This study aimed to evaluate the ability of a newly developed calcium-phosphate desensitizer in dentin permeability reduction and its integration with dentin surface before and after immersion in artificial saliva (AS) under two different dentin surface characteristics; with or without the collagen exposure. Human dentin discs treated by EDTA to expose collagen fibrils or EDTA/NaOCl to expose plain dentin surface were subjected to a calcium-phosphate desensitizer (Teethmate Desensitizer; TMD), while non-desensitizer treatment served as control. TMD application showed the occlusion in dentinal tubules and reduction in dentin permeability up to 92%, regardless of dentin surface characteristics. After AS immersion, permeability reduction percent (PR%) significantly increased in EDTA/NaOCl pretreatment (p<0.05). Newly-formed crystallites were observed on desensitizer treated dentin and EDTA/NaOCl pretreatment control group, whereas the crystallites did not exist on EDTA pretreatment control group. Ultrasonication revealed the integration of the calcium-phosphate rich layer of desensitizer on dentin surface after AS immersion.

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The use of paper points with additional air-blowing for removing excessive adhesive and evaporating residual water/solvent would be effective in producing higher bond strength for the tested one-step self-etch adhesives and fewer blister formations in deeper regions of the post space.

We evaluated the effect of phytic acid on matrix metalloproteinase (MMP)‐ or cysteine cathepsin (CC)‐mediated dentin degradation. Demineralized dentin beams were divided into five groups (n = 12) and treated with 1%, 2%, or 3% phytic acid or with 37% phosphoric acid. Untreated demineralized beams served as controls. After incubation for 1 or 3 wk, dry mass loss was determined and aliquots of incubation media were analysed for cross‐linked telopeptide of type I collagen (ICTP) fragments for MMP‐mediated and c‐terminal telopeptide of type I collagen (CTX) for cathepsin‐k‐mediated degradation. The direct effect of phytic acid was evaluated using MMP activity assay. Data were analysed using repeated‐measures anova. ICTP releases with 1% and 2% phytic acid treatment were statistically significantly lower than those following phosphoric acid treatment at 3 wk. The CTX release for phytic acid‐treated beams at 3 wk was not significantly different from that of untreated control beams, but it was significantly lower than that of phosphoric acid‐treated beams. Their MMP activities at 3 wk were not significantly different from those of the controls but they were significantly lower than those seen for phosphoric acid‐treated beams. Compared to phosphoric acid, phytic acid treatment resulted in a reduced dentinal host‐derived endogenous enzymatic activity and collagen degradation.

The purpose was to evaluate the effect of air-drying dentin surfaces on the microtensile bond strength (μTBS) of a solvent-free onestep adhesive (Bond 1 SF). Twelve human molars were ground with 600-grit SiC paper. Before applying bonding agent, the dentin surface was rinsed with distilled water and blot-dried with tissue paper, followed by air-drying for 0, 3, 30, and 60 s using with a dental air syringe. After applying and curing Bond 1 SF, resin composite was incrementally built up. Specimens were then stored in distilled water for 24 h and then μTBSs were measured at a cross-head speed of 1 mm/min. Higher μTBS were observed when the dentin surface was air-dried for 3 s (33.2±6.8MPa)>0 s (26.7±4.5MPa)>30 s (22.6±5.5MPa)=60 s (20.4±5.0MPa). The results suggested that prolonged air-drying of the dentin surface removed water and decreased the bond strengths of Bond 1 SF.

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