Metabolic Nanoregulator Remodels Gut Microenvironment for Treatment of Inflammatory Bowel Disease

被引:10
|
作者
Xu, Ting [3 ]
Ning, Xiaogang [4 ]
Wu, Jiayan [1 ,2 ]
Wang, Qian [3 ]
Wang, Zhifei [5 ]
Chen, Zhiqing [3 ]
Tang, Xiaoxian [3 ]
Bai, Peirong [5 ]
Pu, Kanyi [1 ,2 ]
Li, Liping [6 ,7 ]
Zhang, Ruiping [3 ]
机构
[1] Nanyang Technol Univ, Sch Chem, Chem Engn & Biotechnol, Singapore 637457, Singapore
[2] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore 637457, Singapore
[3] Fifth Hosp Shanxi Med Univ, Radiol Dept Shanxi Prov Peoples Hosp, Taiyuan 030012, Peoples R China
[4] Shanxi Univ Chinese Med, Sch Chinese Med & Food Engn, Jinzhong 030619, Peoples R China
[5] Third Hosp Shanxi Med Univ, Shanxi Bethune Hosp, Tongji Shanxi Hosp, Shanxi Acad Med Sci, Taiyuan 030032, Peoples R China
[6] Shanxi Med Univ, Sch Basic Med Sci, Taiyuan 030001, Peoples R China
[7] Fifth Hosp Shanxi Med Univ, Taiyuan 030012, Peoples R China
基金
国家重点研发计划;
关键词
inflammatory bowel disease; metabolic regulation; gallium; melanin; systemic strategy; MELANIN; CELLS; IBD;
D O I
10.1021/acsnano.3c11496
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Inflammatory bowel disease (IBD) is strongly related to the occurrence of accumulation of toxic reactive oxygen species (ROS), inflammation of the mucosa, and an imbalance of intestinal microbes. However, current treatments largely focus on a single factor, yielding unsatisfactory clinical outcomes. Herein, we report a biocompatible and IBD-targeted metabolic nanoregulator (TMNR) that synergistically regulates cellular and bacterial metabolism. The TMNR comprises a melanin-gallium complex (MNR) encapsulated within a thermosensitive and colitis-targeting hydrogel, all composed of natural and FDA-approved components. The TMNR confers superior broad-spectrum antioxidant properties, effectively scavenging reactive oxygen species (ROS) and blocking inflammatory signaling pathways. The presence of Ga3+ in TMNR selectively disrupts iron metabolism in pathogenic microorganisms due to its structural resemblance to the iron atom. Additionally, incorporating a thermosensitive injectable hydrogel enables targeted delivery of TMNR to inflammatory regions, prolonging their retention time and providing a physical barrier function for optimizing IBD treatment efficacy. Collectively, TMNR effectively modulates the redox balance of inflamed colonic epithelial tissue and disrupts iron metabolism in pathogenic microorganisms, thereby eliminating inflammation and restoring intestinal homeostasis against IBD. Hence, this work presents a comprehensive approach for precise spatiotemporal regulation of the intestinal microenvironmental metabolism for IBD treatment.
引用
收藏
页码:7123 / 7135
页数:13
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