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                   with viscous bioinks  . SLA leverages photopolymerization to achieve high resolution
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                   (<20 μm)  , critical for replicating intricate microchannel architectures that mimic in

                   vivo vascular networks. Despite its precision, SLA is constrained by material brittleness
                   and  limited  compatibility  with  cell-laden  hydrogels  unless  modified  for

                   biocompatibility.  2PP  stands  out  for  its  sub-200  nm  feature  resolution,  enabled  by

                   nonlinear optical absorption. This technique is ideal for creating nanoscale topographies

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                   that influence cell migration or drug diffusion in cancer models  . However, 2PP’s slow
                   throughput and high operational costs restrict its use to specialized applications. FDM

                   remains  the  most  cost-effective  (<$0.50/cm³)  option  for  rapid  prototyping,  using

                   thermoplastics like PLA or ABS. While FDM is accessible and scalable, its resolution

                   (~100–300  μm)  and  surface  roughness  often  necessitate  post-processing  for

                   microfluidic applications.

                        The selection of an optimal 3D printing modality for tumor modeling demands a

                   systematic evaluation of three critical, interdependent parameters: spatial resolution,

                   which  governs  the  precision  of  microchannel  geometries  and  cellular-scale

                   features; biomaterial compatibility, determining suitability for cell encapsulation, ECM
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                   mimicry, and long-term culture viability  ; and economic feasibility, ensuring a balance
                   between  fabrication  precision,  functional  performance,  and  budget  constraints—

                   particularly crucial for large-scale studies. A comprehensive comparative analysis of

                   these factors (summarized in Table 3) is vital to align fabrication strategies with specific

                   research  objectives,  such  as  replicating  hypoxia  gradients,  vascular  networks,  or

                   metastatic  microenvironments.  Emerging  innovations,  including  hybrid  printing

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                   techniques (e.g., integrating SLA with i3DP) and advanced bioresins  , hold promises
                   for  bridging  current  limitations  in  resolution,  biocompatibility,  and  cost  efficiency,

                   thereby expanding the potential of 3D-printed tumor models.

                        Compared to traditional manufacturing, 3D printing provides exceptional design

                   freedom  and  enables  personalized,  decentralized  production.  It  produces  complex

                   geometries with high precision; its additive nature minimizes material waste, reducing

                   costs  and  environmental  impact   37,55 .  However,  there  are  still  numerous  challenges


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