Delivery of Mir-196c-3p with NIR-II light-triggered gel attenuates cardiomyocyte ferroptosis in cardiac ischemia-reperfusion injury

被引:11
|
作者
Ji, Jing-jing [1 ,4 ]
Chen, Shang-yu [2 ,3 ]
Yang, Zi-wei [1 ]
Zhang, Rui [1 ]
Qian, Ling-lin [1 ]
Jiang, Yu [1 ]
Guo, Jia-qi [1 ]
Wu, Ya [1 ]
Fan, Qu-li [2 ,3 ]
Yao, Yu-yu [1 ,5 ]
Sun, Peng-fei [2 ,3 ]
机构
[1] Southeast Univ, Zhongda Hosp, Dept Cardiol, Med Sch, 87 Dingjiaqiao, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Univ Posts & Telecommun, State Key Lab Organ Elect & Informat Displays, Nanjing 210023, Peoples R China
[3] Nanjing Univ Posts & Telecommun, Inst Adv Mat IAM, Nanjing 210023, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 2, Coll Med, Dept Cardiol, Hangzhou 310009, Zhejiang, Peoples R China
[5] Southeast Univ, Zhongda Hosp, Med Sch, Dept Cardiol, 87 Dingjiaqiao, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Mir-196c-3p; Gel; BTN; Ferroptosis; NIR-II; I; R; LIPID-PEROXIDATION; DRUG-DELIVERY; HYDROGEL; REPAIR;
D O I
10.1016/j.nano.2022.102618
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ferroptosis plays an important role in ischemia-reperfusion (I/R)-induced cardiac injury and there are many defects in current targeted delivery of miRNAs for the treatment of ferroptosis. We herein report a unique hydrogel (Gel) that can be triggered by a near-infrared-II (NIR-II) light with deep tissue penetration and biocompatible maximum permissible exposure (MPE) value for in situ treatment after I/R. The mir-196c-3p mimic (mimics) and photothermal nanoparticles (BTN) were co-encapsulated in an injectable Gel (mimics + Gel/BTN) with NIR-II light-triggered release. Using 1064 nm light irradiation, local microenvironment photothermal-triggered on-demand noninvasive controllable delivery of miRNA was achieved, aiming to inhibit I/R-induced ferroptosis. Consequently, declined ferroptosis in cardiomyocytes and improved cardiac function, survival rate in rats was achieved through the controlled release of Gel/BTN mimics in I/R model to simultaneously inhibit ferroptosis hub genes NOX4, P53, and LOX expression. (c) 2022 Published by Elsevier Inc.
引用
收藏
页数:12
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