Synthesis, Characterization, and Induced Osteogenic Differentiation Effect of Collagen Membranes Functionalized by Polydopamine/Graphene Oxide for Bone Tissue Engineering.

Collagen is one of the most common natural absorbable polymers, which is widely used as a barrier membrane in biomedical fields due to its many desirable biological properties. However, absorbable membranes such as collagen have their own disadvantages such as unpredictable degradation rates, poor rigidity leading to tissue collapse, and limited osteogenic properties and cell adhesion. In this study, a modified collagen membrane with a polydopamine-graphene oxide (PDA/GO) complex was synthesized to improve the characteristics of collagen for bone tissue engineering. The successful synthesis of PDA/GO on collagen membranes was verified using X-ray photoelectron spectroscopy (XPS) and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR). The wettability of PDA/GO-modified collagen membranes was considerably improved based on the characterization by water contact angle compared to the uncoated membranes and surface coatings solely by either PDA or GO. The modified PDA/GO coating also enhanced the mechanical properties such as tensile strength and biodegradation rate of collagen membranes. In addition, the PDA/GO coating effectively enhanced the biocompatibility of collagen membranes as verified by the enhanced proliferation and adhesion of human bone marrow stem cells (hBMSCs). Additionally, the effects of PDA/GO coating on the osteogenic differentiation of hBMSCs on collagen membranes were investigated through alkaline phosphatase (ALP) activity and reverse transcription-quantitative polymerase chain reaction (RT-qPCR). The PDA/GO coating on collagen membranes resulted in a significant increase in osteogenic properties compared with the uncoated collagen membranes. According to the results of the current study, the combination of PDA and GO-modified collagen membranes could be used for bone tissue engineering and biomedical applications.

Evaluation of flexural strength, degree of conversion, and demineralization-prevention properties in adjacent tooth structures of an experimental fissure sealant containing nano-calcium-phosphate compounds.

BACKGROUND: The present study aimed to evaluate the flexural strength, degree of conversion, and demineralization-prevention ability of an experimental fissure sealant containing nano-calcium-phosphate compounds. METHODS: An experimental sealant was formulated using silica and nano hydroxyapatite filler particles. The control group consisted of the DENU Seal (n = 10, each group). The flexural bond strength was evaluated by UTM. DC was evaluated by FTIR. To evaluate the demineralization-prevention ability, Cl V cavities in 10 third molar teeth restored with two sealant products, followed by an acid challenge then the Vickers microhardness test was carried out. RESULTS: The mean flexural strength in the commercial group was higher than the experimental group. However, the mean flexural modulus was not significantly different between the two groups. In the experimental group, DC was significantly higher than the commercial group. Adjacent to the interface, the decrease in microhardness in the experimental group was significantly less than the commercial group. However, on the tooth surface, there were no significant differences between the two groups. In the experimental group, the decrease in microhardness at the interface was less than at the tooth surface, however the situation was opposite in the commercial group. CONCLUSIONS: Incorporating hydroxyapatite into the sealant structure might prevent demineralization, without adverse effects on flexural modulus and degree of conversion.

Design, synthesis, and characterization of a novel dual cross-linked gelatin-based bioadhesive for hard and soft tissues adhesion capability.

Many surgical treatments require a suitable tissue adhesive that maintains its performance in wet conditions and can be applied simultaneously for hard and soft tissues. In the present study, a dual cross-linked tissue adhesive was synthesized by mixing the gelatin methacryloyl (Gel-MA) and gelatin-dopamine conjugate (Gel-Dopa). The setting reaction was based on a photopolymerization process in the presence of a combination of riboflavin and triethanolamine and a chemical cross-linking process attributed to the genipin as a natural cross-linker. Modified gelatin macromolecules were characterized and the best wavelength for free radical generation in the presence of riboflavin was obtained. Tissue adhesives were prepared with 30% hydrogels of Gel-MA and Gel-Dopa with different ratios in distilled water. The gelation occurred in a short time after light irradiation. The chemical, mechanical, physical, and cytotoxicity properties of the tissue adhesives were evaluated. The results showed that despite photopolymerization, chemical crosslinking with genipin played a more critical role in the setting process. Water uptake, degradation behavior, cytotoxicity, and adhesion properties of the adhesives were correlated with the ratio of the components. The SEM images showed a porous structure that could ensure the entry of cells and nutrients into the surgical area. While acceptable properties in most experiments were observed, all features were improved as the Gel-Dopa ratio increased. Also, the obtained hydrogels revealed excellent adhesive properties, particularly with bone even after wet incubation, and it was attributed to the amount of gelatin-dopamine conjugate. From the obtained results, it was concluded that a dual adhesive hydrogel based on gelatin macromolecules could be a good candidate as a tissue adhesive in wet condition.

Repairability of aged dimethacrylate-free ORMOCER-based dental composite resins with different surface roughening methods and intermediate materials.

STATEMENT OF PROBLEM: The repair of damaged composite resin restorations has been recommended as a conservative treatment option. However, a reliable protocol for repairing ORMOCER-based restorations is lacking. PURPOSE: The purpose of this in vitro study was to investigate the effect of different surface roughening methods, repair composite resins, and intermediate materials on the repair bond strength of a dimethacrylate-free ORMOCER-based composite resin. MATERIAL AND METHODS: Cylindrical composite resin specimens (Admira Fusion) were roughened by using hydrofluoric acid (HF) or a diamond rotary instrument. In both groups, 4 types of intermediate materials were used (Monobond-S, Clearfil SE bond [second bottle], Clearfil Universal bond, GC Composite Primer), and then half of the specimens were repaired with a similar composite resin, and the other half with dimethacrylate composite resin (Clearfil-APX). The specimens (n=20) were then subjected to repair bond strength and failure mode evaluation. The data were analyzed by using the Weibull test, 3-way and 1-way ANOVA, and the Tukey honestly significant difference (HSD) test (α=.05). RESULTS: All variables, including the surface roughening method, intermediate material, and repair composite resin, had a significant effect on repair bond strength (P<.001). The lowest repair bond strength values were obtained in the group roughened with HF, prepared with Monobond-S, and repaired with Admira Fusion, and the highest values were obtained in the group roughened with a rotary instrument, prepared with GC Composite Primer, and repaired with Clearfil APX (P<.05). All experimental groups had a lower bond strength than the cohesive and control groups (P<.05). In all experimental groups, the predominant failure modes were adhesive and mixed. CONCLUSIONS: The use of a diamond rotary instrument was a more reliable method of creating roughness, and different intermediate materials based on the clinical situation can be used to repair dimethacrylate-free ORMOCER-based composite resin with similar or different composite resins. However, in general, the highest repair bond strengths were achieved with Clearfil APX-repaired specimens.

Comparison of Bond Strength in the Different Class of Resin Cements to Cast and CAD/CAM Co-Cr Alloys.

OBJECTIVES: Despite the widespread use of resin cements in cementing dental restorations, their bond strength to CAD/CAM base metal alloys is not widely studied. This study aimed to evaluate the microshear bond strength (µSBS) between cobalt-chrome (Co-Cr) alloys fabricated using casting or CAD/CAM methods with three types of resin cements. MATERIALS AND METHODS: Fifty Co-Cr blocks were prepared with CAD/CAM or casting technique. Specimens were divided using primer or not and bonded to three types of resin cements: Panavia F2, RelyX Unicem, and Duo-Link. The differences between the mean µSBS values were analyzed using the two-way ANOVA test and Tukey analysis (α = 0.05). The mode of failure was evaluated using a stereomicroscope. In addition, the specimens were examined by scanning electron microscopy (SEM) based on two received signals: backscattered electrons (SEB) and secondary electrons (SEs). One intact alloy specimen in each group was analyzed by energy-dispersive X-ray spectroscopy (EDX). RESULTS: Most of the specimens in the no-primer group were prematurely debonded. Statistical analyses showed that the interaction between the alloy substrate and cement type was significant (p=0.001). The bond strength of Panavia F2 was significantly higher than Duo-Link in the CAD/CAM group (p=0.001). SEM evaluation confirmed the difference in grain structures, while EDX showed no remarkable difference in the chemical composition of the alloy substrates. CONCLUSION: Alloy fabrication technique may influence the bond strength of resin cements. In the CAD/CAM group, cement containing MDP molecules exhibited higher strength than the etch-and-rinse one.

Effect of Photobiomodulation on Relapse in an Experimental Rapid Maxillary Expansion Model in Rat.

Rapid maxillary expansion (RME) is performed on transversely deficient maxilla. As all orthodontic treatments, retention is important in maintaining therapeutic outcomes. Fixed /removable retainers are used post-RME causing hygiene and compliance problems. Given photobiomodulation's positive effects on the quantity and quality of bone regeneration, its effect on post-RME relapse was studied. Thirty Sprague Dawley rats were randomly divided into group R, non-irradiated RME-treated (n = 12), group P, irradiated RME-treated (n = 12) and group C, non-RME non-irradiated (n = 6). A 1.5 mm metal ring inserted between maxillary incisors at days 0 and 15 was expanded until 1.5 mm space was obtained at day 30. In group P, Ga-Al-As diode laser (810 nm, 100 mW, 4J/cm2 , 30 secs) was applied on days 0, 2, 4, 6, 8, 10, 12 and 14 as predictor variable. The relapse was measured as the space lost between incisors for 30 days after appliance removal (primary outcome variable) and compared with t-test. In week 2, space loss in group P was significantly lower (P < 0.05) than all other groups. The relapse during weeks 2 and 3 was significantly lower in group P than group R. However, no significant difference in relapse amount was found between groups during first and fourth week. There was a significant difference (P < 0.05) between groups in relapse rates (secondary outcome variable) but not in total relapse after 4 weeks. Photobiomodulation proved beneficial in resisting relapse in our study, and it is suggested to be continued until the end of expansion.

Resistance to demineralisation of adjacent enamel and dentine, fluoride release and dentine bond strength of fluoride-containing self-etch adhesive systems.

BACKGROUND: The current study aimed to assess the amount of fluoride released from fluoride-containing dental adhesives and its effect on micro-tensile bond strength (µTBS) and on resistance to demineralisation of dentine and enamel. MATERIAL AND METHODS: Two fluoride-containing dental adhesives, and a fluoride-free adhesive were used as experimental adhesives. After thermal cycling the µ-TBS of adhesives to dentine and the failure mode were assessed. The fluoride release and cross-sectional microhardness (CSMH) of specimens were measured before and after one day, 7 and 28 days of pH-cycling. The data were analysed using one-way ANOVA, Weibull statistics and repeated measures ANOVA. RESULTS: The results indicated a significant difference between the group of FL and both the SE and LBF groups (p≤0.001). The CSMH values of both the dentine and enamel underneath the adhesives was reduced at 28 th day of the pH-cycling compared to the baseline (p≤0.001). From day 1 to day 28, the released fluoride declined in both the fluoride containing dental adhesives (p≤0.001). CONCLUSIONS: Based on the results, the released fluoride from dental adhesives may adversely influence the bond strength and durability of the resin/dentine interface. Moreover, the released fluoride didn't improve the resistance to demineralisation of adjacent enamel and dentine to bond interface. Key words:Fluoride release, micro-tensile bond strength, microhardness, fluoride-containing adhesives.

Degree of conversion and microhardness of bulk-fill dental composites polymerized by LED and QTH light curing units.

OBJECTIVES: The degree of monomer conversion is crucial in determining the mechanical and clinical performance of dental resin composites. This study investigated the polymerization adequacy of two bulk-fill resin composites polymerized by Quartz-Tungsten-Halogen (QTH) and Light Emitting Diode (LED) light curing units at different depths. METHODS: Two bulk-fill resin composites (X-tra Fil; Voco and Tetric N-Ceram Bulk-fill; Ivoclar-Vivadent) with diameters of 7 mm and thicknesses of 1-4 mm were prepared and light-cured by LED or QTH. Then, the degree of conversion (DC) and microhardness of the two bulk-fill composites were evaluated. RESULTS: The microhardness of X-tra fill was significantly higher than that of Tetric N-Ceram polymerized by LED or QTH. The microhardness and DC of X-tra fil exhibited no significant difference among the increments regardless of type of light source. The DC, however, significantly decreased in deep increments for Tetric N-Ceram polymerized by QTH. CONCLUSIONS: The polymerization efficacies of the two bulk-fill composites were different in terms of the depth of cure and type of light source. The DC and microhardness of the X-tra fill bulk-fill composite polymerized by either QTH or LED did not decrease up to a thickness of 4 mm. Thus, new generations of LED light sources are better options for polymerizing the bulk-fill resin composites than QTH.

Debonding Time and Dental Pulp Temperature With the Er, Cr: YSGG Laser for Debonding Feldespathic and Lithium Disilicate Veneers.

Introduction: The removal of ceramic veneers is a time-consuming procedure in a dental office. Little research has been done in alternative removal techniques for ceramic veneers. The objective of this study was to evaluate the removal of feldspathic and lithium disilicate reinforced glass ceramic veneers by Er, Cr: YSGG and to measure debonding time and pulpal temperature increase during veneer removal. Methods: Fifty-seven bovine incisor teeth were prepared and divided into 3 groups. Ceramic specimens with a thickness of 0.7mm, a width of 4mm and a length of 8 mm were fabricated from feldspathic ceramic, lithium disilicate reinforced glass ceramic HT (high translucency) and lithium disilicate reinforced glass ceramic MO (medium opacity) (19 for each group). Specimens were cemented on the labial surface of incisors using resin cement. The Er, Cr: YSGG laser was applied to each specimen at 2.5 W and 25 Hz. Debonding time was measured for each specimen, and the intrapulpal temperature was detected in 3 specimens for each group. Data were analyzed via one-way analysis of variance (ANOVA) at significance level of 0.05 (α = 0.05). Results: Mean debonding time was 103.68 (26.76), 106.58 (47.22) and 103.84 (32.90) seconds for feldspathic, lithium disilicate MO, and lithium disilicate HT respectively. There was no significant statistical difference among the groups (P value = 0.96). The intrapulpal temperature increase was less than 1°C in all groups. Conclusion: Er, Cr: YSGG can successfully be used to efficiently debond feldspathic and lithium disilicate reinforced glass ceramic veneers. There was no significant difference for debonding time among these ceramic materials. During ceramic laminate veneer removal by laser irradiation, no irritating temperature rise was detected.