Efficacy of histotripsy combined with rt-PA in vitro

被引:57
作者
Bader, Kenneth B. [1 ]
Haworth, Kevin J. [1 ,2 ]
Shekhar, Himanshu [1 ]
Maxwell, Adam D. [3 ]
Peng, Tao [4 ]
McPherson, David D. [4 ]
Holland, Christy K. [1 ,2 ]
机构
[1] Univ Cincinnati, Div Cardiovasc Hlth & Dis, Dept Internal Med, Cincinnati, OH USA
[2] Univ Cincinnati, Biomed Engn Program, Cincinnati, OH USA
[3] Univ Washington, Dept Urol, Seattle, WA 98195 USA
[4] Univ Texas Hlth Sci Ctr Houston, Div Cardiovasc Med, Dept Internal Med, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
histotripsy; deep vein thrombosis; passive cavitation imaging; echogenic liposomes; TISSUE-PLASMINOGEN-ACTIVATOR; CATHETER-DIRECTED THROMBOLYSIS; DEEP VENOUS THROMBOSIS; ULTRASOUND-ENHANCED THROMBOLYSIS; VEIN THROMBOSIS; HIGH-INTENSITY; CAVITATION; BUBBLES; EROSION; MECHANISMS;
D O I
10.1088/0031-9155/61/14/5253
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Histotripsy, a form of therapeutic ultrasound that uses the mechanical action of microbubble clouds for tissue ablation, is under development to treat chronic deep vein thrombosis (DVT). We hypothesize that combining thrombolytic agents with histotripsy will enhance clot lysis. Recombinant tissue plasminogen activator (rt-PA) and rt-PA-loaded echogenic liposomes that entrain octafluoropropane microbubbles (OFP t-ELIP) were used in combination with highly shocked histotripsy pulses. Fully retracted porcine venous clots, with similar features of DVT occlusions, were exposed either to histotripsy pulses alone (peak negative pressures of 7-20 MPa), histotripsy and OFP t-ELIP, or histotripsy and rt-PA. Microbubble cloud activity was monitored with passive cavitation imaging during histotripsy exposure. The power levels of cavitation emissions from within the clot were not statistically different between treatment types, likely due to the near instantaneous rupture and destruction of OFP t-ELIP. The thrombolytic efficacy was significantly improved in the presence of rt-PA. These results suggest the combination of histotripsy and rt-PA could serve as a potent therapeutic strategy for the treatment of DVT.
引用
收藏
页码:5253 / 5274
页数:22
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