Xie Yanjun, Huang Yi, Stevenson Hugo C S, Yin Li, Zhang Kaijie, Islam Zain Husain, Marcum William Aaron, Johnston Campbell, Hoyt Nicholas, Kent Eric William, Wang Bowen, Hossack John A
Department of Biomedical Engineering, University of Virginia, 415 Lane Road, Charlottesville, VA, 22908, USA.
Department of Surgery, School of Medicine, University of Virginia, 409 Lane Rd MR4, Charlottesville, VA, 22908, USA.
Ann Biomed Eng. 2025 Jan;53(1):109-119. doi: 10.1007/s10439-024-03609-7. Epub 2024 Sep 9.
The need for safe and effective methods to manage deep vein thrombosis (DVT), given the risks associated with anticoagulants and thrombolytic agents, motivated research into innovative approaches to resolve blood clots. In response to this challenge, sonothrombolysis is being explored as a technique that combines microbubbles, ultrasound, and thrombolytic agents to facilitate the aggressive dissolution of thrombi. Prior studies have indicated that relatively large microbubbles accelerate the dissolution process, either in an in vitro or an arterial model. However, sonothrombolysis using large microbubbles must be evaluated in venous thromboembolism diseases, where blood flow velocity is not comparable. In this study, the efficacy of sonothrombolysis was validated in a murine model of pre-existing DVT. During therapy, microfluidically produced microbubbles of 18 μm diameter and recombinant tissue plasminogen activator (rt-PA) were administered through a tail vein catheter for 30 min, while ultrasound was applied to the abdominal region of the mice. Three-dimensional ultrasound scans were performed before and after therapy for quantification. The residual volume of the thrombi was 20% in animals post sonothrombolysis versus 52% without therapy ( ), indicating a significant reduction in DVT volume. Histological analysis of tissue sections confirmed a reduction in DVT volume post-therapy. Therefore, large microbubbles generated from a microfluidic device show promise in ultrasound-assisted therapy to address concerns related to venous thromboembolism.
鉴于抗凝剂和溶栓剂存在风险,需要安全有效的方法来治疗深静脉血栓形成(DVT),这推动了对解决血凝块创新方法的研究。为应对这一挑战,超声溶栓作为一种将微泡、超声和溶栓剂相结合以促进血栓积极溶解的技术正在被探索。先前的研究表明,相对较大的微泡在体外或动脉模型中可加速溶解过程。然而,使用大微泡的超声溶栓必须在血流速度不可比的静脉血栓栓塞疾病中进行评估。在本研究中,在已存在DVT的小鼠模型中验证了超声溶栓的疗效。治疗期间,通过尾静脉导管给予直径为18μm的微流控产生的微泡和重组组织型纤溶酶原激活剂(rt-PA)30分钟,同时对小鼠腹部区域施加超声。治疗前后进行三维超声扫描以进行定量分析。超声溶栓后动物血栓残余体积为20%,而未治疗组为52%( ),表明DVT体积显著减少。组织切片的组织学分析证实治疗后DVT体积减少。因此,微流控装置产生的大微泡在超声辅助治疗中显示出有望解决与静脉血栓栓塞相关的问题。