Qin Shengping, Caskey Charles F, Ferrara Katherine W
Department of Biomedical Engineering, University of California, 451 East Health Sciences Drive, Davis, CA 95616, USA.
Phys Med Biol. 2009 Mar 21;54(6):R27-57. doi: 10.1088/0031-9155/54/6/R01. Epub 2009 Feb 19.
Microbubble contrast agents and the associated imaging systems have developed over the past 25 years, originating with manually-agitated fluids introduced for intra-coronary injection. Over this period, stabilizing shells and low diffusivity gas materials have been incorporated in microbubbles, extending stability in vitro and in vivo. Simultaneously, the interaction of these small gas bubbles with ultrasonic waves has been extensively studied, resulting in models for oscillation and increasingly sophisticated imaging strategies. Early studies recognized that echoes from microbubbles contained frequencies that are multiples of the microbubble resonance frequency. Although individual microbubble contrast agents cannot be resolved-given that their diameter is on the order of microns-nonlinear echoes from these agents are used to map regions of perfused tissue and to estimate the local microvascular flow rate. Such strategies overcome a fundamental limitation of previous ultrasound blood flow strategies; the previous Doppler-based strategies are insensitive to capillary flow. Further, the insonation of resonant bubbles results in interesting physical phenomena that have been widely studied for use in drug and gene delivery. Ultrasound pressure can enhance gas diffusion, rapidly fragment the agent into a set of smaller bubbles or displace the microbubble to a blood vessel wall. Insonation of a microbubble can also produce liquid jets and local shear stress that alter biological membranes and facilitate transport. In this review, we focus on the physical aspects of these agents, exploring microbubble imaging modes, models for microbubble oscillation and the interaction of the microbubble with the endothelium.
在过去25年中,微泡造影剂及相关成像系统不断发展,最初是用于冠状动脉内注射的手动搅拌液体。在此期间,微泡中加入了稳定壳层和低扩散性气体材料,从而延长了其在体外和体内的稳定性。同时,人们对这些小气泡与超声波的相互作用进行了广泛研究,得出了振荡模型和日益复杂的成像策略。早期研究认识到,微泡回声包含微泡共振频率的倍数频率。尽管由于微泡造影剂的直径在微米量级,单个微泡造影剂无法分辨,但这些造影剂的非线性回声可用于绘制灌注组织区域并估计局部微血管流速。此类策略克服了以往超声血流策略的一个基本局限;以往基于多普勒的策略对毛细血管血流不敏感。此外,共振气泡的声作用会产生有趣的物理现象,这些现象已被广泛研究用于药物和基因递送。超声压力可增强气体扩散,使造影剂迅速破碎成一组较小的气泡,或将微泡驱赶到血管壁。微泡的声作用还可产生液体射流和局部剪切应力,从而改变生物膜并促进物质运输。在本综述中,我们聚焦于这些造影剂的物理特性,探讨微泡成像模式、微泡振荡模型以及微泡与内皮细胞的相互作用。