Chemical analysis of mineral trioxide agregate mixed with hyaluronic acids as an accelerant

Abstract Mineral trioxide aggregate (MTA) has many clinical applications in dentistry; the main drawback is the long setting. The main objective is to investigate and compare the chemical effect of using two commercially available hyaluronic acid hydrogels (HA) instead of distilled water for mixing MTA as an accelerant of setting time. Materials and method: Test materials were divided into three groups; Group 1: (control) mixing MTA with distilled water supplied by the manufacturer; Group 2: mixing MTA with a hybrid cooperative complex of high and low molecular weight HA (Profhilo®); Group 3: mixing MTA with High molecular weight / non-cross-linked HA (Jalupro®). Mixing time, and setting time (initial and final) were determined, Fourier-transform infrared spectroscopy, Energy-dispersive X-ray spectroscopy, Field emission Scanning Electron Microscopy, and X-ray diffraction were performed. Results: mixing time, initial, and final setting time for (MTA + HA) groups were significantly different and lower in comparison to the control group (p < 0.05). This study revealed higher expression of calcium silicate hydrate and calcium hydroxide expression with higher Ca release in the MTA + HA group than the control group. Conclusion: commercially available HA demonstrated better chemical properties when used as a mixing medium for MTA. The Mixing and setting time for MTA + HA group were significantly shorter than those of the control group were. Thus, commercially available HA can be used as a mixing medium for MTA.

Resumo O agregado de trióxido mineral (MTA) tem muitas aplicações clínicas em odontologia, mas a principal desvantagem é a longa presa. O objetivo principal é investigar e comparar o efeito químico do uso de dois hidrogéis de ácido hialurônico (HA) disponíveis comercialmente em vez de água destilada para misturar o MTA como um acelerador do tempo de presa. Materiais e método: Os materiais de teste foram divididos em três grupos: Grupo 1: (controle) misturando o MTA com água destilada fornecida pelo fabricante; Grupo 2: misturando o MTA com um complexo cooperativo híbrido de HA de alto e baixo peso molecular (Profhilo®); Grupo 3: misturando o MTA com HA de alto peso molecular/não reticulado (Jalupro®). Foram determinados o tempo de mistura e o tempo de presa (inicial e final), a espectroscopia de infravermelho com transformada de Fourier, a espectroscopia de raios X com dispersão de energia, a microscopia eletrônica de varredura com emissão de campo e a difração de raios X. Resultados: o tempo de mistura, o tempo de presa inicial e final dos grupos (MTA + HA) foram significativamente diferentes e menores em comparação com o grupo de controle (p < 0,05). Esse estudo revelou maior expressão de silicato de cálcio hidratado e expressão de hidróxido de cálcio com maior liberação de Ca no grupo MTA + HA do que no grupo de controle. Conclusão: a HA disponível comercialmente demonstrou melhores propriedades químicas quando usada como meio de mistura para o MTA. O tempo de mistura e de presa do grupo MTA + HA foi significativamente menor do que o do grupo de controle. Portanto, a HA disponível comercialmente pode ser usada como meio de mistura para o MTA.

A two-step reaction to prepare a fast-hardening strontium-calcium phosphate scaffold in room temperature / 中华创伤骨科杂志

Objective To evaluate a fast-hardening strontium-calcium phosphate scaffold using a two-step reaction in room temperature.Methods The original powder phase consisted of tetracalcium phosphate (TTCP),dicalcium phosphate anhydrous (DCPA) and strontium hydrogen phosphate (DSPA).The liquid phase consisted of 20wt％ citric acid and 12wt％ polyvinylpyrrolidone K-30.Groups were designed as Sr-0,Sr-5,Sr-10,and Sr-20,according to the molar ratios of Sr/(Sr + Ca) being 0,5％,10％,and 20％ in the powder phase,respectively.The ratio 0.5 mL/g in the liquid to solid phase was used for mixing.After the scaffold was prepared,its setting time,compression strength,phase composition and structural morphology,ions release and pH value of the substrates were analyzed.Results Addition of citric acid accelerated the setting reaction.Acceptable setting time was achieved by optimizing composition of the original powder and liquid phases.On the other hand,the compression strength,phase composition and structural morphology were not affected by addition of strontium.In addition,calcium and strontium ions were detected in the substrates,without any significant change in the pH value.Conclusion This two-step reaction can be used to prepare a fast hardening strontium-calcium phosphate scaffold in room temperature.

Microleakage and Shear Bond Strength of Biodentine at Different Setting Time / 대한소아치과학회지

The purposes of this study were to evaluate microleakage of Biodentine, one of the tricalcium silicate based pulp-capping materials, and to compare the shear bond strength between composite resin and Biodentine with different setting times. For microleakage evaluation, 70 bovine teeth were used. Cavities were formed on the labial surfaces and filled with Biodentine. The teeth were divided into seven groups, each consisting of 10 teeth. The specimens were prepared by applying the composite resin on the upper side after different setting times. To evaluate shear bond strength, 210 acrylic resin blocks with central grooves were prepared, and the grooves were filled with Biodentine. The acrylic resin blocks were divided into seven groups of 30 specimens each, and the specimens were prepared by applying the composite resin on the upper side after different setting times.In samples with setting time of 24 hours or longer period, the microleakage between composite resin and Biodentine was reduced significantly while the shear bond strength increased to offset the polymerization shrinkage of the composite resin. Setting Biodentine for more than 24 hours before composite resin restoration would lead to more favorable clinical result.

Effect of mixing method on the working time and setting time of alginate impression materials / 实用口腔医学杂志

Working time of normal setting impression materials was 71 (hand mixing,30 s),66 (Alghamix,20 s) and 53 (Algimax-Ⅱ,8 s) seconds respectively.Working time of fast setting impression materials was 56 (hand mixing,30 s) and 51 (Alghamix 20 s) seconds respectively.Setting time of normal setting impression materials was 163 (hand mixing,30 s),160(Alghamix 20 s) and 124(Algimax-Ⅱ,8 s)seconds respectively.Setting time of fast setting impression materials were 131 (hand mixing,30 s) and121 (Alghamix 20 s) seconds.The working and setting time of normal setting impression materials mixed by hand mixing(30 s) and auto-mixing (Alghamix 20 s;Algimax-Ⅱ,8 s) and fast setting impression materials mixed by hand mixing(30 s) and with auto-mixing using Alghamix (20 s) may satisfly clinical requirement.

Physicochemical Properties of Root Canal Filling Materials for Primary Teeth

Abstract This study evaluated physiochemical proprieties of a calcium hydroxide-based paste (Calen(r)) combined with a zinc oxide cement at different ratios (1:0.5, 1:0.65, 1:0.8 and 1:1). Materials were compared regarding setting time, pH variation, radiopacity, solubility, dimensional changes, flow and release of chemical elements. Data were analyzed statistically by ANOVA and Tukey's test (α=0.05). Longer setting time and higher dimensional changes and solubility values were exhibited by 1:0.65 and 1:0.5 ratios (p<0.05). The 1:0.5 and 1:0.65 ratios exhibited the highest pH values at all time points. All materials exhibited high radiopacity values. Significant differences were found only between 1:0.5 and 1:1 ratios for calcium and zinc release (p<0.05), whereas the amount of zirconium was similar among all groups (p>0.05). Considering the evaluated proprieties, combinations of Calen(r) paste with ZO at 1:0.5 and 1:0.65 ratios had the best results as root canal filling materials for use in primary teeth.

Resumo O objetivo do presente estudo foi avaliar propriedades físico-químicas da pasta à base de hidróxido de cálcio (Calen(r)) combinado com diferentes proporções de óxido de zinco (OZ) (1:0,5 e 1:0,65, 1:0,8 e 1:1) (Calen(r) /OZ). Os materiais foram comparados quanto ao tempo de endurecimento, variação do pH, radiopacidade, solubilidade, alterações dimensionais, escoamento e liberação de elementos químicos. Os dados obtidos foram submetidos à análise de variância (nível de 5% de significância). Maior grau de endurecimento, valores de alterações dimensionais, e solubilidade foram encontrados para Calen(r) /OZ 1:0,65 e 1:0,5. Calen(r) /OZ 1:0,5 e 1:0,65, apresentaram os maiores valores de pH em todos os momentos. Todos os materiais apresentaram valores elevados de radiopacidade com diferenças significativas (p>.05). Foram encontradas diferenças significativas apenas entre Calen(r) /OZ de 1:0,5 e 1:1 na liberação de cálcio e zinco (p< 0,05), enquanto que a quantidade de zircônia foi semelhante entre todos os grupos analisados (p>.05). Em relação às propriedades avaliadas no presente estudo, as combinações de Calen(r) com óxido de zinco nas proporções 1:0,5 e 1:0,65 são mais adequadas como material obturador para os canais radiculares de dentes decíduos.

Cytotoxicity and physical properties of tricalcium silicate-based endodontic materials

OBJECTIVES: The aim of this study was to evaluate the cytotoxicity, setting time and compressive strength of MTA and two novel tricalcium silicate-based endodontic materials, Bioaggregate (BA) and Biodentine (BD). MATERIALS AND METHODS: Cytotoxicity was evaluated by using a 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-5-((phenylamino)carbonyl)-2H-tetrazolium hydroxide (XTT) assay. Measurements of 9 heavy metals (arsenic, cadmium, chromium, copper, iron, lead, manganese, nickel, and zinc) were performed by inductively coupled plasma-mass spectrometry (ICP-MS) of leachates obtained by soaking the materials in distilled water. Setting time and compressive strength tests were performed following ISO requirements. RESULTS: BA had comparable cell viability to MTA, whereas the cell viability of BD was significantly lower than that of MTA. The ICP-MS analysis revealed that BD released significantly higher amount of 5 heavy metals (arsenic, copper, iron, manganese, and zinc) than MTA and BA. The setting time of BD was significantly shorter than that of MTA and BA, and the compressive strength of BA was significantly lower than that of MTA and BD. CONCLUSIONS: BA and BD were biocompatible, and they did not show any cytotoxic effects on human periodontal ligament fibroblasts. BA showed comparable cytotoxicity to MTA but inferior physical properties. BD had somewhat higher cytotoxicity but superior physical properties than MTA.

Effect of five brands of latex gloves on the setting time of polyvinyl siloxane putty impression materials.

Addition silicone impression materials have been used as impression material for more than 20 years. Although they are among the most expensive impression materials, they became popular during the past decade as they have excellent physical properties. Prevention of infection is an important aspect in dental treatment since dental professionals are routinely exposed to the wide variety of microorganisms present in saliva. Gloves are the most common protective measure used during dental treatment. The gloves are mostly made of latex. In this study, we examine how the setting time of three types polyvinyl putty materials were affected by the use of five different brands of latex gloves and one brand of vinyl gloves. Each material was first mixed without wearing gloves according to the manufacturer's instructions. After the stipulated mixing time, the setting time was measured using the Vicat needle. The setting time is measured from the time of mixing till the time that the needle does not produce any indentation on the surface of the material. The putty material was then mixed with gloved hands (using the five different brands of latex gloves in turn) and the setting time was measured. Then the material was mixed with washed gloved hands, and the setting time was measured again. Finally, the material was mixed with vinyl gloved hands and the setting time was measured. The following conclusions were drawn from the study: Reprosil™ and Express™ showed significant variation in the setting time with the latex gloved hands. There was no significant variation in the setting time when material was mixed with unwashed vs washed gloved hands. Vinyl gloves did not significantly affect the setting time of any of the putty impression materials.

Efeito do protocolo de ativação da polimerização e envelhecimento acelerado em algumas propriedades de cimentos resinosos / Effects of polymerization activation protocol and accelerated aging in some resin cements properties

Este estudo teve como objetivo avaliar os efeitos de variações no protocolo de ativação e envelhecimento acelerado em algumas propriedades de cimentos resinosos de polimerização dual. Adicionalmente, investigaram-se os efeitos da variação da temperatura ambiente e envelhecimento acelerado no tempo de trabalho e tempo de presa dos cimentos quando ativados exclusivamente pela reação química. As propriedades avaliadas foram o grau de conversão, determinado por espectrometria no infravermelho com transformada de Fourier (FTIR-ATR), microdureza Knoop, expressa em KHN, e resistência mecânica à tração expressa em MPa. Os tempos de trabalho e tempos de presa foram determinados por um reômetro oscilatório com controle de temperatura da plataforma de teste estabelecida em 24oC ou 37oC. O envelhecimento acelerado foi determinado pela armazenagem dos cimentos, em suas embalagens originais, e após os testes iniciais, em estufa a 37oC por 12 semanas.A variável de modo de ativação foi determinada em 3 níveis. Os cimentos foram manipulados de acordo com as instruções dos fabricantes e ativados por luz imediatamente (controle), ativados por luz após 10 minutos de reação química no escuro (Exp 1) ou mantidos no escuro por 15 minutos, permitindo a reação química, mas sem fotoativação (Exp 2). Os cimentos tiveram suas propriedades avaliadas em função desses diferentes modos de ativação, antes e após o envelhecimento acelerado. Cimento exclusivamente ativado pela reação química foi empregado como controle quando necessário. Os diversos resultados podem ser resumidos em alguns aspectos de interesse. O tempo de trabalho e o tempo de presa de todos cimentos foram afetados significantemente pela temperatura e envelhecimento (p<0.05). O aumento da temperatura acelerou os tempos de trabalho e presa. Os efeitos do envelhecimento foram materiaisdependentes. Alguns materiais apresentaram redução, enquanto outros apresentaram aumento dos tempos de trabalho e presa, independentemente da...

The study aimed to evaluate the effects of curing protocol and accelerated aging on some properties of dual-cure resin cements. Additionally, the effects of different ambient temperature and aging on the working and setting times were investigated when cements were self-cured only. Properties evaluated were degree of conversion as determined by FTIR-ATR spectroscopy, Knoop microhadness as expressed by KHN, and tensile strength as expressed in MPa. Working time and setting time were determined by an oscilating rheometer with controlled temperature stage at either 24oC or 37oC. Accelerated aging was performed by storing the original product kits in an oven at 37oC for 12 weeks after initial testing had been executed. Different curing protocols were established in 3 levels. Cements were manipulated according to the manufacturers instructions and light-activated immediately (control), light-activated after 10 minutes delay of self-curing in the dark (Exp 1), or simply allowed to self-cure for 15 minutes in the dark (Exp 2). Properties were evaluated according to the different curing protocol and both before and after aging. Exclusively self-curing cement was used as control product when appropriate. The results can be summarized in some aspects of interest. The working time and setting time of all products were significantly affected by temperature and aging (p<0.05). Increased temperature resulted in shorter working time and setting time. The effects of aging were material dependent. Some products presented reduced working and setting times, while others behave otherwise, regardless of the temperature. Curing mode and aging significantly affected the properties of the cements (p<0.05). In general, the degree of conversion increased with time after light-activation. The curing delay for 10 minutes caused alterations in the degree of conversion, regardless of aging, for some products, but not all. Aging affected the curing kinectics and general properties of all...

Physical properties of novel composite using Portland cement for retro-filling material / 대한치과보존학회지

OBJECTIVES: The aim of this study was to compare apical sealing ability and physical properties of MTA, MTA - AH-plus mixture (AMTA) and experimental Portland cement - Epoxy resin mixture (EPPC) for a development of a novel retro-filling material. MATERIALS AND METHODS: Forty-nine extracted roots were instrumented and filled with gutta-percha. Apical root was resected at 3 mm and the retro-filling cavity was prepared for 3 mm depth. Roots were randomly divided into 3 groups of 15 roots each. The retro-filling was done using MTA, AMTA, and EPPC as the groups divided. Four roots were used as control groups. After setting in humid condition for 24 hours, the roots were immersed in 1% methylene blue dye solution for 72 hours to test the apical leakage. After immersion, the roots were vertically sectioned and photos were taken to evaluate microleakage. Setting times were measured with Vicat apparatus and digital radiographs were taken to evaluate aluminum equivalent thickness using aluminum step wedge. The results of microleakage and setting time were compared between groups using one-way ANOVA and Scheffe's post-hoc comparison at the significance level of 95%. RESULTS: AMTA and EPPC showed less microleakage than MTA group (p < 0.05). AMTA showed the highest radio-opacity than other groups and the novel EPPC showed 5 mm aluminum thickness radio-opacity. EPPC showed the shortest initial and final setting times than other groups while the MTA showed the longest (p < 0.05). CONCLUSIONS: Under the condition of this study, the novel composite using Portland cement-Epoxy resin mixture may useful for retro-filling with the properties of favorable leakage resistance, radio-opacity and short setting time.

Physical and chemical properties of experimental mixture of mineral trioxide aggregate and glass ionomer cement / 대한치과보존학회지

OBJECTIVES: The purpose of this study was to determine the setting time, compressive strength, solubility, and pH of mineral trioxide aggregate (MTA) mixed with glass ionomer cement (GIC) and to compare these properties with those of MTA, GIC, IRM, and SuperEBA. MATERIALS AND METHODS: Setting time, compressive strength, and solubility were determined according to the ISO 9917 or 6876 method. The pH of the test materials was determined using a pH meter with specified electrode for solid specimen. RESULTS: The setting time of MTA mixed with GIC was significantly shorter than that of MTA. Compressive strength of MTA mixed with GIC was significantly lower than that of other materials at all time points for 7 days. Solubility of 1 : 1 and 2 : 1 specimen from MTA mixed with GIC was significantly higher than that of other materials. Solubility of 1 : 2 specimen was similar to that of MTA. The pH of MTA mixed with GIC was 2-4 immediately after mixing and increased to 5-7 after 1 day. CONCLUSIONS: The setting time of MTA mixed with GIC was improved compared with MTA. However, other properties such as compressive strength and pH proved to be inferior to those of MTA. To be clinically feasible, further investigation is necessary to find the proper mixing ratio in order to improve the drawbacks of MTA without impairing the pre-existing advantages and to assess the biocompatibility.

A study on the material properties of various composite resins for core build-up / 대한치과보존학회지

The purposes of this study were to estimate the material properties of the recently developed domestic composite resins for core filling material (Chemical, Dual A, Dual B; Vericom, Korea) and to compare them with other marketed foreign products (CorePaste, Den-Mat, USA; Ti-Core, Essential Dental Systems, USA; Support, SCI-Pharm, USA). Six assessments were made; working time, setting time, depth of polymerization, flexural strength, bonding strength, and marginal leakage. All items were compared to ISO standards. All domestic products satisfied the minimum requirements from ISO standards (working time: above 90 seconds, setting time: within 5 minutes), and showed significantly higher flexural strength than Core Paste. Dual A and B could, especially, reduce the setting time to 60 seconds when cured with 600 mW/cm2 light intensity. All experimental materials showed 6 mm depth of polymerization. Bond strengths of Ti-Core and Dual B materials were significantly higher than the other materials. Furthermore, three domestic products and Ti-Core could reduce the microleakage effectively.

A study on the material properties of various composite resins for core build-up / 대한치과보존학회지

The purposes of this study were to estimate the material properties of the recently developed domestic composite resins for core filling material (Chemical, Dual A, Dual B; Vericom, Korea) and to compare them with other marketed foreign products (CorePaste, Den-Mat, USA; Ti-Core, Essential Dental Systems, USA; Support, SCI-Pharm, USA). Six assessments were made; working time, setting time, depth of polymerization, flexural strength, bonding strength, and marginal leakage. All items were compared to ISO standards. All domestic products satisfied the minimum requirements from ISO standards (working time: above 90 seconds, setting time: within 5 minutes), and showed significantly higher flexural strength than Core Paste. Dual A and B could, especially, reduce the setting time to 60 seconds when cured with 600 mW/cm2 light intensity. All experimental materials showed 6 mm depth of polymerization. Bond strengths of Ti-Core and Dual B materials were significantly higher than the other materials. Furthermore, three domestic products and Ti-Core could reduce the microleakage effectively.

The thermal expansion compatibility of a new infiltrated ceramic-low-temperat ure compensatory die stone / 实用口腔医学杂志

Objective: To study the thermal expansion compatibili ty of a newly developed low temperature compensatory die stone (CDS) with Al 2O 3 base coping and to determine its setting time and setting expansion rate. Methods: Using HDS (Hieraus Die Stone ) as control. The ther mal expansion compatibility of CDS with Al 2O 3 was determined with TMA method on Du point 2100 thermometer;the setting time and setting expansion rate of CDS were measured with routine technique. Results: CDS showed much smaller thermal expansion with Al 2O 3 base coping than HDS.When the wa ter/powder ratio increased from 0.20 to 0.30,the setting time (h) of CDS increas ed from 12.75?0.7546 to 19.85?0.7472,that of HDS from 12.25?0.7169 to 24.00? 0.8165. The setting expansion of CDS was similar to that of HDS at various water /powder ratio. Conclusion: CDS has suitable thermal expans ion compatibility with Al 2O 3, it also has proper setting time and setting ex pansion rate to meet the clinical needs.