Hydrody-namic method
|
Droplet [27] |
High-throughput, simple chip structure with great flexibility |
Difficult to culture adherent cell, difficult to introduce biochemicals into droplets |
250 µL/h |
75% |
-- |
Inertial [55] |
High throughput, high cell viability, and simple chip |
Only work well under specific flow rates and cell concentrations |
3 mL/min |
84% |
-- |
Vortex [58] |
Has no strict requirement about the properties of cells and fluid |
Require external controller, low single-cell efficiency |
-- |
-- |
Cell rotation 3.5 ± 2.1° s−1
|
Micro-valve [60] |
Reliable and fast for control, suitable for large-scale integration |
Require complex and cumbersome external control devices |
96 cells/chip |
90.6 ± 8% |
-- |
Micro-structure [60] |
Simple for operation, high throughput |
Inflexibility, hard to control specific single-cell |
10000 cells/chip |
90% |
-- |
Electrical method
|
Dielectro-phoresis [20] |
Contactless, high selectivity, label-free |
Require low-conductivity buffer |
3264 pair of cells/chip |
74.2% |
-- |
Electro-osmosis [70] |
Label-free, easy for integrated fabrication |
Low efficiency and accuracy with increased flow rate |
81 cells/chip |
73% |
-- |
Optical method
|
Optical tweezer [12] |
High accuracy and efficiency |
Low throughput, high cost |
-- |
97% |
98% |
ODEP [76] |
Flexible virtual electrodes, label-free, simple and low-cost |
Require low-conductivity solution, opaque substrate |
Scalable |
-- |
-- |
Opto-thermocapillary [77] |
Flexible, can pattern single cells in hydrogel with high viability |
High cost for cumbersome peripherical optical system |
Low |
High |
High |
Acoustic method [23] |
Noninvasive, label-free, good penetrability |
Need piezoelectric substrate for chip fabrication |
High |
-- |
High |
Magnetic method [81] |
Reliable and highly efficient |
Not label-free |
200 µL/min |
> 85% |
> 80% |
Micro-robot-assisted method [84] |
High accuracy, flexible and controllable |
Low throughput |
Low |
High |
-- |