Suppr超能文献

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.

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。

相似文献

3
Dynamics of sonoporation correlated with acoustic cavitation activities.声穿孔的动力学与声空化活动相关。
Biophys J. 2008 Apr 1;94(7):L51-3. doi: 10.1529/biophysj.107.125617. Epub 2008 Jan 22.
4
Control of Acoustic Cavitation for Efficient Sonoporation with Phase-Shift Nanoemulsions.相移纳米乳剂高效声孔作用的声空化控制。
Ultrasound Med Biol. 2019 Mar;45(3):846-858. doi: 10.1016/j.ultrasmedbio.2018.12.001. Epub 2019 Jan 11.
7
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.
8
Ultrasound Imaging of Microbubble Activity during Sonoporation Pulse Sequences.超声造影在声孔脉冲序列期间对微泡活性的成像。
Ultrasound Med Biol. 2019 Mar;45(3):833-845. doi: 10.1016/j.ultrasmedbio.2018.11.011. Epub 2019 Jan 9.
10
Mechanistic Insight into Sonoporation with Ultrasound-Stimulated Polymer Microbubbles.超声刺激聚合物微泡介导声孔效应的机制洞察
Ultrasound Med Biol. 2017 Nov;43(11):2678-2689. doi: 10.1016/j.ultrasmedbio.2017.07.017. Epub 2017 Aug 25.

引用本文的文献

本文引用的文献

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.
5
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.
9
Cavitation microstreaming and stress fields created by microbubbles.微泡产生的空化微流和应力场。
Ultrasonics. 2010 Feb;50(2):273-9. doi: 10.1016/j.ultras.2009.10.002. Epub 2009 Oct 13.
10
Microfoam formation in a capillary.毛细管中微泡沫的形成。
Ultrasonics. 2010 Feb;50(2):260-8. doi: 10.1016/j.ultras.2009.09.028. Epub 2009 Oct 2.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验