Department of Biophysics, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands.
Ultrasound Med Biol. 2010 Feb;36(2):181-91. doi: 10.1016/j.ultrasmedbio.2009.09.009. Epub 2009 Dec 16.
Molecular imaging may provide new insights into the early detection and development of atherosclerosis before first symptoms occur. One of the techniques in use employs noninvasive ultrasound. In the past decade, experimental and clinical validation studies showed that for the microcirculation targeted ultrasound contrast agents, such as echogenic liposomes, microbubbles and perfluorocarbon emulsions, do improve visualization of specific structures. For large arteries, however, successful application is less obvious. In this review, we will address the challenges for molecular imaging of large arteries. We will discuss the problems encountered in the use of targeted ultrasound contrast agents presently available, mainly based on data obtained in flow chambers and animal studies because clinical studies are lacking. We conclude that molecular imaging of activated endothelium in large- and middle-sized arteries by site-specific accumulation of contrast material is still difficult to achieve due to wall shear stress conditions in these vessels.
分子成像技术可能为在出现首发症状之前对动脉粥样硬化的早期检测和发展提供新的见解。目前使用的技术之一是采用非侵入性超声。在过去的十年中,实验和临床验证研究表明,对于针对微循环的超声对比剂,如声振脂质体、微泡和全氟化碳乳剂,确实可以改善特定结构的可视化。然而,对于大动脉,成功的应用并不明显。在这篇综述中,我们将讨论大动脉分子成像的挑战。我们将讨论目前可用的靶向超声对比剂在使用中遇到的问题,主要基于在流动室和动物研究中获得的数据,因为缺乏临床研究。我们的结论是,由于这些血管中的壁切应力条件,通过对比剂的特异性积累来实现大、中动脉中活化的内皮细胞的分子成像仍然具有挑战性。