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International Journal of Bioprinting                              Light-based muscle bioprinting with bioglass




































            Figure 2. Geometry and dimensions of the GelMA-based constructs used for the assessment of printability and resolution (A), for the bioprinting
            experiments using C2C12 cells (B), and for mechanical testing (C). The thin features of the constructs (characteristic widths), used to define the resolution
            limits, are indicated with W  to W .
                              a  e

            manufactured using benchtop SLA-LF 3D Form 3       biological assessment had dimensions of 3.6 mm (length)
            (Formlabs, Somerville, MA, USA) additive manufacturing   × 3.6 mm (width) × 0.8 mm (height).  The parameters
            equipment, using a High Temp FLTHAM02 resin        considered for the bioprinting process were normal layer
            (Formlabs, Somerville, MA, USA). A 0.15-mm thick   exposure time (LT), first layers exposure time (FLT), and
            FEP  film  (ELEGOO,  Shenzhen,  China)  was  cut  and   layer thickness (LTh), which were fixed to 35 s, 60 s, and 50
            placed between the frame and enclosure. A custom-  μm, respectively.
            made build plate was manufactured in aluminum  using
            subtractive manufacturing.                         2.4. Mechanical testing
                                                               The mechanical tensile properties of the hydrogels used in
            2.3. Bioprinted constructs and                     the experiments were evaluated with a Universal Testing
            manufacturing parameters                           Machine (3365 Instron, UK). To prepare the samples
            Three types of constructs (see Figure 2) were designed and   for tensile assays, bone-shape testing constructs were
            fabricated to assess the performance of the bioprinter in   fabricated following ASTM D638 standard with a thickness
            terms of resolution and fidelity, and capability to produce
            adequate GelMA scaffolds for musculoskeletal microtissues   Table 1. Printing parameters used in printing and bioprinting
            and the presence or absence of MBGNs. Figure 2A depicts   experiments
            the first type of construct that contains eight bridges or
            filaments patterns of a length of 2.1 mm and a variation   Parameter  Name            Value
            of the pattern width dictated by the system’s LCD pixel   BLT  Bottom layer exposure   50 s
            resolution, ranging from 35 to 280 μm. An alternative               time
            design was selected (Figure 2B). This second design had   LT   Layer exposure time     37 s
            dimensions of 6.6 mm (length) × 6.6 mm (width) × 1   NBL      Number of bottom layers   2
            mm (height).  Table 1 summarizes the different features   LH      Layer height        50 µm
            evaluated during the assessment. After determining   W        Pattern scaffold widths  W =35 µm, W =70 µm,
                                                                                              a
                                                                                                      b
            which  was  the  thinnest  feature  that  can  be  created  with   x            W =105 µm, W =140 µm,
                                                                                                      d
                                                                                             c
            this process, a second pattern was designed  to be used                         W =175 µm, W = 210 µm,
                                                                                                      f
                                                                                             e
            for cell-laden constructs (Figure 2B). The design used for                      W =245 µm, W = 280 µm
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            Volume 10 Issue 4 (2024)                       553                                doi: 10.36922/ijb.1830
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