Ligustrazine Nanoparticle Hitchhiking on Neutrophils for Enhanced Therapy of Cerebral Ischemia-Reperfusion Injury.
Qingchun MuKai YaoMadiha Zahra SyedaMin ZhangQian ChengYufei ZhangRui SunYuting LuHuamiao ZhangZhicheng LuoHanning HuangXiaojing LiuChunmei LuoXiulong ZhuShuyu WuLiao CuiChunming HuangXiaoyuan ChenLongguang TangPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2023)
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.
Keyphrases
- cerebral ischemia
- subarachnoid hemorrhage
- blood brain barrier
- brain injury
- oxidative stress
- reactive oxygen species
- human health
- ischemia reperfusion injury
- risk assessment
- peripheral blood
- stem cells
- dna damage
- photodynamic therapy
- high dose
- climate change
- bone marrow
- drug induced
- cell therapy
- electronic health record