Hu Yuntong, He Yi, Wang Dingjie, Wei Yingjing, Xing Xiaodong, Xiao Yuhong
Department of Oral Surgery, 920th Hospital of Joint Logistics Support Force, PLA, Teaching Hospital of Kunming Medical University, Kunming, China.
Yunnan Key Laboratory of Stomatology and Department of Dental Research, Kunming Medical University, Kunming, China.
Front Bioeng Biotechnol. 2025 Apr 28;13:1574562. doi: 10.3389/fbioe.2025.1574562. eCollection 2025.
Dental caries is the most common oral disease. In caries-affected dentin (CAD), excessive mineral loss, extensive collagen exposure and collapse, increased enzyme activity, and bacterial residues result in significantly lower resin bonding strength and durability compared to sound dentin (SD). Currently, there are no effective clinical strategies to enhance CAD bonding. Inspired by the excellent wet adhesion capability and collagen affinity of marine mussels, this study aimed to evaluate a mussel-inspired polymerizable monomer (catechol-Lys-methacrylate [CLM]) as a primer to improve CAD bonding performance.
The interactions between CLM and collagen were analyzed Fourier-transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR). Microtensile bond strength, nanoleakage, zymography, and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) were used to assess the bond strength and interface stability. Furthermore, the antibacterial properties of CLM were evaluated using colony-forming units counts, live/dead bacterial staining, and bacterial morphology observation.
FTIR and NMR results showed that CLM was successfully grafted onto CAD collagen through its catechol groups, facilitating subsequent chemical bonding with resin. CLM increased the immediate CAD bond strength by approximately 30% and reduced immediate nanoleakage by approximately 24%, maintaining effectiveness after aging. Moreover, collagen chemical modification by CLM promoted collagen crosslinking, inhibited endogenous enzymatic activity, and conferred antibacterial properties, further enhancing bonding interface stability.
In summary, this study reports the application of a mussel-inspired monomer, CLM, in CAD bonding. During the wet bonding process, CLM not only improves collagen stability but also serves as a molecular bridge between inorganic resin and organic collagen, thereby enhancing both immediate and aged bonding performance. These findings showing promising clinical application potential.
龋齿是最常见的口腔疾病。在龋损牙本质(CAD)中,与健康牙本质(SD)相比,矿物质过度流失、大量胶原蛋白暴露和塌陷、酶活性增加以及细菌残留导致树脂粘结强度和耐久性显著降低。目前,尚无有效的临床策略来增强CAD粘结。受海洋贻贝出色的湿粘附能力和胶原蛋白亲和力的启发,本研究旨在评估一种受贻贝启发的可聚合单体(儿茶酚 - 赖氨酸 - 甲基丙烯酸酯[CLM])作为底漆,以改善CAD粘结性能。
采用傅里叶变换红外光谱(FTIR)和核磁共振(NMR)分析CLM与胶原蛋白之间的相互作用。使用微拉伸粘结强度、纳米渗漏、酶谱分析和十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)来评估粘结强度和界面稳定性。此外,使用菌落形成单位计数、活菌/死菌染色和细菌形态观察来评估CLM的抗菌性能。
FTIR和NMR结果表明,CLM通过其儿茶酚基团成功接枝到CAD胶原蛋白上,促进了随后与树脂的化学键合。CLM使CAD即时粘结强度提高了约30%,即时纳米渗漏减少了约24%,老化后仍保持有效性。此外,CLM对胶原蛋白的化学修饰促进了胶原蛋白交联,抑制了内源性酶活性,并赋予了抗菌性能,进一步增强了粘结界面稳定性。
总之,本研究报道了一种受贻贝启发的单体CLM在CAD粘结中的应用。在湿粘结过程中,CLM不仅提高了胶原蛋白稳定性,还作为无机树脂和有机胶原蛋白之间的分子桥梁,从而增强了即时和老化后的粘结性能。这些发现显示出有前景的临床应用潜力。