van der Hoek Jan L, Snoeijink Tess J, Mirgolbabaee Hadi, Kunst Romaine, Versluis Michel, Arens Jutta, Manohar Srirang, Groot Jebbink Erik
Multi-Modality Medical Imaging Group, TechMed Center, University of Twente, Enschede, The Netherlands.
Department of Medical Imaging, Radboud University Medical Center, Nijmegen, The Netherlands.
Drug Deliv. 2025 Dec;32(1):2505007. doi: 10.1080/10717544.2025.2505007. Epub 2025 May 18.
Transarterial radioembolization (TARE) is an established treatment method for non-resectable liver tumors. One of the challenges of the approach is the accurate prediction of the microsphere biodistribution in the liver. We propose to use ultrasound contrast microbubbles as holmium microsphere precursors, which allows real-time prediction of the microsphere trajectories and biodistribution using dynamic contrast-enhanced ultrasound (DCE-US). The immediate goal in this in vitro study was to investigate the predictive capabilities of microbubbles as microsphere precursors. The study was conducted in an experimental in vitro model which represents the bifurcating right branch of the hepatic artery. A controlled injection of experimental BR-14 ultrasound contrast microbubbles and non-radioactive holmium-165 microspheres was performed in separate consecutive experiments in an arterial flow phantom. The microbubbles and microspheres were collected separately at the outlets of the phantom and counted using a Coulter counter to determine their distribution over the different outlets. The flow profile, the injection velocity, and the catheter position were monitored during the measurements to ensure stability. The results showed a good correlation between the microbubble and the microsphere distributions (p = 0.0038, r = 0.88) measured at the outlets. Differences in the distributions could be attributed to the characteristics of microbubbles and microspheres alone (e.g. particle size and concentration), since critical parameters were kept stable between the two experiments. The current in vitro study provides confidence that the microsphere biodistribution can be predicted using contrast microbubbles. The comparison provided by this study forms a foundation for the development of a DCE-US guided TARE treatment.
经动脉放射性栓塞术(TARE)是一种已确立的不可切除肝肿瘤治疗方法。该方法的挑战之一是准确预测微球在肝脏中的生物分布。我们建议使用超声造影微泡作为钬微球前体,这使得能够使用动态对比增强超声(DCE-US)实时预测微球轨迹和生物分布。这项体外研究的直接目标是研究微泡作为微球前体的预测能力。该研究在一个代表肝动脉右分支分叉的体外实验模型中进行。在动脉血流模型中,分别连续进行了实验性BR-14超声造影微泡和非放射性钬-165微球的控制性注射。在模型出口分别收集微泡和微球,并用库尔特计数器计数,以确定它们在不同出口的分布。测量过程中监测血流剖面、注射速度和导管位置以确保稳定性。结果显示在出口处测量的微泡和微球分布之间具有良好的相关性(p = 0.0038,r = 0.88)。分布差异可能仅归因于微泡和微球的特性(例如粒径和浓度),因为两个实验之间的关键参数保持稳定。当前的体外研究为使用造影微泡预测微球生物分布提供了信心。本研究提供的比较为DCE-US引导的TARE治疗的发展奠定了基础。