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Shuai C et al.

           3.2  Phase composition                              the mechanical loss caused by chemical etching, 1 wt%
                                                               GO was incorporated into the PLLA scaffolds. The
           The phase composition of scaffolds was analyzed using   typical microstructure of GO/PLLA scaffold before
           X-ray diffraction (XRD) within a wide 2θ range of   chemical etching was presented in Figure 4(c). It could
           5°~65° (Figure 3). Results presented typical broadened   be seen that after the addition of GO, the GO/PLLA
           patterns dominated by two diffraction peaks located at   scaffold also exhibited a smooth and dense surface,
           16.6° and 19.1°, which could been ascribed to the semi-
           crystalline nature of PLLA. After NaOH etching process,   showing no obvious differences compared with PLLA
           no new diffraction peaks were detected, demonstrating   scaffold shown in Figure 2(c1). The surface porous
           the NaOH etching process did not lead to phase change.  structure of GO/PLLA-1.0 scaffold was presented in
                                                               Figure 4(d). Similarly, little differences in the micropore
           3.3  Mechanical properties                          structure were observed between the etched GO/PLLA-
                                                               1.0 scaffold and PLLA-1.0 scaffold. The compressive
           Compression tests were performed to quantify the effect
           of chemical etching on the mechanical properties of   stress for GO/PLLA-0, GO/PLLA-0.5, GO/PLLA-1.0,
           the multi-scale porous scaffolds. Figure 4(a) showed   and GO/PLLA-1.5 were 32.2 ± 1.3 MPa, 28.3 ± 1.2
           the representative stress-strain curves of the scaffolds   MPa, 24.5 ± 2.1 MPa, 19.7 ± 2.3 MPa, respectively.
           under compression tests. It could be seen that the stress   Clearly, the incorporation of GO considerably improved
           of PLLA-0 scaffold had a sudden drop at a maximum   the mechanical properties of the etched scaffolds.
           of 20.1 MPa, indicating the brittleness nature of PLLA.   Specifically, the compressive strength of GO/PLLA-1.0
           In comparison, the maximum stress of scaffolds after   scaffold was approximately 41.6% and 10.3% higher
           chemical etching gradually decreased. It was not    than that of PLLA-1.0 scaffold and PLLA-0 scaffold,
           surprising that the chemical etching process had a   respectively. Moreover, the strength of fabricated
           negative effect on the compressive properties of scaffold   scaffolds was comparable to or even higher than that of
                                                                                      [31]
           due to the increased porosity on scaffold surface. The   cancellous bone (4-20 MPa) .
           relationship between the compressive strength on etching   Subsequent indentation tests revealed a similar trend
           time was presented in Figure 4(b). As the etching time   of the hardness with that of compressive strength, as
           increased from 0 h to 1.5 h, the compressive strength   showed in Figure 5. The hardness of PLLA-0 scaffold
           of the scaffolds was considerably decreased by 30.1%   could reach 22.21 ± 0.84 Hv, whereas the porous surface
           from 22.2 ± 1.7 MPa to 15.5 ± 1.5 MPa. It was well   structure by chemical etching impaired the hardness
           known that scaffolds should have adequate mechanical   of scaffolds, e.g. after etching for 1.5 h the hardness
           properties to provide structural support for the new   decreased by 18.7% to 18.05 ± 1.41 Hv in comparison
           tissues after implantation . Therefore, to compensate   to PLLA-0 scaffold. However, the hardness of scaffolds
                                 [8]































                        Figure 3. XRD analysis of the phase composition of the scaffolds with and without chemical etching.

                                       International Journal of Bioprinting (2018)–Volume 4, Issue 2         5
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