Surface functionalized exosomes as targeted drug delivery vehicles for cerebral ischemia therapy

被引:939
作者
Tian, Tian [1 ,2 ,3 ]
Zhang, Hui-Xin [1 ]
He, Chun-Peng [4 ]
Fan, Song [5 ]
Zhu, Yan-Liang [4 ]
Qi, Cui [1 ]
Huang, Ning-Ping [4 ]
Xiao, Zhong-Dang [4 ]
Lu, Zu-Hong [4 ]
Tannous, Bakhos A. [2 ,3 ]
Gao, Jun [1 ]
机构
[1] Nanjing Med Univ, Key Lab Human Funct Genom Jiangsu, Dept Neurobiol, Nanjing 211166, Jiangsu, Peoples R China
[2] Massachusetts Gen Hosp, Dept Neurol, Expt Therapeut & Mol Imaging Lab, Boston, MA 02129 USA
[3] Harvard Med Sch, Boston, MA 02129 USA
[4] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Jiangsu, Peoples R China
[5] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Oral & Maxillofacial Surg, Guangzhou 510120, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Exosomes; Drug delivery; Cerebral ischemia; Curcumin; MESENCHYMAL STEM-CELL; FREE CLICK CHEMISTRY; EXTRACELLULAR VESICLES; IN-VIVO; ALPHA-V-BETA-5; INTEGRINS; MEDIATED DELIVERY; CYCLIC RGD; STROKE; BRAIN; BIODISTRIBUTION;
D O I
10.1016/j.biomaterials.2017.10.012
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The safe and effective delivery of drugs is a major obstacle in the treatment of ischemic stroke. Exosomes hold great promise as an endogenous drug delivery nanosystem for the treatment of cerebral ischemia given their unique properties, including low immunogenicity, innate stability, high delivery efficiency, and ability to cross the blood-brain barrier (BBB). However, exosome insufficient targeting capability limits their clinical applications. In this study, the c(RGDyK) peptide has been conjugated to the exosome surface by an easy, rapid, and bio-orthogonal chemistry. In the transient middle cerebral artery occlusion (MCAO) mice model, The engineered c(RGDyK)-conjugated exosomes (cRGD-Exo) target the lesion region of the ischemic brain after intravenous administration. Furthermore, curcumin has been loaded onto the cRGD-Exo, and administration of these exosomes has resulted in a strong suppression of the inflammatory response and cellular apoptosis in the lesion region. The results suggest a targeting delivery vehicle for ischemic brain based on exosomes and provide a strategy for the rapid and large-scale production of functionalized exosomes. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:137 / 149
页数:13
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