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International Journal of Bioprinting                                Sr-doped printed scaffolds for bone repair

















































            Figure 10. Hematoxylin and eosin (HE) staining of rat kidneys in each scaffold group. Scale bar: 100 μm. Abbreviations: P, polycaprolactone (PCL);
            PSBP, polydopamine (PDA)/strontium (Sr)-doped bioactive glass (SrBG)/polycaprolactone (PCL); SBP, strontium (Sr)-doped bioactive glass (SrBG)/
            polycaprolactone (PCL).



            were statistically analyzed at postoperative months 1, 2,   to the other scaffold groups; new bone tissue gradually
            and 3. The PSBP scaffold displayed the best bone repair   formed in the pores of the stent, and new bone tissue was
            effect (among the scaffold types) relative to the blank group    observed at the defect interface and inside the material. At
            (p < 0.05). The bone mineral density results were consistent   postoperative month 3, the new bone tissue in the PSBP
            with the bone volume fraction analysis.            group was continuous and more widely distributed, and
            3.3.3. HE and Masson staining of rat skull specimens  the area of the new bone was significantly larger than that
            At 1, 2, and 3 months after surgery, the rats were euthanized;   of the blank, P, and SBP scaffold groups (Figure 12).
            skull specimens were collected and analyzed by HE staining   The results of Masson staining are displayed in
            and Masson staining to assess the formation of new bone   Figure 13. At postoperative month 1, the SBP and PSBP
            tissue in the bone defect area. HE staining at postoperative   scaffold groups had more light blue collagen tissue and red
            month 1 revealed that the blank group had more fibrous
            tissue but less new bone tissue in the bone defect area. The   muscle fiber tissue compared to the blank and P scaffold
            P and SBP scaffolds displayed a small amount of new bone   groups. In subsequent months, the neoplastic bone tissue
            in the defect area, while the PSBP scaffold displayed a large   of  each  scaffold  group  further  matured,  exhibiting  dark
            amount of new bone formation. At postoperative month 2,   blue mature collagen, which was most significant in the
            the new bone tissue in the PSBP group was progressively   PSBP scaffold group. These results indicated that PSBP
            darker in color and more widely distributed compared   scaffolds could promote bone defect repair.


            Volume 11 Issue 4 (2025)                       364                            doi: 10.36922/IJB025210211
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