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International Journal of Bioprinting                              Light-based muscle bioprinting with bioglass




            of muscle-like construct  bioprinting using  our  light-  Figure 5A shows the viability of myoblasts cultured in
            based cost-effective printer.                      GelMA constructs, with and without MBGNs, at different
                                                               experimental times as measured in Live/Dead staining
            3.4. Cell viability, alignment, and elongation     assays. A high cell viability was observed immediately after
            Next, we explored the feasibility of the application of our   bioprinting in pristine GelMA constructs (94.76 ±10.7%)
            light-based printer as a bioprinter. For this, we selected a   and GelMA with MBGNs (91.25 ± 7.34%), as confirmed by
            muscle tissue engineering application as a model example.   Live/Dead assays (see Figure 5B). High viability, sustained
            We incorporated C2C12 myoblasts to GelMA-based     through the first 8 days of culture (i.e., viabilities greater
            inks with and without MBGNs. In these bioprinting   than 80%) (Figure 5B), suggested that the bioprinting
            experiments, we focused on analyzing the potential   process did not compromise the main cellular functions.
            effect of low-power laser-assisted bioprinting and the   We did not observe significant differences in cell viability
            incorporation of MBGNs on critical processes such as cell   between GelMA constructs with and without MBGNs at
            proliferation, spreading, metabolic activity, and alignment   the particle concentrations tested. However, significant
            in muscle cell-laden constructs.                   differences in cell viability were observed on day 15,



















































            Figure 5. Bioprinted skeletal muscle GelMA constructs without (control) and with MBGNs. (A) Assessment of the cell viability in the bioprinted constructs
            using Live/Dead staining at different time points (i.e., 1, 3, 6, 9, 12, 15 and 20 days of culture). Scale bar: 200 μm. (B) Cell viability in control constructs
            (black bars) and with MBGNs (gray bars) after 1, 3, 6, 9, 12, 15, and 20 days of culture, as determined by image analysis of the live/dead stained images. *p
            <0.05. (C) Metabolic activity in constructs printed without (black bars) and with MBGNs (gray bars) at different time points (i.e., 1, 3, 6, 9, 12, 15, and 20
            days of culture), as determined by the Presto Blue assay. *p < 0.001.


            Volume 10 Issue 4 (2024)                       558                                doi: 10.36922/ijb.1830
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