Extracellular vesicles for delivering therapeutic agents in ischemia/reperfusion injury

被引:0
|
作者
Zhou, Weihang [1 ]
Jiang, Xinchi [1 ,3 ]
Gao, Jianqing [1 ,2 ,3 ]
机构
[1] Zhejiang Univ, Coll Pharmaceut Sci, State Key Lab Adv Drug Delivery & Release Syst, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Pharm, Hangzhou 310009, Peoples R China
[3] Zhejiang Univ, Hangzhou Inst Innovat Med, Coll Pharmaceut Sci, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
Extracellular vesicles; Extracellular vesicle engineering; Ischemia/reperfusion injury; Nanocarrier; Drug delivery; MESENCHYMAL STEM-CELLS; ISCHEMIA-REPERFUSION INJURY; CEREBRAL-ISCHEMIA; CARDIAC-FUNCTION; EXOSOMES; NANOVESICLES; INFLAMMATION; VEHICLES; PROTECT; TARGET;
D O I
10.1016/j.ajps.2024.100965
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ischemia/reperfusion (I/R) injury is marked by the restriction and subsequent restoration of blood supply to an organ. This process can exacerbate the initial tissue damage, leading to further disorders, disability, and even death. Extracellular vesicles (EVs) are crucial in cell communication by releasing cargo that regulates the physiological state of recipient cells. The development of EVs presents a novel avenue for delivering therapeutic agents in I/R therapy. The therapeutic potential of EVs derived from stem cells, endothelial cells, and plasma in I/R injury has been actively investigated. Therefore, this review aims to provide an overview of the pathological process of I/R injury and the biophysical properties of EVs. We noted that EVs serve as nontoxic, flexible, and multifunctional carriers for delivering therapeutic agents capable of intervening in I/R injury progression. The therapeutic efficacy of EVs can be enhanced through various engineering strategies. Improving the tropism of EVs via surface modification and modulating their contents via preconditioning are widely investigated in preclinical studies. Finally, we summarize the challenges in the production and delivery of EV-based therapy in I/R injury and discuss how it can advance. This review will encourage further exploration in developing efficient EV-based delivery systems for I/R treatment. (c) 2024 Shenyang Pharmaceutical University. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
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页数:20
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