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International Journal of Bioprinting                                               3D-Printed scaffolds



            A                                B                               C
















            Figure 1. Fourier transform infrared of poly(ε-caprolactone) (PCL)/β-tricalcium phosphate (TCP) (A), poly(trimethyl carbonate) (PTMC)/TCP (B), and
            PTMC/PCL/TCP (C) scaffolds with different TCP content.
            A                                B                               C

















            Figure 2. Water contact angle of poly(ε-caprolactone) (PCL)/β-tricalcium phosphate (TCP) (A), poly(trimethyl carbonate) (PTMC)/TCP (B), and PTMC/
            PCL/TCP (C) scaffolds with different TCP content.

            than PCL/TCP scaffolds. Compressive moduli of human   proliferation after 3 days of cultivation compared to only
            compact bone and cancellous bone were 14 – 20 GPa and   1 day. PTMC/PCL/TCP scaffolds indicated slightly higher
            97.8 – 800 MPa, respectively, while compressive modulus   cell  growth  activity than  PCL/TCP  and PTMC/TCP
            of cartilage was 0.4 – 0.8 MPa [32,33] . Therefore, PCL/TCP,   scaffolds. Thus, PCL/TCP, PTMC/TCP, and PTMC/PCL/
            PTMC/TCP, and PTMC/PCL/TCP scaffolds displayed     TCP exhibited low cytotoxicity, increased the proliferation
            lower compressive modulus than human compact bone   of MC3T3-E1 cells, and promoted cell growth.
            and obviously higher compressive modulus than cartilage.
            Moreover, compressive moduli of PCL/TCP and PTMC/    Based on the above measurement, PCL/TCP, PTMC/
            PCL/TCP scaffolds were just within the compressive   TCP,  and PTMC/PCL/TCP  scaffolds  with  25%  TCP
            modulus requirements of cancellous bone. Therefore,   content (PTMC/25%TCP, PCL/25%TCP, and PTMC/
            PCL/TCP and PTMC/PCL/TCP scaffolds are suitable for   PCL/25%TCP) were applied to investigate the degradation,
            use in repairing cancellous bone defects. Meanwhile, TCP   drug -release  property,  cell  proliferation  rate,  and
            promoted the compressive property of scaffolds, and the   implantation. Meanwhile, PCL/10%TCP, PTMC/10%TCP,
            modification of PCL improved the compressive property   and PTMC/PCL/10%TCP were used as the contrast
            of PTMC/PCL/TCP scaffolds.                         controlled samples.

            3.3. Cell cytotoxicity assay                       3.4. Degradation
            PCL/TCP, PTMC/TCP, and PTMC/PCL/TCP scaffolds      All scaffolds displayed M  loss and weight loss in PBS
                                                                                    n
            enhanced cell growth of MC3T3-E1 cells (Figure 6).   (Figure 7A  and  B). PTMC/PCL/TCP scaffolds showed
            All scaffolds displayed no significant differences in cell   the similar weight loss and M  loss pattern as that of
                                                                                         n
            proliferation on day 1. PCL/TCP, PTMC/TCP, and PTMC/  PCL/TCP  scaffolds  after  degradation  for  6 months.
            PCL/TCP scaffolds displayed lower cytotoxicity and higher   PTMC/25%TCP scaffolds displayed similar low weight


            Volume 9 Issue 1 (2023)                        278                      https://doi.org/10.18063/ijb.v9i1.641
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