TABLE 3.
Summary and comparison of microfluidic technologies.
| Approach | Fundamental principle | Applicable objects | Advantages | Limitations |
|---|---|---|---|---|
| Cellular rheology measurement | The deformation of cells in microchannels was measured by hydrodynamics | Blood cells, liver cells and lung cells | Fast measurement speed, high precision and repeatability | The cells need to be treated to obtain a certain cell concentration, and the cells are subject to shear forces, resulting in measurement errors |
| Optical deformation measurement | Stretching cells through two interacting light beams in a microfluidic channel to produce cell deformation | Red blood cells, White blood cells, stem cells, fibroblasts and cancer cells | Fast measurement speed, low sample consumption, low experimental cost, automatable and highly controllable | Multiple parameters cannot be measured simultaneously, special optical equipment is required, and assumptions about cell shape may affect the accuracy of the measurement results |
| Real-time deformability cytometry measurement method | The deformation properties of cells are measured and analyzed by applying different levels of shear force to induce cell deformation and recording the deformation process by a fast imaging system | Cancer cells, immune cells, and red blood cells | Real-time detection, high-throughput measurement, no damage to cells | Shear force may have an impact on the physiological functions of cells, leading to errors in measurement results, and the high cost of equipment and operation limits its popularity in practical applications |