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Recent cell printing systems for tissue engineering





































            Figure 3. Temperature-controlled 3D cell printing process, (a) increasing temperature-controlled (from 4 to 37°C) printing using
            ECM-based bioinks  [48, 49]  and (b) low-temperature (−10°C) cell printing process  [50] .


            shaping ability. It also revealed the successful fabrica-  nozzle  and  reduced  the  damage  of  the  cells  in  the
            tion  of  multi-layered  scaffold  with  significantly  en-  printed  bioink [52] .  Moreover,  the  electric  field  en-
            hanced mechanical properties (10 ± 2.2 MPa of You-  hanced the printing stability and resolution of the dis-
            ng’s  modulus).  For  further  development,  initial  cell   pensed  struts  since  the  electric  force  pulled  down
            viability can be improved, and various types of bioink   the  bioink  and  resulted  in  an  increase  in  the  cohe-
            can be used for low-temperature cell printing.     rence  between  the  layers  and  a  decreased  strut  size.
                                                               However,  there  was  potential  cell  damage  when  the
            3.3 Electric-field Assisted 3D Cell Printing
                                                               high electric field was used, and they reported that the
            Recently, the application of an electric field in cell pri-  limitation  of  the  applied  voltage  with  their  experi-
            nting  was  proposed.  Yeo  et  al. [51]  combined  elec-  mental conditions was less than 2 kV.
            tric-filed  assisted  3D  cell  printing  and  aerosol  cros-
            slinking  process  to  fabricate  a  3D  hybrid  cell-laden   3.4 Hybrid Systems for Mechanically Stable 3D Cell-
                                                               laden Structures
            scaffold.  The  osteoblast-like  cell-laden  fibers  were
            deposited  with  0.16  kV  on  3D  lattice  PCL  struts   As the 3D cell printing was derived from the conven-
            (Figure 4a).  The  initial  cell  viability  was  reasonable   tional 3D printing technology, some researchers have
            (above 80%), and the cells could proliferate for pro-  tried to apply the conventional 3D printing methods to
            longed  culture  period.  The  fibers  maintained  their   the 3D cell printing process. Several papers reported
            shape without dispersion on the hybrid scaffold with a   that  the  melt-plotting  method, one  of  the  most  com-
            significant increase in tensile modulus (4.9 ± 0.6 MPa)   mon methods among non-cell printing processes, was
            compared to alginate mat. Also, Yeo et al. [51]  applied     combined with the cell printing techniques to fabricate
            an  electric  field  to  the  extrusion-based  cell p rinting   and strengthen a cell-laden 3D structure by providing
            that pneumatically printed alginate-based bioink with   a  firm  frame  or  support  for  the  soft  cell-laden  bio-
            human  adipose  stem  cells  with  the  electrical  field   inks [48,53–56] .  In  2012,  Shim  et  al. [53]   used  the  melt-
            (Figure 4b). This reduced the wall shear stress in the   plotting  method  with  a s ynthetic  polymer,  poly  (ε-
            34                          International Journal of Bioprinting (2017)–Volume 3, Issue 1
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