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CMA can still undergo UV crosslinking, and the photoinitiator Irgacure 2959 remains
intact and non-toxic, with good biocompatibility. The resulting 3D printed dressings
exhibited both antibacterial and pro-angiogenic properties, significantly enhancing the
wound healing with complete healing within 17 days, accompanied by hair follicle
regeneration and angiogenesis. This work not only provided a new strategy for creating
highly self-supporting biopolymers inks, but also paved the way for advanced
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personalized wound dressings. Lie Zhu et al. fabricated a multifunctional hydrogel
dressing via DLP technology based on the ECM properties of Acomys (African agouti)
during wound healing. They modified the methyl acryloyl groups of GelMA and
hyaluronic acid (HAMA) with methyl acryloyl, making the molecular chains contain
photosensitive groups, which can undergo free radical polymerization reactions under
the irradiation of photoinitiators and ultraviolet light, forming a covalent cross-linked
network structure. The precise control of the structure, mechanical properties and
biological functions of hydrogels was achieved through the photosensitivity of
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GelMA/HAMA and DLP light-curing printing. Lei Chen et al. fabricated an ECM-
based 3D-printed dermal hydrogel scaffold loaded with Cu-EGCG. Researchers reacted
cell-free ECM (dECM) derived from pigskin with methacrylate anhydride (GMA),
introducing photo-crosslinkable methacrylate groups to form ECMMA (EM). Then it
was mixed with the photoinitiator LAP to prepare bio-ink. Under ultraviolet light (350
nm) irradiation, the double bonds in EM undergo photo-initiated free radical
polymerization reactions, forming covalently cross-linked hydrogels. It was worth
noting that the EM hydrogel used in this study itself also has temperature-sensitive
properties, it was in a sol state at low temperatures and transforms into a gel state near
body temperature. This combination of physical crosslinking and chemical crosslinking
makes the material not only easy to print and form but also possess excellent
mechanical properties and biological activity. This hydrogel scaffold inhibited
excessive inflammation by promoting the macrophages polarization from M1 to M2,
while supporting endothelial cells in forming stable tubular structures essential for
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neovascularization. Chunmao Han et al. used the same method and simultaneously
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