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Bioinspired hydrogel for sustained minocycline release: A superior periodontitis solution

米诺环素 牙周炎 牙科 医学 化学 抗生素 生物化学
作者
Shiyao Liu,Wenqian Zheng,Lina Wang,Yajie Zhang,Kang Feng,Yan Zhang,Haitao Yang,Yao Xiao,Chenxi Sun,Xiqiang Liu,Baoyang Lu,Xuemin Yin
出处
期刊:Materials today bio [Elsevier BV]
卷期号:32: 101638-101638 被引量:6
标识
DOI:10.1016/j.mtbio.2025.101638
摘要

Periodontitis treatment remains challenging due to the limitations of clinical medication therapies, including drug cytotoxicity, poor drug retention, immune imbalances, and epithelial barrier damage. Here, inspired by bioisosterism, we develop a dual-network hydrogel-based drug delivery system (M@PP) with materials structurally similar to minocycline (a commonly used medication). The M@PP hydrogel exhibits optimal mechanical strength and bioadhesion, ensuring sufficient drug retention inside periodontal pockets. The sustained release of minocycline, combined with the hydrogel's acidic microenvironment and the antioxidant functional groups, provides M@PP with excellent biocompatibility, potent antibacterial activity (98.1% against P. gingivalis ), and enhanced anti-inflammatory properties. In vivo studies demonstrate that M@PP regulates macrophage polarization, upregulates anti-inflammatory factors, and promotes the expression of epithelial junction-related cytokines. Additionally, M@PP activates pro-osteogenic mediators, with micro-CT analysis revealing increased trabecular bone density, thickness, and bone reconstruction. RNA sequencing further uncovers its therapeutic mechanisms, highlighting bacterial defense, immune modulation and pro-regenerative signaling. These combined benefits create a favorable immune microenvironment, facilitating epithelial barrier restoration and alveolar bone regeneration, achieving superior therapeutic outcomes compared to commercial products. This study presents a promising localized therapeutic strategy for periodontitis and biofilm-associated disorders. • Developed a multifunctional dual-network hydrogel for targeted periodontitis therapy. • Enhanced minocycline loading and utilization using bioimmune rejection-inspired design principles. • Achieved optimal mechanical strength and bioadhesion for sustained drug release in dynamic oral environments. • Demonstrated antibacterial, anti-inflammatory, immunoregulatory, and regenerative properties. • Outperformed commercial treatments in restoring microbiome-host immune balance and promoting periodontal regeneration.
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