Kim-1 targeted black phosphorus nanoplatforms: Antioxidation and efferocytosis recovery for acute kidney injury treatment

被引:1
作者
Wang, Zhiwen [1 ]
Xie, Ge [2 ,3 ]
Xie, Yue [1 ]
Hu, Mingcun [1 ]
Hu, Qiao [2 ,3 ]
Yang, Min [1 ]
Zhang, Lianbin [2 ,3 ]
Zhu, Jintao [2 ,3 ]
Zhang, Chun [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Nephrol, Wuhan 430022, Peoples R China
[2] Huazhong Univ Sci & Technol HUST, Sch Chem & Chem Engn, State Key Lab Mat Proc & Die & Mold Technol, Minist Educat HUST, Wuhan 430074, Peoples R China
[3] Huazhong Univ Sci & Technol HUST, Sch Chem & Chem Engn, Key Lab Mat Chem Energy Convers & Storage, Minist Educ HUST, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Acute kidney injury; Black phosphorus; Nanoplatform; Antioxidation; Efferocytosis; APOPTOTIC CELLS; REACTIVE OXYGEN; ITACONATE; ULTRATHIN; DISEASE;
D O I
10.1016/j.cej.2024.154207
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Efferocytosis, the clearance of apoptotic cells, is an essential process for resolving inflammation. Current evidence suggests that in acute kidney injury (AKI), the inflammatory cascade triggered by oxidative stress in damaged tissues can impair efferocytosis. This disrupts the clearance of apoptotic cells, exacerbates inflammatory reactions, and ultimately leads to tissue damage. To address this challenge, we developed a novel renal dualtargeting nanoplatform for AKI treatment based on black phosphorus nanosheets (BPNSs). Surface modification with LTH and 4-Octyl itaconate (4OI) endowed BPNSs with both renal tubulars targeting specificity and sustained antioxidant properties. This nanoplatform could effectively target damaged renal tubular epithelial cells, scavenge excess reactive oxygen species (ROS), alleviate oxidative stress, enhance efferocytosis, inhibit inflammatory responses, and ultimately achieve the specific therapeutic goal of AKI.
引用
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页数:17
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