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Microscopic Mechanisms of Sonoporation

机译:声孔的显微镜机制

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摘要

Achieving remote and non-invasive molecular delivery to cells is an area of increasing industrial and academic interest. A focus for current research activity involves ultrasound exposure (insonation) in the presence of contrast agent microbubbles, which is known to enhance membrane permeability and lead to molecular uptake from the locale. Under high ultrasound pressures ( > 0.2MPa), this process (sonoporation) can elicit a number of clinically relevant bioeffects such as direct lysis and apoptosis. Moreover, promising observations of tumour regression have been demonstrated in murine studies. However, whilst speculation regarding the physical mechanisms responsible for membrane permeabilization has been widespread, corroboration has, until very recently remained elusive. Here we present further direct observational evidence that illuminates the dynamical processes relating to individual cavitation events near cells and which, we speculate, provides a cogent explanation for previous statistical studies on insonated cell populations using flow cytometry.
机译:实现对细胞的远程和非侵入性分子递送是越来越多的工业和学术兴趣的领域。目前研究活动的重点涉及在存在造影剂微泡存在的情况下进行超声暴露(令人难以令人知不早),其已知可提高膜渗透性并导致来自区域位的分子摄取。在高超声压力(> 0.2MPa)下,该过程(声孔)可以引发许多临床相关的生物效应,例如直接裂解和细胞凋亡。此外,在小鼠研究中已经证明了对肿瘤回归的有希望的观察。然而,关于负责膜透化的物理机制的猜测是普遍的,但粗化,直到最近仍然难以实现。在这里,我们提出了进一步的直接观察证据,使与细胞附近的单个空化事件有关的动态过程,我们推测,我们推测的是对先前使用流式细胞术的令人敏感细胞群的统计研究提供了易用的解释。

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