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facing  3D  printing  technology  in  the  biomedical  manufacturing  field  (Table  3):

                   adhesive  selection,  suboptimal  product  mechanical  properties,  limited  dimensional

                   accuracy,  powder  agglomeration,  nozzle/distribution  size  constraints,  material
                   limitations, texture/color variations, material longevity, fit/design customization, layer

                   height  issues,  and  construction  failures.  Product  management  areas  like  employee

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                   training, pricing, cybersecurity, and intellectual property also require attention  .
                        Cost-effectiveness and personalization drive 3D printing's adoption in traditional

                   manufacturing, healthcare, and biological research. Particularly SLA—characterized

                   by  layer-by-layer  UV  patterning  in  photopolymer  resins—has  gained  considerable

                   traction for its cost-effectiveness, high resolution, and ease of use  57,58 . Shafique et al.

                   59  demonstrated that low-cost liquid crystal display (LCD) 3D printing achieves 50 μm

                   resolution at faster build rates than conventional methods, enabling scalable production

                   of organ-on-a-chip  devices. In summary, the integration of 3D printing with  tumor

                   microfluidics  substantially  reduces  manufacturing  costs  and  compresses  design-to-

                   validation  cycles  from  months  to  weeks  while  reducing  material  waste  by  40-60%
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                   compared  to  traditional  fabrication  .  Despite  these  advances,  limitations  remain:
                   current  3D  printing  struggles  with  microstructures  <100  µm,  and  restricted

                   manufacturing  precision   60,61   and  insufficient  transparency   62   impede  sample

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                   visualization   (Figure 2).


                   3.  Advanced  Tumor  Modeling:  Integrating  3D  Bioprinting  and  Microfluidic

                   Technologies


                        Conventional  static  culture  systems  often  inadequately  capture  the  intricate

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                   complexity  and  dynamic  nature  of  TME  .  Although  microfluidic  technology  has
                   emerged as a promising solution through the development of tumor-on-chip platforms

                   that overcome these limitations, challenges remain  regarding cost-effectiveness  and

                   scalable production. The integration of 3D printing with microfluidics has consequently

                   become  crucial  for  engineering  biomimetic  tumor  models   64,65 .  This  synergistic
                   approach offers distinct advantages: microfluidic systems enable continuous perfusion


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