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Endoscopic Coregistered Ultrasound Imaging and Precision Histotripsy: Initial Evaluation.内镜共注册超声成像与精确组织粉碎术:初步评估
BME Front. 2022 Jul 1;2022:9794321. doi: 10.34133/2022/9794321. eCollection 2022.
2
Enhancement of Boiling Histotripsy by Steering the Focus Axially During the Pulse Delivery.在脉冲传输过程中轴向引导焦点增强沸腾空化爆破。
IEEE Trans Ultrason Ferroelectr Freq Control. 2023 Aug;70(8):865-875. doi: 10.1109/TUFFC.2023.3286759. Epub 2023 Aug 2.
3
Noninvasive mechanical destruction of liver tissue and tissue decellularisation by pressure-modulated shockwave histotripsy.压力调制式冲击波组织破碎法无创性机械破坏肝脏组织和组织脱细胞化。
Front Immunol. 2023 May 16;14:1150416. doi: 10.3389/fimmu.2023.1150416. eCollection 2023.
4
Comparative Characterization of Nonlinear Ultrasound Fields Generated by Sonalleve V1 and V2 MR-HIFU Systems.Sonalleve V1 和 V2 MR-HIFU 系统产生的非线性超声场的比较特性分析。
IEEE Trans Ultrason Ferroelectr Freq Control. 2023 Jun;70(6):521-537. doi: 10.1109/TUFFC.2023.3261420. Epub 2023 May 25.
5
A Multimodal Phantom for Visualization and Assessment of Histotripsy Treatments on Ultrasound and X-Ray Imaging.一种用于可视化和评估超声和 X 射线成像下的 Histotripsy 治疗的多模态体模。
Ultrasound Med Biol. 2023 Jun;49(6):1401-1407. doi: 10.1016/j.ultrasmedbio.2023.01.019. Epub 2023 Mar 4.
6
Soft Tissue Aberration Correction for Histotripsy Using Acoustic Emissions From Cavitation Cloud Nucleation and Collapse.利用空化云成核和溃灭产生的声发射进行 Histotripsy 的软组织像差校正
Ultrasound Med Biol. 2023 May;49(5):1182-1193. doi: 10.1016/j.ultrasmedbio.2023.01.004. Epub 2023 Feb 8.
7
High intensity focused ultrasound atomization and erosion in healthy and tendinopathic tendons.高强度聚焦超声雾化和侵蚀健康和腱病肌腱。
Phys Med Biol. 2023 Jan 5;68(2). doi: 10.1088/1361-6560/aca9b7.
8
Histotripsy Bubble Dynamics in Elastic, Anisotropic Tissue-Mimicking Phantoms.弹性各向异性组织模拟体中的 Histotripsy 气泡动力学。
Ultrasound Med Biol. 2023 Mar;49(3):853-865. doi: 10.1016/j.ultrasmedbio.2022.11.012. Epub 2022 Dec 26.
9
Mechanical high-intensity focused ultrasound creates unique tumor debris enhancing dendritic cell-induced T cell activation.机械高强度聚焦超声产生独特的肿瘤碎片,增强树突状细胞诱导的 T 细胞激活。
Front Immunol. 2022 Dec 7;13:1038347. doi: 10.3389/fimmu.2022.1038347. eCollection 2022.
10
Initial Assessment of Boiling Histotripsy for Mechanical Ablation of Ex Vivo Human Prostate Tissue.沸腾空化爆破法初步评估用于离体人前列腺组织的机械消融
Ultrasound Med Biol. 2023 Jan;49(1):62-71. doi: 10.1016/j.ultrasmedbio.2022.07.014. Epub 2022 Oct 4.

组织微爆破频谱:技术和仪器的差异与相似性。

The histotripsy spectrum: differences and similarities in techniques and instrumentation.

机构信息

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.

出版信息

Int J Hyperthermia. 2023;40(1):2233720. doi: 10.1080/02656736.2023.2233720.

DOI:10.1080/02656736.2023.2233720
PMID:37460101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10479943/
Abstract

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.

摘要

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。