Platelet-Membrane-Coated Polydopamine Nanoparticles for Neuroprotection by Reducing Oxidative Stress and Repairing Damaged Vessels in Intracerebral Hemorrhage.
Canxin XuYuanbo PanHongchi ZhangYuhao SunYi CaoPengfei QiMingli LiOzioma Udochukwu AkakuruLulu HeChen XiaoBomin SunLiuguan BianJuan LiAiguo WuPublished in: Advanced healthcare materials (2023)
Intracerebral hemorrhage (ICH) has the high morbidity and mortality in the world. Excessive reactive oxygen species (ROS) caused by primary and second brain injury can induce neuron death and inhibit neurological functional recovery after ICH. Therefore, exploring an effective way to noninvasively target hemorrhage sites to scavenge ROS is urgently needed. In spired by the biological function of platelets to target injury vessel and repair injury blood vessels, platelet-membrane-modified polydopamine (Menp@PLT) nanoparticles are developed with targeting to hemorrhage sites of ICH. Results demonstrate that Menp@PLT nanoparticles can effectively achieve targeting to the location of intracranial hematoma. Further, Menp@PLT with excellent anti-ROS properties can scavenge ROS and improve neuroinflammation microenvironment of ICH. In addition, Menp@PLT may play a role in decreasing hemorrhage volume by repairing injury blood vessels. Combining platelet membrane and anti-ROS nanoparticles for targeting brain hemorrhage sites provide a promising strategy for efficiently treating ICH. This article is protected by copyright. All rights reserved.
Keyphrases
- brain injury
- reactive oxygen species
- cerebral ischemia
- dna damage
- subarachnoid hemorrhage
- cell death
- oxidative stress
- cancer therapy
- stem cells
- weight gain
- resting state
- walled carbon nanotubes
- lipopolysaccharide induced
- white matter
- physical activity
- functional connectivity
- lps induced
- induced apoptosis
- heat stress
- ischemia reperfusion injury