The development of nanoscale biomaterials associated with polymers has been growing over the years, due to their important structural characteristics for applications in biological systems. The present study aimed to produce and test polymeric scaffolds composed of polylactic acid (PLA) fibers associated with a 58S bioglass doped with therapeutic ions for use in tissue engineering. Three 58S Bioglass was obtained by the sol-gel route, pure and doped with 5% strontium and cobalt ions. Solutions of 7% PLA was used as control and added the three different bioglass, 4% of 58S bioglass (PLA-BG), 4% bioglass-doped strontium (PLA-BGSr) and 4% bioglass-doped cobalt (PLA-BGCo). Scaffolds were produced through electrospinning process, and was characterized chemical and morphologically. The in vitro tests were performed using mesenchymal cells cultures from femurs of nine rats, grown in osteogenic supplemented total culture medium. After osteoblastic differentiation induction cell viability, alkaline phosphatase activity, total protein content quantification, and visualization of mineralization nodule tests were performed. Analysis of normal distribution used the Shapiro-Wilk test (nanofibers diameter and biological assay). Data were compared using the Kruskal-Wallis nonparametric test (p = 0.05). The bioglasses produced proved to be free of nitrate, chlorinated and nano-sized, with effective incorporation of therapeutic ions in their structure. All materials showed cell viability (>70%), total protein production, and alkaline phosphatase activity. It was possible to develop polylactic acid scaffolds associated with 58S bioglass doped with therapeutic ions without cytotoxicity. Scaffolds characteristics appear to sustain its application in bone tissue engineering.
The objective was to synthesize and characterize fine polycaprolactone (PCL) fibers associated with a new 58S bioglass obtained by the precipitated sol-gel route, produced by the electrospinning process in order to incorporate therapeutic ions (Mg and Li). In PCL/acetone solutions were added 7% pure bioglass, bioglass doped with Mg(NO 3 ) 2 and Li 2 CO 3 and were subjected to electrospinning process. The fibers obtained were characterized morphologically, chemically and biologically. The results
Objective. The aim of this study was to evaluate the optical property changes after staining of precured (PC) and light-cured (LC) composites. Materials and Methods. Specimens were prepared using different LC composites (GrandioSO—Voco, Filtek Z350-3M/ESPE, Opallis—FGM, and Kalore—GC) and four PC blocks (Grandio Blocs—Voco, Lava Ultimate—3M ESPE, Brava Block—FGM, and Cerasmart—GC) from the same manufacturers (n = 20). Baseline color, gloss, translucency, and fluorescence were evaluated. The staining protocol was performed for 15 days, and the final optical properties were reevaluated. Results. The changes in each property were calculated (ΔGloss, ΔTranslucency, ΔFluorescency, ΔE ∗ 00). Data were analyzed by ANOVA and Tukey’s test (α = 5%). Changes in all properties were observed after staining for all materials, with darkening and reduction of gloss, fluorescence, and translucency. Nonsignificant differences were observed between the light-cured and precured materials of the same manufacturer for ΔG and ΔT, but significant differences existed for ΔF and ΔE ∗ 00. For ΔF, the only significant differences were observed between Brava Block and Opallis (smaller). For ΔE ∗ 00, only the light-cured composites GrandioSO and Z350 showed significantly less change than the corresponding blocks. Precured composites were affected the same way as light-cured ones by the staining in relation to the reduction of gloss and translucency. Conclusion. A higher reduction in fluorescence was observed for only one brand of block and was similar for the others. The two brands of light-cured materials showed less staining, while for the others, the staining was similar. The effects of staining vary according to the composite formulation.
Objetives: this study aimed to fabricate electrospun-based polyetherimide (PEI) fibers, under controlled parameters, and to perform a diameter analysis for potential mechanical improvement of dental materials. Material and Methods: PEI pallets (0.75 g) were dissolved in 2 mL of chloroform and then processed by electrospinning, under a flow rate of 1mLh1 , three different electrical voltages (10kV, 15kV and 20kV) and three distances (10 cm, 15 cm and 18 cm) between the needle tip and collector. These parameter combinations resulted in nine experimental groups that were analyzed using scanning electron microscopy (SEM) and image processing program for diameter measurement. Statistical analysis was performed using two-way ANOVA with post-hoc Tukey (5% significance). Results: from SEM images it was possible to observe formation of solid, misaligned and flawless defect-free fibers. And from the statistical analysis, distance (p = 0,0026) and the electric tension (p = 0,0012) showed a significant difference, but not for interaction between then (p = 0,4486). Conclusion: thus, it can be concluded that there is a possibility of the morphology control of PEI electrospun fibers, such as diameter, that can be used for a variety of applications such as incorporation in dental materials in order to improve its properties. Keywords Electrospinning technique; Fibers; Polyetherimide; Polymer.
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