Page 13 - manuscript_ijb05590
P. 13

high-throughput  drug  screening,  thereby  facilitating  personalized  medicine  and

                   improving the prediction of optimal therapeutic regimens.

                        Beyond conventional applications, this combined approach has unlocked unique

                   capabilities in specialized tumor research. For instance, in microgravity biology, 3D-

                   printed microfluidic systems overcome critical limitations of traditional culture flasks

                   and plates—such as medium leakage and bubble formation—while offering superior

                                                                                                     74
                   biocompatibility and experimental control. Leveraging this advantage, Silvani et al.
                   employed  such  a  platform  to  subject  glioblastoma  (GBM)  and  endothelial  cells  to

                   simulated  microgravity  for  24  hours,  enabling  mechanistic  investigation  of  cellular

                   adaptation  and  mechanical  signaling  pathways  in  response  to  altered  gravitational

                   forces.



                   4. Applications in Drug Screening and Therapeutic Development


                        Preclinical development of cancer therapies typically involves testing potential

                                                        1
                   anticancer drugs in tumor cell cultures  . The lack of suitable models hinders therapeutic
                   strategy development. Researchers have developed diverse in vitro cancer models—

                   Transwell-based  2D  platforms,  3D  organoids,  hybrid  platforms,  and  microfluidic

                   systems—to  simulate  tumor  tissue  and  serve  as  drug  research  platforms   75–78 . As

                   understanding of cancer biology deepens and microtechnologies advance, microfluidic

                   technology is increasingly utilized in the detection, diagnosis, and treatment of cancer.

                   Its inherent advantages—minimal sample volume, high sensitivity, rapid processing—

                   overcome limitations of traditional tumor cultures lacking dynamic conditions, tissue-

                   tissue  interfaces,  organ-level  structures,  and  fluid  flow   79,80 .  These  advancements

                   overcome critical limitations of conventional models while positioning microfluidics at
                   the forefront of cancer diagnostics and therapeutic development.


                        The comparative advantages and disadvantages of leading technologies—PDMS

                   microfluidics versus 3D bioprinting—for tumor therapy applications are systematically

                   evaluated  in  Table  4,  highlighting  their  distinct  application  strategies,  drug  testing


                                                            12
   8   9   10   11   12   13   14   15   16   17   18