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microfluidic-3D printing technologies through mechanistic analysis of core principles

                   and developmental trajectories. Distinctively, this review adopts a deliberately clinical

                   lens—evaluating  how  these  platforms  directly  address  oncology  practice  gaps,
                   including  generating  patient-specific  tumor  models  for  therapy  personalization  and

                   liquid biopsy diagnostics at clinically actionable thresholds. Moreover, we uniquely

                   concentrate  on  3D-printed  microfluidic  systems  engineered  explicitly  for  tumor

                   pathophysiology,  dissecting  cancer-tailored  architectures  like  perfusable  vascular

                   networks  and  metastasis  models  with  tumor-derived  bioinks.  We  specifically  map

                   applications across physiologically relevant tumor modeling, therapeutic screening, and

                   high-sensitivity biomarker diagnostics using 3D-printed microfluidic platforms. Finally,

                   we provide a forward-looking perspective addressing current technical constraints and

                   emerging frontiers including transformative 4D/5D bioprinting paradigms.



                   2. Fundamental Principles of Microfluidic and 3D Bioprinting Technologies


                   2.1 Characteristics of Microfluidic Technology
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                        Microfluidics  manipulates  minute  fluid  volumes  (10   to  10   liters)  through
                   microscale  channels  (tens  to  hundreds  of  micrometers)   39 .  Commercial  devices

                   primarily  utilize  glass,  PDMS,  and  thermoplastics  for  their  mechanical  stability,

                   chemical inertness, and biocompatibility  40,41 . Three principal fabrication techniques

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                   are summarized below and in Table 2  : (1) Micromolding: the most accessible method
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                   requiring minimal equipment, ideal for phase-transition biomaterials like hydrogels  .
                   (2) Photolithography:     employing       photochemical      processes      (photo-

                   degradation/polymerization) to achieve geometrically complex quasi-planar networks

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                   with  superior  design  flexibility  .  (3) 3D  printing:  offering  unparalleled  material
                   diversity  and  spatial  freedom  through  unrestricted  nozzle  movement,  enabling

                   biomimetic  vascular  networks  and  organ-on-a-chip  architectures  unattainable  via
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                   conventional techniques  .

                        As  previously  established,  microfluidics  involves  studying  and  manipulating
                   fluids  at  submillimeter  scales.  Unlike  macroscale  systems  where  gravity  dominates


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