Papadopoulou Virginie, Evgenidis Sotiris, Eckersley Robert J, Mesimeris Thodoris, Balestra Costantino, Kostoglou Margaritis, Tang Meng-Xing, Karapantsios Thodoris D
Department of Bioengineering, Imperial College London, London, UK; Environmental & Occupational Physiology Lab., Haute Ecole Paul Henri Spaak, Brussels, Belgium.
Department of Chemistry, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Colloids Surf B Biointerfaces. 2015 May 1;129:121-9. doi: 10.1016/j.colsurfb.2015.03.027. Epub 2015 Mar 24.
Vascular gas bubbles are routinely observed after scuba dives using ultrasound imaging, however the precise formation mechanism and site of these bubbles are still debated and growth from decompression in vivo has not been extensively studied, due in part to imaging difficulties. An experimental set-up was developed for optical recording of bubble growth and density on tissue surface area during hyperbaric decompression. Muscle and fat tissues (rabbits, ex vivo) were covered with nitrogen saturated distilled water and decompression experiments performed, from 3 to 0bar, at a rate of 1bar/min. Pictures were automatically acquired every 5s from the start of the decompression for 1h with a resolution of 1.75μm. A custom MatLab analysis code implementing a circular Hough transform was written and shown to be able to track bubble growth sequences including bubble center, radius, contact line and contact angles over time. Bubble density, nucleation threshold and detachment size, as well as coalescence behavior, were shown significantly different for muscle and fat tissues surfaces, whereas growth rates after a critical size were governed by diffusion as expected. Heterogeneous nucleation was observed from preferential sites on the tissue substrate, where the bubbles grow, detach and new bubbles form in turn. No new nucleation sites were observed after the first 10min post decompression start so bubble density did not vary after this point in the experiment. In addition, a competition for dissolved gas between adjacent multiple bubbles was demonstrated in increased delay times as well as slower growth rates for non-isolated bubbles.
使用超声成像技术在水肺潜水后经常能观察到血管气泡,然而这些气泡的确切形成机制和位置仍存在争议,并且由于成像困难,体内减压过程中气泡的生长尚未得到广泛研究。开发了一种实验装置,用于在高压减压过程中对组织表面积上气泡的生长和密度进行光学记录。将肌肉和脂肪组织(离体兔)用氮气饱和的蒸馏水覆盖,并以1巴/分钟的速率进行从3巴到0巴的减压实验。从减压开始每隔5秒自动采集一次图像,持续1小时,分辨率为1.75微米。编写了一个实现圆形霍夫变换的自定义MatLab分析代码,结果表明该代码能够跟踪气泡生长序列,包括气泡中心、半径、接触线和接触角随时间的变化。结果显示,肌肉和脂肪组织表面的气泡密度、成核阈值和脱离尺寸以及聚并行为存在显著差异,而临界尺寸后的生长速率正如预期的那样受扩散控制。在组织基质上的优先位点观察到异质成核现象,气泡在这些位点生长、脱离,新的气泡依次形成。减压开始后前10分钟后未观察到新的成核位点,因此在实验的这一点之后气泡密度没有变化。此外,相邻多个气泡之间对溶解气体的竞争表现为延迟时间增加以及非孤立气泡的生长速率减慢。