In vivo acoustic contrast enhancement via simultaneous production and injection of microfluidic-produced microbubbles

A. Dixon, A. Dhanaliwala, Dan Lin, Johnny L. Chen, A. Klibanov, J. Hossack
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引用次数: 1

Abstract

Microbubble production by microfluidic devices for ultrasound contrast enhancement allows for precise control over microbubble diameter but at the cost of low production rate and poor microbubble stability. In this work, we investigated whether microbubbles produced by a microfluidic device could provide sufficient ultrasound contrast enhancement when directly injected into the mouse tail vein. Microfluidic-produced microbubbles composed of nitrogen gas and stabilized with 10% dextrose and 3% bovine serum albumin were injected for 10 seconds into the tail vein of wild type C57BL/6 mice. Short-axis ultrasound images of the right and left ventricle were acquired at 12.5 MHz and image intensity over time was analyzed. Microbubble production rates ranged between 2.5×105 and 8.3×105 microbubbles/s, and microbubble diameters were between 9.1 and 19 μm. In all cases, microbubbles were observed in both the right and left ventricle, although the average contrast enhancement was approximately 13.5 dB lower in the left ventricle than in the right ventricle. All mice survived the procedure with no observable respiratory or heart rate distress. The results of this work suggest that on-site production and immediate administration to the murine vasculature may eliminate the necessity for high microbubble production rates, long-term stability, or small microbubble diameters.
通过同时产生和注射微流体产生的微泡来增强体内声学对比
微流控装置产生的微泡用于超声造影剂增强,可以精确控制微泡直径,但代价是产生速率低,微泡稳定性差。在这项工作中,我们研究了由微流体装置产生的微泡直接注射到小鼠尾静脉后是否能提供足够的超声造影剂增强。用10%葡萄糖和3%牛血清白蛋白稳定的由氮气组成的微流体制备的微泡注入野生型C57BL/6小鼠尾静脉,持续10秒。在12.5 MHz下获取左、右心室短轴超声图像,分析图像强度随时间的变化。微泡产率为2.5×105 ~ 8.3×105微泡/s,微泡直径为9.1 ~ 19 μm。在所有病例中,右心室和左心室均可见微泡,尽管左心室的平均对比度增强比右心室低约13.5 dB。所有的小鼠都存活了下来,没有明显的呼吸或心率窘迫。这项工作的结果表明,现场生产和立即给药到小鼠脉管系统可能消除对高微泡产量、长期稳定性或小微泡直径的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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