基因沉默
声动力疗法
光动力疗法
癌症研究
材料科学
U87型
小干扰RNA
体内
癌细胞
血脑屏障
遗传增强
体外
胶质母细胞瘤
转染
细胞培养
纳米技术
癌症
化学
医学
生物
基因
神经科学
中枢神经系统
内科学
生物化学
生物技术
有机化学
遗传学
作者
Yunxia Li,Ying Liu,Jiaqing Xu,Dandan Chen,Tingting Wu,Yu Cao
标识
DOI:10.1021/acsami.3c03001
摘要
Fabrication of ingenious nanomedicines to penetrate the blood–brain barrier (BBB) and blood–brain–tumor barrier (BBTB) for efficient glioblastoma (GBM) therapy remains a big challenge. In this work, macrophage–cancer hybrid membrane-camouflaged nanoplatforms were fabricated for target gene silencing-enhanced sonodynamic therapy (SDT) of GBM. The J774.A.1 macrophage cell membrane and the U87 glioblastoma cell membrane were fused to create a hybrid biomembrane (JUM) with good BBB penetration and glioblastoma targeting capability for camouflaging. The ZIF-8 nanoparticles were synthesized for indocyanine green (ICG) and HIF-1α siRNA encapsulation (ICG-siRNA@ZIF-8, ISZ) with a high loading efficiency. After accumulation in the tumor sites, the pH sensitivity of the nanoplatform enabled release of ICG and HIF-1α siRNA in the tumor cells. Then, the expression of HIF-1α could be efficiently inhibited by the released HIF-1α siRNA to increase the SDT efficiency under hypoxic conditions. In vitro and in vivo experiments revealed that ISZ@JUM showed good BBB penetration and brain tumor-targeting capability and could achieve effective gene silencing-enhanced SDT, demonstrating great promise for clinical applications.
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