EFFECT OF NATURALLY DERIVED COLLAGEN CROSS-LINKERS ON DENTIN BONDING AT CLINICALLY RELEVANT EXPOSURE TIMES

牙本质 蒸馏水 胶粘剂 材料科学 抗坏血酸 牙科粘接 牙科 戊二醛 复合数 复合材料 万能试验机 粘结强度 化学 色谱法 极限抗拉强度 医学 食品科学 图层(电子)
作者
Nabawy Alrobeigy
出处
期刊:Egyptian dental journal 卷期号:63 (1): 859-869
标识
DOI:10.21608/edj.2017.75036
摘要

Purpose: To investigate the effect of treatment the demineralized dentin with two naturally derived collagen cross-linking agents on resin-dentin shear bond strength using three clinically relevant treatment times.Materials and methods: 60 mid-coronal dentin specimens were randomly divided into two divisions (n=30) and either was treated with one of two cross-linking agents: 25% grape seed extract (GSE) and 25% ascorbic acid (ASA). The teeth of each division were further divided into three groups (n=10) according to the time of cross-linking agent application: 30 sec, 60 sec, and 90 sec. Additionally, 10 teeth were used as a control group (no treatment). After cross-linkers treatment and adhesive application, composite (Filtek Z250 XT) cylinders (3 mm diameter × 2 mm length) were built on all dentin surfaces. All specimens were stored in distilled water for 24 hours at 37˚C and then subjected to shear stress in a universal testing machine. Failure patterns were observed using a light microscope at 10X. The micromorphology of the fractured surfaces of selected specimens was evaluated using SEM. SBS data (MPa) were statistically analyzed by two-way ANOVA and t-test.Results: Both cross-linking agents resulted in a significant (P<0.0001) increase in resin-dentin SBS in comparison to control, regardless of application time. SBS values of both cross-linking agents were significantly increased by increasing their application time from 30 to 90 sec, while they were not affected, between other treatment times. There was no significant (P = 0.5) differences in SBS values between the two cross linkers at each corresponding treatment time.Conclusions: Resin-dentin SBS can be improved after treatment of demineralized dentin by GSE, and ASA cross-linking agents at a clinically relevant treatment times.

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