Physics of Fluids Group, MIRA Institute for Biomedical Technology and Technical Medicine, MESA Institute for Nanotechnology, University of Twente, 7500 AE, Enschede, The Netherlands.
Proc Natl Acad Sci U S A. 2014 Feb 4;111(5):1697-702. doi: 10.1073/pnas.1312171111. Epub 2014 Jan 21.
Acoustically sensitive emulsion droplets composed of a liquid perfluorocarbon have the potential to be a highly efficient system for local drug delivery, embolotherapy, or for tumor imaging. The physical mechanisms underlying the acoustic activation of these phase-change emulsions into a bubbly dispersion, termed acoustic droplet vaporization, have not been well understood. The droplets have a very high activation threshold; its frequency dependence does not comply with homogeneous nucleation theory and localized nucleation spots have been observed. Here we show that acoustic droplet vaporization is initiated by a combination of two phenomena: highly nonlinear distortion of the acoustic wave before it hits the droplet and focusing of the distorted wave by the droplet itself. At high excitation pressures, nonlinear distortion causes significant superharmonics with wavelengths of the order of the droplet size. These superharmonics strongly contribute to the focusing effect; therefore, the proposed mechanism also explains the observed pressure thresholding effect. Our interpretation is validated with experimental data captured with an ultrahigh-speed camera on the positions of the nucleation spots, where we find excellent agreement with the theoretical prediction. Moreover, the presented mechanism explains the hitherto counterintuitive dependence of the nucleation threshold on the ultrasound frequency. The physical insight allows for the optimization of acoustic droplet vaporization for therapeutic applications, in particular with respect to the acoustic pressures required for activation, thereby minimizing the negative bioeffects associated with the use of high-intensity ultrasound.
由液态全氟碳组成的对声音敏感的乳液液滴有可能成为高效的局部药物输送、栓塞治疗或肿瘤成像系统。这些相变型乳液在声激活下变成泡沫状分散体的物理机制,即声致液滴蒸发,尚未得到很好的理解。液滴的激活阈值非常高;其频率依赖性不符合均相成核理论,并且已经观察到局部成核点。在这里,我们表明声致液滴蒸发是由两种现象共同引发的:在声波撞击液滴之前的高度非线性失真,以及液滴本身对失真波的聚焦。在高激励压力下,非线性失真会导致波长与液滴尺寸相当的显著超谐波。这些超谐波对聚焦效应有很大贡献;因此,所提出的机制也解释了观察到的压力阈值效应。我们使用超高速摄像机在成核点位置上获取的实验数据验证了我们的解释,发现与理论预测非常吻合。此外,所提出的机制解释了迄今为止与声频率有关的成核阈值的反直觉依赖性。这种物理洞察力使得可以针对治疗应用优化声致液滴蒸发,特别是在激活所需的声压方面,从而最大限度地减少与高强度超声使用相关的负面生物效应。