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International Journal of Bioprinting                      3D-printed scaffolds for TMJ fibrocartilage regeneration






















































            Figure 4. 3D-printed scaffolds for TMJ disc fibrocartilage regeneration. (A) 3D-printed PCL scaffolds of TMJ disc based on the 3D laser scanning data. The
            size of PCL microstrands (300 μm) and interstrand distance (300 μm) and the relative microstrand density parallel to the alignment direction compared
            with the perpendicular direction (2:1) were determined to closely approximate the native tensile properties. (B) Spatial control of connective tissue growth
            factor (CTGF) throughout the scaffolds and transforming growth factor beta 3 (TGF-β3) in the intermediate zone. (C) After a 6-week culture with human
            mesenchymal stem/progenitor cells, the CTGF and TGF-β3 microsphere-embedded scaffold showed type I collagen throughout the scaffold and aggrecan
                                                                                      [75]
            in the intermediate zone. Reproduced with permission from Legemate K, Tarafder S, Jun Y, et al., J Dent Res, 95: 800–7 . (D) Microcomputed tomography
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            analysis and cross-section images of PCL scaffold modified with a PEGDA shell (upper) and a PEGDA core (lower). (from ref.  licensed under Creative
            Commons Attribution license.) (E) Schematic illustration of the construction process of the composite scaffolds. (from ref.  licensed under Creative
                                                                                            [80]
            Commons Attribution license).
               Another approach to modify the PCL scaffold is to   third disc. After 3 months, histological analysis showed
            immerse the 3D-printed PCL scaffold in the PVA hydrogel   no degenerative changes in the mandibular condyle, and
            solution, and network crosslinking is achieved after   ingrowth of fibrous tissue was observed around the PCL. A
            three freeze-thaw cycles . The  in vitro study showed   probable explanation was that the gaps between PVA and
                                [79]
            that the PVA-PCL scaffold possessed non-cell-adhesive   PCL provided spaces for fibrous tissue ingrowth, which
            nature, desirable surface smoothness (friction coefficient   was thought to be an advantage of the PVA-PCL scaffold.
            at 0.0662), similar porosity, compressive property, and   Although the PCL and PU scaffolds usually had smooth
            viscoelasticity as a natural TMJ disc. The PVA-PCL scaffold   surfaces, they lacked the desired ability to promote cell
            was then implanted in the goats to replace the lateral one-  adhesion and growth. To address this challenge, Yi et al.
                                                                                                           [80]

            Volume 9 Issue 5 (2023)                        266                         https://doi.org/10.18063/ijb.761
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