牙周炎
上睑下垂
葡萄糖酸
生物膜
葡萄糖氧化酶
糖尿病
医学
化学
坏死性下垂
过氧化氢酶
药理学
炎症
氧化应激
内科学
生物化学
炎症体
内分泌学
生物
细胞凋亡
程序性细胞死亡
细菌
生物传感器
遗传学
作者
Rongbing Tang,Yanrong Ren,Yueting Zhang,Mengying Yin,Xinyu Ren,Qiangyuan Zhu,Cen Gao,Wei Zhang,Guangxiu Liu,Bin Liu
标识
DOI:10.1016/j.mtbio.2023.100678
摘要
Diabetic periodontitis is a major complication of diabetes, which has a deep involvement in teeth loss and more serious systematic diseases, including Alzheimer's disease, atherosclerosis and cancers. Diabetic periodontitis is difficult to treat because of recalcitrant infection and hyperglycemia-induced tissue dysfunction. Current treatments fail to completely eliminate infection due to the diffusion-reaction inhibition of biofilm, and ignore the tissue dysfunction. Here, we design a glucose-driven transformable complex, composed of calcium alginate (CaAlg) hydrogel shell and Zeolitic imidazolate framework-8 (ZIF-8) core encapsulating Glucose oxidase (GOx)/Catalase (CAT) and Minocycline (MINO), named as CaAlg@MINO/GOx/CAT/ZIF-8 (CMGCZ). The reaction product of glucose-scavenging, gluconic acid, could dissolve ZIF-8 core and transform CMGCZ from inflexible to flexible, facilitating the complex to overcome the diffusion-reaction inhibition of biofilm. Meanwhile, reduced glucose concentration could ameliorate the pyroptosis of macrophages to decrease the secretion of pro-inflammatory factors, thereby reducing inflamm-aging to alleviate periodontal dysfunction.
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