血脑屏障
微气泡
生物物理学
材料科学
药物输送
体内
转铁蛋白受体
靶向给药
渗透
纳米技术
转铁蛋白
化学
超声波
膜
医学
生物
生物化学
中枢神经系统
内分泌学
生物技术
放射科
作者
Anshuman Dasgupta,Tao Sun,Elena Rama,Alessandro Motta,Yongzhi Zhang,Chanikarn Power,Diana Moeckel,Stecia‐Marie Fletcher,Mirjavad Moosavifar,Roman A. Barmin,Céline Porte,Eva Miriam Buhl,Céline Bastard,Roger M. Pallares,Fabian Kießling,Nathan McDannold,Samir Mitragotri,Twan Lammers
标识
DOI:10.1002/adma.202308150
摘要
Microbubbles (MB) are widely used for ultrasound (US) imaging and drug delivery. MB are typically spherically shaped, due to surface tension. When heated above their glass transition temperature, polymer-based MB can be mechanically stretched to obtain an anisotropic shape, endowing them with unique features for US-mediated blood-brain barrier (BBB) permeation. It is here shown that nonspherical MB can be surface-modified with BBB-specific targeting ligands, thereby promoting binding to and sonopermeation of blood vessels in the brain. Actively targeted rod-shaped MB are generated via 1D stretching of spherical poly(butyl cyanoacrylate) MB and via subsequently functionalizing their shell with antitransferrin receptor (TfR) antibodies. Using US and optical imaging, it is demonstrated that nonspherical anti-TfR-MB bind more efficiently to BBB endothelium than spherical anti-TfR-MB, both in vitro and in vivo. BBB-associated anisotropic MB produce stronger cavitation signals and markedly enhance BBB permeation and delivery of a model drug as compared to spherical BBB-targeted MB. These findings exemplify the potential of antibody-modified nonspherical MB for targeted and triggered drug delivery to the brain.
科研通智能强力驱动
Strongly Powered by AbleSci AI