“…HD methods mainly use the shape and the size of the bioparticles to manipulate them; therefore, mainly HD devices have been proposed for separation and sorting of (bio)particles by size [16-18,21-27,29-31,33-35,37-39,114,115] and shape [19,18,20,28,40]. Separation by size includes (i) enrichment of low-concentrated cancer cells from the peritoneal wash [114], separation of plasma from whole blood [115] using filtration, (ii) separation of white blood cells (WBCs) and RBCs [17], separation of plasma from whole blood [17], separation of parasites from human blood [19], capturing of circulating tumor cells (assisted by affinity-based cell culture) using DLD, (iii) separation of RBCs and WBCs [22] and separation of U937 (human leukemic monocyte lymphoma cell line) cells at different phase using hydrophoresis, (iv) enrichment of leukocyte [30] using PFF, and (v) separation of Escherichia coli from RBCs, separation of WBCs, MCF-7 and MDA-MB-231 breast cancer cells [116], focusing of Jurkat and MCF7 (a breast carcinoma cell line) [38], separation of HeLa and MCF cells [34], focusing of HeLa and Jurkat cells [39], separation of plasma from whole blood [117] using inertial microfluidics.…”