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International Journal of Bioprinting                                  3D-printed contractive pennate muscle





















































            Figure 4. Contraction simulation of pennate and parallel muscle models. (A) Boundary condition settings for mechanical simulation. (B) Contraction
            displacement and strain of respective pennate and parallel muscle models.


            long axis on total deformation was also investigated for   employed as bioinks for 3D printing. Phosphate-buffered
            microstructural design optimization. As a result, the   saline (PBS; Corning, United States of America [USA])
            compression force was applied along the direction of the   was utilized for washing cells and tissues. Growth medium
            pennate angle on the model to simulate the force output   (GM) was composed of 89% Dulbecco’s modified Eagle’s
            of the pennate myotubes. The total deformation and   medium (DMEM, Corning, USA), 10% fetal bovine
            equivalent strain of the model were then calculated. Finally,   serum (FBS; FSP500; Excell, China), and 1% penicillin-
            the deformation performance of muscle models, including   streptomycin solution (PS; PB180120; Procell, China).
            macro and microparameters, was evaluated based on the   Differentiation medium (DM) was composed of 89%
            simulation results (Figure 4B).                    DMEM, 10% horse serum (HS; SH30074.02; Cytiva, USA),
                                                               1% PS, 1 mg/mL 6-aminocaproic acid (ACA; A7824-25G;
            2.3. Materials                                     Sigma-Aldrich, USA), and 50 ng/mL insulin-like growth
                                                               factor (IGF-1; I8830; Solarbio, China). Trypsin-EDTA
            C2C12  mouse  skeletal  myoblasts  (CL-0044;  Pricella,   (25200072; Gibco, USA) was applied to digest cells from
            China) under five passages, gelatin methacryloyl   petri dishes. The Live/Dead Viability/Cytotoxicity Kit
            (GelMA; GM-60; EFL, China), and lithium phenyl-2,4,6-  (L3224; Invitrogen, USA), consisting of calcein AM and
            trimethylbenzoylphosphinate (LAP; EFL, China) were   ethidium homodimer-1 (EthD-1), was exploited for

            Volume 10 Issue 6 (2024)                       249                                doi: 10.36922/ijb.4371
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