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International Journal of Bioprinting                                Dual tuning of 3D-printed SilMA hydrogel

















































            Figure 8. In vivo cartilage formation effect. Histological staining (HE, Safranin O, and Alcian Blue) and immunohistochemical staining images for Col-
            II and Col-I of each group. Scale bar: 100 µm; magnification: 200×. Abbreviations: Col I, collagen I; Col II, collagen II; HE, hematoxylin and eosin; NF,
            nanofibers; PEO, poly(ethylene oxide); SilMA, silk methacryloy.

            As shown in  Figure S7, the groups with PEO-induced   PEO-induced porosity and NF reinforcement to enhance
            porosity exhibited significantly higher Col-II and Col-I   their  cartilage tissue regeneration  performance. The
            immunopositivity and average optical density compared to   innovative water-in-water emulsification strategy created
            non-porous controls, especially for the PEO/1%NF/SilMA   a porous architecture that significantly increased the
            group. These observations coincided with the quantitative   average pore diameter (by over 100%) and overall porosity
            GAG measurements and chondrogenic gene expression   (75%), albeit with a significant reduction in mechanical
            analysis.  However, due to the limitations of the animal   properties. The incorporation of homogenized NFs
            model, these results were still unable to demonstrate which   effectively compensated for this mechanical deficit without
            group had a better effect on cartilage formation under   substantially compromising porosity, while concurrently
            the weight-bearing environment. In addition, it is worth   improving the 3D printability of SilMA/PEO hydrogels.
            noting that the materials prepared in this study mainly   Results demonstrated  that the  3D  printed  grid-like
            contain only  one  type  of bioactive substance,  SF. This   PEO/2%NF/SilMA  group  had  compressive strength and
            simplified composition offers a simpler system for future   elastic  modulus comparable to pure  SilMA  hydrogels
            mechanistic studies.                               but with enhanced biological functionality. Remarkably,
                                                               the  PEO/NF/SilMA  hydrogels  exhibited  improved
            4. Conclusion                                      biocompatibility and marked upregulation of chondrogenic
            This study successfully developed a dual-strategy approach   genes (COL2A1,  ACAN, and  SOX9), particularly in
            for modifying 3D-printed SilMA hydrogels, combining   the  PEO/1%NF/SilMA  group.  In vivo  subcutaneous


            Volume 11 Issue 4 (2025)                       293                            doi: 10.36922/IJB025140118
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