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用于牙科的抗菌肽-聚合物共轭物

Antimicrobial Peptide-Polymer Conjugates for Dentistry.

作者信息

Xie Sheng-Xue, Song Linyong, Yuca Esra, Boone Kyle, Sarikaya Rizacan, VanOosten Sarah Kay, Misra Anil, Ye Qiang, Spencer Paulette, Tamerler Candan

机构信息

University of Kansas (KU), Lawrence, Kansas.

University of Kansas (KU), Lawrence, Kansas, and Yildiz Technical University, Istanbul, Turkey.

出版信息

ACS Appl Polym Mater. 2020 Mar 13;2(3):1134-1144. doi: 10.1021/acsapm.9b00921. Epub 2020 Jan 2.

Abstract

Bacterial adhesion and growth at the composite/adhesive/tooth interface remain the primary cause of dental composite restoration failure. Early colonizers, including , play a critical role in the formation of dental caries by creating an environment that reduces the adhesive's integrity. Subsequently, other bacterial species, biofilm formation, and lactic acid from demineralize the adjoining tooth. Because of their broad spectrum of antibacterial activity and low risk for antibiotic resistance, antimicrobial peptides (AMPs) have received significant attention to prevent bacterial biofilms. Harnessing the potential of AMPs is still very limited in dentistry-a few studies have explored peptide-enabled antimicrobial adhesive copolymer systems using mainly nonspecific adsorption. In the current investigation, to avoid limitations from nonspecific adsorption and to prevent potential peptide leakage out of the resin, we conjugated an AMP with a commonly used monomer for dental adhesive formulation. To tailor the flexibility between the peptide and the resin material, we designed two different spacer domains. The spacer-integrated antimicrobial peptides were conjugated to methacrylate (MA), and the resulting MA-AMP monomers were next copolymerized into dental adhesives as AMP-polymer conjugates. The resulting bioactivity of the polymethacrylate-based AMP conjugated matrix activity was investigated. The antimicrobial peptide conjugated to the resin matrix demonstrated significant antimicrobial activity against . Secondary structure analyses of conjugated peptides were applied to understand the activity differential. When mechanical properties of the adhesive system were investigated with respect to AMP and cross-linking concentration, resulting AMP-polymer conjugates maintained higher compressive moduli compared to hydrogel analogues including polyHEMA. Overall, our result provides a robust approach to develop a fine-tuned bioenabled peptide adhesive system with improved mechanical properties and antimicrobial activity. The results of this study represent a critical step toward the development of peptide-conjugated dentin adhesives for treatment of secondary caries and the enhanced durability of dental composite restorations.

摘要

细菌在复合树脂/粘合剂/牙齿界面的粘附和生长仍然是牙科复合树脂修复失败的主要原因。早期定植菌,包括……,通过创造一个降低粘合剂完整性的环境,在龋齿形成中起关键作用。随后,其他细菌种类、生物膜形成以及……产生的乳酸会使相邻牙齿脱矿。由于抗菌肽(AMPs)具有广谱抗菌活性且抗生素耐药风险低,因此在预防细菌生物膜方面受到了广泛关注。在牙科领域,利用抗菌肽的潜力仍然非常有限——一些研究主要通过非特异性吸附探索了含肽抗菌粘合剂共聚物体系。在当前的研究中,为了避免非特异性吸附的局限性并防止肽从树脂中潜在泄漏,我们将一种抗菌肽与一种用于牙科粘合剂配方的常用单体进行了共轭。为了调整肽与树脂材料之间的柔韧性,我们设计了两个不同的间隔域。将整合了间隔域的抗菌肽与甲基丙烯酸酯(MA)共轭,然后将所得的MA-AMP单体作为AMP-聚合物共轭物共聚到牙科粘合剂中。研究了基于聚甲基丙烯酸酯的AMP共轭基质活性的生物活性。与树脂基质共轭的抗菌肽对……表现出显著的抗菌活性。应用共轭肽的二级结构分析来理解活性差异。当研究粘合剂体系相对于AMP和交联浓度的力学性能时,所得的AMP-聚合物共轭物与包括聚甲基丙烯酸羟乙酯在内的水凝胶类似物相比,保持了更高的压缩模量。总体而言,我们的结果提供了一种稳健的方法来开发一种具有改善的力学性能和抗菌活性的精细生物活性肽粘合剂体系。这项研究的结果代表了朝着开发用于治疗继发龋和提高牙科复合树脂修复耐久性的肽共轭牙本质粘合剂迈出的关键一步。

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