药物输送
药理学
间充质干细胞
医学
缺血
神经炎症
脂质体
冲程(发动机)
脑缺血
化学
病理
炎症
免疫学
内科学
生物化学
有机化学
工程类
机械工程
作者
Yun-Fei Dong,Yao-Sheng Li,Hui Liu,Lu Li,Juanjuan Zheng,Zefeng Yang,Yuankai Sun,Zhi-Wei Du,Donghang Xu,Ni Li,Xinchi Jiang,Jianqing Gao
标识
DOI:10.1016/j.jconrel.2024.06.017
摘要
The precise and targeted delivery of therapeutic agents to the lesion sites remains a major challenge in treating brain diseases represented by ischemic stroke. Herein, we modified liposomes with mesenchymal stem cells (MSC) membrane to construct biomimetic liposomes, termed MSCsome. MSCsome (115.99 ± 4.03 nm) exhibited concentrated accumulation in the cerebral infarcted hemisphere of mice with cerebral ischemia-reperfusion injury, while showing uniform distribution in the two cerebral hemispheres of normal mice. Moreover, MSCsome exhibited high colocalization with damaged nerve cells in the infarcted hemisphere, highlighting its advantageous precise targeting capabilities over liposomes at both the tissue and cellular levels. Leveraging its superior targeting properties, MSCsome effectively delivered Dl-3-n-butylphthalide (NBP) to the injured hemisphere, making a single-dose (15 mg/kg) intravenous injection of NBP-encapsulated MSCsome facilitate the recovery of motor functions in model mice by improving the damaged microenvironment and suppressing neuroinflammation. This study underscores that the modification of the MSC membrane notably enhances the capacity of liposomes for precisely targeting the injured hemisphere, which is particularly crucial in treating cerebral ischemia-reperfusion injury.
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