被中性粒细胞吞噬的超声造影剂表现出声学活性

P. Dayton, J. Lindner, J. Chomas, K. Morgan, S. Simon, A. Lum, D. May, M. Coggins, K. Ferrara
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引用次数: 7

摘要

超声造影剂是由薄脂质或白蛋白壳组成的微泡,里面充满空气或高分子量气体。这些微泡用于对比增强超声(CEU)评估器官灌注。在炎症区域,微泡被粘附在静脉壁上的活化中性粒细胞完整地吞噬。作者假设微泡在吞噬作用后仍具有声学活性。因此,他们通过在不同声压下重复单脉冲超声的直接显微镜观察,评估了被吞噬微泡和游离微泡的物理反应。超声波会引起气泡体积的振荡。用高速成像系统记录超声过程中的微泡,并分析直径-时间曲线以确定吞噬作用。尽管细胞内环境增加了微泡所经历的粘弹性阻尼,但被吞噬的微泡保留了它们的声活性。在高声强脉冲(>1 MPa)下,被吞噬的微泡扩大到初始半径的500%,偶尔会导致中性粒细胞破裂。在声压为-240 kPa、脉冲重复频率为10 kHz的条件下,主辐射力将被吞噬的微泡移动了100微米的距离,从而提供了声活动的进一步证据。作者得出结论,被吞噬的微泡表现出粘弹性阻尼,但容易受到声破坏。它们可以产生与自由微泡相同数量级的非线性回声。这些结果表明,CEU可以通过检测被活化的中性粒细胞吞噬的微泡发出的声信号来识别和评估炎症区域。此外,微泡在高声压下的快速膨胀可能提供一种在特定部位破裂中性粒细胞或药物胶囊的方法,从而导致药物的递送。
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Ultrasound contrast agents phagocytosed by neutrophils demonstrate acoustic activity
Ultrasound contrast agents are microbubbles composed of a thin lipid or albumin shell filled with air or a high molecular weight gas. These microbubbles are used for contrast-enhanced ultrasound (CEU) assessment of organ perfusion. In regions of inflammation, microbubbles are phagocytosed intact by activated neutrophils adherent to the venular wall. The authors hypothesized that microbubbles remain acoustically active following phagocytosis. Accordingly, they assessed the physical responses of both phagocytosed and free microbubbles by direct microscopic observation during delivery of repetitive single pulses of ultrasound at various acoustic pressures. Insonation results in oscillation in the bubbles volume. Microbubbles were optically recorded during insonation with a high-speed imaging system and diameter-time curves were analyzed to determine the effect of phagocytosis. Phagocytosed microbubbles retained their acoustic activity, although the intracellular environment increased viscoelastic damping experienced by microbubbles. With a pulse of high acoustic intensity (>1 MPa), phagocytosed microbubbles expanded up to 500% of their initial radii, which occasionally resulted in neutrophil rupture. Primary radiation force displaced phagocytosed microbubbles a distance of 100 microns with an acoustic pressure of -240 kPa and a pulse repetition frequency of 10 kHz, thus providing further evidence of acoustic activity. The authors conclude that phagocytosed microbubbles exhibit viscoelastic damping and yet are susceptible to acoustic destruction. They can generate non-linear echoes on the same order of magnitude as free microbubbles. These results indicate that CEU may be used to identify and assess regions of inflammation by detecting acoustic signals from microbubbles that are phagocytosed by activated neutrophils. In addition, the rapid expansion of a microbubble at high acoustic pressure may present a means to rupture a neutrophil or drug capsule at a specific site, resulting in delivery of a drug.
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