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

牙周膜干细胞 再生(生物学) 牙周炎 牙科 材料科学 化学 细胞生物学 医学 生物化学 碱性磷酸酶 生物
作者
Jingjing Wei,K. Wang,Yongkai Li,Jiao Huang,Ping Deng,Xianbo Xia,Cong Yang,Ling Xu,Jilei Xu
出处
期刊:Bioactive Materials [Elsevier BV]
卷期号:53: 459-479 被引量:5
标识
DOI:10.1016/j.bioactmat.2025.07.001
摘要

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, in vitro and in vivo 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. • MCDs promoted osteogenic differentiation of hPDLSCs under inflammation by activating the PI3K-AKT signaling pathway. • MCDs@IGF-1 effectively delivered IGF-1, preserved its bioactivity and reduced the trypsin-induced degradation. • The Gel/MCDs@IGF-1 hydrogel system sequentially releases MCDs and IGF-1. • This system enhanced bone regeneration in a rat model of periodontitis, offering a promising treatment strategy.
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