Division of Gastroenterology, Department of Medicine, University of Washington, Seattle, WA, USA.
Center for Industrial and Medical Ultrasound, Applied Physics Laboratory, University of Washington, Seattle, WA, USA.
Int J Hyperthermia. 2023;40(1):2233720. doi: 10.1080/02656736.2023.2233720.
Since its inception about two decades ago, histotripsy - a non-thermal mechanical tissue ablation technique - has evolved into a spectrum of methods, each with distinct potentiating physical mechanisms: intrinsic threshold histotripsy, shock-scattering histotripsy, hybrid histotripsy, and boiling histotripsy. All methods utilize short, high-amplitude pulses of focused ultrasound delivered at a low duty cycle, and all involve excitation of violent bubble activity and acoustic streaming at the focus to fractionate tissue down to the subcellular level. The main differences are in pulse duration, which spans microseconds to milliseconds, and ultrasound waveform shape and corresponding peak acoustic pressures required to achieve the desired type of bubble activity. In addition, most types of histotripsy rely on the presence of high-amplitude shocks that develop in the pressure profile at the focus due to nonlinear propagation effects. Those requirements, in turn, dictate aspects of the instrument design, both in terms of driving electronics, transducer dimensions and intensity limitations at surface, shape (primarily, the -number) and frequency. The combination of the optimized instrumentation and the bio-effects from bubble activity and streaming on different tissues, lead to target clinical applications for each histotripsy method. Here, the differences and similarities in the physical mechanisms and resulting bioeffects of each method are reviewed and tied to optimal instrumentation and clinical applications.
自二十年前问世以来,组织微爆破——一种非热机械组织消融技术——已经发展出一系列方法,每种方法都具有独特的增强物理机制:固有阈值组织微爆破、激波散射组织微爆破、混合组织微爆破和沸腾组织微爆破。所有方法都利用短而高振幅的聚焦超声脉冲,以低占空比发射,并且都涉及在焦点处激发剧烈的气泡活动和声流,将组织分割到亚细胞水平。主要区别在于脉冲持续时间,从微秒到毫秒不等,以及所需的超声波形形状和相应的峰值声压,以实现所需类型的气泡活动。此外,大多数类型的组织微爆破都依赖于高强度激波的存在,这些激波是由于非线性传播效应在焦点处的压力分布中产生的。这些要求反过来又决定了仪器设计的各个方面,包括驱动电子设备、换能器尺寸和表面强度限制、形状(主要是-数)和频率。优化的仪器设备与气泡活动和流对不同组织的生物效应相结合,为每种组织微爆破方法带来了目标临床应用。在这里,我们回顾了每种方法的物理机制和由此产生的生物效应的异同,并将其与最佳仪器设备和临床应用联系起来。