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     The mussel-inspired assisted apatite mineralized on PolyJet material for artificial bone scaffold
           biocompatibility  of  materials  is  extremely  important.   osteogenic differentiation potential which is an important
           The cell proliferation of the hMSCs cultured on M, MP,   key to determine if the bone formation process is ongoing.
           MHA,  and  MPHA  for  1,  3,  and  7  days  was  evaluated   Figure  7  shows  cells  growing  on  MPHA  can  express
           by  PrestoBlue  assay  (Figure  5).  The  result  shows  that   the  most ALP  levels,  and  the ALP  expression  level  of
           absorbance of MED610 object with PDA coatings (MP   MED610 object without coatings was lowest. The results
           and MPHA) is higher than Ctl and without PDA coatings   demonstrate that MED610 object with PDA/HA coating
           (M  and  MHA).  Besides,  the  MED610  object  without   helps to improves the osteogenic differentiation potential
           any coatings shows the lowest absorbance. In addition,   of stem cells.
           the hMSCs cultured on MED610 object with both PDA
           coatings reveals a higher area of cell adhesion and are flat   4. Discussion
           with an intact, well-defined morphology (Figure 6). These   MED610  is  a  biocompatible  3D  printing  photocurable
           results point that MED610 object with PDA coatings can   material  commonly  used  in  medical  and  dental  fields
           improve its biocompatibility, making it more suitable as a   requiring  precise  visualization  and  patient  contact.
           biomedical material.
                                                               Although  this  material  is  suitable  for  over  30  days’
           3.3 Osteogenic Differentiation                      skin contact and up to 24 h mucosal membrane or bone
                                                               contact, it can be more widely used if it can be enhanced
           The hMSCs cultured on M, MP, MHA, and MPHA for 3
           and 7 days were analyzed the ALP activity to evaluate the
                                                              Figure 5. The cell proliferation of human mesenchymal stem cells
                                                              cultured on the MED610 substrate with various coatings for 1, 3,
           Figure  3.  Surface  scanning  electron  microscope  images  of  the   and 7 days.
           MED610 substrate with various coatings.
                                                              Figure 6. Surface scanning electron microscope images of human
           Figure 4. Vickers hardness of the MED610 substrate with various   mesenchymal stem cells cultured on the MED610 substrate with
           coatings.                                          various coatings. Cells are indicated by red arrows.
           86                          International Journal of Bioprinting (2019)–Volume 5, Issue 2





