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Binding dynamics of targeted microbubbles in response to modulated acoustic radiation force.

机译:响应于调制的声辐射力,目标微泡的结合动力学。

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摘要

Detection of molecular targeted microbubbles plays a foundational role in ultrasound-based molecular imaging and targeted gene or drug delivery. In this paper, an empirical model describing the binding dynamics of targeted microbubbles in response to modulated acoustic radiation forces in large vessels is presented and experimentally verified using tissue-mimicking flow phantoms. Higher flow velocity and microbubble concentration led to faster detaching rates for specifically bound microbubbles (p < 0.001). Higher time-averaged acoustic radiation force intensity led to faster attaching rates and a higher saturation level of specifically bound microbubbles (p < 0.05). The level of residual microbubble signal in targeted experiments after cessation of radiation forces was the only response parameter that was reliably different between targeted and control experiments (p < 0.05). A related parameter, the ratio of residual-to-saturated microbubble signal (Rresid), is proposed as a measurement that is independent of absolute acoustic signal magnitude and therefore able to reliably detect targeted adhesion independently of control measurements (p < 0.01). These findings suggest the possibility of enhanced detection of specifically bound microbubbles in real-time, using relatively short imaging protocols (approximately 3 min), without waiting for free microbubble clearance.
机译:分子靶向微泡的检测在基于超声的分子成像和靶向基因或药物递送中起着基础性作用。在本文中,提出了一个经验模型,该模型描述了目标微气泡对大血管中调制的声辐射力的响应的结合动力学,并使用组织模拟流模型进行了实验验证。较高的流速和微气泡浓度导致特定结合的微气泡的分离速度更快(p <0.001)。较高的时间平均声辐射力强度导致更快的附着速率和更高的特定结合微气泡饱和度(p <0.05)。在目标实验中,停止辐射力后残留微气泡信号的水平是唯一可靠地在目标实验和对照实验之间不同的响应参数(p <0.05)。提出了一个相关参数,即残余气泡与饱和微气泡信号的比率(Rresid)作为一种测量,该测量与绝对声学信号的大小无关,因此能够独立于控制测量而可靠地检测目标粘附力(p <0.01)。这些发现表明,可以使用较短的成像方案(约3分钟)实时增强对特定结合的微气泡的检测,而无需等待自由的微气泡清除。

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