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     International Journal of Bioprinting                               DLP-printed scaffold for bone regeneration
            Figure 8. Histological and immunohistochemistry evaluation of the new blood vessels in the defect site at week 4. (A) Fluorescent staining (CD31 and
            OPN) of newly formed bone at week 4. (B) The mean fluorescent intensity of CD31. (C) Hematoxylin–eosin staining of newly formed bone at week 4.
            Data were analyzed using one-way ANOVA and are shown as mean ± standard deviation (*p < 0.05, **p < 0.01, ***p < 0.001, n = 3). (NB, new bone; IM,
            implanted materials; BM, bone marrow; BV, blood vessel.)
            Therefore, it has become an attractive strategy to induce   progression of ECO. Furthermore, owing to their excellent
            ECO in situ through the properties of the material itself .   structure, the 3D-printed scaffold also supported the access
                                                        [50]
            Sun et al. prepared an injectable, poly (glycerol sebacate)-  of bone tissue and blood vessels, providing a novel material
            co-poly (ethylene glycol)/polyacrylic acid (PEGS/PAA)   design for ECO-based bone regeneration.
            hydrogels to induce a hypoxia-mimicking environment and   The GelMA/PMAA scaffold possessed better elasticity
            subsequently recapitulate ECO via in situ iron chelation .   and compression strength compared to the conventional
                                                        [37]
            However, injectable hydrogels cannot be prepared directly   GelMA scaffold, increasing early mechanical stability and
            as pre-designed macroscopic structures.
                                                               meeting the  mechanical requirements  of  inclusive bone
               In our study,  GelMA/PMAA scaffolds promoted the   defects. In terms of surface structure, the 3D printing
            expression of HIF-1α by chelating iron ions with the carboxyl   technology could help the scaffold to achieve the co-
            group of PMAA, thus reducing the consumption of HIF-1α   existence of macropores and micropores, as compared to
            by PHD and allowing for better chondrocyte differentiation   only micropores in the conventional injectable hydrogel,
            and vascular regeneration. The scaffolds also overcame the   which is essential for the occurrence of osteoconductivity.
            disadvantages  of  exogenous  factors and allowed  smooth   In addition, the introduction of PMAA not only improved
            Volume 9 Issue 5 (2023)                        123                         https://doi.org/10.18063/ijb.754
     	
