Durable Dentin Bonding with Multifunctional Methacrylated Proanthocyanidins.

IF 5.7 1区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
V Hass,N Wickerhauser,N Desch,Y Li,R Wang,Z Peng,Y Wang
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Abstract

The degradation of dentin bonding interfaces by enzymes, either originating from the dentin matrix or produced by oral biofilms, contributes to the failure of composite restorations. Proanthocyanidins (PAs) are effective collagen crosslinkers that help preserve collagen, but their interference with adhesive polymerization impairs clinical applications. Methacrylate-functionalized PA (MAPA) was developed as a polymerizable collagen crosslinker, designed to strengthen collagen while copolymerizing with adhesives. This study evaluated the effects of MAPA-containing adhesives on dentin-bonding properties, including collagen crosslinking within bonding interfaces (via sodium dodecyl sulfate-collagen hybridizing peptide assay), microtensile bond strength (µTBS), and collagenolytic activity (in situ zymography) at 24 h and after 2 y (2Y), as well as on biofilm inhibition. Two adhesives, Scotchbond Universal and Prime&Bond Elect, were modified with MAPA or PA at 0%, 5%, and 10% concentrations. Human molar dentin surfaces were bonded and restored using composite resin, then sectioned into sticks or slabs for µTBS and in situ zymography at 24 h or 2Y. Additional specimens were evaluated for biofilm formation (Streptococcus mutans) using live/dead staining, MTT assay, and colony-forming unit counts. Data were analyzed using 2-way analysis of variance and Games-Howell set at 5%. Results showed that MAPA effectively enhanced chemical crosslinking within bonding interfaces without affecting µTBS at 24 h (P > 0.05). Notably, 5%MAPA significantly stabilized bonding interfaces over 2Y (P > 0.05) compared with other groups. All MAPA groups demonstrated a significant reduction in collagenolytic activity (P < 0.05), with 5%MAPA maintaining this effect after 2Y (P > 0.05). In addition, MAPA reduced biofilm formation. MAPA's capacity to copolymerize with adhesives while forming strong chemical interactions with collagen creates a durable, chemically integrated polymer-collagen complex that resists enzymatic degradation and inhibits cariogenic bacterial activity. Incorporating MAPA into adhesives stabilizes bonding interfaces and provides antibiofilm benefits, offering a promising approach to extending the longevity of composite restorations.
与多功能甲基丙烯酸基原花青素的持久牙本质结合。
来自牙本质基质或口腔生物膜的酶降解牙本质结合界面是复合修复失败的原因之一。原花青素(PAs)是一种有效的胶原交联剂,有助于保存胶原蛋白,但它们对粘接剂聚合的干扰妨碍了临床应用。甲基丙烯酸酯功能化PA (MAPA)是一种可聚合的胶原交联剂,可在与粘合剂共聚的同时增强胶原。本研究评估了含mapa的粘合剂对牙本质键合特性的影响,包括在键合界面内的胶原交联(通过十二烷基硫酸钠-胶原杂交肽测定)、微拉伸键合强度(µTBS)、24小时和2 y后的胶原溶解活性(原位酶谱法),以及对生物膜的抑制作用。两种粘合剂,Scotchbond Universal和Prime&Bond Elect,分别用0%、5%和10%浓度的MAPA或PA进行改性。使用复合树脂粘合和修复人磨牙本质表面,然后在24 h或2Y时切片成棒状或板状进行微TBS和原位酶谱分析。使用活/死染色、MTT测定和菌落形成单位计数对其他标本进行生物膜形成(变形链球菌)评估。数据分析采用2-way方差分析,game - howell设为5%。结果表明,MAPA有效增强了键合界面内的化学交联,但不影响24 h时的µTBS (P < 0.05)。值得注意的是,与其他组相比,5%MAPA在2Y内显著稳定了键合界面(P < 0.05)。所有MAPA组的胶原溶解活性均显著降低(P < 0.05), 5%的MAPA在2Y后仍保持这种作用(P < 0.05)。此外,MAPA减少了生物膜的形成。MAPA与粘合剂共聚的能力,同时与胶原蛋白形成强烈的化学相互作用,形成持久的,化学整合的聚合物-胶原蛋白复合物,抵抗酶降解,抑制龋齿细菌活性。将MAPA加入粘合剂中可以稳定粘合界面,并提供抗生物膜的好处,为延长复合修复体的使用寿命提供了一种有希望的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Dental Research
Journal of Dental Research 医学-牙科与口腔外科
CiteScore
15.30
自引率
3.90%
发文量
155
审稿时长
3-8 weeks
期刊介绍: The Journal of Dental Research (JDR) is a peer-reviewed scientific journal committed to sharing new knowledge and information on all sciences related to dentistry and the oral cavity, covering health and disease. With monthly publications, JDR ensures timely communication of the latest research to the oral and dental community.
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