内吞作用
胞饮病
血脑屏障
体内
膜
阿霉素
体外
细胞生物学
药物输送
细胞
材料科学
癌症研究
纳米技术
生物物理学
化学
医学
神经科学
中枢神经系统
生物
生物化学
化疗
生物技术
外科
作者
Huajian Chen,Jingsen Ji,Li Zhang,Chunling Luo,Taoliang Chen,Yuxuan Zhang,Chengcheng Ma,Yiquan Ke,Jihui Wang
出处
期刊:Small
[Wiley]
日期:2024-02-23
被引量:4
标识
DOI:10.1002/smll.202306714
摘要
Abstract The blood–brain barrier (BBB) contains tightly connected brain microvascular endothelial cells (BMECs) that hinder drug delivery to the brain, which makes brain tumors difficult to treat. Previous studies have shown that nanoparticles coated with tumor cell membranes selectively target their homologous tumors. Therefore, this study investigated whether bEnd.3‐line BMEC membrane‐coated nanoparticles with poly(lactide‐ co ‐glycolide)‐poly(ethylene glycol)‐based doxorubicin‐loaded cores (BM‐PDs) can be used to target BMECs and cross the BBB. In vitro, the BM‐PDs effectively target BMECs and cross a BBB model. The BM‐PDs enter the BMECs via macropinocytosis, clathrin‐mediated endocytosis, caveolin‐mediated endocytosis, and membrane fusion, which result in excellent cellular uptake. The BM‐PDs also show excellent cellular uptake in brain tumor cells. In vivo, the BM‐PDs target BMECs, cross the BBB, accumulate in brain tumors, and efficiently kill tumor cells. Therefore, the proposed strategy has great therapeutic potential owing to its ability to cross the BBB to reach brain tumors.
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