Magnetic sorting using magnetic beads has become a routine methodology for the separation of key cell populations from biological suspensions. Due to the inherent ability of magnets to provide forces at a distance, magnetic cell manipulation is now a standardized process step in numerous processes in tissue engineering, medicine, and in fundamental biological research. Herein we review the current status of magnetic particles to enable isolation and separation of cells, with a strong focus on the fundamental governing physical phenomena, properties and syntheses of magnetic particles and on current applications of magnet-based cell separation in laboratory and clinical settings. We highlight the contribution of cell separation to biomedical research and medicine and detail modern cell separation methods (both magnetic and non-magnetic). In addition to a review of the current state-of-the-art in magnet-based cell sorting, we discuss current challenges and available opportunities for further research, development and commercialization of magnetic particle-based cell separation systems.

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A first order transition from a paramagnetic-austenite phase to a ferromagnetic-martensite phase occurring in off-stoichiometry single crystals of Ni 2 MnGa at 313 K presents unique features due to the multifunctional character of the magnetic shape memory alloy. A remarkable magnetocaloric effect, associated with an entropy change up to ΔS≈−86 J kg−1 K−1 and an adiabatic temperature change ΔT≈2.2 K, accompanied by mechanical strain Δε⩾3% have been observed in samples subjected to changes of the applied magnetic field ΔH=4×106 A∕m (≈5 T). The effects of magnetic field, temperature, and stress on the entropy variationΔS are quantified and compared.

The microstructure and the room-temperature hysteretic magnetic properties of sputtered, 10 nm thin films of equiatomic binary alloys of CoPt and FePt were characterized using transmission electron microscopy (TEM) and a superconducting quantum interference device (SQUID) magnetometer. A transformation from an atomically disordered, face-centered-cubic structure to the L10 ordered structure occurred during postdeposition annealing and was characterized using digital analysis of dark-field TEM images. The transformation was observed to follow first-order nucleation and growth kinetics, and the ordered volume fraction transformed was quantified at numerous points during the transformation. The ordered volume fraction was then compared to the magnetic coercivity data obtained from the SQUID magnetometer. In contrast to the relationship most commonly described in the literature, that the highest coercivity corresponds to a two phase ordered/disordered mixture, the maximum value for coercivity in this study was found to correspond to the fully ordered state. Furthermore, in samples that were less than fully ordered, a direct relationship between ordered volume fraction and coercivity was observed for both CoPt and FePt. The proposed mechanism for the high coercivity in these films is an increasing density of magnetic domain wall pinning sites concurrent with an increasing fraction of ordered phase.