High‐Throughput Sorting and Single‐Cell Mechanotyping by Hydrodynamic Sorting‐Mechanotyping Cytometry

Abstract The existence of many background blood cells hinders the accurate identification of circulating tumor cells (CTCs) in the blood of cancer patients. To unlock this limitation, a hydrodynamic sorting‐mechanotyping cytometry (HSMC) integrated with a sorting‐concentration chip and a detection chip is proposed for simultaneously achieving the high‐throughput cell sorting and the multi‐parameter mechanotyping of the sorted tumor cells. The HSMC adopts the spiral inertial microfluidics for label‐free sorting of cells in a high‐throughput manner, allowing the efficient enrichment of tumor cells from the large background blood cells. Then, the sorted cells are concentrated by the concentration unit and finally passed through the detection unit for hydrodynamic deformation. The HSMC has a high throughput for sorting and detection and can successfully reveal the differences in the cellular mechanical properties. After characterizing and optimizing the single chips, the identification of white blood cells (WBCs) and three types of tumor cells (A549, MCF‐7, and MDA‐MB‐231 cells) is successfully achieved. The identification accuracies for WBCs and different tumor cells are all larger than 94%, while the highest identification accuracy is up to 99.2%. This study envisions that the HSMC will offer an avenue for the analysis of single cell intrinsic mechanics in clinical medicine.