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     International Journal of Bioprinting                          Scaffolds printed with light sheet stereolithography
                         A
                                                    D
                         B
                         C
            Figure 3. (A-C) Microscope images of the built scaffolds at three different exposure values show the size and distribution of strut and pore. The
            square shows a zoom-in region from the same pictures. (D) Overall view of the complete scaffold shown in (C). Fractures are generated during
            manipulation.
            printing conditions. Exposure, exposure time, and laser   size within the scaffold. It has been demonstrated that
            power define the printing conditions that can be tuned in   the scaffold can be functionalized for different cell types.
            our system to modify the strut size and the printing time of   Furthermore, specific properties  can be improved  by
            the scaffold. Balancing those parameters can significantly   modifying the size distribution of the pores within the
            reduce the printing time and deliver the greatest throughput   scaffold . Furthermore, the precision of the available
                                                                     [27]
            in terms of resolution and precision. For example, the strut   scanning systems has greatly increased, which benefits
            size of the scaffolds shown in Figure 3B and C was increased   scaffold fabrication in pore size control and uniformity.
            up to 43.4 ± 1.9 μm (n = 6), inducing the reduction of the   To illustrate, we fabricated two scaffolds of different
            pore size down to 36.2±1.5 μm at a constant strut spacing.   strut spacing. Figure 4A shows the fluorescence image of
            Furthermore, structures built with LS-SLA depict large   a scaffold with a pore size of 68 ± 2.5 μm (n = 11), and
            surface fabrication. Two-D stitched images of the scaffolds   Figure 4B shows the scaffold that exhibits a pore size of
            shown  in  Figure  3  demonstrate  that  LS-SLA  can  build   149.9 ± 2.3 μm (n = 10). Microspheres (diameter ranging
            structures of large area and simultaneously conserves   from 63 μm to 75 μm) were pipetted with PBS within both
            microscale struts (<50 μm). Figure 3D shows a 2D stitched   scaffolds  and imaged  with fluorescence  microscopy  as
            image of the scaffold shown in Figure 3C with a measured   depicted by the red circles in Figure 4. The microspheres
            area of 19.09 mm × 18.83 mm. At the smallest strut size,   stress the porous characteristics of the scaffolds fabricated
            12.8 μm, the strut length-to-width ratio was l/w = 1696 for   with LS-μ-SL. On one side, the microspheres were filtered
            a scaffold with an area of 21.37 × 20.59 mm².      out or kept in suspension by the small pores of the
                                                               scaffold (Figure 4A). On the other side, the microspheres
            3.2. Pore size control and uniformity              flowed within the pores of the scaffold since the pore size
            In practical terms, it is easier to fix the exposure conditions   was ≈ 2 times larger than the diameter of the microspheres
            with respect to the desired resolution and steer the LS along   in (Figure 4B). In general, the results presented in Figure 4
            the scanning area. Steering the LS allows illuminating at   mimic the property of permeability in highly porous
            different positions and consequently controlling the pore   scaffolds.
            Volume 9 Issue 2 (2023)                         33                      https://doi.org/10.18063/ijb.v9i2.650
     	
