. The substituted HAs can be present better bioactivity for supplying ions with potential to stimulate bone neoformation in grafted sites. This study described the synthesis, characterization and comparison of a range of substituted and co-substituted nHAs contained Sr2+, Mg2+ or Zn2+. Then, it developed bone cement based on HAs with better cytotoxicity results, associated with DCPA, gelatin and chitosan. The nHAs were physicochemically characterized using different techniques. The co-precipitation method was effective for synthesizing HAs with nanometric dimensions. Compared to pure nHA, the diffractograms, FTIR spectra and lattice parameters of the substituted and co-substituted nHAs showed changes, indicating that the incorporation of cations resulted in distortions of the HA lattice. MTT tests demonstrated that the all synthesized nHAs were not cytotoxic after direct contact with fibroblasts (L929) and pre-osteoblasts (MC3T3) cultures. MTT results suggest that Mg2+/Sr2+ and Zn2+/Sr2+ co-substituted nHAs seem to induce more proliferation of fibroblastic and osteoblastic than pure and Mg2+, Sr2+ and Zn2+ substituted nHAs. Bone cements developed showed self-hardening and washout resistance. Also, they Exhibited high wettability and ion release profile with non-toxic concentrations of Ca2+, Sr2+, Mg2+ and Zn2+, range within indicated doses to stimulate the proliferation of osteoblasts. The cement exhibited excellent in vitro cytocompatibility in fibroblastic, endothelial and osteoblastic cell cultures. Cement containing Mg2+/Sr2+ co-substituted nHAs showed better results of the cell viability. After 24 hours of indirect contact with L929 fibroblast culture, the cell growth in the C2 group was highest than all study groups (P <0.01). In EA.hy926 endothelial culture, the cell viability of the C3 group was significantly highest than all other groups after 24 hours (p <0.001). The indirect cytotoxicity in MC3T3 pre-osteoblastic culture revealed that after 48 hours, the C3 group showed the greatest cell viability than all the study groups (p <0.01). The tube formation assay suggests that all cement have angiogenic potential, being that the cements containing Zn2+ / Sr2+ co-substituted nHAs exhibited significantly better results (p < 0,001). Despite being necessary to perform a more significant number of biocompatibility tests, the incorporation of ions into the nHA lattice, which are recognized for affects angiogenesis and osteogenesis, may have resulted in the development of bone cements with the potential to promoting bone regeneration.

Estudio comparativo de la bioactividad de dos materiales biocerámicos / Comparative Study of the Bioactivity of Two Bioceramic Materials

RESUMEN Los materiales a base de silicato de calcio han demostrado ser bioactivos debido a su capacidad para producir apatita carbonatada biológicamente compatible. El objetivo de este estudio fue analizar la bioactividad de Biodentine™ y MTA Repair HP® en contacto con discos de dentina humana, que se obturaron y dividieron aleatoriamente para formar cuatro grupos: grupo 1 Biodentine™, grupo 2 MTA Repair HP®, grupo control positivo MTA Angelus® y grupo control negativo IRM®, los cuales se incubaron en solución PBS durante 10 días, para posterior análisis por medio de MEB-EDS y Espectroscopía Raman. Los tres materiales a base de silicato de calcio analizados en este estudio demostraron ser bioactivos pues al entrar en contacto con una solución a base de fosfato desencadenaron la precipitación inicial de fosfato de calcio amorfo, que actúa como precursor durante la formación de apatita carbonatada.

ABSTRACT Calcium silicate-based materials have been shown to be bioactive due to their ability to produce biologically compatible carbonated apatite. The objective of this study was to analyze the bioactivity of Biodentine ™ and MTA Repair HP® in contact with human dentine discs, which were sealed and divided randomly to form four groups: group 1 Biodentine™, group 2 MTA Repair HP®, positive control group MTA Angelus® and negative control group IRM®, which were incubated in PBS solution for 10 days, for a subsequent analysis by means of MEB-EDS and Raman spectroscopy. The three calcium-based materials analyzed in this study proved to be bioactive because upon contact with a phosphate-based solution they were triggered at the onset of amorphous calcium phosphate, as the precursor during the formation of carbonated apatite.

Effect of iontophoresis on fluoride uptake in enamel with artificial caries lesion

Abstract: Iontophoresis is a noninvasive technique, based on the application of a constant low-intensity electric current to facilitate the release of a variety of drugs, whether ionized or not, through biological membranes. The objective of this research was to evaluate the effect of iontophoresis using different electric current intensities on the uptake of fluoride in dental enamel with artificial caries lesions. In this in vitro operator-blind experiment, bovine enamel blocks (n = 10/group) with caries-like lesions and predetermined surface hardness were randomized into 6 groups: placebo gel without fluoride applied with a current of 0.8 mA (negative control), 2% NaF gel without application of any current, and 2% NaF gel applied with currents of 0.1, 0.2, 0.4 and 0.8 mA. Cathodic iontophoresis was applied for 4 min. The concentration of loosely bound fluoride (calcium fluoride) and firmly bound fluoride (fluorapatite) was determined. The results were analyzed by the nonparametric Kruskal-Wallis and Dunn tests. Iontophoresis at 0.8 mA, combined with the application of fluoridated gel (2% NaF), increased fluoride uptake in enamel with caries-like lesions, as either calcium fluoride or fluorapatite.

Fluoride release and uptake in enhanced bioactivity glass ionomer cement ("glass carbomer™") compared with conventional and resin-modified glass ionomer cements

Abstract Objectives To study the fluoride uptake and release properties of glass carbomer dental cements and compare them with those of conventional and resin-modified glass ionomers. Materials and Methods Three materials were used, as follows: glass carbomer (Glass Fill), conventional glass ionomer (Chemfil Rock) and resin-modified glass ionomer (Fuji II LC). For all materials, specimens (sets of six) were matured at room temperature for time intervals of 10 minutes, 1 hour and 6 weeks, then exposed to either deionized water or sodium fluoride solution (1000 ppm in fluoride) for 24 hours. Following this, all specimens were placed in deionized water for additional 24 hours and fluoride release was measured. Results Storage in water led to increase in mass in all cases due to water uptake, with uptake varying with maturing time and material type. Storage in aqueous NaF led to variable results. Glass carbomer showed mass losses at all maturing times, whereas the conventional glass ionomer gained mass for some maturing times, and the resin-modified glass ionomer gained mass for all maturing times. All materials released fluoride into deionized water, with glass carbomer showing the highest release. For both types of glass ionomer, uptake of fluoride led to enhanced fluoride release into deionized water. In contrast, uptake by glass carbomer did not lead to increased fluoride release, although it was substantially higher than the uptake by both types of glass ionomer. Conclusions Glass carbomer resembles glass ionomer cements in its fluoride uptake behavior but differs when considering that its fluoride uptake does not lead to increased fluoride release.

Enhanced bioactive properties of BiodentineTM modified with bioactive glass nanoparticles

Abstract Objective To prepare nanocomposite cements based on the incorporation of bioactive glass nanoparticles (nBGs) into BiodentineTM (BD, Septodent, Saint-Maur-des-Fosses Cedex, France) and to assess their bioactive properties. Material and Methods nBGs were synthesised by the sol-gel method. BD nanocomposites (nBG/BD) were prepared with 1 and 2% nBGs by weight; unmodified BD and GC Fuji IX (GIC, GC Corporation, Tokyo, Japan) were used as references. The in vitro ability of the materials to induce apatite formation was assessed in SBF by X-ray diffraction (XRD), attenuated total reflectance with Fourier transform infrared spectroscopy (ATR-FTIR), and scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) analysis. BD and nBG/BD were also applied to dentine discs for seven days; the morphology and elemental composition of the dentine-cement interface were analysed using SEM-EDX. Results One and two percent nBG/BD composites accelerated apatite formation on the disc surface after short-term immersion in SBF. Apatite was detected on the nBG/BD nanocomposites after three days, compared with seven days for unmodified BD. No apatite formation was detected on the GIC surface. nBG/BD formed a wider interfacial area with dentine than BD, showing blockage of dentine tubules and Si incorporation, suggesting intratubular precipitation. Conclusions The incorporation of nBGs into BD improves its in vitro bioactivity, accelerating the formation of a crystalline apatite layer on its surface after immersion in SBF. Compared with unmodified BD, nBG/BD showed a wider interfacial area with greater Si incorporation and intratubular precipitation of deposits when immersed in SBF.

Una década de monitoreo de plomo en sangre en niños escolares del área metropolitana de Monterrey, NL / A decade of lead monitoring in schoolchildren in the metropolitan area of Monterrey NL, Mexico

Objetivo. Establecer las concentraciones de plomo (Pb) en sangre en niños escolares de 1998 y 2008, así como su asociación con factores de riesgo. Material y métodos. Se llevó a cabo un monitoreo de Pb en sangre de niños de entre 6 y 12 años que cursan educación primaria en 17 escuelas diferentes, ubicadas en distintas zonas del área metropolitana de Monterrey, de 1998 a 2008. Resultados. Se obtuvieron niveles séricos de 9.6 ± 3.0 (µg/dL rango de 3.18 a 20.88) en 1998 y de 4.5±4.8 µg/dL (rango de 3.3 a 53.7) en 2008, lo que mostró una disminución de 2.1 veces en nivel de Pb (p<0.01). Conclusiones. La reducción de los niveles séricos de Pb demuestran los mejores controles ambientales e industriales y probablemente el éxito de retirar el Pb de la gasolina durante los años noventa.

Objective. To establish the blood lead concentration and associated risk factors in schoolchildren during 1998 and 2008. Materials and methods. A blood lead screening was conducted in schoolchildren of 6-12 years of age, enrolled in 17 elementary schools of the metropolitan area of Monterrey, México, during 1998 and 2008. Results. The mean blood lead level were 9.6 ± 3.0 (µg/dL range of 3.18 to 20.88) in 1998 and 4.5±4.8 µg/dL (range of 3.3 to 53.7) showing a 2.1-times reduction in blood lead levels (p<0.01). Conclusions. This reduction in blood lead levels demonstrate environmental and industrial control improvements and the benefits of fading out the leaded gasoline during the 1990's.

Enamel crystals of mice susceptible or resistant to dental fluorosis: an AFM study

Objective: This study aimed to assess the overall apatite crystals profile in the enamel matrix of mice susceptible (A/J strain) or resistant (129P3/J strain) to dental fluorosis through analyses by atomic force microscopy (AFM). Material and Methods: Samples from the enamel matrix in the early stages of secretion and maturation were obtained from the incisors of mice from both strains. All detectable traces of matrix protein were removed from the samples by a sequential extraction procedure. The purified crystals (n=13 per strain) were analyzed qualitatively in the AFM. Surface roughness profile (Ra) was measured. Results: The mean (±SD) Ra of the crystals of A/J strain (0.58±0.15 nm) was lower than the one found for the 129P3/J strain (0.66±0.21 nm) but the difference did not reach statistical significance (t=1.187, p=0.247). Crystals of the 129P3/J strain (70.42±6.79 nm) were found to be significantly narrower (t=4.013, p=0.0013) than the same parameter measured for the A/J strain (90.42±15.86 nm). Conclusion: enamel crystals of the 129P3/J strain are narrower, which is indicative of slower crystal growth and could interfere in the occurrence of dental fluorosis. .

Use of laser fluorescence in dental caries diagnosis: a fluorescence x biomolecular vibrational spectroscopic comparative study

The aim of this work was to verify the existence of correlation between Raman spectroscopy readings of phosphate apatite (∼960 cm−1), fluoridated apatite (∼575 cm−1) and organic matrix (∼1450 cm−1) levels and Diagnodent® readings at different stages of dental caries in extracted human teeth. The mean peak value of fluorescence in the carious area was recorded and teeth were divided in enamel caries, dentin caries and sound dental structure. After fluorescence readings, Raman spectroscopy was carried out on the same sites. The results showed significant difference (ANOVA, p<0.05) between the fluorescence readings for enamel (16.4 ± 2.3) and dentin (57.6 ± 23.7) on carious teeth. Raman peaks of enamel and dentin revealed that ∼575 and ∼960 cm−1 peaks were more intense in enamel caries. There was significant negative correlation (p<0.05) between the ∼575 and ∼960 cm−1 peaks and dentin caries. It may be concluded that the higher the fluorescence detected by Diagnodent the lower the peaks of phosphate apatite and fluoridated apatite. As the early diagnosis of caries is directly related to the identification of changes in the inorganic tooth components, Raman spectroscopy was more sensitive to variations of these components than Diagnodent.

O objetivo desse estudo foi verificar por meio da espectroscopia Raman, a existência de correlação entre os níveis de apatita fosfatada (∼960 cm−1), apatita fluoretada (∼575 cm−1) e matriz orgânica (∼1450 cm−1) e as leituras do Diagnodent® em diferentes estágios de cárie dental em dentes humanos extraídos. O valor médio do pico de fluorescência na área da cárie foi anotado e os dentes divididos em cárie de esmalte, dentina e dente hígido. Após as leituras de fluorescência, foi realizada a espectroscopia Raman nos mesmos sítios. Os resultados mostraram diferença significante (ANOVA p<0,05) entre as leituras de fluorescência para esmalte (16,4 ± 2,3) e dentina (57,6 ± 23,7) nos dentes cariados. Os picos Raman para esmalte e dentina evidenciaram que os picos ∼575 e ∼960 cm−1 foram mais intensos em cárie de esmalte. Houve correlação negativa e significante (p<0,05) entre os picos ∼575 e ∼960 cm−1 e cárie de dentina. Pode-se concluir que quanto maior a fluorescência detectada pelo Diagnodent menor o pico da apatita fosfatada e fluoretada. O diagnóstico precoce da cárie está diretamente relacionado com a identificação de mudanças nos componentes inorgânicos do dente, assim a espectroscopia Raman foi mais sensível para variações desses componentes quando comparada ao Diagnodent.

Color agreement between nanofluorapatite ceramic discs associated with try-in pastes and with resin cements

The aim of this study was to evaluate the in vitro color agreement between nanofluorapatite ceramic discs (e.max Ceram / Ivoclar Vivadent / A2) associated with try-in pastes and those bonded with resin cements (Vitique / DMG/ try-in shade A2½ and cement shade A2½, Variolink II / Ivoclar Vivadent / try-in shade A1 and cement shade A1, and Choice 2 / Bisco / try-in shade A2 and cement shade A2), and to evaluate the shade stability of the discs bonded with resin cements. The shades of composite resin discs (Lliss / FGM / A2) and nanofluorapatite ceramic discs with try-in pastes or cements were evaluated according to the Vita Classical shade guide by a digital spectrophotometer (Micro EspectroShade, MHT) immediately after placing the try-in pastes or resin cements between composite resin discs and ceramic discs. Other evaluations were performed at 2, 5, and 6 day intervals after cementation with the resin cements. All ceramic discs that received try-in pastes presented an A2 shade. There was no statistical difference in the shade of the ceramic specimens fixed with different cements at the different intervals, as evaluated by the Friedman test (p > 0.05). Two try-in pastes presented shade compatibility with those recommended by the manufacturers. There was no similarity of shades between the ceramic discs with try-in pastes and those with the respective resin cements. Shade stability was observed in ceramic discs with resin cements within the intervals evaluated.

Flexural strength of fluorapatite-leucite and fuorapatite porcelains exposed to erosive agents in cyclic immersion

OBJECTIVE: The aim of this study was to evaluate the fexural strength of two porcelain materials (IPS d.SIGN and IPS e.max Ceram) exposed to erosive agents. MATERIAL AND METHODS: One hundred and twenty bar-shaped specimens were made from each of fuorapatite-leucite porcelain (IPS d.SIGN) and fuorapatite porcelain (IPS e.max Ceram) and divided into 8 groups of 15 specimens each. Six groups were alternately immersed in the following storage agents for 30 min: deionized water (control), citrate buffer solution, pineapple juice, green mango juice, cola soft drink and 4 percent acetic acid. Then, they were immersed for 5 min in deionized water at 37ºC. Seven cycles were completed, totalizing 245 min. A 7th group was continuously immersed in 4 percent acetic acid at 80ºC for 16 h. The final, 8th, group was stored dry at 37ºC for 245 min. Three-point bending tests were performed in a universal testing machine. The data were analyzed statistically by 2-way ANOVA, Tukey's HSD test and t-test at signifcance level of 0.05. RESULTS: The fexural strengths of all groups of each porcelain after exposure to erosive agents in cyclic immersion did not differ signifcantly (p>0.05). For both types of porcelain, dry storage at 37ºC yielded the highest fexural strength, though without signifcant difference from the other groups (p>0.05). The fexural strengths of all groups of fuorapatite porcelains were signifcantly higher (p<0.05) than those of the fuorapatite-leucite porcelains. CONCLUSIONS: This study demonstrated that the erosive agents evaluated did not affect the fexural strength of the tested dental porcelains.

Repair of critical-size defects with autogenous periosteum-derived cells combined with bovine anorganic apatite/collagen: an experimental study in rat calvaria

The aim of this study was to evaluate the bone repair using autogenous periosteum-derived cells (PDC) and bovine anorganic apatite and collagen (HA-COL). PDC from Wistar rats (n=10) were seeded on HA-COL discs and subjected to osteoinduction during 6 days. Critical-size defects in rat calvarias were treated with blood clot (G1), autogenous bone (G2), HA-COL (G3) and HA-COL combined with PDC (G4) (n=40), and then analyzed 1 and 3 months after surgeries. Radiographic analysis exhibited no significant temporal change. G1 and G2 had discrete new marginal bone, but the radiopacity of graft materials in G2, G3 and G4 impaired the detection of osteogenesis. At 3 months, histopathological analysis showed the presence of ossification islets in G1, which was more evident in G2, homogeneous new bone around HA-COL in G3 and heterogeneous new bone around HA-COL in G4 in addition to moderate presence of foreign body cells in G3 and G4. Histomorphometric analysis showed no change in the volume density of xenograft (p>0.05) and bone volume density in G2 was twice greater than in G1 and G4 after 3 months (p<0.05), but similar to G3. The PDC did not increase bone formation in vivo, although the biomaterial alone showed biocompatibility and osteoconduction capacity.

O objetivo deste estudo foi avaliar o reparo ósseo usando células derivadas de periósteo (PDC) e apatita inorgânica e colágeno bovinos (HA-COL). PDC de ratos Wistar (n=10) foram semeadas sobre discos de HA-COL e osteoinduzidas por 6 dias. Defeitos de tamanho crítico em calvárias de ratos foram tratados com coágulo sanguíneo (G1), osso autógeno (G2), HA-COL (G3) ou HA-COL associado a PDC (G4) (n=40) e analisados em 1 e 3 meses após as cirurgias. Análise radiográfica não exibiu mudança temporal significante, G1 e G2 tiveram aumento discreto de novo osso marginal, entretanto a radiopacidade dos materiais de enxerto em G2, G3 e G4 prejudicou a detecção de osteogênese. Análise histopatológica mostrou em 3 meses ilhotas de ossificação em G1 que foi maior em G2, novo osso homogêneo ao redor de HA-COL em G3 e novo osso heterogêneo ao redor de HA-COL em G4 além da presença moderada de células gigantes de corpo estranho em G3 e G4. Análise histomorfométrica mostrou a densidade de volume inalterada do xenoenxerto (p>0,05) e a densidade de volume de novo osso em G2 duas vezes maior que G1 e G4 após 3 meses (p<0,05), mas similar a G3. PDC não aumentaram a formação óssea in vivo apesar do biomaterial sozinho ter apresentado biocompatibilidade e capacidade osteocondutora.

Análisis histológico de implantes de apatita carbonatada porosa de síntesis seca y células de médula ósea de porcino / Análise histológica de implantes de apatita carbonatada porosa de síntese seca e células da medula óssea de suínos / Histological analysis of implanted porus carbonated apatite of dry synthesis embedded with porcine bone marrow cells

La apatita carbonatada (CAp) constituye uno de los principales componentes del tejido óseo. Después de sintetizar CAp por precipitación de soluciones acuosas y por reacción del estado sólido, se tomó material poroso de CAp de síntesis seca previamente embebido con células de medula ósea, y se implantó subcutáneamente y en defectos óseos creados en porcinos. En este artículo se muestra la descripción y el análisis de los cortes histológicos de muestras del material implantado. Los resultados obtenidos indicaron que el material no genera rechazo, es reabsorbido por actividad de los osteoclastos del individuo receptor y es reemplazado por tejido óseo neoformado. El tipo de osificación con el que se regenera el tejido óseo en las perforaciones creadas y reemplazadas y no reemplazadas con CAp, es la osificación membranosa la cual se describe. Las diferencias cuantitativas observadas en los controles y tratamientos respecto del área total del material indican su alta biodegradación, aparentemente explicable por una mayor actividad osteoclástica y/o una respuesta de asimilación mejorada por la presencia de células potencialmente osteogénicas del propio individuo. Esta hipótesis se refuerza por el mayor número de vasos sanguíneos encontrados en los implantes subcutáneos previamente embebidos con células madre de la médula ósea. Según los criterios evaluados, CAp poroso de síntesis seca presenta excelente biocompatibilidad, osteoinducción y osteoconducción, características que se potencian cuando el material es pre-embebido con células de médula ósea...

Carbonated apatite (CAp) constitutes one of the principal inorganic components of the osseous tissue. After synthetising of CAp by reaction of the solid state, the ceramic was treated with porcine bone marrow progenitors and then implanted subcutaneously and in created osseous defects. This article shows the description and analysis of histological samples. Results indicated that the material does not generate rejection; it is re-absorbed by the recipient's osteoclasts activity and then is replaced by biologically synthesised bone. Membranous ossification is described to be responsible for the regeneration of osseous tissue in artificially created defects, with or without being filled with CAp. The quantitative differences between controls and treatments in respect of the total area covered by the material indicate its high biodegradability, probably due to a major osteoclastic activity and/or an improved assimilative response, given the presence of potentially osteogenic cells of the own individual. This hypothesis is reinforced by the observation of more blood vessels in subcutaneous implants previously treated with bone marrow cells. According to the evaluated criteria, porous CAp of dry synthesis shows excellent biocompatibility, osteoinductivity and osteoconductivity, characteristics that are promoted when the material is pre-treated with osteoprogenitors from the bone marrow...

A apatita carbonatada (CAP) é um componente importante do tecido ósseo. Depois de sintetizar CAP por precipitação a partir de soluções aquosas e reação em estado sólido, foi colhido material poroso de CAP de síntese seca previamente embebidas com células da medula óssea, e foi introduzida no tecido subcutâneo e em defeitos ósseos criados em suínos. Este artígo mostra a descrição e a análise dos cortes histológicos de amostras do material implantado. Os resultados obtidos indicaram que este não gera rejeiçao, é reabsorvido pela atividade dos osteoclastos do receptor individual e é substituído por tecido ósseo neoformado. O tipo de ossificação com que é regenerada o tecido óssea nas perfurações criados e substituído e não substituído com CAP, é a ossificação membranosa que se descreve. As diferenças quantitativas observadas nos controles e tratamentos ao respeito da área total do material indicam sua alta biodegradação, aparentemente explicável por uma maior atividade osteoclástica e/o uma resposta de assimilação melhorada pela presença de células potencialmente osteogénicas do própio individuo. Esta hipótese é reforçada pelo maior número de vasos sanguíneos encontrados nos implantes subcutáneos previamente embebidas com células madre da medula óssea. Segundo os criterios de avaliação, CAP poroso de síntese seca mostra excelente biocompatibilidade, osteoindução e osteocondução, características que aumentam quando o material é pré-embebida com células da médula óssea...

Concentraçäo de flúor no esmalte humano, após profilaxia com jato de bicarbonato ou taça de borracha, seguidos da aplicaçäo tópica de flúor em gel / Concentration of fluoride in human dental enamel, after the prophylaxis with bicarbonate jet or rubber cup, following topical application of fluoride gel

Estudou-se o efeito do tipo de profilaxia na reatividade do flúor tópico, com o esmalte dental humano. As concentraçöes de fluoreto de cálcio (CaF2) e apatita fluoretada (FA) foram determinadas no esmalte, após a profilaxia com jato de bicabornato (PROFI IIr) ou taça de borracha, seguidas de aplicaçäo tópica de fúor em gel. Os resultados obtidos mostraram que formou-se mais CaF2 sobre o esmalte, devido a profilaxia com jato de bicarbonato do que com taça de borracha, embora näo tenha sido observada uma diferença estatisticamente significativa. Com relaçäo à concentraçäo de FA, observou-se nas regiöes mais internas do esmalte uma maior concentraçäo em funçäo da profilaxia com jato de bicarbonato, porém sem significado estatístico

Reatividade dos dentifrícios fluoretados comercializados no Brasil com o esmalte dental humano / The reactivity of fluorated dentifrices sold in Brazil to the human dental enamel

A reatividade dos dentifrícios fluoretados com o esmalte dental humano foi avaliada «in vitro¼. As concentrações de flúor total, fluoreto de cálcio e apatita fluoretada, foram determinadas no esmalte após a reação com as soluções dos dentifrícios. A capacidade de formar estes produtos variou amplamente quando os dentifrícios foram comparados. Estes resultados foram discutidos em termos do potencial caristático dos mesmos