Polyvinylpyrrolidone as a primer for resin-dentin bonding.

OBJECTIVE: This study aimed to investigate the effects of polyvinylpyrrolidone (PVP)-containing primer (PCP) on dentin bonding. METHODS: PVP and anhydrous ethanol were used to prepare the PCPs, which were prepared at concentrations of 0.5%, 1%, and 2% (w/v). These PCPs were subsequently applied to the dentin surface, denoted as E1, E2, and E3, respectively. In the control group, no primer was applied. Following the treatment, the dentin surfaces were subjected to analysis using Fourier-transform infrared spectroscopy (FTIR), and the micro-tensile bond strength (MTBS) was evaluated. The failure mode, nanoleakage, and bonding longitudinal section were observed utilizing scanning electron microscopy (SEM). Additionally, the effect of PCPs on matrix metalloproteinases (MMPs) activity was analyzed through an in situ zymography test. Data were subjected to statistical analysis using ANOVA tests (α = 0.05). RESULTS: Significant alterations in the infrared resonances associated with collagen cross-linking within the collagen matrix were observed across all PCP groups. The application of PCP demonstrated a noteworthy enhancement in micro-tensile bond strength (MTBS) compared to group C (p < 0.05). Notably, group C exhibited the lowest MTBS (41 ± 7.7 MPa), whereas group E2 demonstrated the highest MTBS (66 ± 11.9 MPa). Even after undergoing aging, the MTBS of the PCP groups remained superior to that of group C (p < 0.05). The resin tag length in the PCP groups was found to be greater than that of group C, and the occurrence of nanoleakage was comparatively lower in the PCP groups, both before and after aging. Additionally, PCP exhibited a dose-dependent inhibition of matrix metalloproteinases (MMPs) activity, which was statistically significant (p < 0.05). CONCLUSIONS: The utilization of PCP Primer exhibits notable enhancements in bond strength, mitigates nano-leakage, and suppresses enzyme activity within the hybrid layer.

Etch-mineralizing treatment to improve dentin bonding.

Objectives This study aimed to investigate the effect of etch-mineralizing solution as a dentin treatment agent on dentin bonding. Methods This study designed four kinds of etch-mineralizing solutions (EMs) by adding sodium fluoride in 35% phosphoric acid aqueous solution with four different concentrations (5, 10, 20, and 30 mg/ml), and named F1, F2, F3 and F4, respectively. 35% phosphoric acid gel treatment was the control group. SEM, EDS, FTIR and microhardness tests were performed on the treated dentin. Shear bond strength was measured before and after aging. Nanoleakage was also evaluated. Fracture mode was researched after SBS testing. The antibacterial properties of treated dentin were also investigated through live/dead staining of biofilms. Results The smear layer was removed and mineralization substances were observed on the dentin surface and tubule, and no obvious collagen fibers were observed compared with the control group. FTIR spectrums showed that the ratios of phosphate/collagen on EMs treated dentin surfaces were significantly increased (P < 0.05). F2 group had the highest bonding strength (32.14 ± 7.33 MPa) and microhardness (66.08 ± 10.58), while the control group had the lowest bonding strength (21.81 ± 4.03 MPa) and microhardness (42.34 ± 7.08) (p < 0.05), and excellent bonding strength caused more cohesive fracture. Experimental groups showed less nanoleakage than group C (P < 0.05). Moreover, experimental groups had better antiaging performance and antibacterial properties than the control group (p < 0.05). Conclusion EMs treatment not only improved dentin bonding and antibacterial ability, but also remineralized dentin with autologous mineral elements. Clinical significance The treatment provides a novel therapeutic strategy for obtaining ideal dentin bonding strength and prolonging the longevity of the restoration.

Enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation.

Zirconia is a superior implant material owing to its high mechanical strength, durable corrosion resistance, superior aesthetic effect and excellent biocompatibility. However, the bioactivity of zirconia surfaces remains a great challenge for implant osseointegration. A titania (TiO2) coating was innovatively synthesized on the surface of zirconia by infiltration in a suspension of zirconium oxychloride and titania for dense sintering. Subsequently, the coating was subjected to ultraviolet (UV) light to enhance the biological inertness of zirconia. Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and contact angle analysis were conducted to confirm the surface characteristics. Afterwards, in vitro assessments of cell adhesion, proliferation and osteogenic differentiation of MC3T3-E1 cells were performed. Zirconia samples were implanted into rat femurs to assess biocompatibility and host tissue response in vivo. Micro-CT evaluation and histological testing were conducted. After UV irradiation, the content of hydroxyl groups and hydrophilicity of TiO2-modified zirconia were significantly increased. The results of in vitro experiments showed that TiO2-modified zirconia subjected to UV light could promote cell proliferation and spreading, enhance ALP activity and the degree of mineralization, and upregulate osteogenesis-related genes. Furthermore, in vivo assessments confirmed that UV-irradiated TiO2-modified zirconia implants maximized the promotion of osseointegration. TiO2-modified zirconia after UV treatment will have broad clinical application prospects in improving the osseointegration of zirconia implants.