Datta Saurabh, Coussios Constantin-C, Ammi Azzdine Y, Mast T Douglas, de Courten-Myers Gabrielle M, Holland Christy K
Department of Biomedical Engineering, University of Cincinnati, Cincinnati, OH, USA.
Ultrasound Med Biol. 2008 Sep;34(9):1421-33. doi: 10.1016/j.ultrasmedbio.2008.01.016. Epub 2008 Apr 18.
Ultrasound has been shown previously to act synergistically with a thrombolytic agent, such as recombinant tissue plasminogen activator (rt-PA) to accelerate thrombolysis. In this in vitro study, a commercial contrast agent, Definity, was used to promote and sustain the nucleation of cavitation during pulsed ultrasound exposure at 120 kHz. Ultraharmonic signals, broadband emissions and harmonics of the fundamental were measured acoustically by using a focused hydrophone as a passive cavitation detector and used to quantify the level of cavitation activity. Human whole blood clots suspended in human plasma were exposed to a combination of rt-PA, Definity and ultrasound at a range of ultrasound peak-to-peak pressure amplitudes, which were selected to expose clots to various degrees of cavitation activity. Thrombolytic efficacy was determined by measuring clot mass loss before and after the treatment and correlated with the degree of cavitation activity. The penetration depth of rt-PA and plasminogen was also evaluated in the presence of cavitating microbubbles using a dual-antibody fluorescence imaging technique. The largest mass loss (26.2%) was observed for clots treated with 120-kHz ultrasound (0.32-MPa peak-to-peak pressure amplitude), rt-PA and stable cavitation nucleated by Definity. A significant correlation was observed between mass loss and ultraharmonic signals (r = 0.85, p < 0.0001, n = 24). The largest mean penetration depth of rt-PA (222 microm) and plasminogen (241 microm) was observed in the presence of stable cavitation activity. Stable cavitation activity plays an important role in enhancement of thrombolysis and can be monitored to evaluate the efficacy of thrombolytic treatment.
先前的研究表明,超声可与溶栓剂(如重组组织型纤溶酶原激活剂(rt-PA))协同作用,加速溶栓过程。在这项体外研究中,使用了一种商业造影剂Definity,以在120 kHz的脉冲超声照射期间促进并维持空化核的形成。通过使用聚焦水听器作为被动空化探测器,对超谐波信号、宽带发射以及基波的谐波进行声学测量,并用于量化空化活动的水平。将悬浮于人体血浆中的人体全血凝块,在一系列超声峰-峰压力幅值下,暴露于rt-PA、Definity和超声的组合中,这些压力幅值的选择是为了使凝块暴露于不同程度的空化活动中。通过测量治疗前后凝块质量损失来确定溶栓效果,并将其与空化活动程度相关联。还使用双抗体荧光成像技术,在存在空化微泡的情况下,评估rt-PA和纤溶酶原的穿透深度。对于接受120 kHz超声(峰-峰压力幅值为0.32 MPa)、rt-PA和由Definity形成的稳定空化核处理的凝块,观察到最大质量损失(26.2%)。在质量损失与超谐波信号之间观察到显著相关性(r = 0.85,p < 0.0001,n = 24)。在存在稳定空化活动的情况下,观察到rt-PA(222微米)和纤溶酶原(241微米)的最大平均穿透深度。稳定空化活动在增强溶栓作用中起重要作用,并且可以通过监测来评估溶栓治疗的效果。