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International Journal of Bioprinting                         Application and prospects of 3D printable microgels

















































            Figure 4. 3D Bioprinting of macroporous materials based on entangled hydrogel microstrands. (A) Sizing of the bulk tyramine-modified hyaluronic
            acid (HA-TYR) hydrogels using grids with aperture diameter of 40, 100, and 500 µm. (B, C) 3D printing schematic of HA-TYR bioinks. The cell-laden
            microgels can be printed through a 0.61-mm nozzle and stabilized by secondary crosslinking [(from ref.  licensed under Creative Commons Attribution
                                                                              [96]
            4.0 license)]. (D) The bulk hydrogel forms a microchain structure after mechanical crushing, and has moldability, stability in aqueous solutions, porosity,
            printability. (E) A bioink can be created by embedding cells in bulk hydrogel before sizing that results in a spatial deposition of cells inside the gel phase.
            Alternatively, cells can be mixed in between the already prepared entangled microstrands, so cells occupy the space outside the gel phase [(from ref.
                                                                                                            [97]
            licensed under Creative Commons Attribution 4.0 license)].
            networks: a solid but brittle microgel network and a soft   that the mechanical properties of microgels are sufficient to
            hydrogel network. As a result, this P-DN microgel exhibits   meet the needs of most 3D bioprinting, while also having
            exceptional stretchability. The viscosity, yield stress, and   strong customizability.
            strength of this microgel increase with increasing particle
            concentration, and its fracture toughness is capable of   The flow of hydrogel–microgel during the process of
            reaching 3000 J m −2[98] . Seymour et al. reported a strategy   3D bioprinting differs significantly from the liquid flow of
            involving the mixing of two microgels (GelMA: gelatin)   ordinary hydrogels. In order to achieve an ideal printing
            and the removal of the gelatin microgel after crosslinking,   effect,  there are  still  many  challenges  to be  addressed.
            which resulted in a final microgel with controllable pore   To address this issue, Xin et al. utilized thiol-epoxy PEG
            size by manipulating the mixing ratio and diameter of the   microgel  as biological  ink  and studied  ways to  improve
            two microgels . According to the experimental results,   printing performance . They first constructed microgels in
                       [89]
                                                                                [67]
            these microgels showed a decrease in storage modulus as   three different sizes (single disperse 100 μm, single disperse
            the pore ratio increased, with the highest (pure GelMA   150 μm, and multiple disperse 200 μm) for testing and
            microgel) and lowest ratio (40:60) storage moduli being   found that single disperse microgel could be easily printed
            4.5 ± 1.0 kPa and 177 ± 26 Pa, respectively . It can be seen   by nozzles with diameters of 200–400 μm, while multiple
                                             [89]

            Volume 9 Issue 5 (2023)                         95                         https://doi.org/10.18063/ijb.753
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