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International Journal of Bioprinting                               Bioprinted liver dECM/GelMA tumor model






















































            Schematic 1. Schematic diagram of the technological approach for this research. Abbreviations: GelMA, gelatin methacrylate; HepG2, human hepatocellular
            carcinoma; LAP, lithium phenyl-2,4,6-trimethylbenzoylphosphinate; 3D, three-dimensional.



            2.2. Preparation and characterization of gelatin   infrared  (FTIR)  spectra of  freeze-dried GelMA were
            methacrylate and decellularized extracellular matrix   obtained using a NICOLET iS50 (Thermo Fisher Scientific,
            Initially, 10 g of gelatin was dissolved in 100 mL of   USA) equipped with a diamond attenuated total reflection
            phosphate-buffered saline (PBS) at 60°C, followed by   module, analyzing  the  functional groups  within  the
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            the slow addition of 3 mL of methacrylic anhydride and   wavenumber range of 4000–500 cm . Thermogravimetric
            stirring at 50°C for 3 h. The reaction was terminated by   analysis was conducted to investigate the thermal weight
            the addition of 500 mL of PBS. The resulting mixture was   loss behavior of gelatin and GelMA (~10 mg). The analysis
            dialyzed against deionized water for 3 days (molecular   was performed under a nitrogen atmosphere, with a gas
            weight: 12–14 kDa). After dialysis, the solution was filtered   flow rate of 50 mL/min and a heating rate of 10°C/min, up
            through a 0.22 µm membrane, and the filtrate was collected,   to a final temperature of 500°C.
            pre-frozen at –80°C, then freeze-dried for 2 days and stored   The preparation of dECM was carried out by combining
            at –20°C in a sealed container. Finally, 20 mg of gelatin   chemical detergent and enzymatic treatment. Initially, 500
            methacrylate (GelMA) sample was dissolved in 1 mL of   g wet liver tissue samples were cut into 10 × 10 mm  pieces
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            deuterium oxide for  proton  nuclear  magnetic  resonance   and cleaned with ultrapure water for 30 min. Subsequently,
            analysis  to  verify  the synthesis.  The Fourier-transform   the samples were treated with a 1% sodium dodecyl sulfate

            Volume 11 Issue 4 (2025)                       394                            doi: 10.36922/IJB025160142
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