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[基质金属蛋白酶抑制剂的研究进展]

[Progress on matrix metalloproteinase inhibitors].

作者信息

Lingling Jia, Qianbing Wan

机构信息

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, Dept. of Prosthetics, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China.

出版信息

Hua Xi Kou Qiang Yi Xue Za Zhi. 2017 Apr 1;35(2):208-214. doi: 10.7518/hxkq.2017.02.019.

Abstract

Continuing advances in dentin bonding technology and adhesives revolutionized bonding of resin-based composite restorations. However, hybrid layers created by contemporary dentin adhesives present imperfect durability, and degradation of collagen matrix by endogenous enzymes is a significant factor causing destruction of hybrid layers. Bond durability can be improved by using enzyme inhibitors to prevent collagen degradation and to preserve integrity of collagen matrix. This review summarizes progress on matrix metalloproteinase inhibitors (including chlorhexidine, ethylenediaminetetraacetic acid, quaternary ammonium salt, tetracycline and its derivatives, hydroxamic acid inhibitors, bisphosphonate derivative, and cross-linking agents) and suggests prospects for these compounds.

摘要

牙本质粘结技术和粘结剂的不断进步彻底改变了树脂基复合修复体的粘结方式。然而,当代牙本质粘结剂形成的混合层耐久性欠佳,内源性酶对胶原基质的降解是导致混合层破坏的重要因素。使用酶抑制剂来防止胶原降解并维持胶原基质的完整性可提高粘结耐久性。本文综述了基质金属蛋白酶抑制剂(包括氯己定、乙二胺四乙酸、季铵盐、四环素及其衍生物、异羟肟酸抑制剂、双膦酸盐衍生物和交联剂)的研究进展,并对这些化合物的应用前景进行了展望。

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