Reducing Cancer Cell Adhesion using Microtextured Surfaces

For the past century, trypsin has been the primary method of cell dissociation, largely without any major changes to the process. Enzymatic cell detachment strategies for large‐scale cell culturing processes are popular but can be labor‐intensive, potentially lead to the accumulation of genetic mutations, and produce large quantities of liquid waste. Therefore, engineering surfaces to lower cell adhesion strength could enable the next generation of cell culture surfaces for delicate primary cells and automated, high‐throughput workflows. In this study, a process for creating microtextured polystyrene (PS) surfaces to measure the impact of microposts on the adhesion strength of cells is developed. Cell viability and proliferation assays show comparable results in two cancer cell lines between micropost surfaces and standard cell culture vessels. However, cell image analysis on microposts reveals that cell area decreases by half, and leads to an average twofold increase in cell length per area. Using a microfluidic‐based method up to a seven times greater percentage of cells are removed from micropost surfaces than the flat control surfaces. These results show that micropost surfaces enable decreased cell adhesion strength while maintaining similar cell viabilities and proliferation as compared to flat PS surfaces. Cancer cells are grown on microtextured polystyrene surfaces in order to study the impacts of surface texture alone on cell growth and cell adhesion. Microposts result in changes to cell shape and size, as well as reduced cell–surface adhesion strength, while cell viability and proliferation remain the same as on standard, flat surfaces.