Analysis of pH, calcium ion release, and energy dispersive spectroscopy of a bioceramic root canal dressing

Abstract This study compared the pH and calcium ion release of calcium silicate- (Bio-C Temp) and calcium hydroxide-based (Ultracal XS) medications. Intracanal remnants of both medications were also evaluated using SEM-EDS after the removal protocol. Thirty-five bovine teeth were prepared. Fifteen were filled with Bio-C Temp and 15 with Ultracal XS. Five remained without intracanal medication (control group). Five samples from each experimental time (i.e.. 24, 72, and 168 hours) were used to measure pH and calcium ions release using a digital pH meter and microplate reader, respectively. Afterward, the peaks of the chemical elements composing both medications were analyzed in SEM-EDS. One-way ANOVA and Tukey's post hoc test analyzed the pH and calcium ion release data. Student's t-test compared the medications in each experimental time. SEM-EDS described the percentage of chemical elements in the samples. Bio-C Temp and Ultracal XS showed a significant pH increase from 24 to 168 hours (p<0.05). Ultracal XS showed a higher pH value at 24 hours than Bio-C Temp (p<0.05) but were similar at 72 and 168h (p > 0.05). Calcium ion release did not depend on the experimental period (p > 0.05). Bio-C Temp showed lower calcium ions release than Ultracal XS at 24 hours (p<0.05). SEM-EDS analyses showed the remains of both medications, but the concentration of Si, Al, and W ions was present only in the calcium silicate-based medication. Bio-C Temp presented alkaline pH and a satisfactory calcium ion release over the time. The remaining of both medications were present after the protocols for paste removal.

Resumo Este estudo comparou o pH e a liberação de íons cálcio de medicações intracanais a à base de silicato de cálcio (Bio-C Temp) e à base de hidróxido de cálcio (Ultracal XS). Remanescentes de ambas as medicações também foram avaliados usando microscopia eletrônica de varredura e espectroscopia de dispersão de energia após o protocolo de remoção. Trinta e cinco dentes bovinos foram preparados. Quinze dentes foram preenchidos com Bio-C Temp e 15 com Ultracal XS. Cinco permaneceram sem medicação intracanal (grupo controle). Cinco amostras de cada tempo experimental (ou seja, 24, 72 e 168 horas) foram usadas para medir o pH e a liberação de íons de cálcio usando um medidor de pH digital e um leitor de microplacas, respectivamente. Em seguida, os picos dos elementos químicos que compõem os dois medicamentos foram analisados ​​em microscopia eletrônica de varredura e por espectroscopia de dispersão de energia. Os testes One-way ANOVA e post hoc de Tukey analisaram os dados de pH e liberação de íons cálcio. O teste t de Student comparou as medicações em cada tempo experimental. A microscopia eletrônica de varredura e a espectroscopia de dispersão de energia descreveu a porcentagem de elementos químicos nas amostras. O Bio-C Temp e o Ultracal XS mostraram um aumento significativo de pH de 24 a 168 horas (p<0,05). O Ultracal XS apresentou um valor de pH mais alto em 24 horas do que o Bio-C Temp (p<0,05), mas foi semelhante em 72 e 168h (p > 0,05). A liberação de íons cálcio não dependeu do período experimental (p> 0,05). O Bio-C Temp apresentou menor liberação de íons de cálcio do que Ultracal XS em 24 horas (p<0,05). As análises de microscopia eletrônica de varredura e espectroscopia de dispersão de energia mostraram remanescentes de ambas as medicações, mas a concentração de íons Si, Al e W estavam presentes apenas na medicação à base de silicato de cálcio. O Bio-C Temp apresentou pH alcalino e maior liberação de íons cálcio. Remanescentes de ambas as medicações estiveram presentes após os protocolos de remoção da pasta.

Calcium inhibits penetration of Alzheimer's Aß1 -42 monomers into the membrane.

Calcium ion regulation plays a crucial role in maintaining neuronal functions such as neurotransmitter release and synaptic plasticity. Copper (Cu2+ ) coordination to amyloid-ß (Aß) has accelerated Aß1-42 aggregation that can trigger calcium dysregulation by enhancing the influx of calcium ions by extensive perturbing integrity of the membranes. Aß1-42 aggregation, calcium dysregulation, and membrane damage are Alzheimer disease (AD) implications. To gain a detail of calcium ions' role in the full-length Aß1-42 and Aß1-42 -Cu2+ monomers contact, the cellular membrane before their aggregation to elucidate the neurotoxicity mechanism, we carried out 2.5 µs extensive molecular dynamics simulation (MD) to rigorous explorations of the intriguing feature of the Aß1-42 and Aß1-42 -Cu2+ interaction with the dimyristoylphosphatidylcholine (DMPC) bilayer in the presence of calcium ions. The outcome of the results compared to the same simulations without calcium ions. We surprisingly noted robust binding energies between the Aß1-42 and membrane observed in simulations containing without calcium ions and is two and a half fold lesser in the simulation with calcium ions. Therefore, in the case of the absence of calcium ions, N-terminal residues of Aß1-42 deeply penetrate from the surface to the center of the bilayer; in contrast to calcium ions presence, the N- and C-terminal residues are involved only in surface contacts through binding phosphate moieties. On the other hand, Aß1-42 -Cu2+ actively participated in surface bilayer contacts in the absence of calcium ions. These contacts are prevented by forming a calcium bridge between Aß1-42 -Cu2+ and the DMPC bilayer in the case of calcium ions presence. In a nutshell, Calcium ions do not allow Aß1-42 penetration into the membranes nor contact of Aß1-42 -Cu2+ with the membranes. These pieces of information imply that the calcium ions mediate the membrane perturbation via the monomer interactions but do not damage the membrane; they agree with the western blot experimental results of a higher concentration of calcium ions inhibit the membrane pore formation by Aß peptides.

Synthesis of silver-containing calcium aluminate particles and their effects on a MTA-based endodontic sealer.

OBJECTIVE: To synthetize calcium aluminate (C3A) and silver-containing C3A particles (C3A+Ag) testing their effects on the properties of a MTA-based endodontic sealer in comparison to an epoxy resin- and a calcium silicate-based sealer. METHODS: Pure C3A and C3A+Ag particles were synthesized by a chemical method and characterized using XRD to identify crystalline phases. SEM/EDS analysis investigated morphology, particle size, and elemental composition of particles. Setting time, flow, radiopacity, water sorption and solubility of commercial and modified sealers were evaluated according to ISO 6876/2012. The pH and ions release were measured using a pHmeter and a microwave induced plasma optical emission spectrometer. The inhibition of biofilm growth was evaluated by confocal laser scanning microscopy (CLSM). Data were rank transformed and analyzed by ANOVA and Tukey test (P<0.05). RESULTS: The C3A particles showed an irregular grain agglomerated structure with voids and pores. In C3A+Ag particles, Ag modified the material morphology, confirming the deposition of Ag. The physicochemical properties of the modified MTA-based sealer were similar to the commercial material, except for the significant increase in Ca+2 release. However, there was no Ag release. Setting time, flow, radiopacity, water sorption and solubility were adequate for all materials. All the materials showed alkaline pH. Antibiofilm effect was improved in the presence of C3A particles, while the biofilm inhibition was lower in the presence of Ag. SIGNIFICANCE: The modified sealer presented improved antibiofilm properties and calcium release, without dramatic effects on the other characteristics. It is expected a positive effect in its antimicrobial behavior.

Determinación de la dureza total en agua con EDTA empleando una solución amortiguadora inodora de borato / Total hardness water determination by EDTA using a olorless buffer borate

La determinación de Dureza Total con EDTA en agua usando una solución amortiguadora de amonio pH 10 tiene la desventaja de generar vapores de gas amoníaco que suelen ser molestos o ser potencialmente dañinos para el sistema respiratorio del operario. El objetivo de este estudio fue utilizar una solución amortiguadora inodora de borato pH 10 en sustitución de una solución amortiguadora de amonio a pH 10 para la determinación de la dureza total en agua por la metodología de la norma COVENIN 2408-86 y determinar si existía diferencia estadísticamente significativa entre ambos procedimientos. Se determinó la Dureza Total usando la solución amortiguadora inodora de borato en 13 muestras de agua con diferentes grados de dureza (suave, dura y muy dura); los resultados obtenidos se compararon con los valores del procedimiento de referencia. La solución amortiguadora permitió una visualización rápida y definida del punto final durante la ejecución de la determinación volumétrica, los resultados mostraron que no existe diferencia estadísticamente significativa (p≤0,05) en los valores de dureza al emplear ambas soluciones amortiguadoras. Se concluyó que el empleo de la solución amortiguadora inodora de borato para la cuantificación de dureza total en agua es una alternativa a la solución amortiguadora de amonio.

Total Hardness determination EDTA in water using ammonium buffer solution pH 10 has the disadvantage of generating ammonia gas vapors are usually upset or be potentially harmful to the respiratory system operator. The aim of this study was to use a buffer solution pH 10 borate odorless replacing ammonium buffer solution at pH 10 for the determination of total water hardness in the methodology of COVENIN 2408-86 standard and determine whether there was difference statistically significant between the two procedures. Total Hardness was determined using borate buffer odorless in 13 water samples with different degrees of hardness (soft, hard and very hard); the results obtained were compared with the reference method values. The buffer allowed rapid and sharp display of the end point during the execution of the volumetric determination, the results showed that there was no statistically significant difference (p≤ 0,05) in hardness values by using two buffers. It was concluded that the use of borate buffer odorless for quantification of total hardness water is an alternative to the ammonium buffer.

Ph e liberação de cálcio de materiais forradores / Ph and calcium Ion release of pulp-capping materials

Objetivo: Avaliar o pH e liberação de íons cálcio dos materiais forradores a base de hidróxido de cálcio não fotopolimerizável (Hydro C), um fotopolimerizável (Biocal) e MTA. Os materiais foram manipulados e inseridos em tubos de 1 cm de comprimento e 1 mm de diâmetro. Os tubos foram preenchidos e imediatamente imersos em frascos contendo 10 mL de água deionizada. Os tubos foram removidos dos frascos depois de 10 minutos, 24, 48 horas, 7, 15 e 30 dias, e a liberação de íons cálcio e hidroxila foi mensurada com um pHmetro e espectrofotômetro de absorção atômica, respectivamente. Os dados foram comparados pela análise de variância a dois critérios, e as comparações individuais pelo teste de Tukey-Kramer, com nível de significância de 5%. Com relação a liberação de íons calcio, no periodo de 10 minutos ocorreram diferenças significantes (P<0,05) nas comparações do MTA com os outros dois materiais. Nos períodos de 24 e 48 horas os três materiais se diferenciaram estatisticamente (P<0,05) entre si. Na análise de 7 e 15 dias ocorreram diferenças significantes (P<0,05) nas comparações entre: MTA e Biocal, e no confronto entre Hydro C e Biocal. Na avaliação de 30 dias as diferenças significantes (P<0,05) ocorreram nas comparações do MTA com os demais materiais. Com relação ao pH, no período de 10 minutos e 24 horas não ocorreram diferenças significantes (P>0,05). Nos períodos de 48 horas ocorreu diferença estatística (P<0,05) nas comparações do BioCal com os outros dois materiais. Na análise de 7 dias ocorreu diferença significante (P<0,05) na comparação entre MTA e Biocal. Na avaliação de 15 dias ocorreram diferenças significantes (P<0,05) na comparação do Hidro C com os demais materiais. Na análise de 30 dias ocorreram diferenças significantes (P>0,05) nas comparações. Conclui-se que todos os materiais foram capazes de liberar íons cálcio e hidroxila.

Objective: Evaluate the pH and calcium ion release from the pulp-capping materials based on calcium hydroxide does not light-cured (Hydro), a light-cured (Biocal) and MTA. The materials were manipulated and inserted into tubes of 1 cm in length and 1 mm in diameter. The tubes were completed and immediately immersed in vials containing 10 mL of deionized water. The tubes were removed from bottles after 10 minutes, 24, 48 hours, 7, 15 and 30 days, and calcium and hydroxyl ions release was measured with an atomic absorption spectrophotometer and pHmetro, respectively. The data were compared by analysis of variance on two criteria, and individual comparisons by Tukey-Kramer test with significance of 5%. Regarding the calcium ion release, in period of 10 minutes there were significant differences (P<0 .05) MTA comparisons with the other two materials. During periods of 24 and 48 hours the three materials have differentiated statistically (P<0 .05) among themselves. Analysis of 7 and 15 days there were significant differences (P<0 .05) in the comparisons between: MTA and the confrontation between Biocal and Hydro C and Biocal. 30 days evaluation of significant differences (P<0 .05) occurred in MTA comparisons with other materials. With regards to pH, within 10 minutes and 12:0 am not significant differences occurred (P>0 .05). During periods of 48 hours there was statistical difference (P0 .05) in BioCal's comparisons with the other two materials. In During periods of 48 hours there was statistical difference (P<0 .05) in BioCal's comparisons with the other two materials. Analysis of 7 days there was significant difference (P<0 .05) in the comparison between MTA and Biocal. In 15 days trial significant differences occurred (P<0 .05) in comparison with the other's Hydro C materials. In the analysis of significant differences occurred 30 days (P<0 .05) in the comparisons. It is concluded that all materials were able to release calcium ions and hydroxyl.

Estudo do pH de três diferentes pastas de hidróxido de cálcio / Study of pH of three different pastes calcium hydroxide

OBJETIVO: O objetivo deste estudo foi avaliar o pH e difusão de íons cálcio da pasta de hidróxidode cálcio e propilenoglicol, a partir de três marcas comerciais. Foram utilizados quatro grupos, cada umcom dez dentes humanos (G1=Inodon®, G2=Biodinâmica®, G3=Farmadoctor, G4=controle).MATERIAL E MÉTODO: Os dentes foram preparados e os grupos 1, 2 e 3 preenchidos com asrespectivas pastas; o grupo controle sem pasta. A análise do pH foi feita por medidor de pH e amedição da difusão dos íons cálcio pelo método colorimétrico, com tempos de 0 e 48 horas, 7, 14, 21e 28 dias. A análise estatística foi realizada utilizando os testes ANOVA a dois critérios com medidasrepetidas, modelo fatorial completo, comparações múltiplas de Tukey HSD, teste de normalidade deKolmogorov-Smirnov, coeficiente de correlação de Pearson. O nível de significância foi de 5% com ouso do software SPSS 15.0. RESULTADOS: Os resultados mostraram que, independentemente dostempos analisados, para a média dos valores do pH houve diferença estatística entre os grupos (P<0,05),sendo que o grupo controle apresentou a menor média de pH diferindo dos outros três. Na difusão deíons cálcio observou-se diferenças significativas na média do G4 e demais grupos (p<0.05). Em 48horas a maior média ocorreu no grupo G1, em 7, 14 e 21 dias no G2 e em 28 dias no G1.CONCLUSÕES: Não houve diferença no pH dos grupos experimentais; a difusão de íons de cálciofoi maior no G1 e G2, com tendência crescente somente no G1.

OBJECTIVE: The purpose of this study was to evaluate the pH and dissemination of calciumions in the folder of calcium hydroxide and propylene from three trademarks (Inodon, Biodinâmicaand Farmadoctor). Four groups of specimens were used, each containing ten human teeth (GI –Inodon; G2 – Biodinâmica; G3 –Farmadoctor; G4 - control). The teeth were prepared and groups1, 2 and 3 satisfied with their portfolios and the control group without portfolio. pH was measuredby a pH meter and the diffusion of calcium ions was measured by the colorimetric method (0 and48 hours, 7, 14, 21 and 28 days). The statistical analysis was performed using the tests on twocriteria ANOVA with repeated measures, full factorial design, multiple comparisons of Tukey’sHSD, test of normality of Kolmogorov-Smirnov, Pearson’s correlation coefficient. The level ofsignificance was 5% with the use of the software SPSS 15.0. RESULTS: The results showedthat, regardless of time tested, for the average values of pH was no statistical difference betweenthe groups (P <0.05), while the control group had the lowest average Ph. In the disseminationof calcium ions there was significant differences in average for the G4 and other groups (P<0.05). In 48 hours at higher average occurred in the group G1, 7, 14 and 21 days in G2 and28 days in G1. CONCLUSION: There was no difference in the pH of experimental groups, thediffusion of ions of calcium was higher in G1 and G2, with only growing trend in G1.