Microfluidic Cell Co-Culture Platform With Liquid Fluorocarbon as the Cell Separator
Cell co-culture platforms are essential tools for investigating inter-cellular communication and cellular activities among different cell populations. Microfluidic cell co-culture platforms offer several advantages over their conventional counterparts, including precise control over the cellular microenvironment, low cost, and high throughput. Previously, we have developed microfluidic devices using a hydraulically/pneumatically controlled polydimethylsiloxane (PDMS) valve barrier to separate distinct cell populations in culture, providing a means for manipulation and specific treatment of each cell type with different reagents [1]. After releasing the barrier, different cell populations can interact with each other while being observed using real-time imaging. However, the solid PDMS valve barrier is not truly reversible, as any cells/cell processes underneath the barrier will likely undergo physical damage when the valve barrier is activated.