RESUMEN

OBJECTIVE: Several materials have been developed to preserve pulp vitality. They should have ideal cytocompatibility characteristics to promote the activity of stem cells of human exfoliated deciduous teeth (SHED) and thus heal pulp tissue. OBJECTIVE: To evaluate the cytotoxicity of different dilutions of bioceramic material extracts in SHED. METHODOLOGY: SHED were immersed in αMEM + the material extract according to the following experimental groups: Group 1 (G1) -BBio membrane, Group 2 (G2) - Bio-C Repair, Group 3 (G3) - MTA Repair HP, Group 4 (G4) - TheraCal LC, and Group 5 (G5) - Biodentine. Positive and negative control groups were maintained respectively in αMEM + 10% FBS and Milli-Q Water. The methods to analyze cell viability and proliferation involved MTT and Alamar Blue assays at 24, 48, and 72H after the contact of the SHED with bioceramic extracts at 1:1 and 1:2 dilutions. Data were analyzed by the three-way ANOVA, followed by Tukey's test (p<0.05). RESULTS: At 1:1 dilution, SHED in contact with the MTA HP Repair extract showed statistically higher cell viability than the other experimental groups and the negative control (p<0.05), except for TheraCal LC (p> 0.05). At 1:2 dilution, BBio Membrane and Bio-C showed statistically higher values in intra- and intergroup comparisons (p<0.05). BBio Membrane, Bio-C Repair, and Biodentine extracts at 1:1 dilution showed greater cytotoxicity than 1:2 dilution in all periods (p<0.05). CONCLUSION: MTA HP Repair showed the lowest cytotoxicity even at a 1:1 dilution. At a 1:2 dilution, the SHED in contact with the BBio membrane extract showed high cell viability. Thus, the BBio membrane would be a new non-cytotoxic biomaterial for SHED. Results offer possibilities of biomaterials that can be indicated for use in clinical regenerative procedures of the dentin-pulp complex.

Asunto(s)

Compuestos de Aluminio , Materiales Biocompatibles , Compuestos de Calcio , Proliferación Celular , Supervivencia Celular , Cerámica , Pulpa Dental , Combinación de Medicamentos , Ensayo de Materiales , Óxidos , Silicatos , Células Madre , Diente Primario , Humanos , Diente Primario/efectos de los fármacos , Silicatos/química , Silicatos/toxicidad , Silicatos/farmacología , Supervivencia Celular/efectos de los fármacos , Compuestos de Calcio/química , Compuestos de Calcio/farmacología , Compuestos de Calcio/toxicidad , Células Madre/efectos de los fármacos , Factores de Tiempo , Óxidos/química , Óxidos/toxicidad , Proliferación Celular/efectos de los fármacos , Pulpa Dental/efectos de los fármacos , Pulpa Dental/citología , Cerámica/química , Cerámica/toxicidad , Compuestos de Aluminio/química , Compuestos de Aluminio/toxicidad , Materiales Biocompatibles/química , Materiales Biocompatibles/farmacología , Análisis de Varianza , Reproducibilidad de los Resultados , Bismuto/química , Bismuto/toxicidad , Bismuto/farmacología , Células Cultivadas , Valores de Referencia , Sales de Tetrazolio , Xantenos/química , Oxazinas

RESUMEN

CONTEXT: Bismuth complexes with dithiocarbamate ligands have attracted attention because of their biological applications, such as antimicrobial, antileishmanial, and anticancer properties. These complexes have high cytotoxic activity against cancer cells, being more active than the standard drugs cisplatin, doxorubicin, and tamoxifen. In the present study, we investigated the ability of some DFT methods to reproduce the geometries and NMR spectra of the Bi(III) dithiocarbamate complexes, selected based on their proven antitumor activity. Our investigation revealed that the M06-L/def2-TZVP/ECP/CPCM method presented good accuracy in predicting geometries, while the TPSSh/def2-SVP/ECP/CPCM method proved effective in analyzing the 13C NMR spectra of these molecules. In general, all examined methods exhibited comparable performance in predicting 1H NMR signals. METHODS: Calculations were performed with the Gaussian 09 program using the def2-SVP and def2-TZVP basis sets, employing relativistic effective core potential (ECP) for Bi and using the CPCM solvent model. The exchange-correlation functionals BP86, PBE, OLYP, M06-L, B3LYP, B3LYP-D3, M06-2X, TPSSh, CAM-B3LYP, and ωB97XD were used in the study. Geometry optimizations were started from crystallographic structures available at the Cambridge Structural Database. The theoretical results were compared with experimental data using the mean root-mean-square deviation (RMSD), mean absolute deviations (MAD), and linear correlation coefficient (R2).

Asunto(s)

Antineoplásicos , Teoría Funcional de la Densidad , Espectroscopía de Resonancia Magnética , Tiocarbamatos , Antineoplásicos/química , Antineoplásicos/farmacología , Tiocarbamatos/química , Espectroscopía de Resonancia Magnética/métodos , Bismuto/química , Complejos de Coordinación/química , Complejos de Coordinación/farmacología , Modelos Moleculares , Humanos

RESUMEN

This work describes the development of a membraneless, self-powered immunosensor exploiting a photoelectrochemical system based on two photoelectrodes for cardiac troponin I (cTn). An electrode based on CaBi2Ta2O9 combined with bismuth oxyiodides (BiOI/Bi4O5I2/Bi5O7I) was modified with the cTnI antibody (anti-cTnI) and applied in a photoelectrochemical cell as a photoanode. To perform the cTnI detection exploiting a self-powered photoelectrochemical setup, the immunosensor (anti-cTnI/BiOI/Bi4O5I2/Bi5O7I/CaBi2Ta2O9/FTO) was coupled to a photoelectrochemical cell containing a photocathode based on CuBi2O4 (CBO/FTO) for zero-biased photoelectrochemical immunosensing of cardiac troponin I (cTnI) biomarker. For comparison purposes, the photoanode was applied for cTnI detection in a three-electrode electrochemical cell. The spectroscopic, structural, and morphological characteristics of the photoelectrochemical (PEC) materials were evaluated using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD). Electrochemical impedance spectroscopy (EIS) measurements were performed in the presence and absence of light to investigate the effects of photons on the charge transfer resistance of the photoanode. The influence of the cTnI biomarker on the photoelectrochemical response of the anti-cTnI antibody-modified photoelectrochemical platform (anti-cTnI/BiOI/Bi4O5I2/Bi5O7I/CaBi2Ta2O9/FTO) was evaluated by measuring the photocurrent of the system. The immunosensor presented a linear response ranging from 1 pg mL-1 to 200 ng mL-1 as well as a mean recovery percentage between 95.7% and 108.0% in real human serum samples for the cTnI biomarker.

Asunto(s)

Técnicas Biosensibles , Técnicas Electroquímicas , Humanos , Técnicas Electroquímicas/métodos , Inmunoensayo/métodos , Bismuto/química , Técnicas Biosensibles/métodos , Troponina I , Biomarcadores , Dioxigenasa FTO Dependiente de Alfa-Cetoglutarato

RESUMEN

Calcium silicate-based materials are used to block the communication between the root canal and the periodontal ligament space. This brings the materials into contact with tissues and the potential for local and systemic elemental release and movement. The aim of the study was to evaluate the elemental release of bismuth from ProRoot MTA in contact with connective tissues after 30 and 180 days as well as any accumulation in peripheral organs using an animal model. Tricalcium silicate and hydroxyapatite containing 20% bismuth oxide (HAp-Bi) were used as controls. The null hypothesis was that bismuth migrates from tricalcium silicate-based materials when associated with silicon. The materials were examined using scanning electron microscopy, energy dispersive spectroscopy (SEM/EDS) and X-ray diffraction prior to implantation as well as using SEM/EDS, micro X-ray fluorescence and Raman spectroscopy after implantation to assess elemental presence in surrounding tissues. Histological analysis was used to evaluate the changes in tissue architecture and inductively coupled plasma mass spectrometry (ICP-MS) was used to investigate the elemental deposition. For the systemic investigation, routine blood analysis was performed and organs were obtained to evaluate the presence of bismuth and silicon using ICP-MS after acid digestion. In the histological analysis of the implantation sites, macrophages and multinucleated giant cells could be observed after 30 days which after 180 days became a chronic infiltrate; although, no major differences were identified in red and white blood cell analyses and biochemical tests. Implantation altered the materials as observed in the Raman analysis and bismuth was detected both locally and within kidney samples after both periods of analysis, indicating the potential for accumulation of bismuth in this organ. Smaller amounts of bismuth than observed in the kidney were also detected in blood, liver and brain for the ProRoot MTA and HAp-Bi after 180 days. Bismuth was released from the ProRoot MTA locally and was detected systemically and in samples without silicon; thus, the null hypothesis was rejected. The bismuth release demonstrated that this element accumulated both locally and systemically, mainly in the kidneys in comparison with brain and liver regardless of the material base.

Asunto(s)

Óxidos , Silicio , Ratas , Animales , Óxidos/química , Ratas Wistar , Bismuto/química , Ensayo de Materiales , Compuestos de Calcio/química , Silicatos/química , Combinación de Medicamentos , Compuestos de Aluminio/química , Microscopía Electrónica de Rastreo

RESUMEN

Calcium silicate-based cements have diverse applications in endodontics. This study aimed to evaluate the antibiofilm action, biocompatibility, morphological structure, chemical composition and radiopacity of Five Mineral Oxides (5MO), Mineral Trioxide Aggregate Repair High Plasticity (MTA Repair HP), and Mineral Trioxide Aggregate (MTA) cements. MTT analysis was used to test the antibiofilm action of these cements against five anaerobic microorganisms, and test their biocompatibility with mouse macrophage (RAW 264.7) and osteoblasts (MG-63) cultures. Their morphological structure and chemical composition were evaluated by scanning electron microscopy (SEM) coupled to energy dispersion X-ray spectroscopy (EDX), and the phase analysis was performed by X-ray diffraction (XRD). Conventional radiography was used to assess the radiopacity of the cements. 5MO, MTA Repair HP and MTA were effective against Porphyromonas gingivalis, Parvimonas micra, Fusobacterium nucleatum and Prevotella intermedia, they were biocompatible with macrophages and osteoblasts after 5 min of contact, and they had adequate radiopacity to be used clinically. Bismuth oxide (Bi2O3) is used as a radiopacifier in MTA and 5MO, and calcium tungstate, in MTA Repair HP. Titanium dioxide (TiO2) (ANATASE) is responsible for the antimicrobial action and biocompatibility of 5MO.

Asunto(s)

Compuestos de Aluminio , Compuestos de Calcio , Animales , Ratones , Compuestos de Aluminio/química , Compuestos de Aluminio/farmacología , Bismuto/química , Compuestos de Calcio/química , Compuestos de Calcio/farmacología , Cementos Dentales/farmacología , Combinación de Medicamentos , Ensayo de Materiales , Microscopía Electrónica de Rastreo , Minerales , Óxidos/química , Óxidos/farmacología , Silicatos/química , Silicatos/farmacología

RESUMEN

Recently, halides (silver halides, AgX; perosvkite halides, ABX3) and oxyhalides (bismuth oxyhalides, BiOX) based nanomaterials are noticeable photocatalysts in the degradation of organic water pollutants. Therefore, we review the recent reports to explore improvement strategies adopted in AgX, ABX3 and BiOX (X = Cl, Br and I)-based photocatalysts in water pollution remediation. Herein, the photocatalytic degradation performances of each type of these photocatalysts were discussed. Strategies such as tailoring the morphology, crystallographic facet exposure, surface area, band structure, and creation of surface defects to improve photocatalytic activities of pure halides and BiOCl photocatalysts are emphasized. Other strategies like metal ion and/or non-metal doping and construction of composites, adopted in these photocatalysts were also reviewed. Furthermore, the way of production of active radicals by these photocatalysts under ultraviolet/visible light source is highlighted. The deciding factors such as structure of pollutant, light sources and other parameters on the photocatalytic performances of these materials were also explored. Based on this literature survey, the need of further research on AgX, ABX3 and BiOX-based photocatalysts were suggested. This review might be beneficial for researchers who are working in halides and oxyhalides-based photocatalysis for water treatment.

Asunto(s)

Bismuto , Nanoestructuras , Bismuto/química , Catálisis , Luz , Nanoestructuras/química , Plata/química

RESUMEN

This paper revises the use of polymer nanocomposites to attenuate high-energy electromagnetic radiation (HE-EMR), such as gamma radiation. As known, high-energy radiation produces drastic damage not only in facilities or electronic devices but also to life and the environment. Among the different approaches to attenuate the HE-EMR, we consider the use of compounds with a high atomic number (Z), such as lead, but as known, lead is toxic. Therefore, different works have considered low-toxicity post-transitional metal-based compounds, such as bismuth. Additionally, nanosized particles have shown higher performance to attenuate HE-EMR than those that are micro-sized. On the other hand, materials with π-conjugated systems can also play a role in spreading the energy of electrons ejected as a consequence of the interaction of HE-EMR with matter, preventing the ionization and bond scission of polymers. The different effects produced by the interactions of the matter with HE-EMR are revised. The increase of the shielding properties of lightweight, flexible, and versatile materials such as polymer-based materials can be a contribution for developing technologies to obtain more efficient materials for preventing the damage produced for the HE-EMR in different industries where it is found.

Asunto(s)

Nanocompuestos/química , Polímeros/química , Bismuto/química , Fenómenos Electromagnéticos , Rayos gamma , Ensayo de Materiales/métodos , Tamaño de la Partícula , Protección Radiológica/métodos

RESUMEN

Two new bismuth(III) complexes, [BiL1Cl2] (1) and [BiL2Cl2] (2), in which L1 is (2-hydroxy-4-6-di-tert-butylbenzyl-2-pyridylmethyl)amine and L2 is 2,4-diiodo-6-((pyridine-2-ylmethylamino)methyl)phenol, were synthesized and characterized by elemental and conductivity analyses, atomic absorption spectrometry, infrared and 1H NMR spectroscopies. The molecular structure of 1 reveals that the NN'O ligand forms a 1:1 complex with bismuth through coordination via the nitrogen of the aliphatic amine, the nitrogen of the pyridine ring and the oxygen of the phenolate. The coordination sphere is completed with two chloride anions in a distorted square pyramidal geometry. Bismuth exhibits the same coordination mode in compound 2. The cytotoxic activity of 1 and 2 was investigated in a chronic myelogenous leukemia cell line. The complexes are approximately three times more potent than the corresponding free ligands, with the IC50 values 0.30 and 0.38 µM for complex 1 and 2, respectively. To address the cellular mechanisms underlying cell demise, apoptosis was quantified by flow cytometry analysis. From 0.1 µM, both complexes induce apoptosis and there is a remarkable concentration-dependent increase in the population of cells in apoptosis. The complexes were also evaluated against Gram-positive and Gram-negative bacteria. Both inhibited the bacterial growth in a concentration-dependent way, with remarkable activity in some of the tested strains, for example, complex 2 was more active than its free ligand against all bacterial strains and approximately fourteen times more potent against S. dysenteriae and S. typhimurium.

Asunto(s)

Antibacterianos/farmacología , Antineoplásicos/farmacología , Complejos de Coordinación/farmacología , Antibacterianos/síntesis química , Antineoplásicos/síntesis química , Apoptosis/efectos de los fármacos , Bacterias/efectos de los fármacos , Bismuto/química , Complejos de Coordinación/síntesis química , Ensayos de Selección de Medicamentos Antitumorales , Humanos , Células K562 , Ligandos , Pruebas de Sensibilidad Microbiana , Estructura Molecular , Fenoles/síntesis química , Fenoles/farmacología , Piridinas/síntesis química , Piridinas/farmacología

RESUMEN

The cytotoxic and genotoxic effects of commercial endodontic sealers (AH Plus, Sealer 26 and Endomethasone N) incorporated with nanostructured silver vanadate decorated with silver nanoparticles (AgVO3 - at concentrations 2.5, 5, and 10%) on human gingival fibroblast (HGF), and the silver (Ag+ ) and vanadium (V4+ /V5+ ) ions release were evaluated. Cytotoxicity, cell death, and genotoxicity tests were carried out with extract samples of 24-hr and 7-days. The release of Ag+ and V4+ /V5+ was evaluated. Cytotoxicity in HGF was caused by AH Plus (AP) with 5 and 10% of AgVO3 (83.84 and 67.49% cell viability, respectively) with 24-hr extract (p < 0.05), as well as all concentrations of AP with 7-days extract (p < 0.05 -AP 0% = 73.17%; AP 2.5% = 75.07%; AP 5% = 70.62%; AP 10% = 68.46% cell viability). The commercial sealers Sealer 26 (S26) and Endomethasone N (EN) were cytotoxic (p < 0.05 - S26 0% = 34.81%; EN 0% = 20.99% cell viability with 7-days extract). AP 10% with 7-days extract induced 32% apoptotic cells in HGF (p < 0.05). Genotoxic effect was not observed. The AP groups released more Ag+ , while S26 and EN released more V4+ /V5+ in 24 hr. The Ag+ can be cytotoxic. In conclusion, the cytotoxicity caused to HGF can be attributed by the commercial sealers and enhanced by incorporation of AgVO3 , was not observed genotoxic effect, and apoptosis was induced only by AH Plus 10% 7-days extract. Ag+ can influence cell viability.

Asunto(s)

Antibacterianos/química , Bismuto/química , Hidróxido de Calcio/química , Fibroblastos/citología , Encía/citología , Materiales de Obturación del Conducto Radicular/química , Plata/química , Vanadio/química , Antibacterianos/farmacología , Apoptosis/efectos de los fármacos , Materiales Biocompatibles/química , Línea Celular , Supervivencia Celular/efectos de los fármacos , Daño del ADN/efectos de los fármacos , Dexametasona/química , Combinación de Medicamentos , Liberación de Fármacos , Resinas Epoxi/química , Formaldehído/química , Humanos , Hidrocortisona/química , Iones/química , Plata/farmacología , Relación Estructura-Actividad , Timol/análogos & derivados , Timol/química , Titanio/química

RESUMEN

A promising use of bismuth nanoparticles (BiNPs) for different biomedical applications leads to a search for the elucidation of their toxicity mechanisms, since toxicity studies are still at early stage. In the current study, cytotoxic effects of BiNPs produced by laser ablation in solution (LASiS) was investigated in the murine macrophage line RAW 264.7. The cells were exposed to 0.01-50 µg ml-1 of BiNPs for 24 and 48 h and then cytotoxicity assays were performed. Decrease of MTT conversion to formazan and of cell attachment were observed with no effects on cell proliferation. No loss of membrane integrity or significant changes of ROS and RNS levels were observed in exposed cells. Foremost, increased phagocytic activity and DNA repair foci occurred for cells exposed to BiNPs. These effects are important findings that must be considered in the case of biomedical application of BiNPs, since inappropriate macrophages activation and inactivation may lead to immunotoxicity. Bismuth nanoparticles (BiNPs) produced by laser ablation in solution and stabilized with BSA decrease enzyme-dependent MTT conversion to formazan and increase phagocytic activity and DNA repair foci in murine macrophage line RAW 264.7 when exposed to 50 µg ml-1. These effects are findings that should be considered in the case of biomedical application of BiNPs, since inappropriate macrophages activation and inactivation may lead to immunotoxicity.

Asunto(s)

Bismuto/toxicidad , Formazáns/química , Macrófagos/efectos de los fármacos , Nanopartículas del Metal/química , Células RAW 264.7/efectos de los fármacos , Animales , Bismuto/química , Adhesión Celular , Ciclo Celular , Proliferación Celular , Supervivencia Celular , ADN/efectos de los fármacos , Daño del ADN/efectos de los fármacos , Reparación del ADN , Rayos Láser , Macrófagos/citología , Ratones , Fagocitosis , Células RAW 264.7/citología , Especies Reactivas de Oxígeno , Sales de Tetrazolio/química , Tiazoles/química

RESUMEN

This study aimed to synthesize Bi2Fe4O9 and apply it to the degradation of tartrazine yellow dye. Bi2Fe4O9 was synthesized using the solid-state reaction and the Pechini method. The materials obtained were characterized using X-ray diffraction (XRD), visible ultraviolet spectroscopy (UV-Vis) and field emission scanning electron microscopy (FEG). The microscopic images revealed a morphological difference between the two materials in which the material obtained by the Pechini method is the most porous and have the largest surface area. The pellet obtained by the Pechini method was seen to have a lower bandgap value when compared with the sample solid state reaction. In the photocatalysis tests, the best performance was also that of the material obtained by the Pechini method, with 99.34% degradation, while the material obtained by solid state reaction showed 85.86% in 120 minutes. The solution degraded with the material obtained by the Pechini method presented 81.66% of mineralization while the solution with the material obtained by solid state reaction showed 60.97% of mineralization. The results confirmed that the material obtained by both syntheses is able to maintain its effectiveness after 10 repetitions of the photocatalytic process, proving to be promising for waste treatment in the industrial field.

Asunto(s)

Bismuto/química , Colorantes/análisis , Compuestos Férricos/química , Tartrazina/análisis , Aguas Residuales/química , Contaminantes Químicos del Agua/análisis , Purificación del Agua/métodos , Catálisis , Compuestos Férricos/síntesis química , Microscopía Electrónica de Rastreo , Difracción de Rayos X

RESUMEN

Calcium aluminate cement (CAC) has been highlighted as a promising alternative for endodontic use aiming at periapical tissue repair. However, its effects on dental pulp cells have been poorly explored. OBJECTIVE: This study assessed the impact of calcium chloride (CaCl2) and bismuth oxide (Bi2O3) or zinc oxide (ZnO) additives on odontoblast cell response to CAC. METHODOLOGY: MDPC-23 cells were exposed for up to 14 d: 1) CAC with 2.8% CaCl2 and 25% ZnO (CACz); 2) CAC with 2.8% CaCl2 and 25% Bi2O3 (CACb); 3) CAC with 10% CaCl2 and 25% Bi2O3 (CACb+); or 4) mineral trioxide aggregate (MTA), placed on inserts. Non-exposed cultures served as control. Cell morphology, cell viability, gene expression of alkaline phosphatase (ALP), bone sialoprotein (BSP), and dentin matrix protein 1 (DMP-1), ALP activity, and extracellular matrix mineralization were evaluated. Data were compared using ANOVA (α=5%). RESULTS: Lower cell density was detected only for MTA and CACb+ compared with Control, with areas showing reduced cell spreading. Cell viability was similar among groups at days one and three (p>0.05). CACb+ and MTA showed the lowest cell viability values at day seven (p>0.05). CACb and CACb+ promoted higher ALP and BSP expression compared with CACz (p<0.05); despite that, all cements supported ALP activity. Matrix mineralization were enhanced in CACb+ and MTA. CONCLUSION: In conclusion, CAC with Bi2O3, but not with ZnO, supported the expression of odontoblastic phenotype, but only the composition with 10% CaCl2 promoted mineralized matrix formation, rendering it suitable for dentin-pulp complex repair.

Asunto(s)

Compuestos de Aluminio/química , Compuestos de Aluminio/farmacología , Compuestos de Calcio/química , Compuestos de Calcio/farmacología , Cementos Dentales/química , Cementos Dentales/farmacología , Pulpa Dental/citología , Pulpa Dental/efectos de los fármacos , Fosfatasa Alcalina/análisis , Fosfatasa Alcalina/efectos de los fármacos , Animales , Bismuto/química , Bismuto/farmacología , Cloruro de Calcio/química , Cloruro de Calcio/farmacología , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Combinación de Medicamentos , Expresión Génica/efectos de los fármacos , Ensayo de Materiales , Ratones , Odontoblastos/efectos de los fármacos , Óxidos/química , Óxidos/farmacología , Reproducibilidad de los Resultados , Silicatos/química , Silicatos/farmacología , Factores de Tiempo , Óxido de Zinc/química , Óxido de Zinc/farmacología

RESUMEN

Abstract Calcium aluminate cement (CAC) has been highlighted as a promising alternative for endodontic use aiming at periapical tissue repair. However, its effects on dental pulp cells have been poorly explored. Objective: This study assessed the impact of calcium chloride (CaCl2) and bismuth oxide (Bi2O3) or zinc oxide (ZnO) additives on odontoblast cell response to CAC. Methodology: MDPC-23 cells were exposed for up to 14 d: 1) CAC with 2.8% CaCl2 and 25% ZnO (CACz); 2) CAC with 2.8% CaCl2 and 25% Bi2O3 (CACb); 3) CAC with 10% CaCl2 and 25% Bi2O3 (CACb+); or 4) mineral trioxide aggregate (MTA), placed on inserts. Non-exposed cultures served as control. Cell morphology, cell viability, gene expression of alkaline phosphatase (ALP), bone sialoprotein (BSP), and dentin matrix protein 1 (DMP-1), ALP activity, and extracellular matrix mineralization were evaluated. Data were compared using ANOVA (α=5%). Results: Lower cell density was detected only for MTA and CACb+ compared with Control, with areas showing reduced cell spreading. Cell viability was similar among groups at days one and three (p>0.05). CACb+ and MTA showed the lowest cell viability values at day seven (p>0.05). CACb and CACb+ promoted higher ALP and BSP expression compared with CACz (p<0.05); despite that, all cements supported ALP activity. Matrix mineralization were enhanced in CACb+ and MTA. Conclusion: In conclusion, CAC with Bi2O3, but not with ZnO, supported the expression of odontoblastic phenotype, but only the composition with 10% CaCl2 promoted mineralized matrix formation, rendering it suitable for dentin-pulp complex repair.

Asunto(s)

Humanos , Ratones , Compuestos de Calcio/farmacología , Compuestos de Calcio/química , Compuestos de Aluminio/farmacología , Compuestos de Aluminio/química , Cementos Dentales/farmacología , Cementos Dentales/química , Pulpa Dental/citología , Pulpa Dental/efectos de los fármacos , Óxidos/farmacología , Óxidos/química , Factores de Tiempo , Óxido de Zinc/farmacología , Óxido de Zinc/química , Bismuto/farmacología , Bismuto/química , Ensayo de Materiales , Cloruro de Calcio/farmacología , Cloruro de Calcio/química , Expresión Génica/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Reproducibilidad de los Resultados , Silicatos/farmacología , Silicatos/química , Combinación de Medicamentos , Fosfatasa Alcalina/análisis , Fosfatasa Alcalina/efectos de los fármacos , Odontoblastos/efectos de los fármacos

RESUMEN

The incorporation of nanoparticles into endodontic sealers aims at increasing antimicrobial activity of the original material. Aim. The aim of this study is to incorporate the nanostructured silver vanadate decorated with silver nanoparticles (AgVO3, at 2.5%, 5%, and 10%) into three endodontic sealers and evaluate the antibacterial activity of freshly sealers, surface topography and chemical composition, and setting time. Material and Methods. The AgVO3 was incorporated into AH Plus, Sealer 26, and Endomethasone N at concentrations 0%, 2.5%, 5%, and 10% (in mass). The antibacterial activity of freshly sealers was assessed by direct contact with Enterococcus faecalis and CFU/mL count (n=10), surface topography, and chemical composition were measured by SEM/EDS, and the setting time was measured by Gillmore needle (n=10). The Kruskal-Wallis and Dunn statistical tests were applied (α=0.05). Results. All groups of sealers evaluated inhibited E. faecalis (p>0.05). The incorporation of AgVO3 altered the atomic proportions between components of the endodontic sealers, and the percentage of silver (Ag) and vanadium (V) increased proportionally to the concentrations of AgVO3. Topography analysis showed differences in components distribution on the surface of the specimens. The sealers incorporated with AgVO3 of AH Plus presented a lower setting time than the control group (p<0.05). For Sealer 26 and Endomethasone N, the incorporation of AgVO3 increased the setting time in relation to control group (p<0.05). Conclusions. The modification of endodontic sealers by AgVO3 increased the atomic percentage of Ag and V proportionally to the concentration of the nanomaterial and changed the atomic percentage of the sealer components and setting times. It cannot be affirmed that the AgVO3 promote differences in the antimicrobial activity of freshly sealers, and further investigations of the antimicrobial activity of the set sealers should be carried out.

Asunto(s)

Antibacterianos , Bismuto , Hidróxido de Calcio , Enterococcus faecalis/crecimiento & desarrollo , Nanoestructuras/química , Materiales de Obturación del Conducto Radicular , Compuestos de Plata , Vanadatos , Antibacterianos/farmacología , Bismuto/química , Bismuto/farmacología , Hidróxido de Calcio/química , Hidróxido de Calcio/farmacología , Dexametasona/química , Dexametasona/farmacología , Combinación de Medicamentos , Formaldehído/química , Formaldehído/farmacología , Humanos , Hidrocortisona/química , Hidrocortisona/farmacología , Materiales de Obturación del Conducto Radicular/química , Materiales de Obturación del Conducto Radicular/farmacología , Compuestos de Plata/química , Compuestos de Plata/farmacología , Timol/análogos & derivados , Timol/química , Timol/farmacología , Vanadatos/química , Vanadatos/farmacología

RESUMEN

OBJECTIVES: Addition of aluminum fluoride (AlF3) to MTA was tested to inhibit dental discoloration. MATERIALS AND METHODS: MTA Angelus with 0, 5, 15, and 45% AlF3 were tested. The set cements were characterized using scanning electron microscopy, energy-dispersive spectroscopy, and X-ray diffraction. Radiopacity and setting time were analyzed according to ANSI/ADA 57 and ASTM C266-08. Volume change was evaluated using volumetric micro-CT analysis. The pH and calcium ion release were assessed after 3 and 24 h and 28 days. Dental discoloration in contact with the cements was assessed after 24 h and 28 and 90 days of contact with bovine and human dentine. Tissue reaction to subcutaneous implantation in rats was examined after 30 and 60 days. RESULTS: AlF3 altered the microstructure of MTA. The addition of 5% AlF3 did not significantly alter the radiopacity, setting time, and volume change (p > 0.05). pH and calcium ion release significantly increased with addition of AlF3 (p > 0.05). All the tested proportions of AlF3 prevented the dental darkening verified for MTA Angelus in bovine and human teeth. AlF3 did not interfere in inflammatory response of MTA in all periods of analysis; otherwise, lower amounts showed less intense inflammatory infiltrate. CLINICAL RELEVANCE: AlF3 prevents destabilization of bismuth oxide and consequent tooth darkening, frequently verified in clinical practice when using white MTA. CONCLUSIONS: The use of 5% of AlF3 in combination to MTA resulted in a cement that did not result in dental discoloration and did not affect significantly physical, chemical, and biological properties.

Asunto(s)

Compuestos de Aluminio/química , Bismuto/química , Fluoruros/química , Óxidos/química , Silicatos/química , Animales , Bovinos , Esmalte Dental/efectos de los fármacos , Combinación de Medicamentos , Humanos , Concentración de Iones de Hidrógeno , Técnicas In Vitro , Ensayo de Materiales , Microscopía Electrónica de Rastreo , Espectrometría por Rayos X , Propiedades de Superficie , Difracción de Rayos X

RESUMEN

Photocatalytic degradation of p-Cresol was evaluated using the mixed oxide Bi2O3/TiO2 (containing 2 and 20% wt. Bi2O3 referred as TB2 and TB20) and was compared with bare TiO2 under simulated solar radiation. Materials were prepared by the classic sol-gel method. All solids exhibited the anatase phase by X-ray diffraction (XRD) and Raman spectroscopy. The synthesized materials presented lower crystallite size and Eg value, and also higher surface area as Bi2O3 amount was increased. Bi content was quantified showing near to 70% of theoretical values in TB2 and TB20. Bi2O3 incorporation also was demonstrated by X-ray photoelectron spectroscopy (XPS). Characterization of mixed oxides suggests a homogeneous distribution of Bi2O3 on TiO2 surface. Photocatalytic tests were carried out using a catalyst loading of 1 g L-1 under simulated solar light and visible light. The incorporation of Bi2O3 in TiO2 improved the photocatalytic properties of the synthesized materials obtaining better results with TB20 than the unmodified TiO2 under both radiation sources.

Asunto(s)

Bismuto/química , Cresoles/análisis , Luz , Titanio/química , Contaminantes Químicos del Agua/análisis , Catálisis , Fotólisis , Luz Solar , Propiedades de Superficie

RESUMEN

This study evaluated physicochemical properties, cytotoxicity and bioactivity of MTA Angelus (MTA), calcium silicate-based cement (CSC) and CSC with 30% Ytterbium oxide (CSC/Yb2O3). Setting time was evaluated using Gilmore needles. Compressive strength was evaluated in a mechanical machine. Radiopacity was evaluated using radiographs of materials and an aluminum scale. Solubility was evaluated after immersion in water. Cell viability was evaluated by means of MTT assay and neutral red staining, and the mineralization activity by using alkaline phosphatase activity and Alizarin Red staining. The data were submitted to ANOVA, Tukey and Bonferroni tests (5% significance). The bioactive potential was evaluated by scanning electron microscopy. The materials presented similar setting time. MTA showed the lowest compressive strength. MTA and CSC/Yb2O3 presented similar radiopacity. CSC/Yb2O3 showed low solubility. Saos-2 cell viability tests showed no cytotoxic effect, except to 1:1 dilution in NR assay which had lower cell viability when compared to the control. ALP at 1 and 7 days was similar to the control. MTA and CSC had greater ALP activity at 3 days when compared to control. All the materials present higher mineralized nodules when compared with the control. SEM analysis showed structures suggesting the presence of calcium phosphate on the surface of materials demonstrating bioactivity. Ytterbium oxide proved to be a properly radiopacifying agent for calcium silicate-based cement since it did not affected the physicochemical and biological properties besides preserving the bioactive potential of this material.

Asunto(s)

Bismuto/química , Compuestos de Calcio/química , Cementos Dentales/química , Óxidos/química , Silicatos/química , Iterbio/química , Compuestos de Aluminio/química , Supervivencia Celular , Fenómenos Químicos , Fuerza Compresiva , Ensayo de Materiales , Microscopía Electrónica de Rastreo , Solubilidad , Coloración y Etiquetado

RESUMEN

Bismuth vanadate (BiVO4) powders were successfully synthesized in presence of EDTA via microwave irradiation and used as photocatalysts in the oxidation reaction of rhodamine B (rhB) under visible light. Different concentrations of EDTA (0.5 to 10%) to chelate Bi3+ ions were employed on the BiVO4 synthesis. Under the presence of EDTA, a monoclinic crystalline structure was obtained, whereas a mixture of monoclinic and tetragonal phases was observed in the absence of EDTA. In addition, the use of different EDTA concentrations promoted the formation the different shapes of particles. The BiVO4 sample synthesized with low concentration of EDTA (0.5%) exhibited about 85% of rhB decolorization in 300 min at pH 7.5. Therefore, this high efficiency can be attributed to a combination of intrinsic properties such as the morphology type and monoclinic structure of BiVO4 particles.

Asunto(s)

Bismuto/química , Colorantes/química , Ácido Edético/química , Rodaminas/química , Vanadatos/química , Catálisis , Luz , Microscopía Electrónica de Rastreo , Microondas , Oxidación-Reducción , Polvos , Soluciones/química , Contaminantes Químicos del Agua/química

RESUMEN

Monoclinic bismuth oxide (α-Bi2 O3 ) has attractive optical properties and, therefore, its photoluminescence (PL) behavior has been increasingly explored. Besides this fact, the influence of synthesis methods on PL properties of α-Bi2 O3 still requires research. This paper describes the influence of precipitation (PPT) and microwave-assisted hydrothermal (MAH) methods on PL properties of acicular α-Bi2 O3 microcrystals. The synthesis method promoted structural modifications on α-Bi2 O3 , in particular PPT increased the density of oxygen vacancies significantly. As a result, the PL properties of samples were different depending on the method of synthesis. PPT samples presented their maximum PL emission at 1.91 eV (red), while MAH samples had their maximum at 2.61 eV (blue). These results indicate the possibility of controlling PL properties of α-Bi2 O3 by simply choosing the adequate synthesis method.

Asunto(s)

Bismuto/química , Técnicas de Química Sintética/métodos , Colorantes Fluorescentes/síntesis química , Técnicas de Química Sintética/instrumentación , Color , Colorantes Fluorescentes/química , Luminiscencia , Microondas , Agujas

RESUMEN

Abstract This study evaluated physicochemical properties, cytotoxicity and bioactivity of MTA Angelus (MTA), calcium silicate-based cement (CSC) and CSC with 30% Ytterbium oxide (CSC/Yb2O3). Setting time was evaluated using Gilmore needles. Compressive strength was evaluated in a mechanical machine. Radiopacity was evaluated using radiographs of materials and an aluminum scale. Solubility was evaluated after immersion in water. Cell viability was evaluated by means of MTT assay and neutral red staining, and the mineralization activity by using alkaline phosphatase activity and Alizarin Red staining. The data were submitted to ANOVA, Tukey and Bonferroni tests (5% significance). The bioactive potential was evaluated by scanning electron microscopy. The materials presented similar setting time. MTA showed the lowest compressive strength. MTA and CSC/Yb2O3 presented similar radiopacity. CSC/Yb2O3 showed low solubility. Saos-2 cell viability tests showed no cytotoxic effect, except to 1:1 dilution in NR assay which had lower cell viability when compared to the control. ALP at 1 and 7 days was similar to the control. MTA and CSC had greater ALP activity at 3 days when compared to control. All the materials present higher mineralized nodules when compared with the control. SEM analysis showed structures suggesting the presence of calcium phosphate on the surface of materials demonstrating bioactivity. Ytterbium oxide proved to be a properly radiopacifying agent for calcium silicate-based cement since it did not affected the physicochemical and biological properties besides preserving the bioactive potential of this material.

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Resumo Este estudo avaliou as propriedades físico-químicas, citotoxicidade e bioatividade do MTA Angelus (MTA), cimento à base de silicato de cálcio (CSC) e CSC com 30% de óxido de itérbio (CSC/Yb2O3). O tempo de presa foi avaliado usando agulhas Gilmore. A resistência à compressão foi avaliada em uma máquina mecânica. A radiopacidade foi avaliada utilizando radiografias dos materiais e uma escala de alumínio. A solubilidade foi avaliada após imersão em água. A viabilidade celular foi avaliada por meio do ensaio MTT e coloração de vermelho neutro (NR), e a atividade de mineralização por meio da atividade da fosfatase alcalina e a coloração com Vermelho de Alizarina. Os dados foram submetidos aos testes ANOVA, Tukey e Bonferroni (5% de significância). O potencial bioativo foi avaliado por microscopia eletrônica de varredura. Os materiais apresentaram tempo de presa semelhante. O MTA mostrou menor resistência à compressão. MTA e CSC/Yb2O3 apresentaram radiopacidade semelhante. CSC/Yb2O3 apresentou menores valores de solubilidade. A viabilidade celular realizada pelos ensaios de MTT e NR não revelaram efeitos ctotóxicos em todas as diluições, exceto na diluição 1:1 no NR, o qual mostrou baixa viabilidade celular (p<0.05) em todos materiais testados quando comparado ao controle. A atividade de ALP em 1 e 7 dias foi similar ao controle (p>0.05). MTA e CSC tiveram significante aumento na atividade de ALP aos 3 dias quando comarados ao controle (p>0.05). Todos os materiais apresentaram grande produção de nódulos mineralizados quando comparados ao controle (P<0.05). A análise da SEM mostrou estruturas que sugerem a presença de depósitos de fosfato de cálcio na superfície dos materiais demonstrando bioatividade. O Yb2O3 mostrou ser um agente radiopacificador adequado em cimentos à base de silicato de cálcio uma vez que não afetou as propriedades físico-químicas e biológicas e ainda preservou o potencial bioativo desse material.

Asunto(s)

Óxidos/química , Iterbio/química , Bismuto/química , Silicatos/química , Compuestos de Calcio/química , Cementos Dentales/química , Solubilidad , Coloración y Etiquetado , Ensayo de Materiales , Microscopía Electrónica de Rastreo , Supervivencia Celular , Compuestos de Aluminio/química , Fuerza Compresiva , Fenómenos Químicos