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International Journal of Bioprinting                            3D-printed bone scaffolds and biofilm formation




















































            Figure 6. Morphology analysis of bacterial biofilm formation and EPS visualized by SEM. Images (a) and (b) show designs SP-B and SD-B under 6000×
            magnification, respectively. Images (c) and (d) were extracted from the same field of (a) and (b) at a higher magnification of 16,000×, showing the SP-B
            and SD-B designs, respectively. The experiment was performed two times, and a representative field for each sample is shown. The scale bar is 10 µm for
            (a) and (b) and 5 µm for (c) and (d).
            with  scaffolds  of  different  material  composition,    The roughest surface was shown on the SD-B scaffold with
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            drug-induced scaffolds,  or composite scaffolds with   an Sa of 21.69 ± 0.54 µm and an Sq of 26.14 ± 0.68 µm.
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            antibacterial properties,  there are no studies examining   This significantly huge difference is attributed to the fact
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            the biofilm formation on different geometrical design of   that the surface roughness is highly dependable on the
            tissue engineering scaffold.                       geometry complexity, the limitations of the 3D printing
                                                               technique, and its printing parameters. 47,48
            3.3. Scaffold characterization
                                                                  There was no significant effect of porosity on surface
            3.3.1. Surface roughness                           roughness, except for the case of SP structure with lower
            In order to examine other factors that may influence the   porosity showing significantly reduced surface roughness
            biofilm formation on each design, a further investigation   (P < 0.05). Considering the correlation between surface
            considering surface roughness and pore size was    roughness and bacterial biofilm formation in crystal
            performed.  Figure 7 presents the surface roughness   violet assay results (Figure 4) for each individual design,
            for  each  scaffold  design.  The  results  show  a significant   a consistent trend was observed where higher surface
            variability in  surface  roughness  between the  different   roughness increases bacterial adhesion.  Although the RE
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            designs. The least surface roughnesses of 1.68 ± 0.17 µm   designs showed contradictory results when correlated with
            Sa and 2.16 ± 0.21 µm Sq were noted in the RD-A scaffold.   the crystal violet results where a rougher surface led to a


            Volume 10 Issue 1 (2024)                       332                          https://doi.org/10.36922/ijb.1768
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