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非空化靶向微泡介导的单细胞声孔效应

Non-Cavitation Targeted Microbubble-Mediated Single-Cell Sonoporation.

作者信息

Liu Xiufang, Zhang Wenjun, Jing Yanshu, Yi Shasha, Farooq Umar, Shi Jingyao, Pang Na, Rong Ning, Xu Lisheng

机构信息

College of Medicine and Biological Information Engineering, Northeastern University, 195 Innovation Road, Shenyang 110016, China.

Paul C. Lauterbur Research Center for Biomedical Imaging, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.

出版信息

Micromachines (Basel). 2022 Jan 11;13(1):113. doi: 10.3390/mi13010113.

Abstract

Sonoporation employs ultrasound accompanied by microbubble (MB) cavitation to induce the reversible disruption of cell membranes and has been exploited as a promising intracellular macromolecular delivery strategy. Due to the damage to cells resulting from strong cavitation, it is difficult to balance efficient delivery and high survival rates. In this paper, a traveling surface acoustic wave (TSAW) device, consisting of a TSAW chip and a polydimethylsiloxane (PDMS) channel, was designed to explore single-cell sonoporation using targeted microbubbles (TMBs) in a non-cavitation regime. A TSAW was applied to precisely manipulate the movement of the TMBs attached to MDA-MB-231 cells, leading to sonoporation at a single-cell level. The impact of input voltage and the number of TMBs on cell sonoporation was investigated. In addition, the physical mechanisms of bubble cavitation or the acoustic radiation force (ARF) for cell sonoporation were analyzed. The TMBs excited by an ARF directly propelled cell membrane deformation, leading to reversible perforation in the cell membrane. When two TMBs adhered to the cell surface and the input voltage was 350 mVpp, the cell sonoporation efficiency went up to 83%.

摘要

声孔效应利用超声波并伴随微泡空化来诱导细胞膜的可逆破坏,已被开发为一种有前景的细胞内大分子递送策略。由于强烈空化对细胞造成的损伤,很难在高效递送和高存活率之间取得平衡。在本文中,设计了一种由行波表面声波(TSAW)芯片和聚二甲基硅氧烷(PDMS)通道组成的行波表面声波装置,以探索在非空化状态下使用靶向微泡(TMB)进行单细胞声孔效应。应用行波表面声波精确操纵附着在MDA-MB-231细胞上的靶向微泡的运动,从而在单细胞水平上实现声孔效应。研究了输入电压和靶向微泡数量对细胞声孔效应的影响。此外,还分析了气泡空化或声辐射力(ARF)对细胞声孔效应的物理机制。由声辐射力激发的靶向微泡直接推动细胞膜变形,导致细胞膜出现可逆穿孔。当两个靶向微泡附着在细胞表面且输入电压为350 mVpp时,细胞声孔效应效率高达83%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe8/8780975/8de53600654e/micromachines-13-00113-g001.jpg

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