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Ligustrazine Nanoparticle Hitchhiking on Neutrophils for Enhanced Therapy of Cerebral Ischemia‐Reperfusion Injury.

Authors :
Mu, Qingchun
Yao, Kai
Syeda, Madiha Zahra
Zhang, Min
Cheng, Qian
Zhang, Yufei
Sun, Rui
Lu, Yuting
Zhang, Huamiao
Luo, Zhicheng
Huang, Hanning
Liu, Xiaojing
Luo, Chunmei
Zhu, Xiulong
Wu, Shuyu
Cui, Liao
Huang, Chunming
Chen, Xiaoyuan
Tang, Longguang
Source :
Advanced Science; 7/6/2023, Vol. 10 Issue 19, p1-10, 10p
Publication Year :
2023

Abstract

Ischemic stroke is a refractory disease that endangers human health and safety owing to cerebral ischemia. Brain ischemia induces a series of inflammatory reactions. Neutrophils migrate from the circulatory system to the site of cerebral ischemia and accumulate in large numbers at the site of inflammation across the blood–brain barrier. Therefore, hitchhiking on neutrophils to deliver drugs to ischemic brain sites could be an optimal strategy. Since the surface of neutrophils has a formyl peptide receptor (FPR), this work modifies a nanoplatform surface by the peptide cinnamyl‐F‐(D)L‐F‐(D)L‐F (CFLFLF), which can specifically bind to the FPR receptor. After intravenous injection, the fabricated nanoparticles effectively adhered to the surface of neutrophils in peripheral blood mediated by FPR, thereby hitchhiking with neutrophils to achieve higher accumulation at the inflammatory site of cerebral ischemia. In addition, the nanoparticle shell is composed of a polymer with reactive oxygen species (ROS)‐responsive bond breaking and is encased in ligustrazine, a natural product with neuroprotective properties. In conclusion, the strategy of hitching the delivered drugs to neutrophils in this study could improve drug enrichment in the brain, thereby providing a general delivery platform for ischemic stroke or other inflammation‐related diseases. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21983844
Volume :
10
Issue :
19
Database :
Complementary Index
Journal :
Advanced Science
Publication Type :
Academic Journal
Accession number :
164763718
Full Text :
https://doi.org/10.1002/advs.202301348