微气泡
体内
内吞作用
药物输送
脂质体
细胞毒性
内化
生物医学工程
阿霉素
超声波
材料科学
靶向给药
灌注
声穿孔
生物物理学
纳米技术
医学
体外
细胞
化学
化疗
生物
生物化学
外科
放射科
生物技术
作者
Yoonjee C. Park,Chentian Zhang,Sudong Kim,Graciela Mohamedi,Carl Beigie,Jon O. Nagy,R. Glynn Holt,Robin O. Cleveland,Noo Li Jeon,Joyce Y. Wong
标识
DOI:10.1021/acsami.6b09071
摘要
Microbubbles have been used in ultrasound-assisted drug delivery to help target solid tumors via blood vessels in vivo; however, studies to understand the phenomena at the cellular level and to optimize parameters for ultrasound or microbubbles in vivo are challenging and expensive to perform. Here, we utilize microfluidic microvessels-on-a-chip that enable visualization of microbubble/ultrasound-dependent drug delivery to microvasculature. When exposed to pulsed ultrasound, microbubbles perfused through microvessels-on-a-chip were observed to stably oscillate. Minimal cellular damage was observed for both microbubbles and untargeted doxorubicin-encapsulating liposomes (DOX-liposomes) perfused through chip microvessels. In contrast, passive and ultrasound-assisted perfusion of integrin-targeted DOX-liposomes induced cytotoxicity, which was only significantly enhanced for ultrasound-assisted perfusion when microbubbles were coperfused. These results suggest that stably oscillating microbubbles enhance targeted DOX-liposome internalization/cytotoxicity largely by stimulating integrin receptor endocytosis. Furthermore, our study demonstrates the utility of our microvessels-on-a-chip as a screening platform for optimizing drug dosage, targeting ligands and drugs.
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