Rojas Juan D, Dayton Paul A
Joint Department of Biomedical Engineering, University of North Carolina and North Carolina State University, Chapel Hill, North Carolina, USA.
Joint Department of Biomedical Engineering, University of North Carolina and North Carolina State University, Chapel Hill, North Carolina, USA.
Ultrasound Med Biol. 2019 Jan;45(1):192-207. doi: 10.1016/j.ultrasmedbio.2018.08.017. Epub 2018 Oct 26.
Phase-change contrast agents (PCCAs) possess advantages over microbubble contrast agents, such as the ability to extravasate and circulate longer in the vasculature that could enhance the diagnostic capabilities of contrast-enhanced ultrasound. PCCAs typically have a liquid perfluorocarbon (PFC) core that can be vaporized into echogenic microbubbles. Vaporization of submicron agents filled with liquid PFCs at body temperature usually requires therapeutic pressures higher than typically used for diagnostic imaging, but low-boiling-point PCCAs using decafluorobutane or octafluoropropane can be vaporized using pressures in the diagnostic imaging regime. Low-boiling-point PCCAs produce a unique acoustic signature that can be separated from tissue and bubble signals to make images with high contrast-to-tissue ratios. In this work, we explore the effect of pulse length and concentration on the vaporization signal of PCCAs and a new technique to capture and use the signals to make high contrast-to-tissue ratio images in vivo. The results indicate that using a short pulse may be ideal for imaging because it does not interact with created bubbles but still produces strong signals for making images. Furthermore, it was found that capturing PCCA vaporization signals produced higher contrast-to-tissue ratio values and better depth of penetration than imaging the bubbles generated by droplet activation using conventional contrast imaging techniques. The resolution of the vaporization signal images is poor because of the low frequency of the signals, but their high sensitivity may be used for applications such as molecular imaging, where the detection of small numbers of contrast agents is important.
相变造影剂(PCCA)相较于微泡造影剂具有诸多优势,例如能够渗出并在脉管系统中循环更长时间,这可增强超声造影的诊断能力。PCCA通常具有液态全氟化碳(PFC)核心,该核心可汽化为产生回声的微泡。在体温下,填充液态PFC的亚微米剂的汽化通常需要高于诊断成像常用压力的治疗压力,但使用十氟丁烷或八氟丙烷的低沸点PCCA可在诊断成像压力范围内汽化。低沸点PCCA产生独特的声学特征,可与组织和气泡信号分离,以生成具有高对比组织比的图像。在这项工作中,我们探究了脉冲长度和浓度对PCCA汽化信号的影响,以及一种捕获和利用这些信号在体内生成高对比组织比图像的新技术。结果表明,使用短脉冲进行成像可能是理想的选择,因为它不与生成的气泡相互作用,但仍能产生用于成像的强信号。此外,研究发现,捕获PCCA汽化信号比使用传统造影成像技术对液滴激活产生的气泡进行成像能产生更高的对比组织比值和更好的穿透深度。由于信号频率较低,汽化信号图像的分辨率较差,但其高灵敏度可用于分子成像等应用,在这些应用中检测少量造影剂很重要。