血管内超声声滴汽化清除溶解氧的研究。

Kevin J Haworth, Bryan H Goldstein, Karla P Mercado-Shekhar, Rohan Srivastava, P Arunkumar, Haili Su, Ellena M Privitera, Christy K Holland, Andrew N Redington
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引用次数: 4

摘要

声学液滴汽化(ADV)已被提出用于几种治疗应用。冠状动脉介入治疗缺血组织再灌注时减少溶解氧(DO)可抑制活性氧的产生,挽救心肌。本研究的目的是确定血管内超声(IVUS)是否可以触发ADV并降低DO。采用高速振荡和微流体制造技术制备全氟戊烷乳液。高速振动导致多分散液滴分布,其直径从小于1微米到大于16微米不等。微流体制造产生的液滴尺寸范围更窄,直径在8.0微米到9.6微米之间。在IVUS暴露引发ADV之前和之后测量液体的DO含量。采用双工b模式和被动空化成像来评估ADV的成核。暴露于临床IVUS系统后,观察到ADV的回声增强。在流动幻象中,当注入通过高速震动形成的液滴时,测量到IVUS换能器远端DO降低了20%。在静态流体系统中,当微流控芯片制造的液滴暴露于IVUS中时,DO含量降低了11%。这些结果表明,使用临床IVUS系统通过ADV降低DO是可行的。未来的研究将评估ivus核ADV的潜在治疗效果和增加DO清除强度的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dissolved Oxygen Scavenging by Acoustic Droplet Vaporization using Intravascular Ultrasound.

Dissolved Oxygen Scavenging by Acoustic Droplet Vaporization using Intravascular Ultrasound.

Dissolved Oxygen Scavenging by Acoustic Droplet Vaporization using Intravascular Ultrasound.

Dissolved Oxygen Scavenging by Acoustic Droplet Vaporization using Intravascular Ultrasound.

Modification of dissolved gas content by acoustic droplet vaporization (ADV) has been proposed for several therapeutic applications. Reducing dissolved oxygen (DO) during reperfusion of ischemic tissue during coronary interventions could inhibit reactive oxygen species production and rescue myocardium. The objective of this study was to determine whether intravascular ultrasound (IVUS) can trigger ADV and reduce DO. Perfluoropentane emulsions were created using high-speed shaking and microfluidic manufacturing. High-speed shaking resulted in a polydisperse droplet distribution ranging from less than 1 micron to greater than 16 microns in diameter. Microfluidic manufacturing produced a narrower size range of droplets with diameters between 8.0 microns and 9.6 microns. The DO content of the fluids was measured before and after ADV triggered by IVUS exposure. Duplex B-mode and passive cavitation imaging was performed to assess nucleation of ADV. An increase in echogenicity indicative of ADV was observed after exposure with a clinical IVUS system. In a flow phantom, a 20% decrease in DO was measured distal to the IVUS transducer when droplets, formed via high-speed shaking, were infused. In a static fluid system, the DO content was reduced by 11% when droplets manufactured with a microfluidic chip were exposed to IVUS. These results demonstrate that a reduction of DO by ADV is feasible using a clinical IVUS system. Future studies will assess the potential therapeutic efficacy of IVUS-nucleated ADV and methods to increase the magnitude of DO scavenging.

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