微气泡
血脑屏障
胶质母细胞瘤
药物输送
阿霉素
体外
体内
聚焦超声
脑瘤
癌症研究
超声波
靶向给药
声穿孔
化学
生物医学工程
医学
药理学
化疗
病理
中枢神经系统
内科学
生物
生物化学
放射科
生物技术
有机化学
作者
Chuanshi He,Zhisheng Wu,Min Zhuang,Xiangyu Li,Shucheng Xue,Shaofeng Xu,Jinshun Xu,Zhe Wu,Man Lu
标识
DOI:10.1186/s12951-023-02074-z
摘要
Glioblastoma is the most common type of brain tumor. Due to the presence of the blood-brain barrier, the effects of chemotherapy have been unsatisfactory. The combination of focused ultrasound and microbubbles to reversibly open the blood-brain barrier is now considered a key factor in improving treatment outcomes of glioblastoma. In this study, we developed bionic drug delivery microbubbles, which in combination with focused ultrasound had an obvious inhibitory effect on glioblastoma. We extracted the brain microvascular cell membranes, combined them with lipid components, and loaded them with superparamagnetic iron oxide and doxorubicin to prepare biomimetic drug delivery microbubbles (FeDOX@cellMBs). We demonstrated that FeDOX@cellMBs retained the intrinsic properties of loading, such as magnetic properties and drug toxicity, both in vitro and in vivo. FeDOX@cellMBs exhibited good tumor targeting and uptake under the combined action of magnetic and focused ultrasound. Importantly, the FeDOX@cellMBs demonstrated excellent internal stability and effectively inhibited tumor growth in orthotopic glioblastoma mice. Finally, organ H&E staining confirmed that FeDOX@cellMBs were safe for use. In conclusion, FeDOX@cellMBs successfully penetrated the blood-brain barrier and effectively inhibited glioblastoma growth under the combined effects of focused ultrasound and magnetic stimulation. These results provide a new approach for the treatment of glioblastoma, with implications for future clinical translation.
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