Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration

被引:96
作者
Wang, He [1 ]
Chang, Xiaowei [2 ]
Ma, Qian [1 ]
Sun, Boyang [1 ]
Li, Han [1 ]
Zhou, Jinmin [1 ]
Hu, Yiyao [1 ]
Yang, Xiaoyu [1 ]
Li, Jie [1 ]
Chen, Xin [2 ]
Song, Jinlin [1 ]
机构
[1] Chongqing Med Univ, Chongqing Key Lab Oral Dis & Biomed Sci, Chongqing Municipal Key Lab Oral Biomed Engn Highe, Coll Stomatol, Chongqing 401147, Peoples R China
[2] Xi An Jiao Tong Univ, Inst Polymer Sci Chem Engn, Sch Chem Engn & Technol, Dept Chem Engn, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
Periodontal bone regeneration; Diabetes mellitus; Bioinspired; Hydrogel; Drug delivery; GROWTH-FACTORS; DIFFERENTIATION; OSTEOGENESIS; STRATEGIES; HYDROGEL; MELLITUS; REPAIR;
D O I
10.1016/j.bioactmat.2022.08.029
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Diabetes mellitus (DM) aggravates periodontitis, resulting in accelerated periodontal bone resorption. Disordered glucose metabolism in DM causes reactive oxygen species (ROS) overproduction resulting in compromised bone healing, which makes diabetic periodontal bone regeneration a major challenge. Inspired by the natural bone healing cascade, a mesoporous silica nanoparticle (MSN)-incorporated PDLLA (poly(DL-lactide))-PEG-PDLLA (PPP) thermosensitive hydrogel with stepwise cargo release is designed to emulate the mesenchymal stem cell "recruitment-osteogenesis" cascade for diabetic periodontal bone regeneration. During therapy, SDF-1 quickly escapes from the hydrogel due to diffusion for early rat bone marrow stem cell (rBMSC) recruitment. Simulta-neously, slow degradation of the hydrogel starts to gradually expose the MSNs for sustained release of metformin, which can scavenge the overproduced ROS under high glucose conditions to reverse the inhibited osteogenesis of rBMSCs by reactivating the AMPK/beta-catenin pathway, resulting in regulation of the diabetic microenvironment and facilitation of osteogenesis. In vitro experiments indicate that the hydrogel markedly restores the inhibited migration and osteogenic capacities of rBMSCs under high glucose conditions. In vivo results suggest that it can effectively recruit rBMSCs to the periodontal defect and significantly promote periodontal bone regeneration under type 2 DM. In conclusion, our work provides a novel therapeutic strategy of a bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration.
引用
收藏
页码:324 / 339
页数:16
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