Study of the chemical interaction between a high-viscosity glass ionomer cement and dentin

Abstract Objective To investigate the chemical interactions between a high-viscosity glass ionomer cement (GIC) (KetacTM Molar Easymix, 3M ESPE, Seefeld, Bavaria, Germany) and human dentin. It was also analyzed the dynamics of GIC setting mechanism based on the time intervals required for the GIC and the GIC mixed with dentin to achieve stability. Material and Methods Each constituent of GIC - powder (P) and liquid (L) - and powdered dentin (D), as well as the associations P+L, D+L, and P+L+D in the concentrations of 29%, 50%, 65%, 78%, 82%, and 92% of GIC were analyzed with Fourier transform infrared (FTIR) and Raman spectroscopy. Results New optical absorption bands and/or Raman bands, which were not present in P, L, or D, were observed in the associations. The concentrations of 29% and 50% of GIC showed higher interaction, revealing that the amount of dentin influences the formation of new optical absorption or scattering bands. FTIR bands showed that the setting time to achieve bond stability was longer for the high-viscosity GIC (38±7 min) than for the sample with 29% of GIC (28±4 min). Conclusions The analysis revealed the formation of new compounds or molecular rearrangements resulting from the chemical interactions between GIC and dentin. Moreover, this study provides an effective method to evaluate the dynamics of the setting mechanism of GICs.

Effect of the Bis-Dimethylamino Benzydrol Coinitiator on the Mechanical and Biological Properties of a Composite

Abstract To examine the effect of the alternative coinitiator 4,4'bis dimethylamino benzydrol (BZN) in degree of conversion (DC), mechanical and biological properties of experimental composites. The coinitiator BZN was used in three concentrations (0.2, 0.5 and 1.2%), and the coinitiator DMAEMA was used as control at the same concentrations as above. The molar concentration of camphorquinone (CQ) and coinitiators was kept constant (1:1). The composites were manipulated and submitted to microhardness test (VHN), flexural and compressive strength (in MPa), elastic modulus (GPa), DC (FT-IR) and in vitro cytotoxicity (against 3T3 fibroblastic cells) of the experimental resins. Data were subjected to two-way ANOVA and Tukey post-test (α=0.05). The experimental composite resin with BZN showed higher DC values compared to control DMAEMA groups. For the mechanical properties, microhardness values were higher in BZN groups; flexural strength and elastic modulus were similar between all the groups. Compressive strength for groups BZN0.5 and DMAEMA0.5 were not statistically different, being the lowest values attributed to group BZN0.2. The experimental resins with BZN and DMAEMA were considered nontoxic against 3T3 fibroblasts. The inclusion of the coinitiator BZN in experimental composites was considered nontoxic against 3T3 fibroblast cells, without compromising DC and mechanical properties.

Resumo Analisar o efeito do co-iniciador alternativo 4,4'bisdimetilaminobenzidrol (BZN) no grau de conversão (GC) e nas propriedades mecânicas e biológicas de resinas compostas experimentais. O co-iniciador BZN foi utilizado em três concentrações (0,2, 0,5 e 1,2), e o co-iniciador DMAEMA como controle, nas mesmas concentrações acima. A concentração molar entre canforoquinona (CQ) e os co-iniciadores foi mantida constante (1:1). As resinas compostas foram manipuladas e submetidas aos testes de microdureza (VHN), resistência à compressão e flexural (em MPa), módulo de elasticidade (em GPa), GC (em %, por meio de espectroscopia micro-Raman e FTIR com KBr), citotoxicidade in vitro (frente às células fibroblásticas 3T3) das resinas experimentais. Os resultados foram submetidos ao teste ANOVA 1 fator e pós-teste de Tukey (α=0,05). As resinas compostas experimentais com o BZN apresentaram GC e propriedades mecânicas satisfatórias, além de serem consideradas atóxicas a fibroblastos 3T3. A inclusão do co-iniciador BZN à resina composta foi considerada não tóxica frente a células fibroblásticas 3T3 e sem comprometer o grau de conversão e as propriedades mecânicas da mesma.

Glycerol Salicylate-based Pulp-Capping Material Containing Portland Cement

The purpose of this study was to evaluate the water sorption, solubility, pH and ability to diffuse into dentin of a glycerol salicylate-based, pulp-capping cement in comparison to a conventional calcium hydroxide-based pulp capping material (Hydcal). An experimental cement was developed containing 60% glycerol salicylate resin, 10% methyl salicylate, 25% calcium hydroxide and 5% Portland cement. Water sorption and solubility were determined based on mass changes in the samples before and after the immersion in distilled water for 7 days. Material discs were stored in distilled water for 24 h, 7 days and 28 days, and a digital pHmeter was used to measure the pH of water. The cement's ability to diffuse into bovine dentin was assessed by Raman spectroscopy. The glycerol salicylate-based cement presented higher water sorption and lower solubility than Hydcal. The pH of water used to store the samples increased for both cements, reaching 12.59±0.06 and 12.54±0.05 after 7 days, for Hydcal and glycerol salicylate-based cements, respectively. Both cements were able to turn alkaline the medium at 24 h and sustain its alkalinity after 28 days. Hydcal exhibited an intense diffusion into dentin up to 40 µm deep, and the glycerol salicylate-based cement penetrated 20 µm. The experimental glycerol salicylate-based cement presents good sorption, solubility, ability to alkalize the surrounding tissues and diffusion into dentin to be used as pulp capping material.

O objetivo deste estudo foi avaliar a sorção e solubilidade em água, pH e habilidade de difusão na dentina de um cimento para capeamento pulpar à base de glicerol salicilato e compará-lo a um cimento comercial para capeamento pulpar à base de hidróxido de cálcio (Hydcal). Um cimento experimental contendo 60% de resina de glicerol salicilato, 10% de salicilato de metila, 25% de hidróxido de cálcio e 5% de cimento Portland foi formulado. Sorção e solubilidade em água foram determinadas a partir da alteração na massa de espécimes antes e após a imersão em água destilada por 7 dias. Discos dos cimentos foram armazenados em água destilada por 24h, 7 dias e 28 dias e o pH da água foi aferido após cada período. A habilidade de difundir-se no interior de dentina bovina foi avaliada por espectroscopia Raman. O cimento à base de glicerol salicilato apresentou maior sorção e menor solubilidade em comparação com o Hydcal. O pH da água de armazenamento dos espécimes aumentou para ambos os cimentos, chegando a 12,59±0,06 e 12,54±0,05 após 7 dias, para o Hydcal e o cimento à base de glicerol salicilato, respectivamente. Os cimentos foram capazes de promover a alcalinização do meio após 24h e sustentaram a alcalinidade após 28 dias. Hydcal exibiu intensa difusão na dentina até 40 μm de profundidade e o cimento à base de glicerol salicilato penetrou 20 μm. O cimento experimental à base de glicerol salicilato apresentou adequada sorção, solubilidade, habilidade de alcalinizar o meio e difundir-se no interior da dentina para uso como um material para capeamento pulpar.

Raman spectroscopy in determination of forsythin content / 第二军医大学学报

Objective: To compare the two parameters in Raman spectroscopy quantitative analysis, so as to confirm the optimal one. Methods: The ratios of peak intensity and peak area were taken as parameters in quantitative analysis. The contents of forsythin in forsythia suspense leaves gathered at different time points from different regions were analyzed with laser Raman spectroscopy. When the ratio of the peak intensity was taken as parameter, the Raman peak of forsythin (ρΛr-H [1 319.1 cm-1]) and the peak of methanol (νasCH3-O [2 974. 7 cm-1]) were selected as quantitative peak and internal standard reference peak in the confocal micro-Raman spectra of forsythin methanol solution. When the ratio of the peak area was taken as parameter, the Raman peak of forsythin ( ρΛr-H [1 319.1 cm-1]) and the peak of methanol (νsCH3-O[3 020. 9 cm-1]) were selected. The ratios of intensity and area were taken as ordinate, and the content of forsythin was taken as abscissa. The two standard curves were plotted and the linear and recoveries were compared. Results: Both parameters had good linear relationship with forsythin concentration, with the correlation coefficients being 0.998 0 and 0.997 6; the recoveries were 100.04%-101.30% and the recycling was complete. The linear fitting of the results with two parameters were measured, and the regression equation was C2=1.030 4C 1=0.033 1, r=0.999 6. The results obtained with the two parameters were accurate and were largely identical. Conclusion: Both the relative peak intensity and the ratio of the peak area can be used as parameters for forsythin quantitative analysis with Raman spectroscopy. And the two parameters can obtain largely identical results. Raman spectroscopy with internal standard is a simple and rapid method for quantitative analysis of forsythin, and it can be used for quantitative analysis for Chinese herbs.

Algorithms of Raman spectrium analysis in fast identification of counterfeit hypoglycemic agents / 第二军医大学学报

Objective: To investigate the applicability of portable Raman spectroscopy for fast identification of counterfeit hypoglycemic agents. Methods: The Raman spectra of 6 hypoglycemic agents, their corresponding reference standards and 12 common pharmaceutical excipients were detected by BW&-Tek i-Raman portable spectrometer. The spectra were analyzed by three algorithms, namely, the minimized summation of first derivative of subtraction spectra algorithm, local straight-line screening (LSLS) algorithm, and modified LSLS (MLSLS) algorithm. Results: Among the three algorithms, MLSLS algorithm showed the best performance, with the total sensitivity, specificity, accuracy and efficiency being 96.77% , 97.20% , 99.29%, and 96.02%, respectively. Conclusion: The MLSLS algorithm, which is based on infrared spectroscopy, can be adapted to identify suspected counterfeit drugs based on portable Raman spectroscopy.