Hello ! I am presently working on a microfluidic chip aiming at capturing hundreds of cells in an array of capture chambers. To inject the cells inside the platform, we use either 1) small reservoirs filled with the cell solution (1 mL) plugged to our chip through Tygon tubing or 2) 200 µL pipette tips filled with the cell solution direclty put in the chip inlets. Both systems are then hooked to a pressure controller to create flow. However, we encounter a very high amount of cell sedimentation directly at the chip inlets, causing loss of object and improper injection inside the platform. Any ideas to overcome these problems would be very useful. Thanks !

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