Chen Yuwen, Li Rong, Li Bo, Li Ka, Hao Ying
West China Hospital, Sichuan University/West China School of Nursing, Sichuan University, Chengdu, 610041, Sichuan Province, China; Laboratory of Heart Valve Disease, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan Province, China.
Antibiotics Research and Re-evaluation Key Laboratory of Sichuan Province, Sichuan Industrial Institute of Antibiotics, School of pharmacy, Chengdu University, Chengdu, 610106, Sichuan Province, China.
Int J Biol Macromol. 2024 Mar;261(Pt 1):129751. doi: 10.1016/j.ijbiomac.2024.129751. Epub 2024 Jan 26.
Porous hydrogels as scaffolds have great potential in tissue engineering. However, there are still challenges in preparing porous hydrogels with tunable pore size and controlled porosity. Here, we successfully established a photoinduced gas-foaming method of porous hydrogels with controlled macro-micro-nano multiscale. A diazirine (DZ)-modified gelatin (GelDZ) biomaterial was prepared by introducing photocrosslinked DZ group into gelatin. Upon exposure to 365 nm UV light, DZ could be converted to the active group carbene, which could randomly insert into OH, NH, or CH bonds to form covalent crosslinks. GelDZ generated N by photodegradation and formed gas-induced porous hydrogels by intermolecular crosslinking without initiator. The loose porous structure of the hydrogel can promote the infiltration of host cells and blood vessels, which was conducive to tissue repair. The interfacial crosslinking of photoactivated GelDZ with tissue proteins imparted adhesion properties to the hydrogel. GelDZ also possessed photoreduction ability, which can reduce silver ions from metal precursors to silver nanoparticles (Ag NPs) in situ, and showed great antibacterial activity due to the sustained release of Ag NPs. GelDZ-Ag NPs prepared by in situ photoreaction can effectively inhibit wound infection and promote skin wound healing, providing a new strategy for designing porous hydrogel in tissue engineering.
多孔水凝胶作为支架材料在组织工程领域具有巨大潜力。然而,制备具有可调孔径和可控孔隙率的多孔水凝胶仍面临挑战。在此,我们成功建立了一种具有可控宏观 - 微观 - 纳米多尺度的多孔水凝胶光诱导气体发泡方法。通过将光交联的重氮丙啶(DZ)基团引入明胶,制备了一种重氮丙啶修饰的明胶(GelDZ)生物材料。在365 nm紫外光照射下,DZ可转化为活性基团卡宾,其能随机插入OH、NH或CH键形成共价交联。GelDZ通过光降解产生N₂,并在无引发剂的情况下通过分子间交联形成气体诱导的多孔水凝胶。水凝胶松散的多孔结构可促进宿主细胞和血管的浸润,有利于组织修复。光活化的GelDZ与组织蛋白的界面交联赋予了水凝胶粘附性能。GelDZ还具有光还原能力,可将金属前驱体中的银离子原位还原为银纳米颗粒(Ag NPs),并且由于Ag NPs的持续释放而表现出强大的抗菌活性。通过原位光反应制备的GelDZ - Ag NPs能有效抑制伤口感染并促进皮肤伤口愈合,为组织工程中多孔水凝胶的设计提供了一种新策略。