From: Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells
Technology | Key Features | Merits | Demerits | References |
---|---|---|---|---|
Conventional | Cell size; | Simple; | Low capture rate; | [32] |
Cell density; | Low-cost to operate | Low purity; | Â | |
Surface antigen | Â | Low vitality; | Â | |
 DGC | Cell density | Simple; | Low purity; | [33] |
 | Low-cost to operate | Pretreatment method |  | |
 FACS | Surface antigen; | Fast; | Expensive; | [34] |
Fluorescent fuels; | High purity; | High requirements | Â | |
Flow cytometry | Sort multiple cells Simultaneously | Â | Â | |
 MACS | Surface antigen; | Convenient; | Low purity; | [56] |
Magnetic bead; | Less costly; | Not sorting multiple cells | Â | |
Magnetic Fields | Wide application | Â | Â | |
 Affinity lectin separation | Galactose residue; | Low cost; | Low purity | [44] |
SBA | Simple; | Â | Â | |
 | High capture rate |  |  | |
 Microscope operation | Morphology of stained cells | Convenient; | Expensive; | [60] |
 | For single-cell sorting | High demanding |  | |
Novel | Micro-/nanomaterials; | High sensitivity; | Few clinical applications | [64] |
High throughput; | High capture rate; | Â | Â | |
Miniaturization | High purity; | Â | Â | |
 | High vitality |  |  | |
 Microfiltration chips | Cell size; | Not require biomarkers; | Cell clogging; | [85] |
Cell deformability | Simple to operate; | Low purity; | Â | |
 | High throughput | Low vitality |  | |
 DLD microchips | Cell size; | Not require biomarkers; | Large blood samples; | [91] |
Displacements and directions; | Simple to operate; | Cell clogging; | Â | |
 | High capture rate; | Low purity |  | |
 DEP microchips | Dielectric properties; | Simple to operate; | Electrodes easily electrolyze; | [92] |
Inhomogeneous electric field; | For single-cell sorting | Generate some air bubbles; | Â | |
Displacements and directions | Â | Long sorting time | Â | |
 Acoustic chips | Cell size; | Non-contact manipulability; | Demanding equipment; | [130] |
Acoustic contrast factors | High biocompatibility; | Complex sorting | Â | |
 | Gentleness |  |  | |
 Droplet chips | Incompatible multiphase fluids; | Miniaturization; | High cost; | [144] |
Micro-valve control; | Confinement; | Few clinical application | Â | |
Micro-sized droplets | Parallelism | Â | Â | |
 Immunoaffinity microchips | Surface antigen; | High capture rate; | Few clinical applications | |
Immunoaffinity | High purity; | Â | Â | |
 | High vitality |  |  | |
 Static nano-substrates | Surface antigen; | Easy to operate; | Non-specific cells adhesion | |
Immunoaffinity; | High capture rate | Â | Â | |
Nanomaterials; | Â | Â | Â | |
Nanomembranes | Â | Â | Â | |
 Dynamic nano-substrates | Surface antigen; | Reduce WBCs adhesion; | Microbeads easily cluster | |
Immunoaffinity; | Simple and low cost; | Â | Â | |
Magnetic beads | High throughput | Â | Â |