Physical Characterization of Bismuth Oxide Nanoparticle Based Ceramic Composite for Future Biomedical Application.

Employment and the effect of eco-friendly bismuth oxide nanoparticles (BiONPs) in bio-cement were studied. The standard method was adopted to prepare BiONPs-composite. Water was adopted for dispersing BiONPs in the composite. A representative batch (2 wt. % of BiONPs) was prepared without water to study the impact of water on composite properties. For each batch, 10 samples were prepared and tested. TGA (thermogravimetric analysis) performed on composite showed 0.8 wt. % losses in samples prepared without water whereas, maximum 2 wt. % weight losses observed in the water-based composite. Presence of BiONPs resulted in a decrease in depth of curing. Three-point bending flexural strength decreased for increasing BiONPs content. Comparative study between 2 wt. % samples with and without water showed 10.40 (±0.91) MPa and 28.45 (±2.50) MPa flexural strength values, respectively, indicating a significant (p < 0.05) increase of the mechanical properties at the macroscale. Nanoindentation revealed that 2 wt. % without water composites showed significant (p < 0.05) highest nanoindentation modulus 26.4 (±1.28) GPa and hardness 0.46 (±0.013) GPa. Usage of water as dispersion media was found to be deleterious for the overall characteristics of the composite but, at the same time, the BiONPs acted as a very promising filler that can be used in this class of composites.

Biological and physico-mechanical properties of poly (methyl methacrylate) enriched with graphene oxide as a potential biomaterial / Propiedades físicas-mecánicas-biológicas del poli (metilmetacrilato) enriquecido con óxido de grafeno como potencial biomaterial

Objective: To determine the cytotoxicity and effects of graphene oxide (GO) on cellular proliferation of gingival-fibroblasts, pulp-dental cells and human osteoblasts in culture, and to determine the physical, mechanical and biological properties of poly (methyl methacrylate) (PMMA) enriched with GO. Material and Methods: The GO was characterized with SEM. Cytotoxicity and cell proliferation were determined by the MTT bioassay. The physical mechanical tests (flexural strength and elastic modulus) were carried out with a universal testing machine. Sorption and solubility were determined by weighing before and after drying and immersion in water. Porosity was evaluated by visual inspection. Data were analyzed with Student's t-test and Tukey's posthoc ANOVA. Results: The GO has a heterogeneous morphology and a particle size of 66.67±64.76 µm. GO has a slight to no-cytotoxicity (>50-75% viability) at 1-30 days, and at 24 hours incubation of PMMA with GO significantly stimulates osteoblasts (45±8%, p<0.01). The physical and mechanical properties of PMMA with GO increase considerably without altering sorption, solubility and porosity. Conclusion: GO alone or with PMMA has an acceptable biocompatibility, could contribute to cell proliferation, cell regeneration and improve the physical mechanical properties of PMMA.

Objective: To determine the cytotoxicity and effects of graphene oxide (GO) on cellular proliferation of gingival-fibroblasts, pulpdental cells and human osteoblasts in culture, and to determine the physical, mechanical and biological properties of poly (methyl methacrylate) (PMMA) enriched with GO. Material and Methods: T he G O w as c haracterized with SEM. Cytotoxicity and cell proliferation were determined by the MTT bioassay. The physical-mechanical tests (flexural strength and elastic modulus) were carried out with a universal testing machine. Sorption and solubility were determined by weighing before and after drying and immersion in water. Porosity was evaluated by visual inspection. Data were analyzed with Student's t-test and Tukey's post-hoc ANOVA. Results: The GO has a heterogeneous morphology and a particle size of 66.67±64.76 ?m. GO has a slight to no-cytotoxicity (>50-75% viability) at 1-30 days, and at 24 hours incubation of PMMA with GO significantly stimulates osteoblasts (45±8%, p<0.01). The physical and mechanical properties of PMMA with GO increase considerably without altering sorption, solubility and porosity. Conclusion: GO alone or with PMMA has an acceptable biocompatibility, could contribute to cell proliferation, cell regeneration and improve the physical-mechanical properties of PMMA.

Examining the Effect of Radiant Exposure on Commercial Photopolimerizable Dental Resin Composites.

The objective of this study was to evaluate the effect of radiant exposure on the chemical and physical properties of four commercial dental resin composites. The four dental resin composites used were Kalore, Admira, Tetric N-Ceram Bulk Fill, and Filtek Z350 XT. The composites were subjected to three curing protocols: 1000 mW/cm² for 5 s, 1000 mW/cm² for 10 s, and 400 mW/cm² for 25 s. The flexural strength, elastic modulus, water sorption, water solubility, degree of conversion, and polymerization shrinkage were evaluated. The results were analyzed by means of ANOVA and Tukey tests. For Admira and Kalore, significant differences between light exposure protocols were observed for the elastic modulus (p < 0.001), which was higher when a higher amount of radiant exposure was used. For Filtek Z350, differences were only observed for the degree of conversion (p < 0.001), and a higher amount of radiant exposure allowed us to obtain higher values. The Tetric N-Ceram Bulk Fill analysis showed significant differences for the elastic modulus and water sorption (p < 0.001), and specimens that had been subject to a radiant exposure of 10 J/cm² showed a higher elastic modulus. In most cases, the physical and mechanical properties analyzed were not affected by different radiant exposure values. Other resin-based composite (RBC) characteristics seem to have a greater influence on material properties.

In vitro and in vivo biological characterization of poly(lactic acid) fiber scaffolds synthesized by air jet spinning.

Poly(lactic acid) (PLA) is one of the most promising renewable and biodegradable polymers for mimic extracellular matrix for tissue engineering applications. In this work, PLA spun membrane scaffold were successfully prepared by air jet spinning technology. Morphology, mechanical properties, in vitro biocompatibility, and in vitro and in vivo degradation of PLA fibrous scaffold were characterized by X-ray diffraction, Fourier Transform Infrared, and scanning electron microscope (SEM). Morphological results assessed by SEM analyses indicated that PLA scaffolds possessed an average fiber diameter of approximately 0.558 ± 0.141 µm for 7% w/v of PLA and approximately 0.647 ± 0.137 µm for 10% w/v. Interestingly, our results showed that the nanofiber size of PLA scaffold allow structural stability after 100 days of in vitro degradation in Ringer solution where the average fiber diameter were of approximately 0.633 ± 0.147 µm for 7% w/v and approximately 0.645 ± 0.140 µm for 10% w/v of PLA. Mechanical properties of PLA fibers scaffold after in vitro degradation showed decrease in terms of flexibility elongation, and less energy was needed to achieve maximal elastic deformation. The fiber size exerts an influence on the biological response of human Bone Marrow Mesenchymal Stromal Cells as confirmed by MTT assay after 9 days of cell culture and the in vivo degradation assay of 7% w/v and 10% w/v of PLA scaffold, did not demonstrate evidence of toxicity with a mild inflammatory respond. In conclusion, airbrushing technology promises to be a viable and attractive alternative technique for producing a biocompatible PLA nanofiber scaffold that could be considered for tissue engineering regeneration. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 2435-2446, 2018.

Fotopolimerización de resinas compuestas a través de diversos espesores de tejido dental / Light-polymerization of composite resins through different thicknesses of dental tissue

Objetivos: Determinar el espesor de tejido dental a través del cual se presente la fotopolimerización de la resina Prime Dent® con mínimo encogimiento y profundidad de curado adecuada. Método: Se obtuvieron 80 láminas de molares de 1, 2, 3 y 4 mm de espesor (20 por grupo). Se midió la contracción y se calculó el encogimiento de la resina polimerizando (Visilux 2, 3 M) a través de cada lámina (60 s, 400 mW/cm2). Se utilizó la técnica de bonded-disc. Se realizaron pruebas de profundidad de curado, midiendo el espesor de resina polimerizada de acuerdo con la especificación No. 27 ADA. Un grupo control sin tejido dental fue preparado para ambas propiedades. Los datos fueron analizados usando ANOVA con prueba de Tukey (p < 0.001). Resultados: Profundidad de curado: a medida que aumentó el espesor, ésta disminuyó, existiendo diferencia estadísticamente significativa en todos los grupos. El espesor que mostró menor encogimiento, cumpliendo con una profundidad de curado adecuada (ADA marca como valor mínimo, 1 mm) fue de 3 mm. Encogimiento: a medida que aumentó el espesor, éste disminuyó, no existiendo diferencia estadísticamente significativa entre los grupos de 2 y 3 mm. Conclusiones: De acuerdo con los resultados, es posible polimerizar a través de un espesor de 3 mm, por lo que no se recomienda polimerizar a través de un espesor de 4 mm. Es necesario obtener más propiedades mecánicas utilizando diferentes espesores de tejido dental.

Objectives: To determine the thickness of dental tissue through which Prime Dent Resin® might exhibit light-polymerization with minimum shrinkage and suitable curing depth. Method: 80 laminae measuring 1, 2, 3 and 4 mm thickness were obtained from molars (20 laminae per group). Contraction was measured and resin shrinkage was calculated by polymerization (Visilux 2, 3 M) though each lamina (60 s, 400 mW/cm2). Bonded-disk technique was used. Depth of curing tests were undertaken by measuring the thickness of polymerized resin according to ADA's specification number 27. A control group without dental tissue was prepared for both properties. Data were analyzed using ANOVA with Tukey test (p < 0.001). Results: Curing depth: curing depth decreased as thickness increased. All groups revealed statistically significant differences. The thickness that exhibited lesser shrinkage nonetheless meeting with suitable curing depth (ADA establishes minimum value of 1 mm) was the 3 mm group. Shrinkage: as thickness increased, shrinkage decreased; no statistically significant difference was reported for groups 2 and 3 mm. Conclusions: According to obtained results, it is possible to polymerize through a 3 mm thickness, therefore polymerization is not recommended through a 4 mm depth. It will be necessary to obtain further mechanical properties using different thicknesses of dental tissue.

Study of shrinkage-strain and contraction rates of commercial and experimental compomers.

OBJECTIVE: To asses the contraction rate and shrinkage-strain of a new experimental compomer in comparison with four commercial compomers and a flowable composite resin. METHOD: Shrinkage-strain and contraction rate were calculated by measuring the deflection of a disc in a developed instrument using "bonded disk" method. RESULTS: Both shrinkage-strain and contraction rate are reported. Total shrinkage-strain for compomer systems varies from 2.59 to 3.34%, whereas the flowable composite resin showed a value of 3.50%. The contraction rate for compomers varies from 81.60 to 109.80 microm/min, whereas the flowable composite resin obtained 141.6 microm/min. Commercial compomers show a lower contraction rate than the control group, whereas the experimental group only shows statistical differences with a commercial compomer (Dyract AP). SIGNIFICANCE: The shrinkage-strain and contraction rate results for the experimental compomer are as good as those obtained for a commercial flowable compomer and a flowable composite resin. The contraction rates of all compomers could be directly related to polymerization rates. The method used to measure shrinkage-strain and contraction rate is adequate because it simulates conditions in situ. It can be inferred that the contraction rate is directly related to shrinkage-strain.

Calculation of contraction rates due to shrinkage in light-cured composites.

OBJECTIVE: To calculate the contraction rate that results from polymerization shrinkage in photo-cured resins. METHOD: Fourteen materials were irradiated in a previously developed instrument. This instrument uses measurements of deflection using a 'bonded disk' method. Six measurements were made on each material at 20 +/- 2 degrees C and 70 +/- 10% RH. Means and standard deviations were analyzed. RESULTS: Shrinkage-strain and contraction rate are reported. Total shrinkage-strain for photo-polymerized resins (packable and flowable composites) varies between 1.65 and 4.16%. Both are ormocers. The contraction rate for photo-polymerized resins varies between 55.71 and 167.00 microm/min. Packable resins present a lower contraction rate than flowable resins. SIGNIFICANCE: The distance-time graph is linear. The slope of this line is the average velocity. This concept was used to calculate the average contraction rate. The monomer percentage affects the contraction rate, because higher contraction rate means higher percentage of monomer. We can infer that contraction rate bears some relation to polymerization shrinkage.