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Xu, et al.
           2.2.6. Customized software enables the application of   structures, the printing effects of the developed system in
           the desired print control                           terms of temperature-sensitive biological ink, photosensitive
           This software system is divided into two control modes,   biological  ink,  high-temperature  stent  printing,  high-
           (i)  standard  mode:  first  select  the  3D  model  (external   temperature stent and hydrogel composite printing, coaxial
           source  or  built-in  model),  then  perform  layering,  then   printing, and suspension printing will be verified. The related
                                                               printing parameters of the extrusion cell printing process,
           explore process parameters, and finally print the structure   such  as  nozzle  diameter,  printing  speed,  ejection  speed,
           and (ii) Quick mode: prestore the optimized data model   printing path spacing, and height, affect the formability of
           containing printing process information in the common   the  cell  printing  ink  and  the  cell  survival  rate,  as  shown
           database  so  that  users  can  skip  redundant  steps  and   in a previous article [59,60] . Therefore, this research will not
           quickly  start  the  repeated  printing  of  the  model  when   perform further exploration in this area. Initial experiments
           they use it for the 2  time. The printer software interface
                           nd
           enables  the  input  of  required  printing  parameters  and   and prefabricated printing results are described below.
           the  automatic  generation  of  g-codes  to  appropriately   3.1. Printing thermosensitive hydrogels
           move  and  trigger  the  motion  system  and  nozzles.  The
           temperature and UV control interface allow one to set the   To print a 3D complex cell structure with high-resolution,
           nozzle’s temperature, UV curing intensity, and duration.  the cell printing ink needs to improve the gel capacity
                                                               of  the  bioink  by  increasing  the  viscoelasticity  of  the
           2.2.7. Integrated technology for modular and        printing ink to maintain the mechanical properties of the
           collaborative printing                              stacked structure. However, as the viscoelasticity of the
                                                               cell printing ink increases, the shear force that the cells
           Nozzles  that  can  be  quickly  replaced  are  an  important
           foundation  for  modular  combinations  of  nozzles.  The   are  subjected  to  during  the  printing  process  increases,
                                                               thereby reducing the survival rate of the cells. Therefore,
           print head often contains functions such as temperature   controlling  the  viscoelasticity  of  the  cell  printing  ink
           control and extrusion control, so the connection between
           the print head and the main body of the printer has not only   during the printing process and finding the appropriate
           a mechanical connection but also an electronic interface.   viscoelastic interval of the cell printing ink are important
           The  common  mechanical  connection  method  is  screw   steps to achieve good cell 3D printing (good formability
           connection. The connection is firm, but it is inconvenient   and biological performance). Temperature can control the
           to disassemble. Therefore, this study intends to explore   temperature-sensitive material in the gel or sol state and
           a  way  to  quickly  replace  and  combine  multifunctional   then affects the viscoelasticity of the material.
                                                                   The rheological  properties of gelatin,  silica  gel,
           nozzles.  A  quick-release  joint  (a  fixed  method  of
           magnetic attraction and POGO PIN electronic interface)   GelMA,  and  PF127  were  tested  before  printing  to
           was used to connect the motion system and achieve the   determine  the  optimal  printing  temperature  of  the
           signal transmission. When using the magnetic attraction   materials  (Figure  6A-D).  Various  structures  were
           method of plane bonding, if the magnetic attraction is too   printed  using  10%  (w/t)gelatin  at  22°C  and  as  shown
           small,  the  nozzle  will  easily  shake  naturally,  resulting   in Figure 6E. About 40% (w/t) PF127 (Pluronic F-127,
           in poor stability. If the magnetic attraction is too large,   Dow Corning) was printed at 18°C to verify the printer’s
           it is not easy to assemble the nozzles. Therefore, in this   ability to print complex structures (Figure 6F). Gelatin,
                                                               silica gel, nanocellulose, and PF127 material were used
           study, a “⅂”-shaped suspension mode was designed. The
           “convex”  shape  designed  on  the  top  of  the  back  plate   to print (motor-driven piston-based microextrusion) the
           matches  the  “concave”  shape  structure  on  the  back  of   complex  shape  of  the  human  ear  structure,  as  shown
           the nozzle, which not only provides nozzle upward force   in Figure  7A.  The  pneumatic-based  microextrusion
           support but also limits the possibility of swinging from   nozzle  was  also  tested  using  PF127,  GelMA  to  print
           side to side. Using the combination design of magnets   mesh (Figure 7B[i]), cervical stent (Figure 7B[ii]), and
           and the matching design of the POGO PIN, the nozzle   spinal cord (Figure 7B[iii]) structures. The above results
           can be quickly connected and removed from the motion   show  that  the  printed  model  maintains  a  high  fidelity.
                                                               A mixed bioink containing 10% (w/t) gelatin, 1% (w/t)
           system (within 3 s).
                                                               sodium alginate, and cells (1 × 10^6 cells/mL) mL)(the
           3. Initial experiments and prefabrication           rheologicalparameters as shown in Figure 6G was used
           printing results of a single nozzle                 to print the mesh structures (Figure 6H), and the survival
                                                               rate of printed cells (A549, HeLa, NIH3T3 and HUVECs)
           To  further  explore  the  capability  of  this  multifunctional   was tested afterward. After printing, the cell survival rate
           modular 3D bioprinting system, the printability, fidelity, and   exceeded 80% (Figure 6I-M), meeting the requirements
           resolution were subsequently evaluated. To achieve soft and   for  further  use. Actin  staining  results  of  HeLa  cells  as
           hard  materials,  multiscale  fiber  filaments,  and  multiscale   shown in Figure 6N.

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