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International Journal of Bioprinting                            Low-cost quad-extrusion 3D bioprinting system




































































            Figure 5. Cell viability and proliferation study. (A) 3D-printed 20 × 20 mm sample grid with 5% cell-laden GelMA. (B) Close-up of a strand crossing
            region at 48 h with white-dotted curves identifying the boundaries of the printed GelMA. (C-1) FITC fluorescence imaging of printed sample after LIVE
            staining at 24 h. (C-2) FITC fluorescence imaging of printed sample after LIVE staining at 42 h. (C-3) FITC fluorescence imaging of printed sample after
            LIVE staining at 80 h. (D-1) Close-up region of printed sample after 24 h. (D-2) Close-up region of printed sample after 42 h. (D-3) Close-up region of
            printed sample after 80 h. (E-1) LIVE/DEAD image overlay of a small region of the printed sample at 24 h after printing. (E-2) LIVE/DEAD image overlay
            of a small region of the printed sample at 42 h after printing. (E-3) LIVE/DEAD image overlay of a small region of the printed sample at 80 h after printing.

            maximization of the functionality and capabilities of the   3D printer as can be seen in Table 1. These sets of printable
            bioprinter. For example, when printing with four extruders   volumes achievable are relatively large with regard to the
            in a single construct, the printing volume only reduces to   functionalities and capabilities offered in such a compact
            41.8% of the original printing volume of the Ender 3 Pro   and low-cost bioprinter compared to other printers

            Volume 10 Issue 1 (2024)                       303                        https://doi.org/10.36922/ijb.0159
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