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For instance, the click chemic-based all-peptide hydrogel platform proposed by Jianan
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                   Rend  et  al.   as  mentioned  in  the  click  chemical  crosslinking  section,  which  was

                   constructed through a one-step photo-curing reaction, has high-precision 3D printing
                   capabilities,  and  is  loaded  with  human  umbilical  vein  endothelial  cells

                   (HUVECsvegf165+) that overexpress VEGF 165. Thus, the self-continuous release of

                   growth factors can be achieved. This hydrogel not only promotes cell adhesion and

                   migration through the RGDS sequence, but also significantly enhances angiogenesis

                   through the continuous secretion of VEGF 165. Meanwhile, it alleviates endothelial

                   cell  damage  induced  by  high  glucose  by  inhibiting  BaX-mediated  mitochondrial

                   membrane perforation, thereby reducing oxidative stress and inflammation levels. Not

                   only that, this material demonstrates excellent biocompatibility and degradability both

                   in  vivo  and  in  vitro,  and  can  achieve  personalized  shape  adaptation  through  DLP

                   printing technology, meeting the needs of different wound morphologies.

                   Summary and Prospect

                        The repair of diabetic chronic wound was a major challenge in clinical medicine,

                   and  its  complex  pathological  microenvironment  put  forward  multi-dimensional
                   functional  requirements  for  treatment  strategies.  With  its  precise  structure  control

                   achieved through CAD and additive manufacturing technology, combined with good

                   biocompatibility  and  dynamic  microenvironment  regulation  ability,  3D  printed

                   hydrogels  have shown significant  advantages in  diabetic wound repair. The current

                   study, however, still faced a single function module, dynamic response mechanism was

                   imperfect  and  some  challenges  of  the  clinical  translation.  The  long-term

                   biocompatibility and potential immunogenicity of synthetic polymers and crosslinking

                   agents have not been deeply studied. Sterilization methods such as gamma radiation or

                   ethylene oxide may change the structure and biological activity of hydrogels. The high

                   cost of bioinks and professional 3D printers may hinder their wide adoption. Future

                   research  should  focus  on  developing  multifunctional  and  synergistic  intelligent  3D

                   printed hydrogel systems to deeply integrate treatment strategies from the three stages

                   of infection control, inflammation regulation, and tissue remodeling. In addition, 3D


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