Jan L van der Hoek, Tess J Snoeijink, Hadi Mirgolbabaee, Romaine Kunst, Michel Versluis, Jutta Arens, Srirang Manohar, Erik Groot Jebbink
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引用次数: 0
摘要
经动脉放射栓塞(TARE)是一种成熟的治疗不可切除肝肿瘤的方法。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剂微泡作为钬微球前体,它可以使用动态超声造影(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。该研究是在体外实验模型中进行的,该模型代表肝动脉右分支。在不同的连续实验中,在动脉血流模型中对照注射实验性BR-14超声造影剂微泡和非放射性钬-165微球。微泡和微球分别收集在幻影的出口,并使用库尔特计数器计数,以确定它们在不同出口的分布。在测量过程中,监测流量分布、注射速度和导管位置,以确保稳定性。结果表明,在出口处测得的微泡与微球分布具有良好的相关性(p = 0.0038, r = 0.88)。分布的差异可归因于微泡和微球的特性(如粒径和浓度),因为两个实验之间的关键参数保持稳定。目前的体外研究提供了利用对比微泡预测微球生物分布的信心。本研究提供的比较为开发DCE-US引导的TARE治疗奠定了基础。
Ultrasound contrast microbubbles to predict the microsphere distribution during transarterial radioembolization with holmium microspheres, an in vitro proof of concept study.
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.
期刊介绍:
Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.