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本文引用的文献

1
An in vitro study of a phase-shift nanoemulsion: a potential nucleation agent for bubble-enhanced HIFU tumor ablation.一种相移位纳米乳剂的体外研究:一种用于泡增强 HIFU 肿瘤消融的潜在成核剂。
Ultrasound Med Biol. 2010 Nov;36(11):1856-66. doi: 10.1016/j.ultrasmedbio.2010.07.001.
2
Delivery of water-soluble drugs using acoustically triggered perfluorocarbon double emulsions.采用声触发全氟碳双乳液传递水溶性药物。
Pharm Res. 2010 Dec;27(12):2753-65. doi: 10.1007/s11095-010-0277-5. Epub 2010 Sep 25.
3
Delivery of chlorambucil using an acoustically-triggered perfluoropentane emulsion.使用声触发全氟戊烷乳剂递送氯苯丁酸。
Ultrasound Med Biol. 2010 Aug;36(8):1364-75. doi: 10.1016/j.ultrasmedbio.2010.04.019.
4
Dynamics of acoustic droplet vaporization in gas embolotherapy.气体栓塞治疗中声致微泡汽化的动力学
Appl Phys Lett. 2010 Apr 5;96(14):143702. doi: 10.1063/1.3376763. Epub 2010 Apr 7.
5
The role of inertial cavitation in acoustic droplet vaporization.惯性空化在声滴汽化中的作用。
IEEE Trans Ultrason Ferroelectr Freq Control. 2009 May;56(5):1006-17. doi: 10.1109/TUFFC.2009.1132.
6
Numerical simulations of heating patterns and tissue temperature response due to high-intensity focused ultrasound.高强度聚焦超声引起的加热模式和组织温度响应的数值模拟。
IEEE Trans Ultrason Ferroelectr Freq Control. 2000;47(4):1077-89. doi: 10.1109/58.852092.
7
Towards aberration correction of transcranial ultrasound using acoustic droplet vaporization.利用声滴汽化实现经颅超声的像差校正
Ultrasound Med Biol. 2008 Mar;34(3):435-45. doi: 10.1016/j.ultrasmedbio.2007.08.004. Epub 2007 Oct 23.
8
The application of microbubbles for targeted drug delivery.微泡在靶向给药中的应用。
Expert Opin Drug Deliv. 2007 Sep;4(5):475-93. doi: 10.1517/17425247.4.5.475.
9
Acoustic droplet vaporization threshold: effects of pulse duration and contrast agent.声滴汽化阈值:脉冲持续时间和造影剂的影响
IEEE Trans Ultrason Ferroelectr Freq Control. 2007 May;54(5):933-46. doi: 10.1109/tuffc.2007.339.
10
Microbubble expansion in a flexible tube.柔性管中的微泡膨胀。
J Biomech Eng. 2006 Aug;128(4):554-63. doi: 10.1115/1.2206200.

气体栓塞治疗中声学汽化微滴的演变

Evolution of acoustically vaporized microdroplets in gas embolotherapy.

作者信息

Qamar Adnan, Wong Zheng Z, Fowlkes J Brian, Bull Joseph L

机构信息

Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

J Biomech Eng. 2012 Mar;134(3):031010. doi: 10.1115/1.4005980.

DOI:10.1115/1.4005980
PMID:22482690
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3705833/
Abstract

Acoustic vaporization dynamics of a superheated dodecafluoropentane (DDFP) microdroplet inside a microtube and the resulting bubble evolution is investigated in the present work. This work is motivated by a developmental gas embolotherapy technique that is intended to treat cancers by infarcting tumors using gas bubbles. A combined theoretical and computational approach is utilized and compared with the experiments to understand the evolution process and to estimate the resulting stress distribution associated with vaporization event. The transient bubble growth is first studied by ultra-high speed imaging and then theoretical and computational modeling is used to predict the entire bubble evolution process. The evolution process consists of three regimes: an initial linear rapid spherical growth followed by a linear compressed oval shaped growth and finally a slow asymptotic nonlinear spherical bubble growth. Although the droplets are small compared to the tube diameter, the bubble evolution is influenced by the tube wall. The final bubble radius is found to scale linearly with the initial droplet radius and is approximately five times the initial droplet radius. A short pressure pulse with amplitude almost twice as that of ambient conditions is observed. The width of this pressure pulse increases with increasing droplet size whereas the amplitude is weakly dependent. Although the rise in shear stress along the tube wall is found to be under peak physiological limits, the shear stress amplitude is found to be more prominently influenced by the initial droplet size. The role of viscous dissipation along the tube wall and ambient bulk fluid pressure is found to be significant in bubble evolution dynamics.

摘要

本文研究了微管内过热十二氟戊烷(DDFP)微滴的声蒸发动力学以及由此产生的气泡演化。这项工作的动机是一种正在发展的气体栓塞治疗技术,该技术旨在通过使用气泡使肿瘤梗死来治疗癌症。采用理论与计算相结合的方法,并与实验进行比较,以了解演化过程并估计与蒸发事件相关的应力分布。首先通过超高速成像研究瞬态气泡生长,然后使用理论和计算模型来预测整个气泡演化过程。演化过程包括三个阶段:初始的线性快速球形生长,随后是线性压缩椭圆形生长,最后是缓慢的渐近非线性球形气泡生长。尽管与管径相比液滴很小,但气泡演化受管壁影响。发现最终气泡半径与初始液滴半径呈线性比例关系,约为初始液滴半径的五倍。观察到一个幅度几乎是环境条件下两倍的短压力脉冲。该压力脉冲的宽度随液滴尺寸的增加而增加,而幅度的依赖性较弱。尽管发现沿管壁的剪应力上升处于峰值生理极限以下,但剪应力幅度受初始液滴尺寸的影响更为显著。发现沿管壁的粘性耗散和环境体流体压力在气泡演化动力学中起着重要作用。