用硅纳米探针快速监测脑化学的皮升液滴生成

Yan Zhang, Ari Esters, O. Bi, Y. Vlasov
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引用次数: 1

摘要

为了监测神经化学物质,同时最大限度地减少脑损伤,开发了一种微透析系统,其流体通道尺寸为5 μm-半径,可容纳在15x50 μm2的硅神经探针中。利用液滴生成来阻止泰勒色散,以获得高时间分辨率。为了扩大在这样一个空间有限的探针中以超低nL/min流速产生单分散液滴的稳定区域,我们改变了t结角,这一参数通常在考虑较大通道时被忽略。在一系列的实验中,我们发现t结角的增加增加了分离挤压和喷射分割的临界毛细数。通过优化几何结构,我们展示了在硅纳米流体通道中产生单分散的pl体积液滴。有限元分析表明,这些影响是由于压差和粘性剪切力之间的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Picoliter Droplet Generation for Fast Monitoring the Brain Chemistry with Scaled Silicon Nanodyalisis Probe
To monitor neurochemicals while minimizing brain damage, a microdialysis system is developed with fluidic channels scaled to 5 μm-radius to fit into 15x50 μm2 silicon neural probe. Droplet generation is utilized to halt Taylor dispersion to achieve high temporal resolution. To extend the stability region for monodisperse droplet generation in such a space-limited probe at ultra-low nL/min flow rates, we varied the T-junction angle, parameter that is typically omitted from consideration for larger channels. In a series of experiments, we found that increase of the T-junction angle increases the critical capillary number separating squeezing and jetting segmentation regimes. With optimized geometry, we demonstrated generation of monodisperse pL-volume droplets in silicon nanofluidic channels. Finite element analysis indicated that these effects are due to interplay between differential pressure and viscous shear forces.
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