Department of Stomatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Hankou District, Wuhan 430030, People's Republic of China.
J Dent Res. 2011 Aug;90(8):953-68. doi: 10.1177/0022034510391799. Epub 2011 Jan 10.
The limited durability of resin-dentin bonds severely compromises the lifetime of tooth-colored restorations. Bond degradation occurs via hydrolysis of suboptimally polymerized hydrophilic resin components and degradation of water-rich, resin-sparse collagen matrices by matrix metalloproteinases (MMPs) and cysteine cathepsins. This review examined data generated over the past three years on five experimental strategies developed by different research groups for extending the longevity of resin-dentin bonds. They include: (1) increasing the degree of conversion and esterase resistance of hydrophilic adhesives; (2) the use of broad-spectrum inhibitors of collagenolytic enzymes, including novel inhibitor functional groups grafted to methacrylate resins monomers to produce anti-MMP adhesives; (3) the use of cross-linking agents for silencing the activities of MMP and cathepsins that irreversibly alter the 3-D structures of their catalytic/allosteric domains; (4) ethanol wet-bonding with hydrophobic resins to completely replace water from the extrafibrillar and intrafibrillar collagen compartments and immobilize the collagenolytic enzymes; and (5) biomimetic remineralization of the water-filled collagen matrix using analogs of matrix proteins to progressively replace water with intrafibrillar and extrafibrillar apatites to exclude exogenous collagenolytic enzymes and fossilize endogenous collagenolytic enzymes. A combination of several of these strategies should result in overcoming the critical barriers to progress currently encountered in dentin bonding.
树脂-牙本质粘结的耐久性有限,严重影响了牙色修复体的使用寿命。粘结的降解是通过水解未充分聚合的亲水性树脂成分以及富含水的、稀疏的树脂基质的胶原蛋白,由基质金属蛋白酶(MMPs)和半胱氨酸组织蛋白酶引起的。本文综述了过去三年中,不同研究小组为延长树脂-牙本质粘结的耐久性而开发的五种实验策略的数据。它们包括:(1)提高亲水性粘结剂的转化率和酯酶抗性;(2)使用广谱胶原酶抑制剂,包括通过接枝到甲基丙烯酸酯树脂单体的新型抑制剂官能团来产生抗-MMP 粘结剂;(3)使用交联剂来沉默 MMP 和组织蛋白酶的活性,这些酶不可逆地改变其催化/变构结构域的三维结构;(4)用疏水性树脂进行乙醇湿粘结,以完全取代纤维外和纤维内胶原蛋白隔室中的水,并固定胶原酶;(5)使用基质蛋白类似物对充满水的胶原蛋白基质进行仿生再矿化,以逐步用纤维内和纤维外磷灰石取代水,以排除外源性胶原酶并使内源性胶原酶矿化。这些策略的组合应该有助于克服当前在牙本质粘结中遇到的关键障碍。