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Quantification of microfluidic dye mixing using front line tracking in curvature scale space

机译:使用前线跟踪在曲率鳞片空间中进行微流体染料混合的定量

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Microfluidic mixing or mixing at low Reynolds number is dominated by viscous forces that prevent turbulent flow. It therefore differs from conventional mixing(e.g., stirring milk into coffee), as it is driven primarily by diffusion. Diffusion is in turn dependent on(i)the concentration gradient along the interface between two fluids(dye front line)and(ⅱ)the extent of the interface itself. Previously, we proposed an in vivo method to microscopically monitor the mixing interface using Shannon information entropy as mixing indicator and explored the use of length of dye front line as an indirect measure of mixing efficiency. In this work, we present a robust image processing chain supporting quantitative measurements. Based on data from ciliated surfaces mixing dye and water, the dye-water interface front line is extracted automatically using the following processing steps:(i)noise reduction(average filtering)and down sampling in time to reduce compression artifacts;(ⅱ)subtraction imaging with key reference frames in RGB color space to remove background;(ⅲ)segmentation of dye based on color saturation in HSV color space;(ⅳ)extraction of front line;(ⅴ)curve smoothing in curvature scale space(CSS)with an improved Gaussian filter adaptive to the local concentration gradient; and(vi)extraction of length. Evaluation is based on repeated measurements. Reproducibility in unaltered animals is shown using intra- and inter-animal comparison. Future work will include a more comprehensive evaluation and the application to datasets with multiple classes.
机译:在低雷诺数微流体混合或混合是通过粘滞力,以防止湍流支配。因此,从常规的混合不同(例如,牛奶搅拌成咖啡),因为它是由扩散主要驱动。扩散是又取决于(ⅰ)沿两种流体(染料前线)和(ⅱ)的界面本身的程度之间的界面处的浓度梯度。以前,我们在体内方法提出了一种使用信息熵作为混合指标显微镜监测混合接口和探索了使用染料前线的长度作为混合效率的间接量度。在这项工作中,我们提出支撑定量测量鲁棒图像处理链。基于从纤毛表面,所述染料 - 水界面前线被自动提取使用以下处理步骤混合染料和水的数据:(ⅰ)降噪(平均滤波)和向下时间采样,以减少压缩伪像;(ⅱ)减法前线的萃取(ⅳ);(ⅲ)染料的分割基于在HSV颜色空间中的颜色饱和度;与在RGB颜色空间键的参考帧以去除背景成像(ⅴ)在曲率尺度空间(CSS)与曲线平滑改进的高斯滤波器自适应于局部浓度梯度;和(vi)萃取长度。评估是基于重复测量。再现性在未改变的动物使用内和动物间比较而示出。未来的工作将包括一个更全面的评估,并应用到多类数据集。

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