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Inhibition of matrix metalloproteinase activity in human dentin via novel antibacterial monomer

机译:通过新型抗菌单体抑制人牙本质中基质金属蛋白酶的活性

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摘要

Objective. Dentin-composite bond failure is caused by factors including hybrid layer degradation, which in turn can be caused by hydrolysis and enzymatic degradation of the exposed collagen in the dentin. The objectives of this study were to investigate a new antibacterial monomer (dimethylaminododecyl methacrylate, DMADDM) as an inhibitor for matrix metalloproteinases (MMPs), and to determine the effects of DMADDM on both soluble recombinant human MMPs (rhMMPs) and dentin matrix-bound endogenous MMPs. Methods. Inhibitory effects of DMADDM at six mass% (0.1% to 10%) on soluble rhMMP-8 and rhMMP-9 were measured using a colorimetic assay. Matrix-bound endogenous MMP activity was evaluated in demineralized human dentin. Dentin beams were divided into four groups (n = 10) and incubated in calcium- and zinc-containing media (control medium); or control medium + 0.2% chlorhexidine (CHX); 5% 12-methacryloyloxydodecylpyridinium bromide (MDPB); or 5% DMADDM. Dissolution of dentin collagen peptides was evaluated by mechanical testing in three-point flexure, loss of dentin mass, and a hydroxyproline assay. Results. Use of 0.1% to 10% DMADDM exhibited a strong concentration-dependent anti-MMP effect, reaching 90% of inhibition on rhMMP-8 and rhMMP-9 at 5% DMADDM concentration. Dentin beams in medium with 5% DMADDM showed 34% decrease in elastic modulus (vs. 73% decrease for control), 3% loss of dry dentin mass (vs. 28% loss for control), and significantly less solubilized hydroxyproline when compared with control (p < 0.05). Significance. The new antibacterial monomer DMADDM was effective in inhibiting both soluble rhMMPs and matrix-bound human dentin MMPs. These results, together with previous studies showing that adhesives containing DMADDM inhibited biofilms without compromising dentin bond strength, suggest that DMADDM is promising for use in adhesives to prevent collagen degradation in hybrid layer and protect the resin-dentin bond. Published by Elsevier Ltd on behalf of Academy of Dental Materials. All rights reserved.
机译:目的。牙本质复合键失效是由包括杂化层降解在内的因素引起的,而杂化层降解又可能是由于牙本质中暴露的胶原蛋白的水解和酶促降解引起的。这项研究的目的是研究一种新型的抗菌单体(甲基丙烯酸二甲基氨基十二烷基酯,DMADDM)作为基质金属蛋白酶(MMPs)的抑制剂,并确定DMADDM对可溶性重组人MMPs(rhMMPs)和与牙本质基质结合的内源性细菌的作用MMP。方法。使用比色测定法测量了六质量%(0.1%至10%)的DMADDM对可溶性rhMMP-8和rhMMP-9的抑制作用。在脱矿质人牙本质中评估基质结合的内源性MMP活性。牙本质束分为四组(n = 10)并在含钙和锌的培养基(对照培养基)中孵育;或对照培养基+ 0.2%洗必泰(CHX); 5%的12-甲基丙烯酰氧基十二烷基吡啶溴化物(MDPB);或5%DMADDM。牙本质胶原蛋白肽的溶解通过机械测试在三点弯曲,牙本质质量损失和羟脯氨酸分析中进行评估。结果。使用0.1%至10%的DMADDM表现出很强的浓度依赖性抗MMP效应,在5%DMADDM浓度下,对rhMMP-8和rhMMP-9的抑制作用达到90%。与5%DMADDM相比,在含有DMADDM的培养基中的牙本质束显示,弹性模量降低了34%(与之相比,降低了73%),干燥牙本质质量损失了3%(与对照组相比,降低了28%),并且溶解的羟脯氨酸明显少于对照(p <0.05)。意义。新的抗菌单体DMADDM可有效抑制可溶性rhMMP和基质结合型人牙本质MMP。这些结果以及先前的研究表明,含DMADDM的粘合剂可抑制生物膜而不损害牙本质粘合强度,这表明DMADDM有望用于粘合剂中,以防止杂化层中的胶原蛋白降解并保护树脂-牙本质键。由Elsevier Ltd代表牙科材料学院出版。版权所有。

著录项

  • 来源
    《Dental materials》 |2015年第3期|284-292|共9页
  • 作者单位

    Fourth Mil Med Univ, Sch Stomatol, Dept Prosthodont, Xian 710032, Shaanxi, Peoples R China|Univ Maryland, Dept Endodont Prosthodont & Operat Dent, Sch Dent, Baltimore, MD 21201 USA;

    Univ Maryland, Dept Mech Engn, Baltimore, MD 21250 USA;

    Univ Maryland, Dept Endodont Prosthodont & Operat Dent, Sch Dent, Baltimore, MD 21201 USA;

    Univ Maryland, Dept Mech Engn, Baltimore, MD 21250 USA;

    Univ Maryland, Dept Endodont Prosthodont & Operat Dent, Sch Dent, Baltimore, MD 21201 USA|Univ Maryland, Sch Med, Ctr Stem Cell Biol & Regenerat Med, Baltimore, MD 21201 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Dental monomer; Quaternary ammonium; methacrylate; Antibacterial activity; Human dentin; Matrix metalloproteinase inhibitor; Tooth restoration;

    机译:牙科单体季铵盐甲基丙烯酸酯抗菌活性人牙本质基质金属蛋白酶抑制剂牙齿修复;
  • 入库时间 2022-08-18 03:46:53

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