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International Journal of Bioprinting                                 Sr on GO enhances PLLA/PGA scaffold




            of the LG scaffold. As shown in Figure 5a–f, the surface   and subsequently attract PO  to form the apatite layer
                                                                                       3-
                                                                                      4
            of  the  scaffolds  showed  small  holes  due  to  degradation.   deposition.  At the same time, Sr element was also detected
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            There were a number of particles on the surface of the   in the apatite layer deposition on the surface of the LG/
            LG/GP and LG/GPSr1.5 scaffolds, which might be the   GPSr1.5 scaffold, indicating that Sr partially replaced Ca
            apatite layer deposition generated during immersion in   in the apatite layer.  The above results showed that the LG/
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            SBF. The elemental composition of the scaffolds after SBF   GPSr1.5 scaffold had good bioactivity.
            immersion was analyzed by EDS, as shown in Figure 5g–
            i. It was found that the deposition on the surface of the   A scaffold should have good cytocompatibility,
            LG/GP and LG/GPSr1.5 scaffolds was mainly composed   an attribute important for promoting cell growth and
            of Ca  and  P elements.  This indicated that calcium and   proliferation without triggering an immune response. The
            phosphorus crystals grew on the surface of the LG/GP and   cytocompatibility of the LG/GPSr1.5 scaffold was tested
            LG/GPSr1.5 scaffolds after immersion in SBF, because of   and  compared  with  that  of  the  LG  scaffold.  BMSCs  were
            the presence of PDA in scaffold, which was considered   inoculated on the two kinds of scaffolds, and morphology
            to be an effective promoting factor for apatite deposition   of the cells cultured for 1, 3, and 5 days was visualized using
            under physiological conditions. 68,69  The phenolic hydroxyl   SEM. The cells had good adhesion and extension on the
            groups in PDA could sequester Ca  from SBF solution   surface of both LG and LG/GPSr1.5 scaffolds, as shown
                                         2+




















































            Figure 6. BMSCs adhesion on the LG and LG/GPSr1.5 scaffolds (a); statistical results of relative cell adhesion area (b); live/dead cell staining for BMSCs
            on the LG and LG/GPSr1.5 scaffolds (c); statistical results of cell density (d).

            Volume 10 Issue 3 (2024)                       206                                doi: 10.36922/ijb.1829
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