Chitosan-Based Hydrogels as Antibacterial/Antioxidant/Anti-Inflammation Multifunctional Dressings for Chronic Wound Healing.

Due to repeated microbial infection, persistent inflammation, excessive oxidative stress, and cell dysfunction, chronic wounds are difficult to heal, posing a serious threat to public health. Therefore, developing multifunctional wound dressings that can regulate the complex microenvironment of chronic wounds and enhance cellular function holds great significance. Recently, chitosan has emerged as a promising biopolymer for wound healing due to its excellent biocompatibility, biodegradability, and versatile bioactivity. The aim of this review is to provide a comprehensive understanding of the mechanisms of delayed chronic wound healing and discuss the healing-promoting properties of chitosan and its derivatives, such as good biocompatibility, antibacterial activity, hemostatic capacity, and the ability to promote tissue regeneration. On this basis, the potential applications of chitosan-based hydrogels are summarized in chronic wound healing, including providing a suitable microenvironment, eliminating bacterial infections, promoting hemostasis, inhibiting chronic inflammation, alleviating oxidative stress, and promoting tissue regeneration. In addition, the concerns and perspectives for the clinical application of chitosan-based hydrogels are also discussed.

Comparative study on the impact-sliding wear behaviour of CAD/CAM resin-ceramic materials and tooth enamel.

OBJECTIVES: To compare the impact-sliding wear of different CAD/CAM resin-ceramic materials and tooth enamel, and explore the corresponding wear damage mechanism. METHODS: Human tooth enamel (EN), Vita ENAMIC (Vita, VE), Lava Ultimate (3 M, LU), and GC CERASMART (GC, CS) were used in this study. The hardness, elastic modulus, and roughness values of the samples were measured. Further, impact-sliding wear tests were performed in a ball-on-flat configuration with spherical zirconia antagonists and the coefficients of friction (CoF) were recorded simultaneously. Additionally, a white light interferometer was used to determine the volume losses and scanning electron microscopy was used to observe the wear morphology of the wear scars and the damage feature in the vertical sections to clarify the damage mechanism during the impact-sliding wear test. RESULTS: EN exhibited the highest elastic modulus and CoF, followed by VE, LU, and CS. The hardness and roughness of EN and VE were similar and were higher than those of LU and CS. Throughout the wear tests, VE exhibited the highest volume loss, whereas CS exhibited the lowest. The wear damage characteristics of VE were similar to those of EN, displaying brittle fractures of inorganic substances and plastic deformation of organic substances in the impact part, exhibiting plough marks in the sliding parts. In the case of LU and CS, the entire wear areas displayed plastic deformation of the resin matrix, exfoliation of the filler particles, and plough marks. SIGNIFICANCE: Enamel and polymer-infiltrated ceramic network materials exhibit similar wear damage modes. Additionally, the high-density nanocomposite resin material is the most resistant to impact-sliding wear from a tribological perspective.

Effects of Hydrofluoric Acid Concentration and Etching Time on the Bond Strength to Ceramic-coated Zirconia.

PURPOSE: To evaluate the effects of different hydrofluoric acid (HF) concentrations and etching times on the surface topography, roughness, and resin bond strength to ceramic-coated zirconia (CC), and to compare them with the effects of alumina air-abrasion combined with 10-MDP (AA). MATERIALS AND METHODS: AA and CC specimens were divided into 12 groups (N = 10). The CC groups were etched with HF at different concentrations (5% or 9.5%) for various durations (0 min, 1 min, 2 min, 3 min, 5 min or 10 min). The surface morphology was analyzed using SEM. Energy-dispersive x-ray spectroscopy (EDS) and x-ray diffraction (XRD) were performed for chemical and crystalline-phase analyses. Surface roughness (Ra) and shear bond strength (SBS) were recorded and statistically analyzed. RESULTS: The SBS of CC groups initially increased, but then decreased with etching time for both HF acid concentrations. The 9.5% HF group displayed more marked topographical changes and higher Ra compared with the 5% HF group for the same etching period. Mean SBS was lower in the AA group compared with the CC groups etched with 5% HF for 2-10 min and 9.5% HF for 1-3 min (p < 0.05). CONCLUSIONS: Different HF concentrations and etching times influenced the surface topography, roughness, and resin bond strength of/to ceramic-coated zirconia. Etching with 5% HF for 5 min and with 9.5% HF for 2 min, respectively, provided the highest SBS.

Effect of Airborne-Particle Abrasion Protocols and MDP-based Primer on the Bond Strength of Highly Translucent Zirconia.

PURPOSE: To evaluate the effects of airborne-particle abrasion and MDP (methacryloyloxydecyl dihydrogen phosphate)-based primer treatment on the strength of resin bonds to highly translucent zirconia. MATERIALS AND METHODS: Eight groups (n = 20 per group) of specimens were prepared with airborne-particle abrasion treatments (0.1-, 0.3-, or 0.6-MPa pressure) or not (untreated control) and MDP-based primer (treated) or not (untreated). Shear bond strength (SBS) tests were performed on the composite-to-ceramic bonded specimens either with or without thermocycling. After airborne-particle abrasion, the surface topography was evaluated by white light interferometry, and a phase analysis was conducted with x-ray diffraction (XRD). Surface roughness (Ra), surface energy (SE), and SBS measurements were statistically analyzed using either Tukey's HSD or the Kruskal-Wallis test, based on applicability. Lastly, the failure mode was observed by optical microscope and scanning electron microscope. RESULTS: Airborne-particle abrasion resulted in significantly larger Ra (p < 0.05), especially with higher treatment pressures. Treatment with MDP-based primer caused significantly higher SE and SBS than airborne-particle abrasion alone (p < 0.05), both with and without aging. CONCLUSION: MDP-based primer can enhance the bond strength and reduce hydrolytic aging of the bonded interface for highly translucent zirconia, exceeding the effects of airborne-particle abrasion. It is recommended that MDP-based primer treatment be applied with a composite cement containing adhesive phosphate monomer.

Does the bond strength of highly translucent zirconia show a different dependence on the airborne-particle abrasion parameters in comparison to conventional zirconia?

PURPOSE: To compare the effects of airborne-particle abrasion protocols on the surface morphology, the phase transformation and the resin bond strength of highly translucent zirconia (M) and conventional zirconia (Z). METHODS: Thirteen groups (N = 12) of Z and M specimens were prepared. Except for the control group, the specimens were sandblasted with conditions involving different grit sizes (50 µm or 110 µm), treatment times (10 s or 20 s) and pressures (0.1 MPa, 0.3 MPa or 0.6 MPa). The surface morphology was analyzed using scanning electron microscope (SEM) and the phase analysis was conducted with X-ray diffraction (XRD). The Ra and the shear bond strength (SBS) were measured and statistically analyzed, and the failure mode was determined by optical microscope. RESULTS: The surface morphologies were strongly dependent on treatment conditions. Larger particle size and higher pressure resulted in higher Ra for both materials. Longer blasting time resulted in higher Ra for Z but not M. Overall, the SBS increased with increasing Ra; the highest average SBS was achieved by M and exceeded 18 MPa. The monoclinic transformation was not found in any treatment for M, but was found in Z. CONCLUSIONS: Z and M showed different dependence on the airborne-particle abrasion parameters in terms of Ra, SBS and phase transformation. The conditions for maximizing SBS included a 110 µm particle size and 20 s treatment for both, with pressures of 0.3 MPa and 0.6 MPa for the M and Z, respectively.

On the wear behavior and damage mechanism of bonded interface: Ceramic vs resin composite inlays.

Advances in adhesive technologies have increased indications for the use of inlays. Decrease in the bonded interface integrity due to wear has been cited as the main cause of its failure. However, this process of interface degradation and the influence of inlay material on damage mechanism appear to be poorly understood. Thus, we aimed to compare the wear behavior and interface damage between ceramic and resin composite inlays bonded to enamel under sliding contact and use the experimental findings to support recommendation of the appropriate inlay material. Bonded interface specimens involving tooth enamel and either ceramic or resin composite inlays were prepared and subjected to reciprocating wear tests up to 5×104 cycles. The wear track profiles and morphologies were characterized after increments of cyclic sliding contact using white light interferometry and scanning electron microscopy, respectively. Optical microscopy was used to evaluate sub-surface cracks and their propagation within the samples. A finite element analysis was used to analyze the stress distributions of the bonded interfaces. Composite inlays showed higher wear depth than the ceramic in the early stage (N ≤ 5×102 cycles), while no significant difference was found at the later stage. For ceramic inlay a greater portion of the contact load was concentrated in the ceramic structure, which facilitated cracks and chipping of the ceramic inlay, with rather minimal damage in the adjacent interface and enamel. In contrast, for the resin composite inlay there was larger stress concentrated in the adjacent enamel, which caused the development of cracks and their propagation to the inner enamel. The restoration material could contribute to the stress distribution and extent of damage within enamel-inlay bonded interfaces. A tough ceramic appears to be more effective at protecting the residual dental tissue.

Wear and damage at the bonded interface between tooth enamel and resin composite.

OBJECTIVE: To investigate the wear mechanisms and evolution of damage in tooth enamel-resin composite bonded interfaces caused by sliding contact, and to develop an understanding of interface degradation from a tribological viewpoint that supports clinical recommendations for improving interface integrity. METHODS: Reciprocating wear tests were performed on bonded interface samples involving commercial resin composite (Tetric N Ceram Bulk Fill), resin cement (Rely X U200) and tooth enamel using the ball-on-flat configuration. The bonded samples were subjected up to 5 × 104 cycles of sliding contact, and the wear depth and wear track morphology were characterized after increments using white light interferometry and scanning electron microscopy, respectively. Optical microscopy was also used to evaluate cracks and their propagation in the samples. RESULTS: In the early stages of sliding contact, wear evolved most rapidly at the interface, followed by the enamel and the resin composite. Gradually, the difference between the wear depth at the interface and other areas decreased. Furthermore, cracks and brittle fracture appeared in the enamel during the early stages of wear, adjacent to the interface. With continuing cyclic loading, enamel wear manifested primarily as ploughs, with discontinuous pits and peeled material. Cracking decreased to only a few cracks extending to the inner enamel and parallel to the interface. CONCLUSIONS: Cracking and damage occurred in the enamel during the early stages of sliding contact and accelerated by poor margin finishing. Cracks caused by wear under sliding contact could be one of the reasons for secondary caries and tooth discoloration.