TABLE I.
Common cell identification methods | ||||||
---|---|---|---|---|---|---|
Mechanism type | Differential attributes | Technology | Apparatus or applications | References | ||
Physical | Osmotic tolerance | Hypotonic solution | RBC lysis buffer | 15 | ||
Density | Zonal centrifugation | Mononuclear cell isolation buffer | 6, a 16 | |||
Dimension | Inertial force | Size-dependent Hydrodynamic isolation | 31, a17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30 | |||
Filtration | Microfluidic chip/membrane filters | 32, 33, 34, 35 | ||||
Electric susceptibility | Dielectrophoresis/negative dielectrophoresis | DEP/n-DEP chip | 36, 37, 38, 39, 40 | |||
Impedance | Impedance-test | Impedance-based cytometers | 41, 42, 43, a44a | |||
Elasticity | Deformability-test | Deformability-based chip | 34, 45, 46, 47 | |||
Optical-properties | Forward/side scattering | Flow cytometers | 65, 88, 89 | |||
Raman scattering | Raman spectroscopy | 90, 91, 92, 93 | ||||
Chemical/biological | DNA/RNA profiling | Polymerase chain reaction | Fluorescence labelling gel electrophoresis | Q-PCR/EP-PCR | 48, 49, 50, 51 | |
Antibody specificity | Surface adhesion (trapping cells) | channels | Temperature/pH/light-sensitive gel | Trapping target cells at channel wall | 31, 58, 59, 60 | |
structures | Trapping target cells at pillars | 14, a56, a57 | ||||
objects | Trapping target cells at beads | 61a | ||||
Magnetic beads | Magnetic beads | 17, 52, 53, 54, 55 | ||||
Immuno-fluorescence | Flow cytometry | Flow cytometers | 64, 65, 66 | |||
Microscopy | Cell arrays | 67, 68, 69, 70, 71, 72, 73, 74, 75 | ||||
Fluidic cell chips | 6, 76, 77a | |||||
Bio-capability | To form spheroids, endocytose, balance electrolytes | cell chips | 57, 94 | |||
Integrated system | Using a variety of techniques | Automatic/semi-automatic system | 78, 79, a80, 81 |
Research paper using clinical cancer patient blood.