研究目的
To monitor neurochemicals while minimizing brain damage by developing a microdialysis system with scaled fluidic channels for high temporal resolution.
研究成果
Demonstrated generation of monodisperse droplets in silicon channels, with volume controllable within 1-20pL. Found that larger T-junction angles result in larger droplet volumes and higher critical capillary numbers, favoring squeezing over jetting regimes.
研究不足
Scaled channels restrict droplet volume and require sub-nL/min flow rates, making control difficult.
1:Experimental Design and Method Selection:
Developed a microdialysis system with fluidic channels scaled to 5 μm-radius to fit into a silicon neural probe. Utilized droplet generation to halt Taylor dispersion.
2:Sample Selection and Data Sources:
Used water with fluorescent dye as dispersed phase and octanol as continuous phase.
3:List of Experimental Equipment and Materials:
Silicon nanofluidic channels, PDMS layer, capillaries with 250μm ID.
4:Experimental Procedures and Operational Workflow:
Fabricated silicon nanofluidic structures, varied T-junction angle, characterized droplet generation.
5:Data Analysis Methods:
Used computer vision algorithm to extract droplet volume, performed finite element analysis.
独家科研数据包,助您复现前沿成果,加速创新突破
获取完整内容