In Vitro Sonothrombolysis Enhancement by Transiently Stable Microbubbles Produced by a Flow-Focusing Microfluidic Device

被引:26
作者
Dixon, Adam J. [1 ]
Rickel, John Marschner Robert [1 ]
Shin, Brian D. [1 ]
Klibanov, Alexander L. [1 ,2 ]
Hossack, John A. [1 ]
机构
[1] Univ Virginia, Dept Biomed Engn, Charlottesville, VA 22908 USA
[2] Univ Virginia, Sch Med, Div Cardiovasc, Charlottesville, VA 22908 USA
基金
美国国家卫生研究院;
关键词
Thromboembolism; Sonothrombolysis; Microfluidics; Microbubbles; Ultrasound; TISSUE-PLASMINOGEN ACTIVATOR; CAVITATION BUBBLES; CONTRAST AGENTS; RADIATION FORCE; ULTRASOUND; THROMBOLYSIS; CLOT; GENERATION; THROMBOSIS; COLLAPSE;
D O I
10.1007/s10439-017-1965-7
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Therapeutic approaches that enhance thrombolysis by combining recombinant tissue plasminogen activator (rtPA), ultrasound, and/or microbubbles (MBs) are known as sonothrombolysis techniques. To date, sonothrombolysis approaches have primarily utilized commercially available MB formulations (or derivatives thereof) with diameters in the range 1-4 A mu m and circulation lifetimes between 5 and 15 min. The present study evaluated the in vitro sonothrombolysis efficacy of large diameter MBs (d (MB) >= 10 A mu m) with much shorter lifetimes that were produced on demand and in close proximity to the blood clot using a flow-focusing microfluidic device. MBs with a N-2 gas core and a non-crosslinked bovine serum albumin shell were produced with diameters between 10 and 20 A mu m at rates between 50 and 950 x 10(3) per second. Use of these large MBs resulted in approximately 4.0-8.8 fold increases in thrombolysis rates compared to a clinical rtPA dose and approximately 2.1-4.2 fold increases in thrombolysis rates compared to sonothrombolysis techniques using conventional MBs. The results of this study indicate that the large diameter microbubbles with transient stability are capable of significantly enhanced in vitro sonothrombolysis rates when delivered directly to the clot immediately following production by a flow focusing microfluidic device placed essentially in situ adjacent to the clot.
引用
收藏
页码:222 / 232
页数:11
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