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International Journal of Bioprinting                              Droplet-based bioprinting of tumor spheroids




            Table 1. Summary of droplet-based bioprinting technologies
             Droplet-based bioprinting   Main process   Droplet   Cell viability   Advantages  Disadvantages
             method             parameters    diameter   (%)
                                              (μm)
             Thermal inkjet bioprinting  Heat  30–60    75–90      Low cost and high   Low cell viability and ease of
                                                                   throughput          clogging with viscous bioinks
             Piezoelectric inkjet   Waveform,   25–100  70–90      Wide range of droplet diam-  Large shear stress due to rapid
             bioprinting        amplitude, and                     eter and low voltage  change of pressure, satellite
                                frequency of                                           droplets, and nozzle clogging
                                voltage pulse                                          with viscous bioinks
             Electrostatic bioprinting  Frequency of   10–60  ~70  High throughput (up   Low cell viability
                                voltage pulse, vis-                to 2 kHz), suitable for
                                cosity of bioink                   high-viscous bioink, and
                                                                   high precision
             Electrohydrodynamic jet   Voltage, flow rate,  10–1000  >90 (~95)  Low shear stress, adapting   Requirement of high voltage
             bioprinting        distance between                   to highly viscous bioinks,   (5–20 kV), multiple droplets
                                nozzle tip and                     and a wide range of droplet   ejection, and specialized
                                substrate                          diameter            substrate
             Microvalve-based   Pneumatic     100–600   85–95      High cell viability, high fre-  Large droplet diameter and high
             bioprinting        pressure, valve                    quency (up to 1 kHz), and a   shear stress
                                gating time,                       wide range of viscosity
                                nozzle length,
                                and geometry
             Acoustic           Amplitude and   10–200  >90 (90–99)  Nozzle-free, no clogging, no  Complex structures and
             bioprinting        frequency of                       mechanical stress on cells,   complicated operations
                                acoustic wave                      and large spray angle
             Microfluidic bioprinting  Flow rate,   >10  >95       Droplet generation at high   Polydimethylsiloxane (PMDS) is
                                hydrophilicity/                    throughput, controlled   prone to penetration, aging with
                                hydrophobicity of                  composition of droplets,   poor thermal stability
                                pipeline                           and miniaturization


































            Figure 2. Schematic of droplet-based bioprinting technologies. (A) Inkjet bioprinting, including TIJ, PIJ, and EIJ. (B) Electrohydrodynamic jet bioprinting.
            (C) Microvalve-based bioprinting. (D) Acoustic bioprinting. (E) Microfluidic bioprinting.


            Volume 10 Issue 1 (2024)                       110                          https://doi.org/10.36922/ijb.1214
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