Skip to main content
. 2022 Sep 15;122(22):16839–16909. doi: 10.1021/acs.chemrev.1c00798

Table 2. Advantages and Disadvantages of Microfluidic and Various Nonmicrofluidic Methods of Formulation of Topological Microtissues.

method complexity of the generated microtissue size and monodispersity of the generated microtissue throughput complexity of the experimental setup degree of automation of the formulation process organic solvents (potential cytotoxicity)
microwells “0D” structures (no compartments) no size limit; monodispersity low low low; no special equipment required low; manual one-step process (pipetting) no
layer-by-layer (LbL) assembly “0D” structures of core–shell topology (1 cellular compartment) monodispersity and size depending on the process of core generation mode rate low to high depending on the process of core generation moderate; involves a number of manual washing steps (same as the number of shells) no
superhydrophobic surfaces “0D” structures of core–shell topology (2 cellular compartments) >1000 μm (limited by the pipetted volume); monodispersity high low low; no special equipment required low; manual one-step or multistep process (when combined with LbL) no
micropatterning based methods “0D” or “2D” structures of Janus topology (2 cellular compartments) >50 μm; monodispersity high mode rate moderate; requires microfabrication moderate. automation limited; requires calibration/optimization of the setup no
electrospray/electrospinning complex “0D” and “1D” structures of core–shell or Janus topologies (multiple cellular compartments) 200–500 μm; monodispersity high high moderate; requires specialized equipment high; automated process; requires calibration/optimization of the setup no
3D printing of adhesive droplets complex “2D” and “3D” structures of Janus topologies (multiple cellular compartments) >1000 μm; monodispersity moderate moderate to high high; requires specialized equipment and microfabrication high; automated process; requires calibration/optimization of the setup yes/no
microfluidics/microfluidic spinning. Complex “0D”, “1D”, “1.5D”, “2D”, and “3D” structures of core shell and Janus topologies (multiple cellular compartments) 100–500 μm; monodispersity high high to very high high; requires specialized equipment and microfabrication high; automated process; requires calibration/optimization of the setup yes/no