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Relationship between cavitation and loss of echogenicity from ultrasound contrast agents

机译:空化与超声造影剂回声丧失之间的关系

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摘要

Ultrasound contrast agents (UCAs) have the potential to nucleate cavitation and promote both beneficial and deleterious bioeffects in vivo. Previous studies have elucidated the pulse-duration dependent pressure amplitude threshold for rapid loss of echogenicity due to UCA fragmentation. Previous studies have demonstrated that UCA fragmentation was concomitant with inertial cavitation. The purpose of this study was to evaluate the relationship between stable and inertial cavitation thresholds and loss of echogenicity of UCAs as a function of pulse duration. Determining the relationship between cavitation thresholds and loss of echogenicity of UCAs would enable monitoring of cavitation based upon the on-screen echogenicity in clinical applications. Two lipid-shelled UCAs, echogenic liposomes (ELIP) and Definity®, were insonified by a clinical ultrasound scanner in duplex spectral Doppler mode at four pulse durations (“sample volumes”) in both a static system and a flow system. Cavitation emissions from the UCAs insonified by Doppler pulses were recorded using a passive cavitation detection system and stable and inertial cavitation thresholds ascertained. Loss of echogenicity from ELIP and Definity® was assessed within regions of interest on B-mode images. A numerical model based on UCA rupture predicted the functional form of the loss of echogenicity from ELIP and Definity®. Stable and inertial cavitation thresholds were found to have a weak dependence on pulse duration. Stable cavitation thresholds were lower than inertial cavitation thresholds. The power of cavitation emissions was an exponential function of the loss of echogenicity over the investigated range of acoustic pressures. Both ELIP and Definity® lost more than 80% echogenicity before the onset of stable or inertial cavitation. Once this level of echogenicity loss occurred, both stable and inertial cavitation were detected in the physiologic flow phantom. These results imply that stable and inertial cavitation are necessary in order to trigger complete loss of echogenicity acoustically from UCAs and this finding can be used when planning diagnostic and therapeutic applications.
机译:超声造影剂(UCA)具有在体内形成空化并促进有益和有害生物效应的潜力。先前的研究已经阐明了由于UCA碎裂而导致回声性快速丧失的脉搏持续时间依赖性压力幅度阈值。先前的研究表明,UCA碎裂伴随惯性空化。这项研究的目的是评估稳定和惯性空化阈值与UCA的回声丧失之间的关系,作为脉冲持续时间的函数。确定空化阈值和UCA的回声丧失之间的关系将使能够基于临床应用中的屏幕回声来监视空化。临床超声扫描仪以双谱多普勒模式以四个脉冲持续时间(“样本量”)在静态系统和超声系统中对两个带有脂质壳的UCA(回声脂质体(ELIP)和Definity ®)进行声处理。流系统。使用无源气蚀检测系统记录由多普勒脉冲声化的UCA产生的气蚀排放,并确定稳定和惯性的气蚀阈值。在B型图像的目标区域内评估了ELIP和Definity ®产生的回声损失。基于UCA破裂的数值模型预测了ELIP和Definity ®会造成回声丧失的功能形式。发现稳定的和惯性的气蚀阈值对脉冲持续时间的依赖性很弱。稳定的气蚀阈值低于惯性气蚀阈值。空化发射的功率是在所研究的声压范围内回声损失的指数函数。在稳定或惯性空化开始之前,ELIP和Definity ®都损失了80%以上的回声。一旦发生这种水平的回声损失,就可以在生理流模型中检测到稳定和惯性空化。这些结果表明,必须有稳定和惯性的气蚀才能触发UCA完全回声的回声性,这一发现可用于计划诊断和治疗应用。

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