Kotopoulis Spiros, Postema Michiel
Emmy-Noether Group, Institute of Medical Engineering, Department of Electrical Engineering and Information Technology, Ruhr-Universität Bochum, D-44780 Bochum, Germany.
Ultrasonics. 2010 Feb;50(2):260-8. doi: 10.1016/j.ultras.2009.09.028. Epub 2009 Oct 2.
The ultrasound-induced formation of bubble clusters may be of interest as a therapeutic means. If the clusters behave as one entity, i.e., one mega-bubble, its ultrasonic manipulation towards a boundary is straightforward and quick. If the clusters can be forced to accumulate to a microfoam, entire vessels might be blocked on purpose using an ultrasound contrast agent and a sound source. In this paper, we analyse how ultrasound contrast agent clusters are formed in a capillary and what happens to the clusters if sonication is continued, using continuous driving frequencies in the range 1-10 MHz. Furthermore, we show high-speed camera footage of microbubble clustering phenomena. We observed the following stages of microfoam formation within a dense population of microbubbles before ultrasound arrival. After the sonication started, contrast microbubbles collided, forming small clusters, owing to secondary radiation forces. These clusters coalesced within the space of a quarter of the ultrasonic wavelength, owing to primary radiation forces. The resulting microfoams translated in the direction of the ultrasound field, hitting the capillary wall, also owing to primary radiation forces. We have demonstrated that as soon as the bubble clusters are formed and as long as they are in the sound field, they behave as one entity. At our acoustic settings, it takes seconds to force the bubble clusters to positions approximately a quarter wavelength apart. It also just takes seconds to drive the clusters towards the capillary wall. Subjecting an ultrasound contrast agent of given concentration to a continuous low-amplitude signal makes it cluster to a microfoam of known position and known size, allowing for sonic manipulation.
超声诱导形成气泡簇作为一种治疗手段可能会引起人们的兴趣。如果这些簇表现为一个整体,即一个巨型气泡,那么对其进行朝向边界的超声操控将是直接且快速的。如果能够迫使这些簇聚积成微泡,那么使用超声造影剂和声源就有可能故意阻塞整个血管。在本文中,我们分析了在毛细管中超声造影剂簇是如何形成的,以及如果持续超声处理这些簇会发生什么情况,所使用的连续驱动频率范围为1 - 10兆赫兹。此外,我们展示了微泡簇聚现象的高速摄像机拍摄画面。我们观察到在超声到达之前微泡密集群体内微泡形成的以下阶段。超声处理开始后,造影微泡由于二次辐射力而相互碰撞,形成小簇。由于一次辐射力,这些簇在超声波长四分之一的空间内合并。所形成的微泡也由于一次辐射力而朝着超声场方向移动,撞击毛细管壁。我们已经证明,一旦气泡簇形成并且只要它们处于声场中,它们就表现为一个整体。在我们的声学设置下,只需几秒钟就能迫使气泡簇到达相距约四分之一波长的位置。同样只需几秒钟就能将这些簇朝着毛细管壁驱动。对给定浓度的超声造影剂施加连续的低振幅信号会使其聚集成具有已知位置和已知大小的微泡,从而实现超声操控。