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International Journal of Bioprinting                               3D-printed scaffold for biomolecule delivery




















































            Figure 2. Characterization of the gelatin-silica (GS) composite xerogel bulk. (a) Illustration of the experimental procedure for characterizing the bulk-type
            xerogel. (b) optical images of the xerogel bulk produced by gelatin ratio without (upper) and with (bottom) 100 μg/mL of Cyt c as a model protein. Scale
            bars: 5 mm. (c) Attenuated total reflectance Fourier transform infrared (ATR FTIR) spectra display the differences in the interactions between specific
            molecules in silica xerogel, gelatin, and GS composite. (d and e) Degradation (d) and release of Cyt c (e) from xerogel bulk in phosphate-buffered saline
            (PBS) at 37°C for 24 days. All data (n = 8) are presented as the mean ± standard deviation.


            during the hybrid process enhanced the physical stability   controlled release with independently positioned GFs. The
            due to an increase in strength and reduction in shrinkage.   hybridization of GS was achieved by synthesis using the
            Some reports have suggested that organic and inorganic   sol-gel  method  at  room  temperature.  Low-temperature
            composites exhibit improved mechanical properties due to   processing prevents protein denaturation and is useful
            the inorganic networks formed in the organic matrix. 37,43  for multilayer coatings with good physical stability.
                                                               Fluorescence intensity measurements were conducted
               To confirm whether each layer was mixed or      to evaluate the potential intermixing between the two
            separated, each component of the 20 GS was stained   layers during scaffold preparation (Table 1). The intensity
            with fluorescence dyes FITC (first layer: later effect) and   profiles for the green channel (Ch1) and the red channel
            rhodamine (second layer: earlier effect) and then coated   (Ch2) were recorded across the scaffold. The green signal
            on the 3D scaffold. As featured in Figure 4a–e, the layers   (Ch1) exhibited an average intensity of approximately
            have separate colors. This indicates that the double layers   1000–1500 units, while the red signal (Ch2) demonstrated
            were coated separately without mixing on the scaffold.   a higher intensity range of 1000–4000 units. Notably, the
            The developed scaffolds were expected to maintain a   two signals remained confined to their respective layers,

            Volume 10 Issue 6 (2024)                       448                                doi: 10.36922/ijb.4638
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