Chen Xiaoyu, Huang Ning, Wang Danyang, Zhang Miao, Deng Xuyang, Guo Fangze, Yi Bingcheng, Yuan Changqing, Zhou Qihui
Department of Stomatology, The Affiliated Hospital of Qingdao University, Qingdao 266003, China.
School of Stomatology, Qingdao University, Qingdao 266003, China.
ACS Nano. 2024 Jun 4;18(22):14312-14326. doi: 10.1021/acsnano.4c00137. Epub 2024 May 20.
Periodontitis, a prevalent chronic inflammatory disease worldwide, is triggered by periodontopathogenic bacteria, resulting in the progressive destruction of periodontal tissue, particularly the alveolar bone. To effectively address periodontitis, this study proposed a nanoformulation known as CuS@MSN-SCS. This formulation involves coating citrate-grafted copper sulfide (CuS) nanoparticles with mesoporous silica (MSNs), followed by surface modification using amino groups and sulfated chitosan (SCS) through electrostatic interactions. The objective of this formulation is to achieve efficient bacteria removal by inducing ROS signaling pathways mediated by Cu ions. Additionally, it aims to promote alveolar bone regeneration through Cu-induced pro-angiogenesis and SCS-mediated bone regeneration. As anticipated, by regulating the surface charges, the negatively charged CuS nanoparticles capped with sodium citrate were successfully coated with MSNs, and the subsequent introduction of amine groups using (3-aminopropyl)triethoxysilane was followed by the incorporation of SCS through electrostatic interactions, resulting in the formation of CuS@MSN-SCS. The developed nanoformulation was verified to not only significantly exacerbate the oxidative stress of , thereby suppressing bacteria growth and biofilm formation , but also effectively alleviate the inflammatory response and promote alveolar bone regeneration without evident biotoxicity in an rat periodontitis model. These findings contribute to the therapeutic effect on periodontitis. Overall, this study successfully developed a nanoformulation for combating bacteria and facilitating alveolar bone regeneration, demonstrating the promising potential for clinical treatment of periodontitis.
牙周炎是一种在全球范围内普遍存在的慢性炎症性疾病,由牙周病原菌引发,会导致牙周组织尤其是牙槽骨的渐进性破坏。为有效治疗牙周炎,本研究提出了一种名为CuS@MSN-SCS的纳米制剂。该制剂是用介孔二氧化硅(MSNs)包裹柠檬酸盐接枝的硫化铜(CuS)纳米颗粒,然后通过静电相互作用使用氨基和硫酸化壳聚糖(SCS)进行表面改性。该制剂的目的是通过诱导由铜离子介导的ROS信号通路来实现高效的细菌清除。此外,它旨在通过铜诱导的促血管生成和SCS介导的骨再生来促进牙槽骨再生。正如预期的那样,通过调节表面电荷,成功地用MSNs包裹了用柠檬酸钠封端的带负电荷的CuS纳米颗粒,随后使用(3-氨丙基)三乙氧基硅烷引入胺基,接着通过静电相互作用引入SCS,从而形成了CuS@MSN-SCS。经证实,所开发的纳米制剂不仅能显著加剧[具体细菌名称]的氧化应激,从而抑制细菌生长和生物膜形成,而且在大鼠牙周炎模型中能有效减轻炎症反应并促进牙槽骨再生,且无明显的生物毒性。这些发现有助于对牙周炎的治疗效果。总体而言,本研究成功开发了一种用于对抗细菌和促进牙槽骨再生的纳米制剂,展示了在牙周炎临床治疗中的广阔前景。