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




            3.3.2. Micro-CT of rat skull                       ability of the P scaffold was limited. Compared to the P
            In order to evaluate the bone repair effect of the three   scaffold,  the  SBP  scaffold—with  the  addition  of  SrBG—
            scaffolds in vivo, we constructed a bone defect model in SD   displayed bone growth along the composite scaffold in
            rats and performed cranial bone sampling at postoperative   the defective area at month 1, gradually increasing over
            months 1, 2, and 3; micro-CT scanning was performed to   subsequent months until the bone trabeculae covered
            evaluate the repair of the bone defect area. As displayed in   almost 50% of the defective area at the end of month 3,
            Figure 11A, in the blank group, the amount of new bone   indicating that the  addition of  SrBG  could  promote  the
            production in the bone defect area was low at postoperative   repair of bone defects. In contrast, the PSBP scaffold—
            months 1 and 2, and there was still no significant increase   with the addition of PDA—displayed more bone growth
            in new bone tissue at postoperative month 3, indicating   across all time points compared to the P and SBP scaffolds;
            that  the  bone  repair  effect  was  relatively  poor  in  the   the defect area was seen to be significantly filled with bone
            absence of scaffolding implantation. Conversely, in the P   trabeculae at month 1, gradually increasing in subsequent
            scaffold, there was a low amount of new bone production   months until almost complete coverage of the bone
            at  postoperative  month  1,  and  in  months  2  and  3,   defect area with bone trabeculae at the end of month 3.
            increasing new bone tissue was observed, but large bone   The bone volume fraction (Figure 11B) and bone density
            defects remained visible, indicating that the bone repair   (Figure 11C) of the bone defect area in each scaffold group


















































            Figure 9. Hematoxylin and eosin (HE) staining of rat liver 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).


            Volume 11 Issue 4 (2025)                       363                            doi: 10.36922/IJB025210211
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