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基于二甲双胍碳点的成骨和蛋白质递送系统促进牙周炎中的骨再生。

Metformin carbon dots-based osteogenic and protein delivery system to promote bone regeneration in periodontitis.

作者信息

Wei Jingjing, Wang Kai, Li Yongkai, Huang Jiao, Deng Ping, Xia Xianbo, Yang Cong, Xu Ling, Xu Junji

机构信息

College of Stomatology, Chongqing Medical University, 401147, China.

Chongqing Key Laboratory of Oral Diseases, 401147, China.

出版信息

Bioact Mater. 2025 Jul 25;53:459-479. doi: 10.1016/j.bioactmat.2025.07.001. eCollection 2025 Nov.

Abstract

The chronic inflammation in periodontitis suppresses the osteogenic potential of human periodontal ligament stem cells (hPDLSCs), posing a significant challenge to endogenous bone regeneration. To address this, we developed an osteogenic and protein-delivery composite hydrogel system based on metformin carbon dots (MCDs) to enhance the osteogenic potential of hPDLSCs under inflammatory conditions. We successfully synthesized a novel Gel/MCDs@IGF-1 composite hydrogel (Gel) that exhibited excellent biocompatibility and sequentially released MCDs and insulin-like growth factor 1 (IGF-1). First, MCDs were synthesized using a one-step hydrothermal method. MCDs promote the osteogenic differentiation of hPDLSCs under lipopolysaccharide (LPS)-induced inflammatory conditions by activating the PI3K/AKT signaling pathway, and alleviate inflammation. Next, MCDs and IGF-1 were assembled into MCDs@IGF-1 complexes through supramolecular interactions, facilitating efficient IGF-1 delivery and reducing its degradation by trypsin. Furthermore, and studies demonstrated that the Gel/MCDs@IGF-1 composite hydrogel effectively recruited stem cells, exerted early anti-inflammatory effects, increased the osteogenesis of hPDLSCs under inflammatory conditions, and significantly promoted alveolar bone regeneration in a Sprague-Dawley (SD) rat model of periodontitis. In conclusion, MCDs, with their dual roles in promoting osteogenesis and protein delivery, are a promising candidate nanoplatform for periodontitis therapy. Additionally, the MCDs-based sequential release hydrogel system presents a novel material strategy for the treatment of periodontitis.

摘要

牙周炎中的慢性炎症会抑制人牙周膜干细胞(hPDLSCs)的成骨潜能,这对内源性骨再生构成了重大挑战。为了解决这一问题,我们开发了一种基于二甲双胍碳点(MCDs)的成骨和蛋白质递送复合水凝胶系统,以增强炎症条件下hPDLSCs的成骨潜能。我们成功合成了一种新型的Gel/MCDs@IGF-1复合水凝胶(Gel),它具有优异的生物相容性,并能依次释放MCDs和胰岛素样生长因子1(IGF-1)。首先,采用一步水热法合成MCDs。MCDs通过激活PI3K/AKT信号通路促进脂多糖(LPS)诱导的炎症条件下hPDLSCs的成骨分化,并减轻炎症。接下来,MCDs和IGF-1通过超分子相互作用组装成MCDs@IGF-1复合物,促进IGF-1的有效递送并减少其被胰蛋白酶降解。此外, 和 研究表明,Gel/MCDs@IGF-1复合水凝胶有效地募集干细胞,发挥早期抗炎作用,增加炎症条件下hPDLSCs的成骨能力,并在Sprague-Dawley(SD)大鼠牙周炎模型中显著促进牙槽骨再生。总之,MCDs在促进成骨和蛋白质递送方面具有双重作用,是牙周炎治疗中一种有前途的候选纳米平台。此外,基于MCDs的顺序释放水凝胶系统为牙周炎的治疗提供了一种新的材料策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f9/12312117/9654f34ed3bd/ga1.jpg

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