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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Enzymatic biodegradation of HEMA/bisGMA adhesives formulated with different water content.
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Enzymatic biodegradation of HEMA/bisGMA adhesives formulated with different water content.

机译:不同含水量配制的HEMA / bisGMA粘合剂的酶促生物降解。

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Dentin adhesives may undergo phase separation when bonding to wet demineralized dentin. We hypothesized that adhesives exhibiting phase separation will experience enhanced biodegradation of methacrylate ester groups. The objective of this project was to study the effect of enzyme-exposure on the release of methacrylic acid (MAA) and 2-hydroxyethyl methacrylate (HEMA) from adhesives formulated under conditions simulating wet bonding. HEMA/bisGMA(2,2-bis[4(2-hydroxy-3-methacryloyloxy-propyloxy)-phenyl] propane), 45/55 w/w ratio, was formulated with different water content: 0 Wt % (A00), 8 wt % (A08), and 16 wt % (A16). After a three day prewash, adhesive discs were incubated with/without porcine liver esterase (PLE) in phosphate buffer (PB, pH 7.4) at 37 degrees C for 8 days. Supernatants were collected daily and analyzed for MAA and HEMA by HPLC. For all formulations, daily MAA release in the presence of PLE was increased compared to MAA release in PB. HEMA release in the presence of PLE was not detected while HEMA release was consistently measured in PB. A08 and A16 released significantly larger amounts of HEMA compared to A00. Analysis of the cumulative release of analytes showed that the leachables in PLE was significantly increased (p < 0.05) as compared with that released in PB indicating that MAA release was not only formed from unreacted monomers but from pendant groups in the polymer network. However, the levels of analytes HEMA in PB or MAA in PLE were increased in A08 and A16 as compared with A00, which suggests that there could be a greater loss of material in HEMA/bisGMA adhesives that experience phase separation under wet bonding conditions.
机译:当与湿的脱矿质牙本质粘合时,牙本质粘合剂可能会发生相分离。我们假设表现出相分离的胶粘剂将经历甲基丙烯酸酯基团的增强的生物降解。该项目的目的是研究酶暴露对模拟湿粘合条件下配制的胶粘剂释放甲基丙烯酸(MAA)和甲基丙烯酸2-羟乙酯(HEMA)的影响。配制45/55 w / w比的HEMA / bisGMA(2,2-双[4(2-羟基-3-甲基丙烯酰氧基-丙氧基)-苯基]丙烷)丙烷,水含量为0 Wt%(A00), 8重量%(A08)和16重量%(A16)。预洗三天后,将胶粘盘与/不与猪肝酯酶(PLE)在磷酸盐缓冲液(PB,pH 7.4)中于37摄氏度孵育8天。每天收集上清液,并通过HPLC分析其MAA和HEMA。对于所有制剂,与PB中的MAA释放相比,在PLE存在下的每日MAA释放增加。未检测到存在PLE的HEMA释放,而在PB中始终检测到HEMA释放。与A00相比,A08和A16释放的HEMA量明显增加。分析物累积释放的分析表明,PLE中的可浸出物比PB中的可浸出物显着增加(p <0.05),这表明MAA释放不仅由未反应的单体形成,而且由聚合物网络中的侧基形成。但是,与A00相比,A08和A16中PB中PB或MAA中分析物HEMA的水平与A00相比有所增加,这表明在湿粘结条件下经历相分离的HEMA / bisGMA粘合剂中材料的损失可能更大。

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