TABLE 3.
Comparison of the three types of 3-D bioprinting techniques.
Jetting-based | Extrusion-based | Laser-based | |
Printer cost | Low | Moderate | High |
Biomaterial viscosity | Medium | High | Medium to high |
Print speed | Fast (1–10,000 droplets/s) | Slow (10–50 μm/s) | Medium-fast (200–1,600 mm/s) |
Cell viability (%) | 80%–90% | 40%–95% | 95% |
Resolution | High (up to 50 μm) | Moderate (100 μm to millimeters) | High (10–50 μm) |
Cell densities | Low (≤106 cells/ml) | High (cell spheroids) | Medium (≤108 cells/ml) |
Quality of vertical structure | Poor | Good | Fair |
Advantage | High cell viability; High printing speeds; Low cost; Wide availability; Easy operation | High cell densities; High cell viability; Broad selection of biomaterials; High deposition rates; High print speeds; Anatomically correct porous construct generation | Nozzle free; Fast and accurate fabrication; High resolution; High precision; High cell viabilities |
Disadvantage | Low droplet directionality; Nozzle clogging; Limited biomaterials selection; Low cell density and concentration of the ink; Heat and sheer stresses induced damage to cells | Low resolution; Deformation; Encapsulated cell apoptosis; Low cell viability | High cost; Low speed; Low built capability; Possible cytotoxicity; UV induced DNA damage; Low stability and scalability; Limited printing directionality |
Tissue engineering application | Blood vessel, bone, cartilage, neuron, liver | Blood vessel, bone, lungs, liver, cartilage, neuron, muscle, ear, skin, lipid bilayers | Blood vessel, bone, skin, adipose, cardiac tissue |
References | Irvine and Venkatraman (2016), Roseti et al. (2018), Roseti et al. (2017) | Cole et al. (2009), Hasan et al. (2014), Daly et al. (2016), Pillai et al. (2018), Dhawan et al. (2019) | Roseti et al. (2018), Dhawan et al. (2019), Irvine and Venkatraman (2016) |