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脉冲超声暴露介导声孔效应时微泡群动态活动的表征

Characterization of the dynamic activities of a population of microbubbles driven by pulsed ultrasound exposure in sonoporation.

作者信息

Fan Zhenzhen, Chen Di, Deng Cheri X

机构信息

Department of Biomedical Engineering, University of Michigan, 2200 Bonisteel Boulevard, Ann Arbor, Michigan, USA.

Department of Biomedical Engineering, University of Michigan, 2200 Bonisteel Boulevard, Ann Arbor, Michigan, USA.

出版信息

Ultrasound Med Biol. 2014 Jun;40(6):1260-72. doi: 10.1016/j.ultrasmedbio.2013.12.002. Epub 2014 Jan 30.

DOI:10.1016/j.ultrasmedbio.2013.12.002
PMID:24486236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4011999/
Abstract

Ultrasound-driven microbubble activities have been exploited to transiently disrupt the cell membrane (sonoporation) for non-viral intracellular drug delivery and gene transfection both in vivo and in vitro. In this study, we investigated the dynamic behaviors of a population of microbubbles exposed to pulsed ultrasound and their impact on adherent cells in terms of intracellular delivery and cell viability. By systematically analyzing the bubble activities at time scales relevant to pulsed ultrasound exposure, we identified two quantification parameters that categorize the diverse bubble activities subjected to various ultrasound conditions into three characteristic behaviors: stable cavitation/aggregation (type I), growth/coalescence and translation (type II) and localized inertial cavitation/collapse (type III). Correlation of the bubble activities with sonoporation outcome suggested that type III behavior resulted in intracellular delivery, whereas type II behavior caused the death of a large number of cells. These results provide useful insights for rational selection of ultrasound parameters to optimize outcomes of sonoporation and other applications that exploit the use of ultrasound-driven bubble activities.

摘要

超声驱动的微泡活性已被用于在体内和体外短暂破坏细胞膜(声孔效应),以实现非病毒细胞内药物递送和基因转染。在本研究中,我们研究了暴露于脉冲超声的一群微泡的动态行为,以及它们在细胞内递送和细胞活力方面对贴壁细胞的影响。通过系统地分析与脉冲超声暴露相关时间尺度下的气泡活性,我们确定了两个量化参数,这些参数将在各种超声条件下的不同气泡活性分为三种特征行为:稳定空化/聚集(I型)、生长/合并和平移(II型)以及局部惯性空化/崩溃(III型)。气泡活性与声孔效应结果的相关性表明,III型行为导致细胞内递送,而II型行为导致大量细胞死亡。这些结果为合理选择超声参数以优化声孔效应及其他利用超声驱动气泡活性的应用的结果提供了有用的见解。

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本文引用的文献

1
Improving ultrasound gene transfection efficiency by controlling ultrasound excitation of microbubbles.通过控制超声微泡激发来提高超声基因转染效率。
J Control Release. 2013 Sep 28;170(3):401-13. doi: 10.1016/j.jconrel.2013.05.039. Epub 2013 Jun 11.
2
Spatiotemporally controlled single cell sonoporation.时空控制的单细胞声孔法。
Proc Natl Acad Sci U S A. 2012 Oct 9;109(41):16486-91. doi: 10.1073/pnas.1208198109. Epub 2012 Sep 24.
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An in vivo validation of the application of acoustic radiation force to enhance the diagnostic utility of molecular imaging using 3-d ultrasound.利用三维超声的声辐射力增强分子成像的诊断效用的体内验证。
Ultrasound Med Biol. 2012 Apr;38(4):651-60. doi: 10.1016/j.ultrasmedbio.2011.12.005. Epub 2012 Feb 15.
4
Dependence of aggregate formation of microbubbles upon ultrasound condition and exposure time.微泡聚集体形成对超声条件和暴露时间的依赖性。
Annu Int Conf IEEE Eng Med Biol Soc. 2011;2011:5589-92. doi: 10.1109/IEMBS.2011.6091352.
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Controlled permeation of cell membrane by single bubble acoustic cavitation.单泡空化超声致细胞膜受控渗透。
J Control Release. 2012 Jan 10;157(1):103-11. doi: 10.1016/j.jconrel.2011.09.068. Epub 2011 Sep 16.
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Real-time technique for improving molecular imaging and guiding drug delivery in large blood vessels: in vitro and ex vivo results.实时技术提高大型血管内分子成像和药物输送的效果:体外和离体结果。
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Targeted gene transfection from microbubbles into vascular smooth muscle cells using focused, ultrasound-mediated delivery.利用聚焦超声介导传递技术,将靶向基因从微泡转染到血管平滑肌细胞中。
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Microbubble mediated sonoporation of cells in suspension: clonogenic viability and influence of molecular size on uptake.悬浮细胞的微泡介导声孔法转染:集落形成活力和分子大小对摄取的影响。
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Cavitation microstreaming and stress fields created by microbubbles.微泡产生的空化微流和应力场。
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Microfoam formation in a capillary.毛细管中微泡沫的形成。
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