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International Journal of Bioprinting                              Bioprinted tissue-on-a-chip in drug screening






















































            Figure 3. Schematic illustrations of different properties of bioinks. (A) The gel state during fabrication and cell culture. Reproduced with permission

            from ref.  (B) Chemical structure of antioxidant ink and its crosslinking process [from ref.  licensed under Creative Commons Attribution (CC BY)].
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            (C) The printed scaffold and the viability of encapsulated cells: (Ⅰ) the printed process of the bioink, and (Ⅱ) the photographs of live/dead staining [from
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            ref.  licensed under Creative Commons Attribution (CC BY)]. (D) Structure and crosslinking process of this bioink [from ref.  licensed under Creative
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            Commons Attribution (CC BY)].
            remarkable mechanical properties of PCL make it a   hydrogel network. This approach may synchronously
            popular choice for cardiac tissue engineering. The rebound   enhance the mechanical properties and physiological
            characteristic of PCL allows it to withstand the great   relevance of the resulting bioinks. Each component in
            pressure from ventricular systole, and the degradation of   these bioinks retains its functionality without interfering
            PCL lasts for 2–3 years.  Synthetic polymers with lower   with others. Khati et al.  employed succinimidyl valerate-
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            gelation temperatures  can be more easily modified to   polyethylene glycol-succinimidyl valerate to connect
            improve cell adhesion. Although these polymers with both   gelatin and dECM. Gelatin enhanced the rheological
            toxicity and lower cell adhesion may go against cell growth,   properties,  and  dECM  promoted  the  physiological
            they are widely used in osteogenic manufacturing.   correlation of the final bioink. The covalent linkage was
                                                               based on the reaction between the succinimidyl valerate
            3.1.4. An example of the multi-component bioink    group and the amino group. To ensure the stability of the
            Multi-component bioinks are mixed after successive   construct, the enzyme tyrosinase was used to facilitate
            combinations, acquiring a stable and complementary   secondary crosslinking. Moreover, the entire fabrication


            Volume 10 Issue 3 (2024)                       180                                doi: 10.36922/ijb.1951
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