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Anti-proteolytic capacity and bonding durability of proanthocyanidin-biomodified demineralized dentin matrix

机译:原花青素生物改性脱矿牙本质基质的抗蛋白水解能力和结合耐久性

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摘要

Our previous studies showed that biomodification of demineralized dentin collagen with proanthocyanidin (PA) for a clinically practical duration improves the mechanical properties of the dentin matrix and the immediate resin–dentin bond strength. The present study sought to evaluate the ability of PA biomodification to reduce collagenase-induced biodegradation of demineralized dentin matrix and dentin/adhesive interfaces in a clinically relevant manner. The effects of collagenolytic and gelatinolytic activity on PA-biomodified demineralized dentin matrix were analysed by hydroxyproline assay and gelatin zymography. Then, resin-/dentin-bonded specimens were prepared and challenged with bacterial collagenases. Dentin treated with 2% chlorhexidine and untreated dentin were used as a positive and negative control, respectively. Collagen biodegradation, the microtensile bond strengths of bonded specimens and the micromorphologies of the fractured interfaces were assessed. The results revealed that both collagenolytic and gelatinolytic activity on demineralized dentin were notably inhibited in the PA-biomodified groups, irrespective of PA concentration and biomodification duration. When challenged with exogenous collagenases, PA-biomodified bonded specimens exhibited significantly less biodegradation and maintained higher bond strengths than the untreated control. These results suggest that PA biomodification was effective at inhibiting proteolytic activity on demineralized dentin matrix and at stabilizing the adhesive/dentin interface against enzymatic degradation, is a new concept that has the potential to improve bonding durability.
机译:我们以前的研究表明,在临床实用的时间内,用原花青素(PA)对脱矿质牙本质胶原进行生物改性可以改善牙本质基质的机械性能和直接的树脂-牙本质粘合强度。本研究试图以临床相关的方式评估PA生物修饰减少胶原酶诱导的脱矿牙本质基质和牙本质/粘附界面生物降解的能力。通过羟脯氨酸分析和明胶酶谱分析,分析了胶原分解和明胶分解活性对PA-生物改性的脱矿牙本质基质的影响。然后,制备树脂/牙本质结合的标本,并用细菌胶原酶攻击。用2%洗必泰处理的牙本质和未处理的牙本质分别用作阳性对照和阴性对照。评估胶原蛋白的生物降解,粘合标本的微拉伸粘合强度以及断裂界面的微观形态。结果表明,在PA生物修饰的组中,对软化牙本质的胶原蛋白水解和明胶分解活性均受到抑制,而与PA浓度和生物修饰时间无关。当用外源胶原酶攻击时,与未经处理的对照相比,PA生物修饰的结合标本显示出明显更少的生物降解并保持了更高的结合强度。这些结果表明,PA生物改性可有效抑制脱矿的牙本质基质上的蛋白水解活性,并稳定胶粘剂/牙本质界面以防止酶降解,这是一个新的概念,具有改善粘合耐久性的潜力。

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