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仿生寡肽通过矿化形成类似牙釉质的组织和牙本质小管阻塞,用于治疗牙本质过敏症。

Biomimetic oligopeptide formed enamel-like tissue and dentin tubule occlusion via mineralization for dentin hypersensitivity treatment.

机构信息

Department of Periodontology, Nanjing Stomatological Hospital, Medical School of Nanjing University, Nanjing, China.

State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering, Southeast University, Nanjing, China.

出版信息

J Appl Biomater Funct Mater. 2021 Jan-Dec;19:22808000211005384. doi: 10.1177/22808000211005384.

Abstract

OBJECTIVE

Dentin hypersensitivity (DH) is a common oral disease with approximately 41.9% prevalence. Reconstruction of dental hard tissues is the preferred treatment for relieving DH. Here, we applied biomineralization method using oligopeptide simulating cementum protein 1 (CEMP1) to regenerate hard tissues on demineralized dentin.

METHODS

The self-assembly and biomineralization property of the oligopeptide were detected by scanning electron microscopy (SEM), circular dichroism spectroscopy, and transmission electron microscopy. Oligopeptide's binding capacity to demineralized dentin was evaluated by SEM and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR). Remineralization was characterized using SEM, ATR-FTIR, X-ray diffraction, and nanoindentation. Oligopeptide's biocompatibility was evaluated using periodontal ligament cells.

RESULTS

Oligopeptides self-assembled into nano-matrix and templated mineral precursor formation within 24 h. Moreover, oligopeptide nano-matrix bound firmly on demineralized dentin and resisted water rinsing. Then, bound nano-matrix served as a template to initiate nucleation and transformation of hydroxyapatite on demineralized dentin. After 96 h, oligopeptide nano-matrix regenerated an enamel-like tissue layer with a thickness of 15.35 μm, and regenerated crystals occluded dentin tubules with a depth of 31.27 μm. Furthermore, the oligopeptide nano-matrix had good biocompatibility when co-cultured with periodontal ligament cells.

CONCLUSIONS

This biomimetic oligopeptide simulating CEMP1 effectively induced remineralization and reconstructed hard tissues on demineralized dentin, providing a potential biomaterial for DH treatment.

摘要

目的

牙本质敏感症(DH)是一种常见的口腔疾病,患病率约为 41.9%。重建牙体硬组织是缓解 DH 的首选治疗方法。在这里,我们应用生物矿化方法,使用模拟牙骨质蛋白 1(CEMP1)的寡肽来再生脱矿牙本质上的硬组织。

方法

通过扫描电子显微镜(SEM)、圆二色光谱和透射电子显微镜检测寡肽的自组装和生物矿化特性。通过 SEM 和衰减全反射傅里叶变换红外光谱(ATR-FTIR)评估寡肽对脱矿牙本质的结合能力。通过 SEM、ATR-FTIR、X 射线衍射和纳米压痕法对再矿化进行表征。使用牙周膜细胞评估寡肽的生物相容性。

结果

寡肽在 24 小时内自组装成纳米基质并模板化形成矿物前体。此外,寡肽纳米基质牢固地结合在脱矿牙本质上,能抵抗水冲洗。然后,结合的纳米基质作为模板,在脱矿牙本质上启动羟磷灰石的成核和转化。96 小时后,寡肽纳米基质再生了厚度为 15.35μm 的类似釉质的组织层,并使再生的晶体封闭了深度为 31.27μm 的牙本质小管。此外,当与牙周膜细胞共培养时,寡肽纳米基质具有良好的生物相容性。

结论

这种仿生模拟 CEMP1 的寡肽能有效诱导脱矿牙本质的再矿化和硬组织重建,为 DH 治疗提供了一种潜在的生物材料。

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